Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 7
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

We measured the bone-specific alkaline phosphatase (ALP) isoenzyme activity in 67 plasma samples from 14 newborn Holstein calves using both a conventional method (featuring heat inactivation) and a commercial agarose gel electrophoresis (AGE) kit; the relevant isoenzymes were termed bone-specific ALP (BAP) and ALP isoenzyme 3 (ALP3). We explored whether the AGE kit afforded reliable data when used to analyze samples from Holstein calves. The blood was collected from the jugular vein of each calf immediately prior to the first colostrum feeding (pre-feeding), 20 and 40 h after pre-feeding, and on days 4 and 7; whereas three samples (from three calves) were not obtained. The total plasma ALP activity varied widely, exceeding the ranges of reference values. On electrophoresis, 52 of 67 plasma samples (77.6 %) clearly contained both ALP isoenzyme 2 and ALP3, as did control human serum. The total ALP activity of the 52 samples ranged from 166–1989 U/L (median: 1013 U/L), whereas the values for the other 15 samples (22.4%) exhibiting abnormal isoenzyme fractionation ranged from 1014–5118 U/L (median: 1780 U/L). In the 52 plasma samples exhibiting clearly separated isoenzymes, ALP3 and BAP activities were strongly positively correlated as revealed by Deming regression (y = 0.93x + 22.6, p<0.0001) and Bland-Altman analysis (ALP3/BAP activities limit of agreement: −5.1%). Thus, the AGE kit yields useful information on newborn calves, and can replace the conventional method when the total plasma ALP activity is less than approximately 1000 U/L.

Go to article

Authors and Affiliations

R. Onomi
K. Hatate
N. Yamagishi
Download PDF Download RIS Download Bibtex

Abstract

This study details the relationship between maternal plasma oxidant-antioxidant enzymes with colostrum quality, serum gamma glutamyl transferase (GGT), immunoglobulin G (IgG) and IgM concentrations of calves in the different calving seasons. Holstein breed cows between two and eight lactations and their calves were enrolled in the study. Holstein cows calving in winter (n=45) and their calves (n=45) were assigned to the winter group, while cows calving in summer (n=45) and their calves (n=45) were assigned to the summer group. Samples for malondialdehyde (MDA) and glutathione peroxidase (GSH-Px) were collected on day -21±3 before expected calving and also on calving day (Day 0). IgG and the specific gravity of the colostrum were determined after calving. Serum GGT and IgG and IgM were measured before the feeding, with colostrum, of calves (0 hours) and also in the 24th hour following the feeding of colostrum. Plasma MDA levels at -21±3 and 0 days in the summer cows were determined to be higher. GSH-Px activity was higher in the winter cows. IgG levels and the specific gravity of the colos- trum were also higher in the winter cows. Calf IgG levels at the 24th hour of life were higher in the winter cows. In the winter group, IgM levels at 0 and 24 hours were also higher. While MDA was negatively correlated with IgG, IgM, GGT, IgG and the specific gravity of colostrum, GSH-Px activity had a positive correlation with IgG, IgM, GGT, IgG and the specific gravity of colostrum. The observed differences in plasma MDA, GSH-Px, calf serum IgG and IgM levels, and colostrum quality between both groups suggest a possible seasonal effect. The relationship between maternal oxidant-antioxidant enzymes, colostrum quality, and passive calf immunity revealed that these enzymes could be used as indicators in the evaluation of calf health and colos- trum quality.
Go to article

Authors and Affiliations

H.E. Çolakoğlu
1
M.O. Yazlık
1
E.Ç. Çolakoğlu
2
U. Kaya
3
R. Bayramoğlu
4
S. Kurt
5
R. Vural
1
Ş. Küplülü
1

  1. Ankara University, Faculty of Veterinary Medicine, Department of Obstetrics and Gynecology, 06110, Ankara, Turkey
  2. Ankara University, Faculty of Veterinary Medicine, Department of Internal Medicine, 06110, Ankara, Turkey
  3. Hayat Mustafa Kamel University, Faculty of Veterinary Medicine, Department of Biostatistics, 31001, Hatay, Turkey
  4. Veterinary Practitioner, Farm Animal Managament Practicer, Western Thrace, Greece
  5. Dicle University, Faculty of Veterinary Medicine, Department of Obstetrics and Gynecology, 21200, Diyarbakır, Turkey
Download PDF Download RIS Download Bibtex

