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Open Access Case report

Hypovitaminosis A coupled to secondary bacterial infection in beef cattle

Xiuyuan He1*, Yongtao Li2, Meng Li3, Guangmin Jia2, Haiju Dong1, Yanru Zhang1, Cong He1, Chuanqing Wang1, Lixin Deng1 and Yurong Yang1

Author Affiliations

1 College of Animal Science and Veterinary Medicine, Henan Agricultural University, Wenhua Road 95#, Zhengzhou, Henan, 450002, P.R. China

2 Unit of Animal Infectious Diseases, State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Shizishan Street1#, Hubei, Wuhan, 430070, P.R. China

3 College of Veterinary Medicine, South China Agricultural University, Wushan Street483#, Guangdong, Guangzhou, 510642, P.R. China

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BMC Veterinary Research 2012, 8:222  doi:10.1186/1746-6148-8-222


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1746-6148/8/222


Received:24 May 2012
Accepted:22 August 2012
Published:14 November 2012

© 2012 He et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Vitamin A is essential for normal growth, development, reproduction, cell proliferation, cell differentiation, immune function and vision. Hypovitaminosis A can lead to a series of pathological damage in animals. This report describes the case of hypovitaminosis A associated with secondary complications in calves.

Case presentation

From February to March in 2011, 2-and 3-month old beef calves presented with decreased eyesight, apparent blindness and persistent diarrhea occurred in a cattle farm of Hubei province, China. Based on history inspection and clinical observation, we made a tentative diagnosis of hypovitaminosis A. The disease was confirmed as a congenital vitamin A deficiency by determination of the concentrations of vitamin A in serum and feed samples. Furthermore, pathological and microbiological examination showed that the disease was associated with pathogenic Escherichia coli (E. coli) infection and mucosal barriers damage in intestines. The corresponding treatments were taken immediately, and the disease was finally under control for a month.

Conclusions

To our knowledge, this is the first report of hypovitaminosis A coupled to secondary infection of E. coli in beef cattle, advancing our knowledge of how vitamin A affects infection and immunity in animals. This study could also be contributed to scientific diagnosis and treatments of complex hypovitaminosis A in cattle.

Keywords:
Vitamin A; Hypovitaminosis A; Calves; E. coli

Background

Vitamin A is well known to be important for animal growth, development and various physiological processes, such as keeping the normal sight and bone function, especially in neonatal and growing animals [1]. Vitamin A is not synthesized by vertebrates and depends essentially onβ-carotene of green plants in dietary provision [2]. Since the discovery of vitamin A in 1920s, cases have been reported frequently about hypovitaminosis A in animals [3,4]. Many studies have showed that hypovitaminosis A can lead to a series of pathological damage, such as growth stunting, reproductive dysfunction, and low immunity, epithelial keratinization and degeneration, xerophthalmia and night blindness [5-7]. Researchers also demonstrated that vitamin A deficiency can be harmful for protein synthesis and maintenance of normal growth and metabolism, and decrease the body resistance to infection [8,9]. For grazing animals, vitamin A deficiency occurred easily in spring or winter when it lacks of green feed. To date, several investigations have been conducted on vitamin A deficiency in cattle [10-13]. In humans, there has been reported that vitamin A decreased during the acute phase response to bacterial infection [14]. However, the case of vitamin A deficiency in beef calves accompanied by bacterial infections has not yet been reported. In this study, we report on an investigation of vitamin A deficiency with E. coli infection in beef calves, a systematic diagnostic and effective treatment programs conducted on a beef cattle farm, which could be contributed to scientific prevention and control of vitamin A deficiency in cattle.

Case presentation

Case history

In Suizhou of Hubei Province, there is a beef cattle farm with a total of 553 cattle, including 144 cows, 66 pregnant cows, 59 calves and 284 finishing cattle. From February to March in 2011, the symptoms of elevated body temperature, loss of appetite and blurred vision were detected in 12 calves at the age of 2- to 3-month and 4 calves were total blind in April. The cows which produced calves last year could be found mainly lower abdomen edema with 10% morbidity, and 6 of 13 newborn calves appeared illness with 46% morbidity. The cattle diet included 0.5 to 1 kg concentrate feed (53% maize, 18% soybean meal and 29%wheat bran), 3.5 to 5 kg straw, and 15 kg (fresh weight) white lees, without any additives.

