Scholarly article on topic 'Medicinal plants – prophylactic and therapeutic options for gastrointestinal and respiratory diseases in calves and piglets? A systematic review'

Medicinal plants – prophylactic and therapeutic options for gastrointestinal and respiratory diseases in calves and piglets? A systematic review Academic research paper on "Veterinary science"

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Academic research paper on topic "Medicinal plants – prophylactic and therapeutic options for gastrointestinal and respiratory diseases in calves and piglets? A systematic review"

Ayrle et al. BMC Veterinary Research (2016) 12:89 DOI 10.1186/s12917-016-0714-8

BMC Veterinary Research

Medicinal plants - prophylactic and therapeutic options for gastrointestinal and respiratory diseases in calves and piglets? A systematic review


Hannah Ayrle1,2*, Meike Mevissen2, Martin Kaske3, Heiko Nathues4, Niels Gruetzner4, Matthias Melzig5 and Michael Walkenhorst1


Background: Gastrointestinal and respiratory diseases in calves and piglets lead to significant economic losses in livestock husbandry. A high morbidity has been reported for diarrhea (calves < 35 %; piglets < 50 %) and for respiratory diseases (calves < 80 %; piglets < 40 %). Despite a highly diverse etiology and pathophysiology of these diseases, treatment with antimicrobials is often the first-line therapy. Multi-antimicrobial resistance in pathogens results in international accordance to strengthen the research in novel treatment options. Medicinal plants bear a potential as alternative or additional treatment. Based on the versatile effects of their plant specific multi-component-compositions, medicinal plants can potentially act as 'multi-target drugs'. Regarding the plurality of medicinal plants, the aim of this systematic review was to identify potential medicinal plant species for prevention and treatment of gastrointestinal and respiratory diseases and for modulation of the immune system and inflammation in calves and piglets.

Results: Based on nine initial sources including standard textbooks and European ethnoveterinary studies, a total of 223 medicinal plant species related to the treatment of gastrointestinal and respiratory diseases was identified. A defined search strategy was established using the PRISMA statement to evaluate 30 medicinal plant species starting from 20'000 peer-reviewed articles published in the last 20 years (1994-2014). This strategy led to 418 references (257 in vitro, 84 in vivo and 77 clinical trials, thereof 48 clinical trials in veterinary medicine) to evaluate effects of medicinal plants and their efficacy in detail. The findings indicate that the most promising candidates for gastrointestinal diseases are Allium sativum L., Mentha x piperita L. and Salvia officinalis L.; for diseases of the respiratory tract Echinacea purpurea (L.) MOENCH, Thymus vulgaris L. and Althea officinalis L. were found most promising, and Echinacea purpurea (L.) MOENCH, Camellia sinensis (L.) KUNTZE, Glycyrrhiza glabra L. and Origanum vulgare L. were identified as best candidates for modulation of the immune system and inflammation.

Conclusions: Several medicinal plants bear a potential for novel treatment strategies for young livestock. There is a need for further research focused on gastrointestinal and respiratory diseases in calves and piglets, and the findings of this review provide a basis on plant selection for future studies.

Keywords: Medicinal plants, Calves, Piglets, Gastrointestinal diseases, Respiratory diseases

* Correspondence:

department of Livestock Sciences, Research Institute of Organic Agriculture

(FiBL), Ackerstrasse 113, postbox 219, Frick 5070, Switzerland

2Division Veterinary Pharmacology & Toxicology, Department Clinical

Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern,

Laenggassstrasse 124, Bern 3012, Switzerland

Fulllist of author information is available at the end of the article

(3 BioMed Central

© 2016 The Author(s). Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.


A high standard of animal health and welfare is striven in modern livestock husbandries. Health in early life represents a precondition for a superior constitution and results in a high productivity later in life. The mammalian immune system is still immature in the first weeks of life and, in combination with an inappropriate colostral supply, contact to pathogens often results in high morbidity and mortality in young farm animals. Inadequate management including long distance transports, fasting, commingling of individuals from different sources, abrupt changes in diet or incorrect diet, overcrowding of pens, improper climate and suboptimal hygiene are crucially involved in infectious diseases [1-6]. In calves and piglets, the first contact sites for pathogens are the epithelia of the gastrointestinal and respiratory tract. Table 1 shows four of the most important infectious disease complexes in calves and piglets leading to a decreased animal performance and welfare and therefore high economic losses.

In calves and piglets, a variety of pathogens can cause gastrointestinal diseases. Neonatal calf diarrhea represents the most frequent cause of calf losses [2, 7-9] with a mortality of around 55 % in the U.S.A. and in Korea [10] and a morbidity ranging from 12 % in the U.S.A., 23 % in Canada up to 53 % in The Netherlands [1, 7, 11]. Insufficient colostral supply and failure of feeding or improper diet are triggers for diarrhea in calves [12-14]. In suckling and postweaning piglets an infection with enterotoxigenic Escherichia coli strains has been reported to lead to high economic losses as a result of a constant high morbidity and mortality [15]. Verocytotoxin-producing Escherichia coli infections can lead to more seldom but severe edema disease in weaned pigs [16-18]. The prevalence of post-weaning diarrhea has been reported to be 35 % in France

[19], the morbidity was stated to exceed 50 % in Finland

[20] and the mortality can be as high as 25 % without therapy [17]. The incidence of neonatal diarrhea in piglets depends on concentration of antibodies in sow's colostrum. While piglets are protected by the antibodies in sow's milk, the predisposition for postweaning diarrhea increases with weaning. Additional factors to the immuno-logical gap, including abrupt changes in diet, an increase in stomach pH, and changes in the enzymatic and cellular configuration of the intestine lead to dysbiosis [6,17, 21].

Respiratory diseases in calves and piglets have been assessed as one of the most serious diseases with regard to financial losses because of decreased weight gain, costs for veterinary interventions and higher condemnation at slaughter [22]. In fattening calves bovine respiratory disease is a considerable challenge with a morbidity ranging from 49 % in Switzerland to 80 % in the U.S.A. [23, 24]. There is a disposition of the bovine respiratory tract to respiratory diseases. Improper microclimate, noxious gases and distress through transportation are

predisposing factors additionally [25, 26]. Respiratory diseases are also of high importance in pigs. The morbidity rates differ between countries; a morbidity of 10 and 40 % have been reported for Denmark and the U.S.A. respectively [27, 28]. Mortality rates up to 15 % [29] have been reported and attributed with the porcine respiratory disease complex. The interaction of various pathogens as well as housing conditions, management and genetic factors, were reported to cause bronchopneumonia [27, 29].

Antibiotic therapy is often the first-line therapy of diseases of the gastrointestinal and respiratory tract in calves and piglets. A previously published study showed that fattening calves receive antibiotics for 30 days on average. Moreover, calves are frequently treated with reserve antibiotics such as fluorchinolones and cephalosporines of the 3. and 4. generation [30]. In pig production, routine pro-and metaphylactic administration of antimicrobial agents is a widely-used practice in herds suffering from neonatal diarrhea, postweaning diarrhea or edema disease irrespective of increasing ineffectiveness in consequence of bacterial resistance [6]. More than 60 % of the antibiotics used in porcine husbandry are administered by oral group treatment [31]. Data on antimicrobial resistance monitoring indicated that 59 % of porcine Escherichia coli strains from fecal samples showed resistance to at least one antibiotic and 12 % to more than four of the antibiotics that were investigated [32]. With regard to increasing antimicrobial resistance worldwide, the prevailing issue of reducing antibiotics in food producing animals is seeking for novel options to prevent and cure most common and costly diseases. Improved biosecurity and housing conditions, new feeding regimes, vaccinations and the use of disease-resistant breeds are important provisions.

The diverse etiopathology and symptomatology of diseases in young stock is a challenge and demands a multi-targeted therapy. In contrast to chemically synthesized mono-target drugs, multi-target drug characteristics are typical for medicinal plants based on their multi-component composition, which can lead to pleiotropic, synergistic or additive effects in the organism [33, 34]. The broad spectrum of natural products from plants represents a prevailing and widely unemployed potential especially for medication of herbivore and omnivore livestock [35]. Medicinal plants have been used worldwide for prevention and treatment of diseases in human and animals for centuries. Ethnoveterinary research and the underlying documents describing traditional and recent use of medicinal plants [36-38] could be exploited as alternative or as supportive tools to reduce the use of antibiotics in livestock. Additionally, some medicinal plants are known to modulate the immune system and inflammation and could be used as a prophylaxis for infectious diseases.