Abstract

Racecadotril, used as an antidiarrheal drug in humans and some animals such as the dog, inhibits peripheral enkephalinase, which degrades enkephalins and enkephalinase inhibition induces a selective increase in chloride absorption from the intestines. The study material consisted of 46 calves with infectious diarrhea and 14 healthy calves in the age 2-20 days. The calves were divided into eight groups; healthy calves (HG), healthy calves administered racecadotril (HRG), calves with E.coli-associated diarrhea (ECG), calves with E.coli-associated diarrhea administered racecadotril (ECRG), calves with bovine Rotavirus/Coronavirus-associated diarrhea (VG), calves with bovine Rotavirus/Coronavirus-associated diarrhea administered racecadotril (VRG), calves with C. parvum-associated diarrhea (CG) and calves with C. parvum-associated diarrhea administered racecadotril (CRG). Calves in the racecadotril groups received oral racecadotril at a dose of 2.5 mg/kg twice a day for 3 days. A routine clinical examination of all calves was performed. Hemogram and blood gas measurements were made from the blood samples. Standard diarrhea treatment was applied to the HG, ECG, CG, and VG groups. Clinical score parameters such as appetite, feces quality, dehydration, standing and death and some blood gas and hemogram parameters were evaluated to determine the clinical efficacy of racecadotril. Clinical score parameters were determined observationally. Blood gas measurements were performed using a blood gas analyzer. The hemogram was performed using an automated hematologic analyzer. Statistically significant differences were determined in the blood pH, bicarbonate, base deficit, lactate, and total leukocyte count in calves with diarrhea compared to healthy calves. After the treatments, these parameters were found to be within normal limits. At the end of treatment, 42 of the 46 diarrheal calves recovered, while 4 died. We found that racecadotril was effective in improving both clinical recovery and feces consistency in neonatal calves with diarrhea caused by E. coli. As a result, it can be stated that racecadotril, which has an antisecretory effect, is beneficial in the treatment of bacterial diarrhea caused by such as E. coli.
Go to article