Clinical signs

The earliest changes of all affected calves were anorexia, slow growth and weakness. Though clinical signs of affected calves varied, the common presence included mild to severe ataxia, partial blindness or total blindness as judged by avoidance of obstacles, rumen distention and persistent diarrhoea. Even in bright sunlight, some affected calves also lost light reflex. There was also absence of the blink response or eye preservation reflex. Compared to normal cattle, all affected calves had significantly increased defecography and urination. Examination of the eye revealed a dilated and circular pupil in affected calf, but horizontal and oval one in the normal.

Ophtalmological examination

The affected cattle were restrained in six columns for fundus examination and photography. The changes of optic disc, retinal vessels, tapetum nigrum and tapetum lacidum were carefully checked, and the healthy calves were also exampled as control. In healthy calf, the surface of optic disc was flat, and the edge was clear and visible (Figure 1A). No edema, hemorrhage, exudation and disorder of pigment were found in retina (Figure 1B). However, ophthalmoscopic examination of the affected calves revealed that irregular pigmentation was present with varied sizes at local areas in the tapetum nigrum(Figure 1C) and tapetum lucidum (Figure 1D), and more obvious in the tapetum nigrum than in the tapetum lucidum. No other significant abnormality was found.

thumbnailFigure 1. Fundus examination of the healthy and affected calves. In healthy calf, the surface of optic disc is flat, and the edge is clear and visible (Figure 1A). No edema, hemorrhage, exudation and disorder of pigment were found in retina (Figure 1B). The irregular pigmentation was present with varied sizes at local areas in the tapetum nigrum (Figure 1C) and tapetum lucidum (Figure 1D), and more obvious in the tapetum nigrum than in the tapetum lucidum. The black arrow in the figure 1C means that pigmentation was present in the tapetum nigrum and that in the figure 1D means that pigmentation was present tapetum lucidum.

Determination of the content of vitamin A and aflatoxin B1

Through the history inspection and clinical signs, we suspected the disease might be related to vitamin A deficiency, then determined the vitamin A content using the High-performance liquid chromatography (HPLC) in milk and serum after sample preparation [15]. And we also randomly chose five pieces of feed samples and respectively measured the content of vitamin A according to national standard for measuring vitamin A in China. The limitation value of Vitamin A measured by this method in feed was 1000 IU/kg. Results showed that the average vitamin A content in the feed samples was far below the normal value (Table 1). Likewise, vitamin A was deficient in the milk of affected cows and in serums of affected calves [16]. In brief, we could conclude that the lack of Vitamin A in feed attributed to the low content in milk or serums (Table 1).

Table 1. Vitamin A concentration in different samples from clinically affected calves compared to reference values

Moreover, in the cattle farm of China, aflatoxin B1 is the most common aflatoxin and the necessary inspection item in feed. In order to verify whether the disease was related to aflatoxin poisoning, we also measured the aflatoxin B1 [17] and found that the concentration was 8.3 μg/kg in feed far less than the lowest poisoning dose of 100 μg/kg [18], indicating that the disease was not associated with aflatoxin B1 poisoning.

