Skip to main content
Download PDF

Effects of feeding drunken horse grass infected with Epichloë gansuensis endophyte on animal performance, clinical symptoms and physiological parameters in sheep

BMC Veterinary Research volume 13, Article number: 223 (2017) Cite this article

Abstract

Background

Many reports showed that grass-endophyte symbiosis induced livestock poisoned. Yet, there is no study evaluating clinical symptoms and physiological parameters in sheep fed Epichloë gansuensis endophyte-infected grass. The objective of the present study was to investigate these indexes by feeding sheep with endophyte-infected A. inebrians (E+ Group) or endophyte-free A. inebrians (E- Group) drunken horse grass or alfalfa hay (Control Group).

Results

The Epichloë endophyte caused obvious toxicity symptoms in the sheep fed E+ A. inebrians, with 1 of the 5 sheep having died by the 35th day. The feed intake and body weight gain of the E+ Group were significantly less than the E- and control groups (P < 0.05). Serum concentrations of alanine aminotransferase (ALT, 45.5 mmol/L) and aspartate aminotransferase for the E+ group (AST, 139.3 mmol/L) were significantly (P < 0.05) greater than for the E- (ALT, 31.2 mmol/L; AST, 78.6 mmol/L) and control (ALT, 32.6 mmol/L; AST, 56.6 mmol/L) groups at the fifth week; serum concentration of creatinine for the E+ group (63.8 mmol/L) was also significantly (P < 0.05) greater than for E- (56.6 mmol/L) and control groups (58.5 mmol/L). Meanwhile, urine biochemical indices for the E+ group indicated that ketone and occult blood were significantly (P < 0.05) elevated compared to the other groups while urine pH values were significantly (P < 0.05) acidic. The relative weight of heart, brain, liver, lung and kidney for Group E+ were almost two fold more than the other groups, but uterus weight was about half that found for Group E- or Control.

Conclusions

We conclude that the Epichloë endophyte infection is the cause of A. inebrians toxicity to sheep. Interestingly, none of the measured parameters differed significantly between E- and the control groups, which implied that drunken horse grass could be utilized efficiently by sheep when not infected by the Epichloë endophyte.

Background

Drunken horse grass (Achnatherum inebrians) is distributed mainly within the native grasslands of northern and northwestern China. Unfortunately, once infected by a symbiotic fungal endophytes of Epichloë, the grass is a toxic perennial plant and poisonous to grazing animals [1]. On the one hand, grass plants with the endophytic fungus display insect resistance, drought resistance, rapid growth, and strong competitive ability. On the other hand, as noted above, the symbiont produces toxins that cause livestock poisoning, with huge animal productivity losses as a result. Animals fed A. inebrians can display symptoms of intoxication, such as sluggishness, tottering, drooping, and glaring [2]. The horse (Equus caballus), donkey (E. asinus), mule (E. caballus × E. asinus), and rabbit (Oryctolagus cuniculus) are commonly reported to show symptoms of intoxication, but sheep were not significantly intoxicated when dosed with A. inebrians powder [3, 4], which might be the grass without fungal endophytes or rumen fermentation reducing toxicity of endophyte toxins in ruminants but what mechannism is not reported. Previous research has shown that almost 100% of A. inebrians plants in natural rangeland are infected by the endophyte Epichloë gansuensis [5], and that the main alkaloids produced are ergonovine and ergine [6, 7]. A rabbit-feeding trial comparing the effect of endophyte-infected (E+) and endophyte-free (E-) A. inebrians, demonstrated significant clinical intoxication symptoms in animals fed the E+ material [1]. In order to further explore the toxicity status A. inebrians when infected by this endophyte, an experiment was carried out on small-tailed Han sheep (Ovis aries) fed E+ or E- A. inebrians. Resulting clinical symptoms, and physiological or biological effects were observed and analyzed.

Methods

A feeding experiment of 35 days duration was conducted at the Animal Experimental Station of Gansu Agricultural University, China. All research protocols used in the current experiments were approved by the Animal Ethics Committee of Gansu Province, China.