Bibliography

1. Al Mawly J, Grinberg A, Prattley D, Moffat J, Marshall J, French N (2015) Risk factors for neonatal calf diarrhoea and enteropathogen shedding in New Zealand dairy farms. Vet J 203: 155-160.
2. Amaral-Phillips DM, Scharko PB, Johns JT, Franklin S (2006) Feeding and managing baby calves from birth to 3 months of age. Univ Kentucky Coop Ext Serv 1-6.
3. Aydogdu U, Yildiz R, Guzelbektes H, Naseri A, Akyuz E, Sen I (2018) Effect of combinations of intravenous small-volume hypertonic sodium chloride, acetate Ringer, sodium bicarbonate, and lactate Ringer solutions along with oral fluid on the treatment of calf diarrhea. Pol J Vet Sci 21: 273-280.
4. Berchtold J (2009) Treatment of calf diarrhea: intravenous fluid therapy. Vet Clin North Am Food Anim Pract 25: 73-99.
5. Bergmann JF, Chaussade S, Couturier D, Baumer P, Schwartz JC, Lecomte JM (1992) Effects of acetorphan, an antidiarrhoeal enkephalinase inhibitor, on oro‐caecal and colonic transit times in healthy volunteers. Aliment Pharmacol Ther 6: 305-313
6. Björkman C, Svensson C, Christensson B, De Verdier K (2003) Cryptosporidium parvum and Giardia intestinalis in calf diarrhoea in Sweden. Acta Vet Scand 44: 145-152.
7. Boranbayeva T, Karahan AG, Tulemissova Z, Myktybayeva R, Özkaya S (2020) Properties of a new probiotic candidate and lactobacte-rin-TK2 against diarrhea in calves. Probiotics Antimicrob 12: 918-928.
8. Constable PD (2009) Treatment of calf diarrhea: Antimicrobial and ancillary treatments. Vet Clin North Am Food Anim Pract 25: 101-120.
9. Constable PD, Hinchcliff KW, Done SH, Grünberg, W (2016) Veterinary medicine: a textbook of the diseases of cattle, horses, sheep, pigs and goats. 11 th ed., Elsevier Health Sciences, St. Louis, pp:113-137.
10. Coskun A, Sen I, Guzelbektes H, Ok M, Turgut K, Canikli S (2010) Comparison of the effects of intravenous administration of isotonic and hypertonic sodium bicarbonate solutions on venous acid-base status in dehydrated calves with strong ion acidosis. J Am Vet Med 236: 1098-1103.
11. CVMP (2020) List of nationally authorised medicinal products Active substance: racecadotril. EMA/646224/2020.https://www.ema.europa.eu/en/documents/psusa/racecadotrillist-nationally-authorised-medicinal-products-psusa/ 00002602/202003_en.pdf
12. Duval‐Iflah Y, Berard, H, Baumer P, Guillaume P, Raibaud P, Joulin Y, Lecomte JM (1999) Effects of racecadotril and loperamide on bacterial proliferation and on the central nervous system of the newborn gnotobiotic piglet. Aliment Pharmacol Ther 6: 9-14.
13. Eberlin M, Mück T, Michel MC (2012) A comprehensive review of the pharmacodynamics, pharmacokinetics, and clinical effects of the neutral endopeptidase inhibitor racecadotril. Front Pharmacol 3: 93
14. Field M (2003) Intestinal ion transport and the pathophysiology of diarrhea. J Clin Invest 111: 931-943.
15. Fischbach W, Andresen V, Eberlin M, Mueck T, Layer P (2016) A comprehensive comparison of the efficacy and tolerability of racecadotril with other treatments of acute diarrhea in adults. Front Med (Lausanne) 14: 44.
16. Gibbons JF, Boland F, Buckley JF, Butler F, Egan J, Fanning S, Markey BK, Leonard FC (2014) Patterns of antimicrobioal resistance in pathogenic Escherichia coli isolates from cases of calf enteritis during the spring-calves season. Vet Microbiol 170: 73-80.
17. Hinterleitner TA, Petritsch W, Dimsity G, Berard H, Lecomte JM, Krejs GJ (1997) Acetorphan prevents cholera-toxin-induced water and electrolyte secretion in the human jejunum. Eur J Gastroenterol Hepatol 9: 887-891.
18. Hodges K, Gill R (2010) Infectious diarrhea: cellular and molecular mechanisms. Gut Microbes 1: 4-21.
19. Katsoulos PD, Karatzia MA, Dovas CI, Filioussis G, Papadopoulos E, Kiossis E, Arsenopoulos K, Papadopoulos T, Boscos C, Karatzias H (2017) Evaluation of the In-Field Efficacy of Oregano Essential Oil Administration on the Control of Neonatal Diarrhea Syndrome in Calves. Res Vet Sci 115: 478–483.
20. Kumar B, Shekhar P, Kumar N (2010) A clinical study on neonatal calf diarrhoea. Intas Polivet 11: 233-235.
21. Lecomte JM (2000) An overview of clinical studies with racecadotril in adults. Int J Antimicrob Agents 14: 81-87.
22. Malik YS, Kumar N, Sharma K, Sharma R, Kumar HB, Anupamlal K, Kumari S, Shukla S, Chandrahekar KM (2013) Epidemiology and genetic diversity of rotavirus strains associated with acute gastroenteritis in bovine, porcine, poultry and human population of Madhya Pradesh, Central India, 2004–2008. Adv Anim Vet Sci 1: 111-115.
23. Matheson AJ, Noble S (2000) Racecadotril. Drugs 59: 829-835.
24. McGuirk SM (2008) Disease management of dairy calves and heifers. Vet Clin North Am Food Anim Pract 24: 139-153.
25. Megeed KN, Hammam AM, Morsy GH, Khalil FA, Seliem MM, Aboelsoued D (2015) Control of cryptosporidiosis in buffalo calves using garlic (Allium sativum) and nitazoxanide with special reference to some biochemical parameters. Glob Vet 14: 646-655.
26. Muheet AT, Ashraf I, Chhibber S, Soodan JS, Singh R, Muhee A, Nazim K, Majeed A (2018) The use of racecadotril as an effective adjunct therapeutic measure in the management of diarrhea. Pharma innov 7: 610-612.
27. Naylor JM (2009) Neonatal Calf Diarrhea. Food Anim Pract 2009 : 70-77.
28. Ok M, Guler L, Turgut K, Ok U, Sen I, Gunduz IK, Birdane MF, Güzelbektes H (2009) The studies on the aetiology of diarrhoea in neonatal calves and determination of virulence gene markers of Escherichia coli strains by multiplex PCR. Zoonoses Public Health 56: 94-101.
29. Ok M, Sevinc F, Ider M, Ceylan O, Erturk A, Ceylan C, Durgut, MK (2021) Evaluation of clinical efficacy of gamithromycin in the treatment of naturally infected neonatal calves with cryptosporidiosis. Eurasian J Vet Sci 37: 49-54.
30. Ok M, Yildiz R, Hatipoglu F, Baspinar N, Ider M, Üney K, Ertürk A, Durgut MK, Terzi F (2020) Use of intestine-related biomarkers for detecting intestinal epithelial damage in neonatal calves with diarrhea. Am J Vet Res 81: 139-146.
31. Primi MP, Bueno L, Baumer P, Berard H, Lecomte JM (1999) Racecadotril demonstrates intestinal antisecretory activity in vivo. Aliment Pharmacol Ther 6: 3-7.
32. Rachmilewitz D, Karmeli F, Chorev M, Selinger Z (1983) Effect of opiates on human colonic adenylate cyclase activity. Eur J Pharmacol 93: 169-173.
33. Renaud DL, Buss L, Wilms JN, Steele MA (2020) Technical note: Is fecal consistency scoring an accurate measure of fecal dry matter in dairy calves? J Dairy Sci 103: 10709-10714.
34. Renaud DL, Kelton DF, Weese JS, Noble C, Duffield TF (2019) Evaluation of a Multispecies Probiotic as a Supportive Treatment for Diarrhea in Dairy Calves: A Randomized Clinical Trial. J Dairy Sci 102: 4498-4505.
35. Schwartz JC (2000) Racecadotril: a new approach to the treatment of diarrhoea. Int J Antimicrob Agents 14: 75-79.
36. Sen I, Altunok V, Ok M, Coskun A, Constable PD (2009) Efficacy of oral rehydration therapy solutions containing sodium bicarbonate or sodium acetate for treatment of calves with naturally acquired diarrhea, moderate dehydration, and strong ion acidosis. J Am Vet Med Assoc 234: 926-934.
37. Sen I, Guzelbektes H, Yildiz R (2013) Neonatal Calf Diarrhea: Pathophysiology, Epidemiology, Clinic, Treatment and Prevention. Turkiye Klinikleri J Vet Sci 4: 71-8.
38. Singh N, Narayan S (2008) Racecadotril: A novel antidiarrheal. Med J. Armed Forces India 64: 361-362.
39. Smith GW, Berchtold J (2014) Fluid therapy in calves. Vet Clin North Am Food Anim Pract 30: 409-427.
40. Trefz FM, Constable PD, Lorenz I (2015) Quantitative physicochemical analysis of acid‐base balance and clinical utility of anion gap and strong ion gap in 806 neonatal calves with diarrhea. J Vet Intern Med 29: 678-687.
41. Trefz FM, Lorenz I, Lorch A, Constable PD (2017) Clinical signs, profound acidemia, hypoglycemia, and hypernatremia are predictive of mortality in 1,400 critically ill neonatal calves with diarrhea. PLoS One 12: e0182938.
42. Tsukano K, Kato S, Sarashina S, Abe I, Ajito T, Ohtsuka H, Suzuki K (2017) Effect of acetate Ringer’s solution with or without 5% dextrose administered intravenously to diarrheic calves. J Vet Med Sci 79: 795-800.
43. Tsunemitsu H, Smith DR, Saif LJ (1999) Experimental inoculation of adult dairy cows with bovine coronavirus and detection of coronavirus in feces by RT-PCR. Arch Virol 144: 167-175.
44. Turgut K, Ok M (1997) Veteriner Gastroenteroloji. 1st ed., Bahcıvanlar Basımevi, Konya, pp 362-383.
45. Urie NJ, Lombard JE, Shivley CB, Kopral CA, Adams AE, Earleywine TJ, Olson JD, Garry FB (2018) Preweaned Heifer Management on US Dairy Operations: Part V. Factors Associated with Morbidity and Mortality in Preweaned Dairy Heifer Calves. J Dairy Sci 101: 9229-9244.
46. WHO (2007) World Health Organization. Proposal for the inclusion of racecadotril in the WHO model list of essential medicines. WHO Essential medicines list for children: Racecadotril. Paris, France, p 23.
Go to article