Human clinical studies, experimental in vivo, ex vivo and in vitro studies on medicinal plants are available,

Table 1 Challenging infectious diseases in calves and piglets: pathogens, pathophysiology, resulting demands for prophylaxis and therapy

Disease complex Pathogens




Pathophysiology/pathogenesis Demands for prophylaxis and therapy


NeonatalCalf Diarrhea1

Escherichia coli Bovine Coronavirus Rotavirus

Cryptosporidium parvum

Bovine Respiratory Mannheimia haemolytica


PasteureHa multocida

Infectious bovine rhinotracheitis virus

Parainfluenza type 3 virus

Histophilus somni Bovine respiratory syncytialvirus

Mycoplasma bovis Bovine viraldiarrhea virus


NeonatalDiarrhea Escherichia coli Rotavirus

Postweaning Diarrhea3

Clostridium perfringens

Lawsonia intracellularis

Brachyspira spp. Salmonella spp. (Yersinia spp.)

Cryptosporidium spp.

Coronavirus Isospora suis

Porcine Circovirus type 2 Trichuris suis

Oesophagostomum dentatum

Porcine respiratory Pasteurella disease complex4 multocida

Mycoplasma hyopneumoniae

Porcine reproductive and respiratory syndrome virus

Swine influenza virus

Porcine circovirus type 2

secretory/malabsorptive/ maldigestive diarrhea


hypovolemic shock

decrease in temperature

d-lactat acidosis





reluctance to drink

catharral/interstitial/fibrinous bronchopneumonia

increased respiratory rate



nasal discharge




secretory/malabsorbtive/ maldigestive diarrhea








reduced growth rates

suppurative/fibrinous/interstitial bronchopneumonia


nasal discharge











immunostimulant antimicrobial


















immunostimulant antimicrobial



Table 1 Challenging infectious diseases in calves and piglets: pathogens, pathophysiology, resulting demands for prophylaxis and therapy (Continued)

Actinobacillus pleuropneumoniae

(Streptococcus suis)

(Haemophilus parasuis)

increased respiratory rate fever

reduced growth rates runting






1[10-13] 2[3-5, 23, 25] 3[6, 15-18] 4[22, 27, 29]

but there is a lack of comprehensive research for veterinary medicine, especially in young farm animals. Therefore, the purpose of the underlying work is to gain information about potential efficacy of medicinal plants in human and veterinary medicine including in vitro, in vivo and clinical studies.

The aim of this systematic literature review is to identify medicinal plant species or their extracts that are promising candidates for use in diseases of the gastrointestinal and respiratory tract and for stimulation of the immune system and prevention or therapy of inflammation in calves and piglets. Candidate plants should bear a reliable potential for effective treatment and prevention of these diseases. The information obtained can build a basis for state-of-the-art experimental trials and clinical studies with medicinal plants of interest for the treatment of gastrointestinal and respiratory diseases and for the modulation of the immune system and inflammatory processes in calves and piglets.


The design of the systematic review was 'a priori' individually developed according to the recommendations of the PRISMA statement [39, 40] and AMSTAR measurement tool [41]. The research question was designed following the PICOS scheme [39]: the population are calves and piglets in livestock farming, the intervention is a treatment with medicinal plants, the comparator is no treatment, a placebo or standard treatment, the outcome is the effect of the plant, the study design included in vitro, ex vivo, in vivo and clinical trials. The detailed protocol of the systematic review is provided in the Additional file 1.

Selection of plant species

To choose eligible plant species, different initial sources were screened in respect to plant species frequently recommended for the treatment of gastrointestinal diseases, particularly unspecified or infectious diarrhea and gastrointestinal spasms (QA) and respiratory diseases (QR) as well as those plants that have been reported to

modulate the immune system and affect inflammation in infectious diseases (QL). Regarding the intended use of medicinal plants in Western livestock husbandry, potential plant species should be economically available or easy to cultivate in Europe. The initial sources included standard literature, based on traditional empiric knowledge and historical literature of veterinary [42-45], and human phytotherapy [46], peer-reviewed publications of European [47] and in particular Swiss ethnoveterinary medicine [36, 38] and a report of the European Food Safety Authority (EFSA) [48] focusing on the use of plants as feed additives in animal production. All plant species of these sources connected to one or more of the indications were recorded including the used part(s) of plant, the route of administration, the dosage, the contraindications and adverse effects (Additional file 1). Based on the plant species that had been mentioned in at least three different initial sources for the same indication, a preliminary selection was established. This selection was sent to three specialists in European veterinary phytotherapy to capitalize their experience. The experts were asked to comment on the preliminary selection of plant species regarding the most common ones being particularly suitable for treatment and prevention of gastrointestinal and respiratory diseases.

Selection of scientific references Bibliographic search

The chosen plant species were included in the following step. A bibliographic web-based search was conducted based on the recommendations of the PRISMA statement [39, 40] and AMSTAR measurement tool [41]. An introduction in scientific bibliographic literature searches and continuous support was provided by a professional librarian. The bibliographic sources used included PubMed [49] and Web of Science [50]. Both were consulted in the time between 2015-02-16 and 2015-02-19 by one person. The search terms consisted of the Latin name, the common trivial name in English and the pharmaceutical denomination in Latin (e.g. "Foeniculum vulgare" OR "fennel" OR "foeniculi fructus"). In the PubMed keyword search, the results were refined with the subjects 'complementary

medicine! 'dietary supplements! 'systematic review, 'toxicology' and 'veterinary science'. In the PubMed search with MeshTerms, only the Latin name of the plant was used and the subheadings 'adverse effects! 'analysis! 'drug effects! 'microbiology! 'pharmacology! 'therapeutic use! 'therapy' and 'toxicity'. In the Web of Science database! the search was conducted in the research domain 'science technology' and the results were refined with the research areas 'pharmacology! 'infectious diseases! 'toxicology! 'veterinary sciences! 'microbiology! 'gastroenterology! 'integrative complementary medicine! 'general internal medicine! 'respiratory system' and 'virology'. Overall! only peer-reviewed articles written in English or German language and published between 1994 and 2014 were considered for further evaluation to ensure contemporary scientific quality and timeliness of the review. The references found were saved in an EndNote X7 data base [51] and the information on each plant was stored in a separate folder in this database. Duplicates were removed for each plant species.

In some studies more than one plant species was investigated (e. g. a screening of plant species against E. coli [52]). In other studies! more than one indication was considered and investigated (e. g. spasmolytic effect of Plantago lanceolata L. on intestine and trachea [53]). Therefore! the following definition of "reference" was introduced:

reference = indication per plant species per peer-

reviewed publication

Term-list search

A term-list search was conducted within each plant species using the search function in EndNote X7 [51]. Only references containing one of the following predefined keywords occurring in the title or the abstract were included: 'pig*! 'calv*! 'muco*! 'spasmo*! 'anti*' (e.g. antimicrobial! antibacterial! antiviral! antifungal! antioxidant! antinocicep-tive...)! 'wean*! 'intest*! 'gastro*! 'pulmo*! 'broncho*! 'pharma*! 'eff*'(e.g. efficiency! effectivity! effect)! 'bioactiv*! 'constitu*'. References containing the terms 'tumor' or 'cancer' were excluded. The check of the excluded references lowered the risk to exclude relevant references.

Refining with inclusion and exclusion criteria

The remaining references were refined using a selective screening of the title. References remained if the content suffices the objective of the review. Therefore! inclusion criteria were pre-defined by two scientists and lead to an inclusion of all references containing investigations of plants in in vitro! ex vivo! in vivo or clinical studies. Besides these categories! the evaluation included the following inclusion criteria: antibacterial effect! enhancement of antibiotics! antiviral effect! antiprotozoal effect! anti-inflammatory effect! analgesic effect! spasmolytic effect! antiadhesive effect!

astringent effect, secretolytic or mucolytic effect, antitussive effect, and other effects on the gastrointestinal tract, respiratory tract or immune system, treatment of diarrhea, bacterial or viral infections of the gastrointestinal tract or respiratory tract, bronchopneumonia, common cold, cough as well as ingredients, constituents, components of plants and the detection or extraction of them, toxic activity or adverse effects due to a treatment with plants.