Microbiological examination

To obtain the possible bacteria related to the diarrhea in diseased cattle, tissue samples including liver, spleen, lymph nodes, intestine and lungs were prepared and inoculated on blood agar for 18–24 h at 37°C. Rectal swabs were directly inoculated on blood agar. The suspected colonies were picked for smearing, staining and microscopic examination and inoculated onto eosin methylene blue agar medium and MacConkey medium for identification cultivation. Meanwhile, homogenates were inoculated in nutrient broth medium, and cultured for 24 hours in a carbon dioxide incubator with 5% carbon dioxide. Bacterial isolation and identification test showed that bacteria could only be isolated from and rectal swabs and the bacterial isolates were Gram-negative, rod-shaped, slightly rounded at both ends, without mobility by microscopic examination [19]. When grown on ordinary plate, the single colony was neat in edge, centrally uplifted, smooth, transparent and colourless. Furthermore, basic biochemical identification tests showed that the bacteria could ferment a variety of carbohydrates to produce acid and gas, especially ferment lactose rapidly and about half of the bacteria could not breakdown sucrose. MR (Methyl Red) and indole test were positive, the VP (Vogues Proskauer) and citrate experiments were negative, in accordance to the general characteristics of E. coli (Table 2), which further suggested that the isolates were E. coli. In addition, serotyping was performed on all isolates with 25 prevalent E. coli antiserums in China and confirmed the presence of O8 serotype E. coli in rectal swabs. To determine the virulence of these O8 strains, the fifty percent mouse lethal dose (MLD50) titer of no.1 strain was determined by intraperitoneally inoculating six mice in each group with 50 μl of serial 10-fold dilutions E. coli. Results indicated that this strain displayed high pathogenic to mice and LD50 was 5.45 × 109 CFU (Table 3). For investigating the antibiotic susceptibility, the identified isolates were cultivated by streak plate method and the single colonies were picked for three continuous generations. The purified bacteria were inoculated on blood agar dish with 14 kinds of antibiotic discs incubated for 18 hours at 37°C. Results showed that the isolated strains are highly sensitive to amoxicillin, ciprofloxacin, gentamicin and other antibiotics (Table 4).

Table 2. Biochemical properties of the bacterial colonies isolated from intestine and rectal swabs of affected calves

Table 3. Pathological and microbiological findings from five affected calves

Table 4. The antibiotic sensitivity test of E. coli strains isolated from affected calves

Pathological examination

As mentioned above, it was intriguing to find that the affected calves manifested persistent diarrhoea. To exploit the pathological mechanism of diarrhoea, the intestines of healthy and affected calves were isolated and fixed by submerging them in 4% neutral buffered formalin and embedding them in paraffin. Three-micron sections were made before they were stained with hematoxylin and eosin (H&E). Images were obtained on an Olympus BX-50 light microscope at 5-fold original magnifications. Intestine tissues in lesion areas of affected calves showed intestinal capillary congestion, cell necrosis in smooth muscle and exfoliation of epithelial cells in mucosa (Figure 2A). Compared with the affected, the jejunum of the healthy calves showed normal epithelial cell in mucosa and submucosa (Figure 2B).

thumbnailFigure 2. The microscopic examination of jejunum in affected calves compared with the healthy jejunum. (A) Hematoxylin- and eosin-stained sections of jejunum from the healthy calves. Images were obtained on an Olympus BX-50 light microscope at 5-fold original magnifications. The jejunum of the healthy calves showed normal epithelial cell in mucosa and submucosa. (B) The microscopic lesions of jejunum tissues collected from affected calves showed intestinal capillary congestion (arrow a), cell necrosis in smooth muscle (arrow b) and exfoliation of epithelial cells in mucosa (arrow c).

Treatment

Considering the above clinical findings and experimental tests, we took the following measures to treat and control the disease. Firstly, to the affected calves, it is effective for controlling vitamin A deficiency through repeated intramuscular injections of vitamin A or continuous dietary supplementation. The affected cows and calves were intramuscularly administered by vitamins A for a month at the dose of 200000 IU once per day and 50000 IU respectively. Additionally, the severe affected cows and calf was orally treated respectively by 30 ml and 2 ml cod liver oil each day for a month. Secondly, antibacterial drugs, such as amoxicillin, ciprofloxacin and gentamicin were used to control secondary infection of E. coli. Last but not the least, calcium gluconate or glucose and mannitol were intravenously injected to alleviate cerebral edema and intracranial pressure, which contributes to reduce the neurological symptoms of the affected cattle. After one and a half months for treatment, most of mildly affected calves had a recovery of sight and the secondary E. coli infection was also effectively controlled. However, two calves with severe signs were totally blind in the end. In brief, the effect of corresponding treatments confirms also that the disease was attributed mainly to hypovitaminosis A.