Authors and Affiliations

B. Tras
1
M. Ok
2
M. Ider
2
T.M. Parlak
1
R. Yildiz
3
H. Eser Faki
1
Z. Ozdemir Kutahya
4
K. Uney
1

  1. Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Selcuk, Ardicli Neighborhood, 42100, Konya, Turkey
  2. Department of Internal Medicine, Faculty of Veterinary Medicine, University of Selcuk, Ardicli Neighborhood, 42100, Konya, Turkey
  3. Department of Internal Medicine, Faculty of Veterinary Medicine, University of Mehmet Akif Ersoy, Yakakoy, 15030, Burdur, Turkey
  4. Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, University of Cukurova, Fatih Sultan Mehmet Avenue, 01930, Adana, Turkey
Download PDF Download RIS Download Bibtex

Abstract

Calf diarrhea continues to be the major problem of calves in the neonatal period. The effect of zeolites has been increasingly studied in ruminant health in recent years. In the present study, the efficacy of cristobalite, a zeolite, in neonatal calf diarrhea was studied first time. For this purpose, twenty-five neonatal calves with diarrheas were divided into two groups, and Group 1 (n=12) received conventional treatment and Group 2 (n=13) received cristobalite (Zoosorb 10 mg/kg) orally 3 times a day in addition to conventional treatment. Escherichia coli k99 and CS31a, bovine rotavirus and bovine coronavirus were isolated from fecal samples at the beginning of the treatment, on the third day and before discharge. It was determined that the recovery period in Group 2 was 0.95 (20.6%) days shorter than in Group 1 (p<0.05) while no viral agents were found on the fifth day in Group 2, viral shedding continued in 4 of 5 calves in Group 1. In conclusion, the study revealed that cristobalite speeds the recovery time and possibly decreases viral shedding in neonatal calf diarrhea, demonstrating a remarkable efficiency in the treatment.
Go to article