Exclusion criteria were chosen in order to exclude references dealing with other plant species or subspecies than those we focused on, a mixture of different plant species investigated as one single preparation, pathogens affecting only humans, diseases regulated by laws, cultivation or breeding of plants, plant genetics, seeds and fertilizers, regional reservoirs, habitats or demands for growing of plants, plant pathology, plant protection systems or pesticides, ecology, geology, ethology, sociology, the usage of the plant as food, food technology or food-packaging, the use of the plant as a repellent or insecticide, other medical branches, other diseases or apparatuses than mentioned in the inclusion criteria (e.g. dermatology, cardiology, oncology, nephrology, diabetes) as well as other animal classes than mammalians and birds.


Thereby the references were classified into different categories of trial types. Studies investigating diseases occurring naturally in the investigated animal species or in humans were categorized as 'clinical references'. Trials investigating diseases or the effect of plants in animal models were categorized as 'in vivo references'. Studies using pathogens, cell layers or ex vivo models were categorized as 'in vitro references'. Studies investigating the pharmacologic characteristics, constituents or the detection of them were categorized as pharmacognostic references' and the evaluation of plants summarizing other studies as review references'.

In the last step, abstracts of the remaining clinical, in vivo and in vitro references were studied by one person. During this process, further references were excluded because they did not match the predefined selection criteria.

Assessment of clinical, in vivo and in vitro references

The remaining references were assessed by the following characteristics: used plant species, type of reference (clinical, in vivo or in vitro), indication of the reference inspired by the ATCvet classification (QA, QR, QL) [54], animal species used, study design, pharmaceutical form of the plant, type of application, concentration tested, dosage or minimal inhibition concentration and, if available, the tested pathogen.

To assess the potential of the selected plant species, a reconciliation of the demands for prophylaxis and therapy of gastrointestinal and respiratory diseases with the

hypothesized and tested effects of the plants was performed. The demands for prophylaxis and therapy were derived from the pathophysiology of the focused diseases (Table 1). According to these data, plant-derived treatment options should act bacteriostatic or bactericidal, syn-ergistically with antibiotics, antiviral, antiprotozoal, anti-inflammatory, analgesic, immunomodulatory, antidiarrheal, antiadhesive, spasmolytic, astringent, expectorant or anti-tussive (depending on the indication). The conclusion of a trial on the investigated hypothesized effect of the plant species (Additional file 3) was transferred in the following assessment. To compare the potential of the plant species, a scoring system was established. For each significantly proven effect, the plant species one point was given, while for each uncertain effect, zero points were assigned, and for each disproved effect a point was subtracted (for more details see Additional file 1). Clinical studies were given more weight compared to in vivo studies followed by in vitro studies. Clinical studies were given a weight of three, in vivo studies two, and in vitro studies one. The weighted average of the sum of points of the clinical, in vivo, and in vitro scores served as the final score. The scores were used to identify the plant species that are the most efficacious options for related disease complexes.

Score = 3 x (number of proven effects in clinical studies -

number disproof of effects in clinical studies) + 2 x (number of proven effects in in vivo studies -number ofdisproof of effects in in vivo studies) + 1 x (number of proven effects in in vitro studies-number of disproof of effects of in vitro studies)


The procedure of this systematic literature review is visualized in Fig. 1. The screening of ethnoveterinary research and standard phytotherapeutic textbooks (initial sources) led to a total of 223 plant species recommended for the treatment and prophylaxis of gastrointestinal (diarrhea and intestinal spasms) and respiratory diseases in human and animals. A number of 134 different plant species were recommended for QA, 121 for QR and 44 for QL (Additional file 2). A preliminary selection of 29 plant species, recommended in at least three different sources for the same indication, was established. Therefrom, 17 plant species were recommended for QA, 15 for QR and 8 for QL. The specialists review led to an addition of one plant species (Origanum vulgare L.) to the preliminary list including finally 30 plant species. All of these plant species meet the claims for cost-efficiency or cultivability in Europe.

In the subsequent bibliographic search 20,364 references (after removal of duplicates) were found for the 30 plants species (Table 2). During the term-list search, the amount of relevant references led to a reduction of references with 6,800 remaining references. An ensuing

random check of the excluded references confirmed the selected terms. The subsequent screening of titles led to a number of 2,797 eligible references, which were classified into the categories 'clinical references' (243), 'in vivo references' (428), 'in vitro references' (1258), 'pharmacog-nostic references' (704) and 'review references' (164). The terminal screening of the abstracts of all clinical, in vivo and in vitro references revealed a final number of 418 references (77 clinical, 84 in vivo, 258 in vitro) (Additional file 3). Due to the fact that more than one reference could be defined from some studies, the systematic literature research led to a number of 378 studies representing the effects and efficacy of 29 plant species in 418 references. For one plant species, Quercus robur L., no references were found according to the criteria.

A total of 19,077 references were excluded because they did not match the predefined selection criteria. Predominant reasons for exclusion included that the content of title and abstract did not correspond to the focus of the review (e. g. pathogens were not the pathogens of the focused diseases). Other reasons were missing abstracts (in 212 references) or publications that were not peer-reviewed.

From the 418 remaining references, 48 references based on clinical studies were veterinary origin with 19 swine studies, 5 cattle studies, 17 horse studies, and 4 studies in rabbits. A number of 370 references include studies in humans (29 clinical, 84 in vivo and 257 in vitro studies). A number of 77 in vivo references used laboratory rodents (rats, mice, guinea-pigs) and three studies used cats as an animal model. For gastrointestinal indications (QA), 198 references were found, 57 references were related to respiratory diseases (QR), and 163 references aimed at the modulation of the immune system and inflammation processes (QL). Most references coping with the inclusion criteria were found for Echinacea purpurea L. MOENCH. (48 references), Origanum vulgare L. (36 references) Thymus vulgaris L. (36 references), Camellia sinensis (L.) KUNTZE (32 references), and Allium sativum L. (31 references). The required effects of a treatment and the proven effects of the plant species as mono-substances for each indication are shown in Tables 3, 4 and 5. In Table 6, the most promising plant species of the peer-reviewed references according to the scoring system for each indication (QA, QR and QL), as well as the most frequently recommended plant species of the traditional references (Additional file 2) are shown. According to the scoring system, the two most promising plant species are Echinacea purpurea (L.) MOENCH (for QR and QL) and Allium sativum L. (for QA).


There is a large amount of evidence-based knowledge about medicinal plants, represented by 20,364 studies focusing on 30 medicinal plant species from the last

Selection of plant species (223) based on ethnoveterinary research and standard phytotherapeutic textbooks

Fig. 1 Process of the systematic literature review

20 years considering peer-reviewed publications in English or German language. The emergence of multi-drug resistance in human and animal pathogens results in international accordance to strengthen the research in novel treatment options. Medicinal plants and their extracts might be an option to prevent and cure livestock diseases.