Discussion

Vitamin A of grazing animals is totally dependent on exogenous supply. According to previous studies, the minimum requirement of vitamin A in cow is about 30 IU/kg each day, and the demand should be increased by 50% during lactation and pregnancy [13]. The long-term lack of dietary vitamin A or carotene in cow can easily result in hypovitaminosis A in newborn calves [11]. The rapid growth and development of calves need enough vitamin A, through liver storage and extra implements, mainly dependent on breast milk. However, in our current study, beef cattle were fed with rice straw and distillers’ grains for a long time, without green feed, carrots and other vitamin A-rich feed, which resulted in vitamin A deficiency in pregnant and lactation cows. Under normal circumstances, the content of vitamin A in the cattle feed should not be less than 400,000 IU/kg in order to ensure normal growth and development. However, the vitamin A content was 1360 IU/kg in feed of this farm. In the serums of affected calves, the average content of vitamin A was 130 IU/L at the late stage in this farm, far below the normal value [16], confirming this disease was related with vitamin A deficiency in calves.

The blindness disorders are regarded as the typical signs in affected calves of vitamin A deficiency [21,22]. The mechanisms of blindness due to vitamin A deficiency have been explored for many years. In terms of blindness or associated signs, fundus examination plays an important role in the quick diagnosis of hypovitaminosis A. At the early stage of hypovitaminosis A, papilledema is the first sign of changes in the optic disc and is reversible under the experimental conditions. The most representative characteristic, however, is pigmentation with various sizes and shapes on the tapetum nigrum of retina. In this study, no clear papilledema was found, which might be due to the delay of taking photos of fundus. However, the irregular pigmentation was found clearly with varied sizes at local areas in the tapetum nigrum and tapetum lucidum, especially in tapetum nigrum (Figure 1).

Vitamin A plays a significant role in immune system function of animals. In humans, it is well accepted that `vitamin A deficiency impairs innate immunity by impeding normal regeneration of mucosal barriers damaged by infection, and by diminishing the function of immune cells [23,24]. In the case of diarrheal diseases, vitamin A could promote regeneration of damaged mucosal epithelium and enhance the phagocytic activity of neutrophils and macrophages. It has also been shown that vitamin A can reduce the incidence and duration of diarrhea in children [25,26]. In this study, based on the clinical findings, his-pathological changes in intestines and vitamin A determinations, we could conclude that hypovitaminosis A impeded mucosal barriers of intestines and lowered the immunity of cattle which made the cattle more susceptible to E. coli, and the intractable diarrhea of cattle was likely attributed to both hypovitaminosis A and pathogenic E. coli infections, which was in accordance to previous studies [27,28]. Therefore, the corresponding treatment should include vitamin A supplement and antibacterial drugs utilization according the antibiotic susceptibility test. It is intriguing that Rumen distention was present in affected calves, whether it is due to hypovitaminosis A or E. coli infections remains further studies. Further research on E. coli isolates should be performed to identify genetic material encoding for specific virulence factors of E. coli and to demonstrate the effect of vitamin A deficiency on expression of innate immunity-related genes and development of immune cells in gastrointestinal tract of cattle [29].

Conclusions

This report describes a predominant case about hypovitaminosis A coupled to secondary E. coli infection in beef calves. Based on the clinical signs and experimental tests, corresponding measures were taken immediately to make vitamin A recovery at the normal level and to control E. coli infection in intestines of calves. Collectively, the findings provided insights into the important role of vitamin A in the immunity against microbiology infections of animals.

Consent

Orally informed consent was obtained from the owner of cattle farm for publication of this case report and any accompanying images.

Abbreviations

(VA): Vitamin A; (E. coli): Escherichia coli; (HPLC): High-Performance Liquid Chromatography; (MR): Methyl Red; (MLD50): Fifty percent mouse lethal dose.