Animals used and feeding regime

Drunken horse grass, E+ and E- A. inebrians hay, was harvested from the Yuzhong experimental station (N 35°10′, E 103°41′, elevation 1731 m) of Lanzhou University, Gansu, China. To confirm the endophyte infection status, the endophyte was detected by microscopic examination for both E+ and E- plants. Referring to the procedure by Zhang et al. (2011) reported that the alkaloids were determined with Agilent 1100 series high performance liquid chromatography (HPLC) system, ZORBAX - XDB C18 reversed phase chromatographic column, mobile phase flow rate of 1 ml/min, 20 ul, testing with VWD uv monitor [8].

Fifteen 10 to 12 month-old female small-tailed Han sheep were used, and their initial body weights ranged from 17.46 to 22.29 kg. The sheep were randomly divided into 3 groups (E+, E- and control), and each sheep was housed in a metabolic cage (150 cm by 80 cm × 70 cm). Sheep was fed a diet (Table 1) containing E+ or E- A. inebrians hay, and the daily dry matter allowance was calculated as 3% of animal body weight. For the control group, alfalfa hay (Medicago sativa) replaced A. inebrians hay. Animals had free access to water. During a one-week pre-experiment period, and for the five week experiment that followed, the daily diet was divided into three equal parts for feeding to individual animal over the course of the day.

Table 1 Ingredient and chemical composition of experimental diets
Full size table

During the five-week experiment any clinical symptoms were carefully recorded each day. Feed intake and body weight were measured and samples of blood weekly and urine were collected at the end of 5th week. Sheep heart rates were determined with a medical stethoscope, and rectal temperature also was measured using a mercury thermometer. At the end of the experiment, all animals were weighed, and then slaughtered. The heart, liver, spleen, lung, brain, and uterus of each animal were removed and their respective fresh weights immediately recorded.

Sampling procedures

Blood samples were drawn from a jugular vein. To obtain samples, an area around the mid and lower third of the jugular vein was shaved and sterilised, pressure applied, and when vascular engorgement occurred, a double ended hypodermic needle inserted, and blood collected into test tubes, and whole blood samples were centrifuged under 3500 rmp for 15 min to obtain serum for the respective chemical determinations. All serum samples were saved - 75 °C freezer until analysed. Glutamic pyruvic transaminase (ALT), aspartate aminotransferase (AST) and creatinine (Cr) were determined by a 7080 automatic biochemistry analyzer (Hitachi, Japan).

About 200-ml urine was collected using a sterile plastic bag while the sheep was urination on the morning of last three days of 5th week. After collection of urine, 0.5 ml of 40% formaldehyde solution per 100 ml of urine was added and sub-samples were stored at −20 °C. Routine urine analyses were carried out using a BW-200 urine analyzer (Yantai, China), including occult blood, urine protein, and ketone levels and leukocyte counts.

At the end of the experiment after slaughter, viscera were removed and major organs including the heart, liver, spleen, lung, kidney, brain, and uterus dissected out, weighed, and the weight expressed as a percentage of body weight, hereafter referred to as the relative weight of organ.

Statistical analysis

Statistical analyses were performed by a professional statistician using SPSS Version 21.0. Significance was set at P < 0.05. For intake, body weight, heart rate, rectal temprature, ralative weight of organ and serum biochemical parameters, these comparisons were made using one-way ANOVA with Tukey multiple comparisons. For the acidic or positive of urine parameters, the ratio was caluclated and significances were anounced using χ2 test procedure.

Results

Animal clinical symptoms and performance associated with ingestion of Achnatherum Inebrians endophyte

Clinical symptom, feed intake and weight gain

The small-tailed Han sheep used in these feeding experiments appeared to have a severe toxic reaction to E+ A. inebrians, including absent-mindedness, blank stares and stumbling, but not to E- A. inebrians or the control (Table 2), which indicated that the toxicity of A. inebrians was associated with Epichloë endophyte infection.

Table 2 Effects of ingested Achatherum inebrians on clinical symptoms of sheep
Full size table

Additionally, the feed intake of the E+ group was significantly less than E- and control Groups (P < 0.05), while the feed intake of E- and control Groups did not differ significantly (P > 0.05), with the average feed intake of E+ and E- Groups was reduced by 12.50% and 2.7%, respectively, compared to the Control group during the feeding experiments (Table 3).