Evaluation of the search strategy

This systematic review was designed and performed according to the guidelines of the PRISMA statement and AMSTAR measurement tool [39-41]. Due to the fact that we searched for available data on a largely underrepre-sented topic in the last decades, only a small number of

Table 2 Quantifying and categorizing of scientific publications regarding 30 medicinal plants during bibliographic literature research process

Plant species Common Allreferences After keyword Pharmacognostic Reviews After checking Clinical in vivo in vitro and

name imported from search in titles studies of relevance, studies studies ex vivo

WoS1 and PM2 and abstracts regarded for studies

after removal with endnote the assessment

of duplicates of plant species

Achillea millefolium L. yarrow 345 157 14 2 15 2 3 10

Agrimonia eupatoria L. agrimony 73 37 10 0 2 1 0 1

Allium sativum L. garlic 1149 630 24 14 31 9 5 17

Althaea officinalis L. marshmellow 62 29 6 1 6 0 4 2

Camellia sinensis (L). green tea 2052 804 53 21 32 4 6 22


Carum carvi L. caraway 191 95 28 6 5 0 1 4

Cetraria islandica (L.) Icelandic 118 46 8 0 4 1 1 2

ACH. moss

Echinacea purpurea (L.) purple 869 364 45 18 48 14 8 26

MOENCH coneflower

Foeniculum vulgare (L.) fennel 825 308 46 6 18 1 4 13

Glycyrrhiza glabra L. liquorice 597 252 43 8 26 3 7 16

Linum usitatissimum L. linseed 762 227 12 5 7 3 3 1

Malva sylvestris L. wild mallow 243 50 2 2 4 0 3 1

Matricaria recutita L. camomile 908 305 43 7 22 1 7 14

Mentha x piperita L. peppermint 1331 425 35 23 21 8 0 13

Origanum vulgare L. oregano 904 526 42 0 36 10 4 22

Picea abies (L.) H.KARST. norway 1031 153 0 0 1 0 0 1


Pimpinella anisum L. anis 453 147 12 2 12 2 0 10

Plantago lanceolata L. english 532 136 7 2 6 1 0 5


Potentilla erecta (L.) tormentil 49 15 3 2 3 2 0 1


Primula veris L. cowslip 106 23 2 0 1 0 0 1

Quercus robur L. english oak 1210 165 7 0 0 0 0 0

Rubus fruticosus L. blackberry 583 172 34 0 6 0 1 5

Rumex ssp. L. dock 939 208 15 2 11 0 4 7

Salix ssp. L. willow 915 171 20 13 6 0 1 5

Salvia officinalis L. sage 902 372 67 5 20 7 7 6

Sambucus nigra L. elderberry 891 169 19 4 7 1 2 4

Thymus vulgaris L. thyme 831 372 52 3 36 6 2 28

Tussilago farfara L. coltsfoot 101 36 14 0 4 0 1 3

Urtica dioica L. stinging 760 251 16 10 20 1 6 13


Vaccinium myrtillus L. blueberry 632 155 25 7 8 0 4 4

suma 20364 6800 704 164 418 77 84 257

adue to the definition of reference (trial x plant species x indication) the sum may contain some trials more than one time; 1WoS = Web of Science [50]; 2PM = PubMed [49]

veterinary clinical data is currently available. Therefore, research question. Human clinical studies, experimental the search strategy was adapted to gain as much plant spe- in vivo studies with laboratory animals as well as ex vivo cific information as possible and to cope with the complex and in vitro studies were included as well. To avoid the

Plant species Number of Type of Antibacterial Synergism Antiviral Anti Anti Anti Spasmolytic Immuno Antiin Analgesic Hypothesis

references reference with AB protozoal adhesive diarrheal stimulant flammatory proved

+ ? o + ? o + ? o + ? o + ? o + ? o + ? o + ? o + ? o + ? o + ? o

Achillea millefolium L. 6 2 in vitro in vivo + clinical 21 13 42 14

Allium sativum L. 12 in vitro 125 16

9 in vivo + clinical 27 18 29 210 111 112 213

Althaea officinalis L. 2 0 in vitro in vivo + clinical 214

Camellia sinensis (L.) 8 in vitro 615 116 117 1 18

KUNTZE 3 in vivo + clinical 219 220

Carum carvi L. 4 1 in vitro in vivo + clinical 321 122 123

Echinacea purpurea 0 In vitro

(L.) MOENCH 1 in vivo + clinical 124

Foeniculum vulgare 10 in vitro 625 126 127 1 28 129 130

(L.) MILL. 2 in vivo + clinical 131 132

Glycyrrhiza glabra L. 9 4 in vitro in vivo + clinical 433 238 234 135 1 36 139 137 140

Linum usitatissimum L. 0 3 in vitro in vivo + clinical 141 142 143 144

Matricaria recutita L. 9 3 in vitro in vivo + clinical 545 247 446 148

Plant species

Mentha x piperita L.

Origanum vulgare L.

Picea abies (L.) H.KARST.

Pimpinella anisum L.

Plantago lanceolata L.

Potentilla erecta (L.) RAEUSCH.

Rubus fruticosus L.

Rumex ssp. L.

Salix ssp. L.

Salvia officinalis L.

Sambucus nigra L.

Number of Type of Antibacterial references reference

13 in vitro 8

7 in vivo + 1 clinical

21 in vitro 1

8 in vivo + 1 clinical

1 in vitro 1

0 in vivo +


7 in vitro 3

0 in vivo + clinical

1 in vitro

1 in vivo + clinical

0 in vitro

2 in vivo + clinical

1 in vitro

0 in vivo + clinical

4 in vitro 4

1 in vivo + clinical

1 in vitro

0 in vivo +


6 in vitro 5

Synergism Antiviral Anti Anti

with AB protozoaladhesive


Spasmolytic Immuno stimulant

in vivo + 38 clinical

in vitro 18

in vivo + clinical

? o + ? o +


flammatory ?

Analgesic Hypothesis proved

Thymus vulgaris L.

in vitro

1090 19

Plant species

Tussilago farfara L.

Urtica dioica L.

Vaccinium myrtillus L.

Sum of plant species for each effect

Sum of assessments

in vivo + clinical

Number of Type of AntibacterialSynergism Antiviral Anti references reference

Anti Anti Spasmolytic Immuno Antiin

stimulant flammatory

in vitro 1 '

in vivo + clinical

inn vitro 2

in vivo + clinical

in vitro

in vivo + clinical

in vitro 18

in vivo + 6 clinical

in vitro 93

in vivo + 11 clinical

with AB protozoaladhesive diarrheal

o + ?o+?o+ ?o + ?o + ?o + ?o+?o

0 0 2 0 0 0

0 0 2 0 0 3

7 0 0 3 0 0 2 0 0 0 0 0 0 6

0 1 0 0

0 0 1 1 0 0

0 0 0 0

10 0 0 0 6 0 0 3

0 0 0 2

0 0 20 000 00

0 0 3 0 3

Analgesic Hypothesis proved

+ ? o + ? o

0 0 0 0 0 0 0 0 0 6 0 2

0 0 0000 00 1 1 0 0 0 7 0 2

aAssessment = conclusion of a reference on a hypothesized effect; breference = trial x plant species x indication; cparticularly unspecified or infectious diarrhea and gastrointestinal spasms + = reference proves evidently the hypothesized effect; ? = reference shows uncertain hypothesized effect; o = reference does not prove evidently the hypothesized effect

1[147, 148] 2[149—152] 3[153] 4[154] 5[69-76, 155-158] 6[69] 7[63, 66] 8[159] 9[62, 160] 10[63, 64] "[66] 12[77] 13[161, 162] 14[163, 164] 15[165-170] 16[170] 17[171] 18[172] 19[124, 125] 20[124, 173] 21[174-176] 22[177] 23[178] 24[179] 25[175, 176, 180-183] 26[184] 27[185] 28[181] 29[186] 30[187] 31[188] 32[189] 33[143, 190-192] 34[142, 193] 35[145] 36[194] 37[195] 38[196, 197] 39[141] 40[198] 41[199] 42[199] 43[200] 44[201] 45[202] [175, 185,

[244, 246] [247] 66[248] 67[249] 68[175, 250, 251] 69[252, 253] 70[251, 254] 71[255] 72[53] 73[256] 74[257] 75[258] 76[259] 77[180, 260-262] 78[263] 79[264] 80[175, 211, 233, 237, 265] 81[252] 82[266-268] 83[267, 268] i4[269] 85[270] 86[269] 87[268] 88[271] 89[272] 90[52, 118-120, 175, 176, 226, 250, 252,273] 91[274] 92[113, 275,276] 93[277, 278] 94[279] 95[280] 96[191, 281] 97[185, 282] 98[145] 99[283, 284] 100[285] 101[259] 102[286]

03[287] 104[286]

203, 204] 46[205-208] 47[209, 210] 48[189] 49[176, 211-216] 50[217] 51[214] 52[88, 205, 218] 53[219] 54[220] 55[86, 87, 221, 222] 56[223] 57[52, 118, 175, 224-237] 58[238, 239] 59[240] 60[241] 61[242, 243] 62[244] 63[245]