Competing interests

There are non-financial competing interests in this study.

Authors’ contributions

XYH and YTL carried out all works and drafted the manuscript. ML, GMJ, HJD and LXD performed the clinical examination and the course of the case. YRY and YRZ performed the pathological examination. CH and CQW participated in microbiological test in the lab and helped to draft the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The authors would like to thank PhD. Li Yuan for her contribution to antibiotic test experiments, Yongqiang Cao for his help in clinical examination, and Pro. Yanxiu Liu and Wendy Barclay for critically reading the manuscript. The study was supported by National beef cattle industry research system (CARS-38).

References

  1. Clagett-Dame M, Knutson D: Vitamin A in reproduction and development.

    Nutrients 2011, 3(4):385-428. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  2. Oldham ER, Eberhart RJ, Muller LD: Effects of supplemental vitamin A or beta-carotene during the dry period and early lactation on udder health.

    J Dairy Sci 1991, 74(11):3775-3781. PubMed Abstract | Publisher Full Text OpenURL

  3. Booth A, Reid M, Clark T: Hypovitaminosis A in feedlot cattle.

    J Am Vet Med Assoc 1987, 190(10):1305-1308. PubMed Abstract OpenURL

  4. Carrigan MJ, Glastonbury JR, Evers JV: Hypovitaminosis A in pigs.

    Aust Vet J 1988, 65(5):158-160. PubMed Abstract | Publisher Full Text OpenURL

  5. De Risio L, Beltran E, de Stefani A, Holloway A, Matiasek K: Neurological dysfunction and caudal fossa overcrowding in a young cheetah with hypovitaminosis A.

    Vet Rec 2010, 167(14):534-536. PubMed Abstract | Publisher Full Text OpenURL

  6. Clagett-Dame M, DeLuca HF: The role of vitamin A in mammalian reproduction and embryonic development.

    Annu Rev Nutr 2002, 22:347-381. PubMed Abstract | Publisher Full Text OpenURL

  7. Gallina AM, Helmboldt CF, Frier HI, Nielsen SW, Eaton HD: Bone growth in the hypovitaminotic A calf.

    J Nutr 1970, 100(1):129-141. PubMed Abstract | Publisher Full Text OpenURL

  8. See AW, Kaiser ME, White JC, Clagett-Dame M: A nutritional model of late embryonic vitamin A deficiency produces defects in organogenesis at a high penetrance and reveals new roles for the vitamin in skeletal development.

    Dev Biol 2008, 316(2):171-190. PubMed Abstract | Publisher Full Text OpenURL

  9. Stephensen CB: Vitamin A, infection, and immune function.

    Annu Rev Nutr 2001, 21:167-192. PubMed Abstract | Publisher Full Text OpenURL

  10. Donkersgoed JV, Clark EG: Blindness caused by hypovitaminosis A in feedlot cattle.

    Can Vet J 1988, 29(11):925-927. PubMed Abstract | PubMed Central Full Text OpenURL

  11. Hill B, Holroyd R, Sullivan M: Clinical and pathological findings associated with congenital hypovitaminosis A in extensively grazed beef cattle.

    Aust Vet J 2009, 87(3):94-98. PubMed Abstract | Publisher Full Text OpenURL

  12. Millemann Y, Benoit-Valiergue H, Bonnin JP, Fontaine JJ, Maillard R: Ocular and cardiac malformations associated with maternal hypovitaminosis A in cattle.

    Vet Rec 2007, 160(13):441-443. PubMed Abstract | Publisher Full Text OpenURL

  13. Puvogel G, Baumrucker C, Blum JW: Plasma vitamin A status in calves fed colostrum from cows that were fed vitamin A during late pregnancy.

    J Anim Physiol Anim Nutr 2008, 92(5):614-620. Publisher Full Text OpenURL

  14. Stephensen CB, Gildengorin G: Serum retinol, the acute phase response, and the apparent misclassification of vitamin A status in the third National Health and Nutrition Examination Survey.