Table 3 Effects of ingested E+ or E-Achatherum inebrians on feed intake and body weight of han sheep1,2
Full size table

There was a decline in body weight of the E + group within the first week, while body weights of E- sheep were stable and Control sheep slowly increased. The body weight loss of the E+ group compared to E- and Control groups had become statistically significant after the secend week (P < 0.05). Body weight of the E- group was less than that of the Control group, but not significantly so (P > 0.05). The average body weight of E+ sheep (15.0 kg) was 28% lighter than E- sheep (20.9 kg) and 34% lighter than Control sheep (22.9 kg) by the end of the feeding experiments (Table 3).

Heart rate and rectal temperature

E+ exhibited a transitory elevation of heart rate compared to E- and control sheep in week 2 and week 3 (P < 0.05), and after the first two weeks, rectal temperatures of E+ sheep were significantly (P < 0.05) greater than the other two groups. However, heart rates and rectal temperatures of E- and Control sheep did not differ significantly (P > 0.05) at any time (Table 4).

Table 4 Effects of ingested E+ or E- Achnatherum inebrians on heart rate and rectal temperatures of han sheep1, 2
Full size table

Urine parameters

Numbers of sheep with acidic urine were significantly (P < 0.05) higher for E+ A. inebrians-fed sheep than for the E- and control groups. Urine occult blood and ketone levels were also significantly (P < 0.05) elevated in E+ sheep, but urine protein and leukocyte levels did not significantly (P > 0.05) change (Table 5).

Table 5 Effects of ingested E+ or E- Achnatherum inebrians on urine parameters of han sheepa,b,c
Full size table

Serum activity of enzymes and renal function

Ingestion of E+ A. inebrians resulted in significantly (P < 0.05) elevated aspartate aminotransferase activity (AST) compared to E- and Control groups from week 2 onwards. Alanine aminotransferase (ALT) activity and creatinine levels (Cr) were not significantly elevated in E+ animals during the first 4 weeks (P > 0.05), but were increased significantly by the 5th week (P < 0.05) (Table 6).

Table 6 Effects of ingested E+ or E- Achatherum inebrians on selected serum biochemical parameters in han sheep
Full size table

Effects of Achatherum inebrians Endophyte on relative weight of organ

Significant differences in relative weight of organ (P > 0.05) were also observed. Ingestion of E+ A. inebrians raised heart, brain, liver, lung and kidney relative weight of organ, while its for the uterus was decreased (Table 7).

Table 7 Effects of ingested E+ or E- Achatherum inebrians on relative weight of organ of han sheep
Full size table

Discussion

Clinical symptoms

Feeding experiments demonstrated that the small-tailed Han sheep appeared to have a toxic reaction after ingestion of E+ A. inebrians, including absent-mindedness, blank stares and stumbling, but not following ingestion of E- A. inebrians or the control feed. At 35-d one small-tailed Han sheep exhibited poisoning symptoms including mydriasis, neck stiffness, limb tic, nasal mucosa bleeding, and weak breathing. It suffered a hypotensive crisis and its condition worsened, with muscle flaccidity, loss of defecation, abdominal swelling, retention of urine, and ultimately death. These symptoms are similar to the toxicity symptoms of ergonovine and ergine [9,10,11]. Ergonovine poisoning can cause excitement, muscle relaxation and allergic reaction, apparent intelligence depression, gastrointestinal dysfunction and stomach ache. Ergine can cause anesthesia and retroperitoneal fibrosis, urinary tract obstruction and renal failure. Therefore, it was concluded that the sheep fed E+ A. inebrians were poisoned by the alkaloids that are produced by the N. gansuense endophyte symbiont of A. inebrians.

The feed intake of sheep fed E+ A. inebrians was significantly less than those fed E- A. inebrians or the control group, so the endophytic fungi reduce either palatability or feeding drive of the animals, or possibly both. In the first three days of the experiment, the feed intake reduction of the E+ group was very large but then rose slightly, suggesting initial aversion of the sheep to feed containing endophye infected drunken horse grass, followed by gradual acclimation. This is consistent with prevously published findings [12].

Suppression of feed intake of small tailed han sheep offered endophyte infected A. inebrians is consistent with observed body weight loss, so the endophyte infected A. inebrians can be considered a factor in poor body condition of small tailed han sheep. This is consistent with a research report of Blaney [13].