Plant species

Number of Type of Anti-bacterialSynergism AntiviralSpasmolytic Expectorant Antitussive Immuno-stimulant Anti-inflammatory Analgesic Hypothesis

references reference with AB proved

?o+?o + ?o+ ?o + ?o + ?o +

o + ? o + ? o

Achillea millefolium L. 2 in vitro

1 in vivo + cl nical

Agrimonia eupatoria L. 1 in vitro

0 in vivo + cl nical

Allium sativum L. 1 in vitro

0 in vivo + cl nical

Althaea officinalis L. 0 in vitro

4 in vivo + cl nical

Camellia sinensis (L). 0 in vitro

KUNTZE 2 in vivo + cl nical

Cetraria islandica (L.) 0 in vitro

ACH. 1 in vivo + cl nical

Echinacea purpurea (L.) 3 in vitro

MOENCH s in vivo + cl nical

Foeniculum vulgare (L.) 2 in vitro

MILL. 0 in vivo + cl nical

Glycyrrhiza glabra L. 1 in vitro

2 in vivo + cl nical

Mentha x piperita L. 1 in vitro

0 in vivo + cl nical

Pimpinella anisum L. 2 in vitro

0 in vivo + cl nical

Plantago lanceolata L. 1 in vitro

0 in vivo + cl nical

Primula veris L. 1 in vitro

0 in vivo + cl nical

Rubus fruticosus L. 0 in vitro

1 in vivo + cl nical

Rumex ssp. L. 2 in vitro

0 in vivo + cl nical

Salvia officinalis L. 0 2

Sambucus nigra L. Thymus vulgaris L. Tussilago farfara L. Urtica dioica L. Vaccinium myrtillus L.

Sum of plant species for each effect

Sum of assessments

in vitro in vivo + cli in vitro in vivo + cli in vitro in vivo + cli in vitro in vivo + cli in vitro in vivo + cli in vitro in vivo + cli in vitro in vivo + cli in vitro in vivo + cli

nical nical

nical nical

nical 2 9

nical 2

0 0 0 0 0 6 0 0 7 0 0 0 0 0 0 0 0 0 0 1 1 0 0 0 0 0 0 0 0

0 0 0 0 1 2 0 1 2 0 0 2 0 0 4 0 0 1 0 0 2 0 0 1 0 0 3 0 1

0 0 0 0 0 8 0 0 15 0 0 0 0 0 0 0 0 0 0 1 2 0 0 0 0 0 0 0 0

0 0 0 0 1 2 0 1 2 0 0 2 0 0 7 0 0 2 0 0 2 0 0 1 0 0 4 0 2

a Assessment = conclusion of a reference on a hypothesized effect; b reference = trial x plant species x indication; + = reference proves evidently the hypothesized effect; ? = reference shows uncertain hypothesized effect; o = reference does not prove evidently the hypothesized effect

1 [288, 289] 2 [290] 3 [291] 4 [292] 5 [293-296] 6 [297] 7 [298] 8 [297] 9 [299] 10 [300, 301] 11 [103, 301] 12 [302] 13 [94] 14 [96] 15 [302, 303] 16 [96] 17 [95, 304] 18 [305, 306] 19 [307, 308] 20 [309] 21 [140] 22 [139] 23 [89] 24 [310, 311] 25 [53] 26 [312] 27 [313] 28 [314] 29 [315] 30 [293] 31 [316] 32 [300] 33 [317] 34 [191, 318, 319] 35 [113-116, 320, 321] 36 [108] 37 [322] 38 [323] 39 [323] 40 [322, 324, 325] 41 [326] 42 [327]

Table 5 Assessment3 of medicinal plants based on peer-reviewed references'3 of the last 20 years aiming the modulation of the

immune system and inflammation

Plant species Number of references Type of reference Immunostimulant Antiinflammatory Analgesic Hypothesis proved

+ ? o + ? o + ? o + ? o

Achillea millefolium L. 2 in vitro 21

2 in vivo + clinical 12 13 14

Agrimonia eupatoria L. 0 in vitro

1 in vivo + clinical 15

Allium sativum L. 4 in vitro 16 17 28

5 in vivo + clinical 59 1 10

Camellia sinensis (L). KUNTZE 14 in vitro 311 1212

5 in vivo + clinical 213 214 115

Cetraria islandica (L.) ACH. 2 in vitro 216

1 in vivo + clinical 117

Echinacea purpurea (L.) MOENCH 23 in vitro 1618 119 620

13 in vivo + clinical 921 222 123 124

Foeniculum vulgare (L.) MILL. 1 in vitro 125

3 in vivo + clinical 1 26 327

Glycyrrhiza glabra L. 6 in vitro 428 229

4 in vivo + clinical 330 131 132

Linum usita-tissimum L. 1 in vitro 133

3 in vivo + clinical 134 235 1 36

Malva sylvestris L. 1 in vitro 137

3 in vivo + clinical 1 38 239 140

Matricaria recutita L. 5 in vitro 141 442

5 in vivo + clinical 143 144 245 246

Mentha x piperita L. 0 in vitro

1 in vivo + clinical 147

Origanum vulgare L. 1 in vitro 148

6 in vivo + clinical 249 350 151

Pimpinella anisum L. 1 in vitro 152

2 in vivo + clinical 153 154

Plantago lanceolata L. 3 in vitro 355

0 in vivo + clinical

Potentilla erecta (L.) RAEUSCH. 1 in vitro 1 56

0 in vivo + clinical

Rubus fruticosus L. 4 in vitro 457

0 in vivo + clinical

Rumex ssp. L. 1 in vitro 1 58

3 in vivo + clinical 259 260

Salix ssp. L. 4 in vitro 461

1 in vivo + clinical 1 62

Salvia officinalis L. 0 in vitro

7 in vivo + clinical 163 164 165 466 267

Sambucus nigra L. 2 in vitro 1 68 1 69

1 in vivo + clinical 1 70

Table 5 Assessment3 of medicinal plants based on peer-reviewed references' of the last 20 years aiming the modulation of the immune system and inflammation (Continued)

Thymus vulgaris L. 5 4 in vitro in vivo + clinical 172 173 571 274

Tussilago farfara L. 1 0 in vitro in vivo + clinical 175

Urtica dioica L. 4 4 In vitro in vivo + clinical 276 378 277 179 1 80

Vaccinium myrtillus L. 1 2 In vitro in vivo + clinical 1 82 1 81 283

Sum of plant species for each effect in vitro 6 3 0 20 0 0 0 0 0 0 0 0

in vivo + clinical 9 4 6 13 01 12 0 1 1 1 1

Sum of assessments in vitro 29 3 0 56 00 0 0 0 0 0 0

in vivo + clinical 24 4 7 20 01 20 0 1 1 1 1

aAssessment = conclusion of a reference on a hypothesized effect; breference = trial x plant species x indication; + = reference proves evidently the hypothesized effect; ? = reference shows uncertain hypothesized effect; o = reference does not prove evidently the hypothesized effect

1 [328, 329] 2[330] 3[331] 4[331] 5[332] 6[333] 7[334] 8[78, 80] 9[65, 67, 68, 79, 335] 10[79] 11[133, 336, 337] 12[336, 338-348] 13[134, 349] 14[131, 350] 15[351] 16[352, 353] 17[354] 18[99, 100, 355-368] 19[369] 20[102, 370-374] 21[93, 97, 98, 375-380] 22[381, 382] 23[383] 24[384] 25[385] 26[386] 27[386-388] 28[144, 334, 389, 390] 29[391, 392] 30[138, 380, 393] 31[394] 32[394] 33[395] 34[396] 35[397, 398] 36[397] 37[399] 38[400] 39[401, 402] 40[401] 41[403] 42[404-407] 43[408] 44[409] 45[410, 411] 46[410, 412] 47[413] 48[414] 49[415, 416] 50[417-419] 51[420] 52[421] 53[422] 54[423] 55[392, 424, 425] 56[426] 57[427-430] 58[431] 59[432, 433] 60[432, 434] 61[426, 435437] 62[438] 63[439] 64[440] 65[441] 66[442-445] 67[442, 443] 68[446] 69[430] 70[447] 71[436, 448-450] 72[451] 73[451] 74[417,452] 75[453] 76[454, 455] 77[456, 457] 78[138, 458, 459] 79[460] 80[460] 81[344] 82[461] 83[461, 462]

risk of source selection bias, multiple types of sources were used initially: standard textbooks, peer-reviewed publications, a governmental report, and personal communications with experts. The risk of introducing database bias was reduced by using two different and independent databases and by using the Mesh Terms function of PubMed. The selection of the 30 traditionally used plant species may bear a sampling bias. European ethnoveterinary and traditional administrations of medicinal plants were screened to identify promising plant species for the bibliographic search. Due to our strategy, it is likely that frequently studied plant species come up as more promising compared to less frequently studied plants. Additionally, the timeliness of the review excluded studies published before 1994 which may be accepted in science for decades by e.g. the European Scientific Cooperative on Phytotherapy [55]. As a consequence, plants including Malva sylvestris L., Potentilla erecta (L.) RAEUSCH, Primula veris L., Quercus robur L. or Picea abies (L.) H.KARST. appeared less promising, although they are an integral element of traditional medicine.