Authors and Affiliations

U. Ozcan
1
M.G. Sezener
2
B.U. Sayilkan
1
E. Kulluk
1
A. Akman
3
H. Cetiner
1
V.E. Erguden
2
S. Yaman
2
S. Gumusova
4
A. Ciftci
2
Y. Meral
1
D. Dalgın
1

  1. Department of Internal Medicine, Faculty of Veterinary Medicine, Ondokuz Mayis University, TR-55200, Samsun, Turkey
  2. Department of Microbiology, Faculty of Veterinary Medicine, Ondokuz Mayis University, TR-55200, Samsun, Turkey
  3. Samsun Veterinary Control Institute, TR-55200, Samsun, Turkey
  4. Department of Virology, Faculty of Veterinary Medicine,Ondokuz Mayis University, TR-55200, Samsun, Turkey
Download PDF Download RIS Download Bibtex

Abstract

Blastocystis spp. is a parasite that causes intestinal infection in humans and other animals. A few studies have been performed in Turkey on the distribution of Blastocystis in cattle. In this study, fecal samples were collected from 100 calves and subjected to analysis based on an SSU rRNA gene fragment. The overall prevalence of the disease was determined as 15% (15/100). This rate was 14.04% for females and 16.28% for males. In addition, three Blastocystis subtypes were identified: ST10, ST14, and novel subtypes ST25. To our knowledge, the ST25 subtype was reported with this study for the first time in Turkey. The nucleotide sequences (OM920832-OM920839) obtained in this study were deposited in GenBank. The results obtained will be useful for a better understanding of the epidemiology of Blastocystis spp., and its effects on public health.
Go to article

Authors and Affiliations

B. Aslan Çelik
1

  1. Department of Parasitology, Faculty of Veterinary Medicine, Siirt University, Siirt, Turkey
Download PDF Download RIS Download Bibtex

Abstract

Neonatal calf diarrhea (NCD) is one of the most important concerns in cattle production. Escherichia coli is the most important bacterial agent of NCD. Although vaccination and antibiotic treatment are common in NCD, the high antigenic diversity of E. coli and the increase in antibiotic resistance cause difficulties in the control. The study aimed to investigate the rate of E. coli in calf diarrhea, isolate an agent of the NCD E. coli strain, determine antimicrobial resistance, and find out about some surface antigens. Fecal samples (n=115) were analyzed to isolate pathogenic E. coli strains with nine mixed infections; sixty-one strains isolate from fifty diarrhoeic calves. Among the isolates from diseased animals, 22 K99+STa+F41, 3 K99+STa, 3 strains F41, 2 strains Stx1, one strain K99, one strain eae, and one strain Stx2+eae were detected. 27 strains of F17- associated fimbriae have been identified. 17 strains F17a, 6 strains F111, 3 strains F17c, one strain carrying the F17a and F17c gene regions, whereas subfamily typing of one strain could not be performed. Serotypes were determined by molecular and serological methods: 32/61 (52.5%) isolates were O101 and 2/61 (3.3%) isolates were O9 serotypes. But 27 strain serotypes could not be detected. The antibiotic resistance profiles of the isolates were determined by the disc diffusion method. The resistance rates to antibiotics were trimethoprim- sulphamethoxazole 91.7%, ampicillin 86.7%, enrofloxacin 86.7%, gentamicin 45%, tobramycin 41.7%, cefotaxime 3.3%, and ceftazidime 1.7%. Due to increasing antibiotic resistance, prophylaxis is gaining importance. In further research, E. coli surface antigenic structures should be examined in detail, and it should form the basis for vaccine and hyperimmunization studies to be developed.
Go to article