Endophyte infected A. inebrians fed to sheep resulted in significantly elevated levels of urine ketone bodies and occult blood and increased numbers of animals with acidic urine. Ketone bodies are a product of the decomposition of fatty acids, and include acetoacetate, acetone and ß- hydroxybutyric acid [14,15,16]. When their production is greater than the liver can metabolize, the ketones will accumulate to produce acidosis. Under physiological conditions, ketone bodies cannot be detected in animal urine, but they can appear with long-term malnutrition, hunger, long-term anesthesia and after a wound. Ergot alkaloids produced by E+ A. inebrians have effects on the nervous system, with the increased presence of ketone bodies possibly being responsible for long-term anesthesia, but the specific mechanism of action needs further research.

Occult blood is hemoglobin or red blood cells in urine which cannot be observed by the naked eye directly [17, 18]. The bleeding of different parts of the urinary tract, due to hemolytic disease, poisoning [19] or blood transfusion reactions [20], can cause a positive occult blood reaction. In this study, the poisoning of sheep by feeding E+ A. inebrians was very strongly correlated with the positive occult blood reaction, and can be considered a probable cause.

The pH of animal urine is affected by feed properties, and generally herbivore urine is slightly alkaline, but some nutritional metabolic diseases such as ketonemia, or pathogenic heat or malnutrition can make urine acidic [16, 21]. In this study, the observed acidic urine may have been caused by ketone bodies, but the mechanism is still ill-defined.

Liver and renal function

Serum ALT and AST values are used mainly for the detection of liver disease in livestock, and generally the ALT and AST activity of sheep ranges from 25.0 to 70.0 U/L, 40.0 to 123.0 U/L respectively [22]. In the present study, the activities of serum ALT and AST in E+ sheep were significantly higher than the E- or Control sheep. These results for the E+ group were similar to those prevously published [23,24,25,26].

Creatinine is a substance associated with energy metabolism of muscles, and elevation occurs when its discharge is increased. Serum creatinine concentration rises rapidly early in kidney disease [27]. That is consistent with the detected significant increase in the first week of the experiment. The normal range of Serum creatinine is usually less than 150 mmol/L. Reduced creatinine levels are of no clinical significance, but when levels of 250 mmol/L or more are observed, this may inidcate kidney dehydration or heart failure [28].

Relative weight of organ

E+ A. inebrians ingestion brought about higher of brain, liver, lung and kidney, but lower that of the uterus. This result would be expected, given the negative effects in liver and renal function, and more loss of body weight outlined above.

Conclusions

Ingestion of E+ A. inebrians feed by small tailed Han sheep (O. aries) resulted in a range of clinical symptoms and biochemical effects. Ingestion of the endophyte not only made serum indices and urine biochemistry abnormal, but also caused absent-mindedness, blank stares and stumbling. The alkaloid secondary metabolites produced by the Epichloë endophyte infection of A. inebrians are apparently the cause of this toxicity. Interestingly, no significant differences in measured parameters were observed between sheep fed E- A. Inebrians and those fed a diet based on alfalfa, which implies that drunken horse grass could be utilized as an animal feed source if free of the Epichloë endophyte.

Abbreviations

ALT:

Alanine aminotransferase

AST:

Aspartate aminotransferase

Cr:

Creatinine

E-:

Endophyte-free A. inebrians

E+:

Endophyte-infected A. inebrians

References

  1. Li CJ, Nan ZB, Zhang CJ, Zhang CY, Zhang YH. Effects on health of the rabbits fed drunk horse grass. Chin Sci Technol. 2009;11:84–90.

    Google Scholar 

  2. Ren JZ. Northwest grasslands several common poisonous weeds. Gansu Agricultural University Press. 1959;1:9–16.

    Google Scholar 

  3. Wang K, Dang XP. Toxicity test of drunken horse grass to the sheep. China Vet Sci Technol. 1991;21:32–3.

    Google Scholar 

  4. Cao GR, Dang XP, Duan DX, Li SJ, Zhou JH. Drunken horse grass poisoning experiment. China Vet Sci Technol. 1991;21:26–7.

    Google Scholar 

  5. Li CJ, Nan ZB, Gao JH, Tian P. Detection and distribution of Epichloë - Achnatherum inebrians association in China. In: Proc. 5th Int. Epichloë/Grass Interactions Symposium, Arkansas, USA. 2004.

  6. Miles CO, Lane GA, Menna ME, Garthwaite I, Piper EL, Ball OP, Harris PS. High levels of ergonovine and lysergic acid amide in toxic Achnatherum inebrians accompany infection by an Acremonium-like endophytic fungus. J Agric Food Chem. 1996;44:1285–90.