Comparison of traditional phytotherapy with up-to-date knowledge

The most promising plant species of the peer-reviewed publications of the last 20 years were compared to the most common traditional administrations of the initial sources (Table 6). For the most promising plant species 62, 30 and 27 % are also frequently recommended in the initial sources for QA, QR and QL, respectively. The results confirmed the rationale of some traditional

administrations of medicinal plants. Cases where the traditional applications were not confirmed by current studies, may be explained by the fact that only studies published between 1994 and 2014 were considered. Nevertheless, for many of these plant species broad scientific substantiation exists. For example, ESCOP monographs are available for Linum usitatissimum L., Pimpinella anisum L., Cetraria islandica (L.) ACH., Primula veris L. and Salix ssp..

Complexity of varying chemistry

It is important to consider that the amount of active constituents in plants depends on environmental factors. Based on the plant cultivars used climatic and geographic conditions, quality of the soil and method of cultivation and harvest influence the phytochemical composition of the plant and therefore, different amounts of constituents can be found in different batches. The used part of plant, widely divergent post-harvesting processing and methods of extraction and stabilization affect the chemistry of phy-topharmaceuticals [56]. Environmental factors and post harvesting procedures are likely to explain varying effectiveness of a medicinal plant in different studies as reported for Echinacea [57, 58]. Therefore, a direct comparison of the outcome of the studies is difficult especially because of the lack of information regarding the phytochemical composition of the used test material. The use of pharmacopoeia quality in future research would ensure a defined amount of active constituents [59].

Table 6 Promising medicinal plants for treatment and prophylaxis of gastrointestinal and respiratory diseases and for modulation of the immune system and inflammation


Traditional applications in initial sources (number of references recommending the plant for the indication)a

Peer-reviewed references

(sum of points gathered in the scoring system2)b


Respiratory tract

Modulation of immune system and inflammation

Matricaria recutita L. (7) Foeniculum vulgare (L.) MILL. (6)

Potentilla erecta (L.) RAEUSCH (5)

Linum usitatissimum L. (5)

Rubus fruticosus L. (5)

Thymus vulgaris L. (4)

Quercus robur L. (4)

Mentha x piperita L. (4)

Urtica dioica L. (4)

Vaccinium myrtillus L. (4)

Salvia officinalis L. (4)

Carum carvi L. (4)

Camellia sinensis (L.) KUNTZE (4)

Achillea millefolium L. (4)

Thymus vulgaris L. (7)

Pimpinella anisum L. (6)

Althaea officinalis L. (5)

Cetraria islandica (L.) ACH. (5)

Primula veris L. (5)

Foeniculum vulgare (L.) MILL. (4)

Sambucus nigra L. (4)

Malva sylvestris L. (4)

Allium sativum L. (4)

Picea abies (L.) H.KARST. (4)

Echinacea purpurea (L.) MOENCH (2)

Salix sp. L. (2)

Thymus vulgaris L. (1)

Sambucus nigra L. (1)

Urtica dioica L. (1)

Malva sylvestris L. (1)

Plantago lanceolata L. (1)

Allium sativum L. (1)

Tilia cordata MILL/Tlia platyphyllos SCOP. (1) Artemisia absynthum L. (1) Verbascum sp. L. (1) Armoracia rusticana PH. GÄRTN.(!)

Allium sativum L. (41) Mentha x piperita L. (30) Salvia officinalis L. (27) Origanum vulgare L. (24) Camellia sinensis (L.) KUNTZE (18) Matricaria recutita L. (15) Glycyrrhiza glabra L. (14) Thymus vulgaris L. (13) Foeniculum vulgare (L.) MILL. (7) Carum carvi L. (6) Pimpinella anisum L. (6) Rumex sp. L. (6) Urtica dioica L. (6)

Echinacea purpurea (L.) MOENCH (10) Thymus vulgaris L. (10) Althaea officinalis L. (8)

Glycyrrhiza glabra L. (5)

Salvia officinalis L. (5)

Tussilago farfara L. (5)

Urtica dioica L. (5)

Achillea millefolium L. (4)

Camellia sinensis (L.) KUNTZE (4)

Sambucus nigra L. (4)

Echinacea purpurea (L.) MOENCH (41)

Camellia sinensis (L.) KUNTZE (26)

Glycyrrhiza glabra L. (19)

Origanum vulgare L. (19)

Allium sativum L. (18)

Salvia officinalis L. (16)

Urtica dioica L. (15)

Foeniculum vulgare (L.) MILL. (11)

Matricaria recutita L. (11)

Malva sylvestris L. (9)

Rumex sp. L. (9)

1 initial sources = standard literature, based on traditional empiric knowledge and historical literature of veterinary [42-45], and human phytotherapy [46], peer-reviewed publications of European [47] and Swiss ethnoveterinary medicine [36, 38] and a report of the European Food Safety Authority (EFSA) [48] focusing on the use of plants as feed additives in animal production; 2Score = 3 x (number of proven effects in clinical studies - number disproof of effects in clinical studies) + 2 x (number of proven effects in in vivo studies - number of disproof of effects in in vivo studies) + 1 x (number of proven effects in in vitro studies - number of disproof of effects of in vitro studies) agastrointestinal tract: all plant species recommended for QA 4 times or more in the initial sources, ordered by incidence of recommendation by different authors as listed in detail in Additional file 2; arespiratory tract: all plant species recommended for QR 4 times or more in the initial sources, ordered by incidence of recommendation by different authors as listed in detail in Additional file 2; aModulation of immune system and inflammation: includes all plant species recommended for QL 1 time or more in the initial sources, ordered by incidence of recommendation by different authors as presented in file 2 in greater detail; bgastrointestinal tract: includes all plant species gathered for QA with a minimum score of 6 ordered by sum of points the plant species gathered; brespiratory tract: includes all plant species gathered for QR with a minimum score of 4, ordered by sum of points the plant species gathered; bModulation of immune system and inflammation: includes all plant species gathered for QL with a minimum score of 9, ordered by sum of points the plant species gathered; bold letters = plant species recommended in initial sources and in peer-reviewed references for same indication

Relevance for the treatment of livestock diseases

From the 418 references assessed, 46 focused on livestock including 19 clinical references for pigs and five for cattle. Most of these clinical studies used the plants as a feed additive and not as a pharmaceutical. This might be due to complex regulatory affairs exacerbating the licensing and authorization of a medicinal plant or a plant extract as a veterinary drug.

Due to missing information regarding the absorption of orally administered medicinal plant compounds by the gastrointestinal tract, local treatment of gastrointestinal diseases might promising compared to a systemic treatment of respiratory diseases. Effective concentrations of, e.g. essential oils via inhalation may be obtained in the respiratory tract, but it is less practicable when larger herds need to be treated. While pigs as monogastrics might be compared with humans, calves are young ruminants and the biotransformation of plants secondary metabolites in the foresto-mach is not well known. However, in suckling calves plant extracts can be administered by daily milk diet to ensure bypassing the forestomach by oesophagal groove reflex.

We identified only a few recent references and also few traditional recommendations for the indication QR (n = 57) compared to QA (n = 198). Interestingly, similar findings were reported from ethnoveterinary research [47, 60]. One explanation might include the challenge of the treatment of respiratory diseases because systemic effects are needed to obtain the therapeutic effect compared to primarily local effects. Modulation of the immature or deficient immune system of calves and piglets provides a starting-point for the prevention of multifac-torial infectious diseases. In the traditional phytotherapy literature, effects of medicinal plants on the immune system cannot be found frequently. This might be explained by the fact that immunology is a relatively young scientific field that developed rapidly in recent years. In human medicine, some immune stimulating preparations are already available on the market and therefore, a variety of studies is available. In contrast, for livestock, scientific knowledge is not transferred to practical use yet.