    Am J Clin Nutr 2000, 72(5):1170-1178. PubMed Abstract | Publisher Full Text OpenURL

  15. Suzuki J, Katoh N: A simple and cheap methods for measuring serum vitamin A in cattle using only a spectrophotometer.

    Nihon juigaku zasshi 1990, 52(6):1281-1283. PubMed Abstract | Publisher Full Text OpenURL

  16. Wang J: "Veterinary Internal Medicine (4th) Edition". Beijing: China Agricultural Press; 2010:178-181. OpenURL

  17. Stroka J, Petz M, Joerissen U, Anklam E: Investigation of various extractants for the analysis of aflatoxin B1 in different food and feed matrices.

    Food Addit Contam 1999, 16(8):331-338. PubMed Abstract | Publisher Full Text OpenURL

  18. Rasostits OM, Gay CC, Blood DC, Hinchcliff KW: Veterinary medicine. London: W.B. Saunders Co. Ltd; 2000:1684-1688. OpenURL

  19. Kaneene JB, Warnick LD, Bolin CA, Erskine RJ, May K, et al.: Changes in tetracycline susceptibility of enteric bacteria following switching to nonmedicated milk replacer for dairy calves.

    J Clin Microbiol 2008, 46(6):1968-1977. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  20. Hamilton MA, Russo RC: Trimmed Spearman-Karber method for estimating median lethal concentrations in toxicity bioassays.

    Environ Sci Technol 1977, 11(7):714-719. Publisher Full Text OpenURL

  21. Mason CS, Buxton D, Gartside JF: Congenital ocular abnormalities in calves associated with maternal hypovitaminosis A.

    Vet Rec 2003, 153(7):213-214. PubMed Abstract | Publisher Full Text OpenURL

  22. van der Lugt JJ, Prozesky L: The pathology of blindness in new-born calves caused by hypovitaminosis A.

    Onderstepoort J Vet Res 1989, 56(2):99-109. PubMed Abstract OpenURL

  23. Twining SS, Schulte DP, Wilson PM, Fish BL, Moulder JE: Vitamin A deficiency alters rat neutrophil function.

    J Nutr 1997, 127(4):558-565. PubMed Abstract | Publisher Full Text OpenURL

  24. Thurnham DI, Northrop-Clewes CA, McCullough FS, Das BS, Lunn PG: Innate immunity, gut integrity, and vitamin A in Gambian and Indian infants.

    J Infect Dis 2000, 182(Suppl 1):S23-S28. PubMed Abstract | Publisher Full Text OpenURL

  25. Sircar BK, Ghosh S, Sengupta PG, Gupta DN, Mondal SK, et al.: Impact of vitamin A supplementation to rural children on morbidity due to diarrhoea.

    Indian J Med Res 2001, 113:53-59. PubMed Abstract OpenURL

  26. Barreto ML, Santos LM, Assis AM, Araujo MP, Farenzena GG, Santos PA, Fiaccone RL: Effect of vitamin A supplementation on diarrhoea and acute lower-respiratory-tract infections in young children in Brazil.

    Lancet 1994, 344(8917):228-231. PubMed Abstract | Publisher Full Text OpenURL

  27. Yang Y, Yuan Y, Tao Y, Wang W: Effects of vitamin A deficiency on mucosal immunity and response to intestinal infection in rats.

    Nutrition 2011, 27(2):227-232. PubMed Abstract | Publisher Full Text OpenURL

  28. Friedman A, Meidovsky A, Leitner G, Sklan D: Decreased resistance and immune response to Escherichia coli infection in chicks with low or high intakes of vitamin A.

    J Nutr 1991, 121(3):395-400. PubMed Abstract | Publisher Full Text OpenURL

  29. Amit-Romach E, Uni Z, Cheled S, Berkovich Z, Reifen R: Bacterial population and innate immunity-related genes in rat gastrointestinal tract are altered by vitamin A-deficient diet.

    J Nutr Biochem 2009, 20(1):70-77. PubMed Abstract | Publisher Full Text OpenURL