Bibliography

  1. Algammal AM, El-Kholy AW, Riad EM, Mohamed HE, Elhaig MM, Yousef SaA, Hozzein WN, Ghobashy MOI (2020) Genes Encoding the Virulence and the Antimicrobial Resistance in Enterotoxigenic and Shiga-Toxigenic E. coli Isolated from Diarrheic Calves. Toxins 12: 383.
  2. Andersson DI, Hughes D (2011) Persistence of antibiotic resistance in bacterial populations. FEMS Microbiol Rev 35: 901-911.
  3. Bendali F, Bichet H, Schelcher F, Sanaa M (1999) Pattern of diarrhoea in newborn beef calves in south-west France. Vet Res 30: 61-74.
  4. Bertin Y, Martin C, Oswald E, Girardeau J-P (1996) Rapid and specific detection of F17-related pilin and adhesin genes in diarrheic and septicemic Escherichia coli strains by multiplex PCR. J Clinic Microbiol 34: 2921-2928.
  5. Bielaszewska M, Schmidt H, Liesegang A, Prager R, Rabsch W, TschäPe H, Cízek A, Janda J, Bláhová K, Karch H (2000) Cattle can be a reservoir of sorbitol-fermenting Shiga toxin-producing Escherichia coli O157: H− strains and a source of human diseases. J Clin Microbiol 38: 3470-3473.
  6. Boucher HW, Talbot GH, Bradley JS, Edwards JE, Gilbert D, Rice LB, Scheld M, Spellberg B, Bartlett J (2009) Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America. Clin Infect Dis 48: 1-12.
  7. Caffarena RD, Casaux ML, Schild CO, Fraga M, Castells M, Colina R, Maya L, Corbellini LG, Riet-Correa F, Giannitti F (2021) Causes of neonatal calf diarrhea and mortality in pasture-based dairy herds in Uruguay: a farm-matched case-control study. Braz J Microbiol 52: 977-988.
  8. Cengiz S, Adiguzel MC (2020) Determination of virulence factors and antimicrobial resistance of E. coli isolated from calf diarrhea, part of eastern Turkey. Ankara Univ Vet Fak Derg 67: 365-371.
  9. Cho YI, Yoon KJ (2014) An overview of calf diarrhea - infectious etiology, diagnosis, and intervention. J Vet Sci 15: 1-17.
  10. Coura FM, Freitas MD, Ribeiro J, De Leme RA, De Souza C, Alfieri AA, Facury Filho EJ, De Carvalho AU, Silva MX, Lage AP, Heinemann MB (2015) Longitudinal study of Salmonella spp., diarrheagenic Escherichia coli, Rotavirus, and Coronavirus isolated from healthy and diarrheic calves in a Brazilian dairy herd. Trop Anim Health Prod 47: 3-11.
  11. Debroy C, Maddox C (2001) Identification of virulence attributes of gastrointestinal Escherichia coli isolates of veterinary significanc. Anim Health Res Rev 1: 12.
  12. Donovan GA, Dohoo R, Montgomery DM, Bennett FL (1998) Calf and disease factors affecting growth in female Holstein calves in Florida, USA. Prev Vet Med 33: 10.
  13. Dubreuil JD, Isaacson RE, Schifferli DM (2016) Animal Enterotoxigenic Escherichia coli. EcoSal Plus 7: 47.
  14. Fidock DA, Mcnicholas PA, Lehrbach PR (1989) Nucleotide sequence of the F41 fimbriae subunit gene in Escherichia coli B41. Nucleic Acids Res 17: 2849.
  15. Foster DM, Smith GW (2009) Pathophysiology of diarrhea in calves. Vet Clin North Am Food Anim Pract 25: 13-36, xi.
  16. Franck SM, Bosworth BT, Moon HW (1998) Multiplex PCR for enterotoxigenic, attaching and effacing, and Shiga toxin-producing Escherichia coli strains from calves. J Clini Microbiol 36: 1795-1797.
  17. Guler L, Gunduz K, Ok U (2008) Virulence factors and antimicrobial susceptibility of Escherichia coli isolated from calves in Turkey. Zoonoses Public Health 55: 249-257.
  18. Gulliksen SM, Lie KI, Loken T, Osteras O (2009) Calf mortality in Norwegian dairy herds. J Dairy Sci 92: 2782-2795.
  19. Hang BPT, Wredle E, Börjesson S, Sjaunja KS, Dicksved J, Duse A (2019) High level of multidrug-resistant Escherichia coli in young dairy calves in southern Vietnam. Trop Anim Health Prod 51: 1405-1411.
  20. Hur T-Y, Jung Y-H, Choe C-Y, Cho Y-I, Kang S-J, Lee H-J, Ki K-S, Baek K-S, Suh G-H (2013) The dairy calf mortality: the causes of calf death during ten years at a large dairy farm in Korea. Korean J Vet Res 53: 103-108.
  21. Iguchi A, Iyoda S, Seto K, Morita-Ishihara T, Scheutz F, Ohnishi M (2015) Escherichia coli O-genotyping PCR: a comprehensive and practical platform for molecular O serogrouping. J Clini Microbiol 53: 2427-2432.
  22. Jerse AE, Yu J, Tall BD, Kaper JB (1990) A genetic locus of enteropathogenic Escherichia coli necessary for the production of attaching and effacing lesions on tissue culture cells. Proc Nat Acad Sci 87: 7839-7843.
  23. Mohammed S, Marouf S, Erfana AM, El JK, Hessain AM, Dawoud TM, Kabli SA, Moussa IM (2019) Risk factors associated with E. coli causing neonatal calf diarrhea. Saudi J Bio Sci 26: 1084-1088.
  24. Paton AW, Beutin L, Paton JC (1995) Heterogeneity of the amino-acid sequences of Escherichia coli Shiga-like toxin type-I operons. Gene 153: 71-74.
  25. Paton AW, Paton JC, Manning PA (1993) Polymerase chain reaction amplification, cloning and sequencing of variant Escherichia coli Shiga-like toxin type II operons. Microb Pathog 15: 77-82.
  26. Pervez A, Anjum FR, Bukhari AA, Anam S, S. R, Arshad MI (2018) Isolation and virulence genes characterization of diarrheagenic Escherichia coli from calves. Pak Vet J 38: 5.
  27. Prieto A, Lopez-Novo C, Diaz P, Diaz-Cao JM, Lopez-Lorenzo G, Anton C, Remesar S, Garcia-Dios D, Lopez C, Panadero R, Diez-Banos P, Morrondo P, Fernandez G (2022) Antimicrobial susceptibility of enterotoxigenic Escherichia coli from diarrhoeic neonatal calves in Spain. Animals (Basel) 12: 12.
  28. Roosendaal B, Gaastra W, De Graaf FK (1984) The nucleotide sequence of the gene encoding the K99 subunit of enterotoxigenic Escherichia coli. FEMS Microbiol Lett 22: 253-258.
  29. Sekizaki T, Akashi H, Terakado N (1985) Nucleotide sequences of the genes for Escherichia coli heat-stable enterotoxin I of bovine, avian, and porcine origins. Am J Vet Res 46: 909-912.
  30. Shahrani M, Dehkordi FS, Momtaz H (2014) Characterization of Escherichia coli virulence genes, pathotypes and antibiotic resistance properties in diarrheic calves in Iran. Biol Res 47: 13.
  31. Smith DR (2012) Field disease diagnostic investigation of neonatal calf diarrhea. Vet Clin North Am Food Anim Pract 28: 465-481.
  32. Thiry D, Saulmont M, Takaki S, De Rauw K, Duprez J-N, Iguchi A, Piérard D, Mainil JG (2017) Enteropathogenic Escherichia coli O80: H2 in young calves with diarrhea, Belgium. Emerg Infect Dis 23: 3.
  33. To S (1984) F41 antigen among porcine enterotoxigenic Escherichia coli strains lacking K88, K99, and 987P pili. Infect Immun 43: 549-554.
  34. Umpiérrez A, Acquistapace S, Fernández S, Oliver M, Acuña P, Reolón E, Zunino P (2016) Prevalence of Escherichia coli adhesion-related genes in neonatal calf diarrhea in Uruguay. J Infect Dev Ctries 10: 472-477.
  35. Usda (2008) Dairy 2007, Part II: Changes in the U.S. Dairy Cattle Industry, 1991–2007. Fort Collins, CO: 57-60.
  36. Van Boeckel TP, Glennon EE, Chen D, Gilbert M, Robinson TP, Grenfell BT, Levin SA, Bonhoeffer S, Laxminarayan R (2017) Reducing antimicrobial use in food animals. Science 357: 1350-1352.
  37. Wani S, Bhat M, Samanta I, Nishikawa Y, Buchh A (2003) Isolation and characterization of Shiga toxin‐producing Escherichia coli (STEC) and enteropathogenic Escherichia coli (EPEC) from calves and lambs with diarrhoea in India. Lett Appl Microbiol 37: 121-126.
  38. Yu J, Kaper JB (1992) Cloning and characterization of the eae gene of enterohaemorrhagic Escherichia coli O157: H7. Mol Microbiol 6: 411-417.
  39. Yuyama Y, Yoshimatsu K, Ono E, Saito M, Naiki M (1993) Postnatal change of pig intestinal ganglioside bound by Escherichia coli with K 99 fimbriae. J Biochem 113: 488-492.
Go to article