    Article  CAS  Google Scholar 

  7. Li CJ, Nan ZB, Christopher S. Levels and temporal variation of ergot alkaloids in endophyte-infected drunken horse grass, Achnatherum inebrians, in China. In: APS, CPS and MSA Joint Meeting Abstracts, Quebec, Canada. 2006:203–4.

  8. Zhang XX, Li CJ, Nan ZB. Effects of cutting frequency and height on alkaloid production in endophyte-infected drunken horse grass (Achnatherum inebrians). Sci China Life Sci. 2011;54(6):567–71.

    Article  CAS  PubMed  Google Scholar 

  9. Foote A, Harmon D, Strickland J, Bush L, Klotz J. Effect of ergot alkaloids on contractility of bovine right ruminal artery and vein. J Anim Sci. 2011;89:2944–9.

    Article  CAS  PubMed  Google Scholar 

  10. Dänicke S, Diers S. Effects of ergot alkaloids on liver function of piglets as evaluated by the 13C-Methacetin and 13C-α-Ketoisocaproic acid breath test. Toxins. 2013;5:139–61.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Foote AP. Effect of ergot alkaloids on bovine foregut vasculature, nutrient absorption, and epithelial barrier function. PhD Dissertation: University of Kentucky, Lexington; 2013.

    Google Scholar 

  12. Garner GB, Cornell CN. University of Missouri report on fescue research activities (preliminary report). Tall Fescue Toxicosis Workshop, Memphis, Tenn: Proc; 1987.

    Google Scholar 

  13. Blaney BJ, McKenzie RA, Josey BJ, Ryley MJ, Downing JA. Effect of grazing sorghum (Sorghum bicolor) infected with ergot (Claviceps africana) on beef cattle. Aust Vet J. 2000;78:124–5.

    Article  CAS  PubMed  Google Scholar 

  14. Larsen M, Kristensen NB. Effect of a lucerne feeding strategy in the first week postpartum on feed intake and ketone body profiles in blood plasma, urine, and milk in Holstein cows. Acta Agriculturae Scand Section A. 2010;60:239–49.

    CAS  Google Scholar 

  15. Raoofi A, Jafarian M, Safi S, Vatankhah M. Fluctuations in energy-related metabolites during the peri-parturition period in Lori-Bakhtiari ewes. Small Rumin Res. 2013;109:64–8.

    Article  Google Scholar 

  16. Newman JC, Verdin E. Ketone bodies as signaling metabolites. Trends in Endocrinol Metab. 2014;25:42–52.

    Article  CAS  Google Scholar 

  17. Liu CX, Yu GH, Zhang Y. Contrast analysis on urine occult blood tested by urine analyzer and microscope analysis of urine red blood cell. J Southwest Univ Nationalities. 2010;6:20–9.

    Google Scholar 

  18. Xu X, Luo CL, Pu J, Liu Q, Zhang Y. Reliability of dry-chemistry method in detecting urine occult blood. Chongqing Med. 2012;18:1802–4.

    Google Scholar 

  19. Yamanaka K., Yamano Y, Yoshimura Y, Shimoda Y, Endo Y, Endo G. Speciation analysis of arsenic compounds in the serum and urine of a patient with acute arsine poisoning. In: Proc. 16th Int. Conference on Heavy Metals in the Environment, E3S Web of Conferences, Japan. 2013;1:39003.

  20. Tobian AA, Tobian AA, Savage WJ, Tisch DJ, Thoman S, King KE, Ness PM. Prevention of allergic transfusion reactions to platelets and red blood cells through plasma reduction. Transfus. 2011;51:1676–83.

    Article  Google Scholar 

  21. Cartwright MM, Hajja W, Al-Khatib S, Hazeghazam M, Sreedhar D, Li RN, Wong-McKinstry E, Carlson RW. Toxigenic and metabolic causes of ketosis and ketoacidotic syndromes. Crit Care Clin. 2012;28:601–31.

    Article  PubMed  Google Scholar 

  22. Wang MZ. Veterinary clinical differential diagnostics. Beijing: China Agriculture Press; 1992. p. 299–303.

    Google Scholar 

  23. Bond J, Powell JB, Undersander DJ, Moe PW, Tyrrell HF, Oltjen RR. Forage composition and growth and physiological characteristics of cattle grazing several varieties of tall fescue during summer conditions. J Anim Sci. 1984;59:584–93.