This review mainly focused on therapeutic options of medicinal plants. From this point of view, the relevance of possible toxicity, adverse effects or residues in livestock products remains open. Regarding safety aspects Tussilago farfara L. cannot be recommended as a therapeutic medicinal plant due to the presence of toxic pyr-rolizidine alkaloids. Nevertheless, the majority of plant species in this review are consumed by humans as food, spices, luxury foodstuffs or as registered nutraceuticals and pharmaceuticals. If these plant species are safe for ingestion in humans, it might be legitimate to transfer these results to other mammalians with a comparable metabolism (herbivores and omnivores). Under these circumstances, risks for humans based on residues in

products from food-producing animals should be neglect-able. For herbivores and omnivores with a mainly plant-based ration, safety of the most medicinal plant species can be supposed. These species may cope with plant secondary metabolites in a similar way as humans [35].

Promising plant species for gastrointestinal and respiratory diseases and for modulation of the immune system and inflammation

Several trials show the equivalence of plant-derived pharmaceuticals with synthetic ones, but nonetheless there are some trials showing the contrary. Based on the data presented in this review, Allium sativum L., Mentha x piperita L. and Salvia officinalis L. carry a high potential for treatment of gastrointestinal diseases (Table 3). Echinacea purpurea (L.) MOENCH, Thymus vulgaris L. and Althaea officinalis L. may be considered for the treatment of respiratory diseases (Table 4). Regarding the majority of positive results of studies evaluated, Echinacea purpurea (L.) MOENCH, Camellia sinensis (L.) KUNTZE and Glycyrrhiza glabra L. were found to stimulate the immune response (Table 5).

Traditionally, plant species with a high content of tanning agents are administered in diarrhea. Allium sativum L. does not contain tanning agents, but due to its antibacterial, antidiarrheal, anti-inflammatory and immuno-modulatory effects, it may be used for prophylactic and acute treatment in diarrhea of calves and piglets. Eight in vivo and clinical studies were identified for Allium sativum L. proving these effects, and no studies disproving them. A trial conducted with neonatal calves showed that allicin, a main active compound of Allium sativum L., delayed the onset of diarrhea due to Cryptosporidium parvum [61]. Two clinical studies demonstrated anti-diarrheal effects and a reduction of the fecal coliform count by Allium sativum L.. There is also evidence for an improvement of performance in pre-ruminant calves [62, 63]. The immunomodulatory activity of Allium sati-vum L. in pigs [64, 65] and poultry [66, 67] may hold true in immunocompromised calves to support their immune defense. Its antibacterial effects on Escherichia coli and Salmonella ssp. in vitro suggest a high probability of antibacterial activity in vivo [68-75]. Nevertheless, more clinical studies are necessary to investigate antiinfective effects of Allium sativum L. in young farm animals. Al-lium sativum L. has been reported to exhibit anti-inflammatory activity in rats [76]. There is also mechanistic evidence for anti-inflammatory properties as well as immunostimulation showed in three in vitro studies, namely an inhibition of leucocyte migration [77], modulation of interleukin and interferon-gamma expression [78] and a suppression of nitrogen oxide production in macrophages [79]. An anti-inflammatory effect may be useful for the treatment of systemic inflammation

processes often accompanied with diarrhea. Facing animal welfare and regarding efficient synthetic non-steroidal and steroidal anti-inflammatory agents, it is debatable whether there is a need for plant-derived alternatives. While synthetic non-steroidal and steroidal anti-inflammatory agents often produce considerable adverse effects including an inhibition of mucus production [80, 81], medicinal plants compass considerable adverse-effects because they contain several different active compounds which might reduce the potential of unwanted effects [82]. In in vivo tests for acute and chronic toxicity, the maximum tolerance dose and genotoxicity Allium sativum L. was demonstrated to be relatively safe if administered in therapeutic dosages

[83] and if estimated for the animals metabolic body weight

[84]. With respect to food quality, it must be assured that residues of Allium sativum L., responsible for the typical taste of this plant do not result in an altered taste of meat.

To reduce enteral spasm during diarrheal diseases, Mentha x piperita L. might be an efficient treatment option based on three clinical studies in humans, demonstrating efficient spasmolytic activity comparable to butylscopola-mine [85-87]. The underlying mechanism includes inhibition of smooth muscle contractility through the block of calcium influx by menthol [88]. In traditional medicine, Mentha x piperita L. has been used in the therapy of respiratory diseases. Peppermint essential oil showed spasmolytic activity on rat trachea ex vivo [89]. But there are no clinical studies in veterinary medicine for Mentha x piperita L. in respiratory disease. No adverse effects have been reported for Mentha x piperita L. infusions or oral intake of leaves [90]. Excessive inhalation or local application of pure Mentha x piperita L. essential oil was shown to lead to hypersensitivity reactions [56]. Contraindications are severe hepatic damage and cholestasis [43].

Based on this review, the most prominent plant species for stimulation of the immune system is Echinacea purpurea (L.) MOENCH. The main constituents are polysac-charides, alkylamides, caffeic acid esters and polyacetylenes [91]. It has been used in therapy for stimulation of the immune system in human medicine, mainly for prevention of viral infections of the respiratory tract [92]. A total of 23 clinical and in vivo studies revealed multiple effects on the innate and acquired immune system. Echinacea purpurea (L.) MOENCH was shown to increase the immune response towards swine erysipelas vaccination in piglets [93], prevented enveloped virus infections in humans [94] and reduced symptom severity in naturally acquired upper respiratory tract infections in humans [95]. In contrast, seven clinical or in vivo studies reported the absence of the above mentioned effects. For example Echinacea purpurea (L.) MOENCH failed to enhance growth or to show any immu-nomodulatory effect in one study in pigs [96]. Reasons for these negative results may be due to a very small number of individuals, an improper dosage or study design. As

mentioned above, the diversity of non-standardized Echin-acea preparations with varying chemistry is likely to result in different findings. In some studies, the dosage was not reported, and therefore it was not possible to estimate how much plant material or drug equivalent was administered per day. Consequently, due to missing data final conclusions cannot be drawn. Nevertheless, eight in vivo studies reported modulations of immune system and blood cell count, and no studies were found disproving these effects. Different Echinacea species were found to increase the total number of white and red blood cells in mice [97] and horses [98]. Twenty-six in vitro studies demonstrated the underlying mechanisms of immunomodulatory effects of Echinacea purpurea (L.) MOENCH. It was reported to activate macrophages and natural killer cells [99-101] and to modulate several cytokines [102-105]. Echinacea purpurea (L.) MOENCH is known as a safe immunostimulant in humans and several products are available on the market. No reported interactions with other drugs and no toxic effects after overdosage were reported [106]. Possible rare adverse effects such as hypersensitivity reactions are reported, but no adverse effects have been observed during long-term administration [107]. In general, Echinacea purpurea (L.) MOENCH seems to be effective in preventing respiratory diseases and as an early intervention immediately after onset of first symptoms of infectious diseases [95]. However, further veterinary clinical studies need to be performed, especially to evaluate effective dosages.

In human medicine, Thymus vulgaris L. has been already effectively used according to its antitussive and mucolytic effects in the treatment of acute bronchitis, often in combinations with other plant species, e. g. Primula veris L. for its expectorant effects [108-110]. The main active compound of Thymus vulgaris L. is the essential oil containing thymol, geraniol, thujanol and linalool [111]. The above mentioned effects still have to be investigated for veterinary purposes. Nevertheless, an enhancement of the mucociliary clearance in mice was shown in two in vivo studies [112, 113]. This effect was explained by an interaction with beta2 receptors in rat lung tissue [112]. Additionally, three ex vivo studies demonstrated spasmolytic effects of Thymus vulgaris L. on tracheal chains comparable to theophylline [114-116]. The reported anti-inflammatory properties [117] and antibacterial effects found in in vitro studies [118-120] of Thymus vulgaris L. still needs to be investigated in clinical studies. In vivo studies on the toxicology of Thymus vulgaris L. leaf extract showed no toxic potential [121,122]. In summary, the data available support the potential for using Thymus vulgaris L. for treatment of respiratory diseases in livestock.