Authors and Affiliations

M.R. Coşkun
1
M. Şahin
2

  1. Department of Microbiology, Faculty of Veterinary Medicine, Kafkas University, 36100, Kars, Turkey
  2. Department of Microbiology, Faculty of Veterinary Medicine, Kyrgyz-Turkish Manas University, 720038, Bishkek, Kyrgyzstan
Download PDF Download RIS Download Bibtex

Abstract

Diarrhea caused by parasitic agents is common in neonatal calves and leads to significant economic losses in cattle farms worldwide. Cryptosporidium spp. is one of the most frequently detected parasitic agents causing diarrhea in neonatal calves. The aim of this study was to investigate the presence of Cryptosporidium spp. on a dairy farm which a has major diarrhea problem. Samples were collected from calves, cows, drinking bowls, and two different artesian water sources, as well as from the environment. All fecal samples were investigated using Kinyoun acid-fast stained slides and real-time PCR targeting the Cryptosporidium spp. COWP gene. In addition, species identification was performed by nested PCR targeting the Cryptosporidium spp. COWP gene and sequencing. Cryptosporidium spp. was detected in 11 calves (30.55%; 11/36) by real-time PCR and the cows were negative. Among real-time PCR positive samples, only five were also found positive by microscopy. Moreover, Cryptosporidium spp. was found in one of the two artesian water sources and five environmental samples by real-time PCR. Among these positive samples, eight were sequenced. According to the RFLP pattern, BLAST and, phylogenetic analyses, all sequenced samples were Cryptosporidium parvum. These findings show the importance of C. parvum as a cause of calf diarrhea on dairy farms.
Go to article