    Article  CAS  Google Scholar 

  24. Rice RL, Blodgetta DJ, Schuriga GG, Sweckerb WS, Fontenotc JP, Allend VG, Akerse RM. Evaluation of humoral immune responses in cattle grazing endophyte-infected or endophyte-free fescue. Vet Immunol Immunopathol. 1997;59:285–91.

    Article  CAS  PubMed  Google Scholar 

  25. Koontz AF. Effects of Endophyte infected fescue alkaloid ingestion on energy metabolism, nitrogen balance, in situ feed degradation, and Ruminal passage rates. PHD Diss: University of Kentucky, Lexington; 2013.

    Google Scholar 

  26. Stowe H, Stowe HM, Miller M, Burns MG, Calcatera SM, Andrae JG, Aiken GE, Schrick FN, Cushing T, Bridges WC, Pratt SL. Effects of fescue toxicosis on bull growth, semen characteristics, and breeding soundness evaluation. J Anim Sci. 2013;91:3686–92.

    Article  CAS  PubMed  Google Scholar 

  27. Perrone RD, Madias NE, Levey AS. Serum creatinine as an index of renal function: new insights into old concepts. Clin Chem. 1992;38:1933–53.

    CAS  PubMed  Google Scholar 

  28. Yokus B, Cakir D, Kanay Z, Gulten T, Uysal E. Effects of seasonal and physiological variations on the serum chemistry, vitamins and thyroid hormone concentrations in sheep. J Vet Med Ser A. 2006;53:271–6.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors are highly appreciative to Prof. Ruijun Long for his valuable comments on the work, to Prof. Matthew Cory for polishing the English, and Mr. Yao Xiang for helping to format the manuscript.

Funding

This work was supported by the National Key Basic Research Program (973) of China (2014CB138702) and Natural Science Foundation of China (30070546, 31372366).

Availability of data and materials

All data generated or analysed during this study are included in this published article, and also available from the corresponding author on reasonable request.

Author information

Author notes

    Authors and Affiliations

    1. State Key Laboratory of Grassland and Agro-ecosystems, College of Pastoral Agriculture Science and Technology, Lanzhou University, Lanzhou, 730020, China

      Ying Liang, Hucheng Wang, Chunjie Li, Zhibiao Nan & Fadi Li

    2. Second Hospital of Lanzhou University, Lanzhou, 730000, China

      Ying Liang

    Authors
    1. Ying Liang
      View author publications

      You can also search for this author in PubMed Google Scholar

    2. Hucheng Wang
      View author publications

      You can also search for this author in PubMed Google Scholar

    3. Chunjie Li
      View author publications

      You can also search for this author in PubMed Google Scholar

    4. Zhibiao Nan
      View author publications

      You can also search for this author in PubMed Google Scholar

    5. Fadi Li
      View author publications

      You can also search for this author in PubMed Google Scholar

    Contributions

    YL conceived the study and its coordination; YL, HW and CL participated in the design of the study, contacted the collaborating laboratories, and interpreted data; YL and HW wrote the initial draft, and CL, ZN, FL revised the draft critically for intellectual content. All authors read and approved the final manuscript.

    Corresponding author

    Correspondence to Chunjie Li.

    Ethics declarations

    Ethics approval and consent to participate

    It is approved by the Animal Ethics Committee of Gansu Province, China.

    Consent for publication

    Not applicable.

    Competing interests

    The authors declare that they have no competing interests.

    Publisher’s Note

    Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

    Rights and permissions

    Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), 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 (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

    Reprints and permissions

    About this article

    Check for updates. Verify currency and authenticity via CrossMark

    Cite this article

    Liang, Y., Wang, H., Li, C. et al. Effects of feeding drunken horse grass infected with Epichloë gansuensis endophyte on animal performance, clinical symptoms and physiological parameters in sheep. BMC Vet Res 13, 223 (2017). https://doi.org/10.1186/s12917-017-1120-6

    Download citation

    • Received:

    • Accepted:

    • Published:

    • DOI: https://doi.org/10.1186/s12917-017-1120-6

    Keywords

    BMC Veterinary Research

    ISSN: 1746-6148

    Contact us