Camellia sinensis (L.) KUNTZE seems to be useful for treatment of diarrhea as well as for stimulation of the immune system. Main constituents are polyphenolic compounds (up to 25 % catechin derivatives in non-fermented

plants, e.g. epigallocatechin), purine alkaloids (caffeine, theo-bromine, theophylline) and flavonoids [123]. Some clinical studies reported beneficial effects of Camellia sinensis (L.) KUNTZE on gut health as indicated by a reduced prevalence of postweaning diarrhea in piglets, but also a decrease in growth performance [124]. An experimental trial on a diet with Camellia sinensis (L.) KUNTZE whole plant extract revealed a significant decrease of Clostridia counts, but also of Enterococci counts in the feces of piglets compared to a standard diet with antibiotics [125]. Two in vivo studies showed also anti-influenza virus activity in mice [126] and chicken [127], which might be due to an inhibition of virus adsorption [126]. Fifteen in vitro and five in vivo studies demonstrated antioxidative [128-130] and anti-inflammatory [131, 132] effects and a modulation of the immune system [133, 134]. No studies were found disproving these effects. In mice, the intake of a concentrated extract of Camellia sinensis (L.) KUNTZE did not lead to unwanted adverse effects [135]. Despite that Camellia sinensis (L.) KUNTZE is known to be fairly devoid of unwanted effects, some reports on liver damage related to the intake of Camellia sinensis (L.) KUNTZE extract are available [136, 137]. In summary, most reports state that safety of Camellia sinensis (L.) KUNTZE extract can be supposed, if used appropriately to the recommendations [136]. Therefore, Camellia sinensis (L.) KUNTZE bears a reliable potential for prophylaxis and therapy of diseases in calves and piglets.

The main active compound of medicinally used roots of Glycyrrhiza glabra L. is the saponin glycyrrhizin. Furthermore, it contains flavonoids and isoflavonoids, chalcones, cumarins and phytosterols [123]. With regard to the inclusion criteria of this review, no clinical studies focusing on Glycyrrhiza glabra L. could be found. Nevertheless, it was shown to exhibit immunostimulatory effects in vivo, by stimulation of cellular and nonspecific response [138]. In three in vivo and ex vivo models, antitussive [139] and tracheal smooth muscle relaxing activity [140] as well as regulating effects in the gastrointestinal tract were reported [141]. Four in vitro studies demonstrated its antimicrobial [142, 143] and antiviral potential by activation of autophagy [144]. In an assessment of different plant species, Glycyr-rhiza glabra L. exerted the strongest antiviral activity against rotavirus [145]. Due to these versatile effects, Glycyrrhiza glabra L. might be beneficial for prophylaxis and treatment of virus induced diseases of the respiratory- as well as the gastrointestinal tract. Regarding the safety of Glycyrrhiza glabra L., it is important to choose the right dosage due to the hyper-mineralocorticoid-like effects of glycyrrhizin. An acceptable daily dosage of 0.015-0.229 mg glycyrrhizin/kg body weight/day for human and animals was reported [146].


This systematic review identified common medicinal plant species as a potential future therapeutic option for

gastrointestinal and respiratory diseases in calves and piglets. Based on their plant specific multi-component compositions, the versatile effects of medicinal plants as 'multi-target drugs' may bear a potential for the treatment of respiratory and gastrointestinal diseases in calves and piglets. Medicinal plants are unlikely to replace chemical medications as a general rule, but they may be a single or at least a complementary treatment. In concert with housing, feeding and hygiene, medicinal plants are part of a sustainable, natural option for improving animal health and reducing the use of antimicrobials in livestock farming. The results of this review provide support for a need for additional in vitro, in vivo and clinical research focused on phytotherapy for recently emerging and challenging diseases in livestock. While a large amount of peer-reviewed studies about medicinal plant species is available, most of the clinical and experimental studies were performed in humans and experimental animals. More research is needed to evaluate the potential of medicinal plants for treatment of farm animals. The data from this review provide guidance on medicinal plants promising for further investigations in livestock: the most promising candidates for gastrointestinal diseases are Allium sativum L., Mentha x piperita L. and Salvia officinalis L.; for diseases of the respiratory tract, Echinacea purpurea (L.) MOENCH, Thymus vulgaris L. and Althea officinalis L. were found most promising, and Echinacea purpurea (L.) MOENCH, Camellia sinensis (L.) KUNTZE, Glycyrrhiza glabra L. and Origanum vulgare L. were identified as best candidates for modulation of the immune system and inflammation. Based on this review, studies are under way to investigate the effects of promising medicinal plants in calves and piglets.

Additional files

Additional file 1: Protocolof the systematic review. (DOCX 27 kb)

Additional file 2: Plant species recommended for the treatment of gastrointestinaland respiratory diseases in human and animals based on standard textbooks, European peer-reviewed ethnoveterinary publications and an EFSA report. (XLSX 42 kb)

Additional file 3: Assessment of medicinalplants effects in 418 final peer-reviewed references. (XLSX 59 kb)


ATCvet, AnatomicalTherapeutic Chemicalclassification system for veterinary medicine; e.g., exempli gratia (in English: for example); EFSA, European Food Safety Authority; EMA, European Medicines Agency; ESCOP, European Scientific Cooperative On Phytotherapy; MBW, metabolic body weight; pH, pondus Hydrogenii; PICOS, population, intervention, comparator, outcome, study design; QA, preparations used for the treatment of diseases affecting the alimentary tract or metabolism, particularly unspecified or infectious diarrhea and intestinalspasms; QL, immunomodulating agents; QR, preparations for the treatment of diseases in the respiratory system; sp., any species, not specified in detail; ssp., subspecies; WHO, World Health Organization


We want to thank the specialists of veterinary phytotherapy for reviewing the primary list of 29 medicinal plant species, namely Dr. med. vet. Caecilia Brendieck-Worm, Dr. med. vet. Werner Hagmueller and Dr. med. vet. Elisabeth Stoeger. Furthermore, we want to thank Edith Hofer, librarian of the Vetsuisse library, University of Bern, for the continuous and straightforward support; Dr. Stephan Haesler, president of the Swiss Association of the History of Veterinary Medicine, for providing historic veterinary literature and Dr. Christopher Portier for linguistic revision. Special thanks goes to the Swiss retailer Migros for funding this work.


This work was funded by the Swiss retailer Migros (project #500 54). The funding institution were not involved in the study design, collection, analysis and interpretation of the obtained data and in writing the manuscript.

Availability of data and materials

All the data supporting the findings are contained within the manuscript and in the Additional files 1, 2 and 3.

Authors' contributions

HA designed the review, collected, analysed and interpreted the data and wrote the manuscript. MMev participated in the design of the study, in the interpretation and discussion of data and coordinated the writing and reviewing of the manuscript. MK contributed his expert-knowledge on diseases of calves and participated in the interpretation and discussion of data. HN and NG contributed their expert-knowledge on diseases of piglets and participated in the interpretation and discussion of data. MMel contributed his expert-knowledge on pharmaceutical biology and participated in the interpretation and discussion of data. MW participated in the design of the study, in the interpretation and discussion of data and in the writing of the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests'. Consent for publication

Not applicable because this manuscript does not contain any individual persons' data.

Ethics approval and consent to participate

Not applicable for this systematic literature review.

Author details

department of Livestock Sciences, Research Institute of Organic Agriculture (FiBL), Ackerstrasse 113, postbox 219, Frick 5070, Switzerland. 2Division Veterinary Pharmacology & Toxicology, Department Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Laenggassstrasse 124, Bern 3012, Switzerland. 3Department of Farm Animals, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 260, Zurich 8057, Switzerland. 4Department of Clinical Veterinary Medicine, Swine Clinic, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, Bern 3012, Switzerland. 5Dahlem Centre of Plant Sciences, Institute of Pharmacy, Freie Universität Berlin, Koenigin-Luise-Strasse 2 + 4, Berlin 14195, Germany.

Received: 27 November 2015 Accepted: 30 May 2016 Published online: 06 June 2016


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