Bibliography


Arslan MÖ, Sarı B, Kara M, Taşçı GT, İtik Ekinci A, Gündüz N (2012) Research on the Prevalence of Eimeria and Cryptosporidium Species in Cows in Periparturient Period in Kars Region. Kafkas Univ Vet Fak Derg 18: 65-70.
Ayinmode AB, Fagbemi BO (2010) Prevalence of Crypto-sporidium infection in cattle from south western Nigeria. Vet Arh 80: 723-731.
Burgu A (1984) Preliminary studies on the occurrence of Cryptosporidia in calves in Turkey. Ankara Üniv Vet Fak Derg 3: 573-585. Cole DJ (1997) Detection of Cryptosporidium parvum using the Kinyoun acid-fast stain. Proc Annu Conv AAEP 43: 409-410.
Doungmala P, Phuektes P, Taweenan W, Sangmaneedet S, Japa O (2019) Prevalence and species identification of Cryptosporidium spp. In the newborn dairy calves from Muang District, Khon Kaen Province, Thailand. Vet World 12: 1454-1459.
Döşkaya M, Caner A, Deǧirmenci A, Wengenack NL, Yolasığmaz A, Turgay T, Özensoy Töz S, Gürüz Y (2011) Degree and frequency of inhibition in a routine realtime PCR detecting Pneumocystis jirovecii for the diagnosis of Pneumocystis pneumonia in Turkey. J Med Microbiol 60: 937-944.
Elmi T, Gholami S, Rahimi-Esboei B, Garaili Z, Najm M, Tabatabaie F (2017) Comparison of sensitivity of sucrose gradient, Wet mount and formalin-ether in detecting protozoan Giardia lamblia in stool specimens of BALB/c mice. J Pure Appl Microbiol 11: 105-109.
Fayer R, Santín M, Macarisin D (2010) Cryptosporidium ubiquitum n. sp. in animals and humans. Vet Parasitol 172: 23-32.
Guy RA, Payment P, Krull UJ, Horgen PA (2003) R Real-time PCR for quantification of Giardia and Cryptosporidium in environmental water samples and sewage. Appl Environ Microbiol 69(9): 5178-85.
Hamnes IS, Gjerde B, Robertson L (2006) Prevalence of Giardia and Cryptosporidium in dairy calves in three areas of Norway. Vet Parasitol 140: 204-216.
Hatam-Nahavandi K, Ahmadpour E, Carmena D, Spotin A, Bangoura B, Xiao L (2019) Cryptosporidium infections in terrestrial ungulates with focus on livestock: A syste- matic review and meta-analysis. Parasit Vectors 12: 1-23.
Ibrahim HS, Shehab AY, Allam AF, Mohamed MA, Farag HF, Tolba NM (2020) Detection and Molecular Identification of Cryptosporidium Species Among Children with Malignancies. Acta Parasitol. 66 (2): 377-383.
Karakavuk M, Aldemir D, Mercier A, Atalay E, Can H, Murat JB, Döndüren Ö, Can Ş, Özdemir HG, Değirmenci Döşkaya A, Pektaş B, Darde ML, Gürüz AG, Döşkaya M (2018) Prevalence of toxoplasmosis and genetic characterization of Toxoplasma gondii strains isolated in wild birds of prey and their relation with previously isolated strains from Turkey. PLoS One 13: 1-17.
Karakavuk M, Can H, Selim N, Yeşilsiraz B, Atlı E, Atalay E, Demir F, Gül A, Özdemir HG, Alan N, Yalçın M, Özkurt O, Aras M, Çelik T, Can Ş, Değirmenci Döşkaya A, Gürüz AG, Döşkaya M (2021) Investigation of the role of stray cats for transmission of toxoplasmosis to humans and animals living in Izmir, Turkey. J Infect Dev Ctries 15: 155-162.
Kehl KS, Cicirello H, Havens PL (1995) Comparison of four different methods for detection of Cryptosporidium species. J Clin Microbiol 33: 416-418.
Morgan UM, Pallant L, Dwyer BW, Rich G, Thompson RC (1998) Comparison of PCR and microscopy for detection of Cryptosporidium parvum in human fecal specimens: Clinical trial. J Clin Microbiol 36: 995-998.
Muthusamy D, Rao SS, Ramani S, Monica B, Banerjee I, Abraham OC, Mathai DC, Primrose B, Muliyil J, Wanke CA, Ward HD, Kang G (2006) Multilocus genotyping of Cryptosporidium sp. isolates from human immunodeficiency virus-infected individuals in South India. J Clin Microbiol 44: 632-634.
Naciri M, Lefay M, Mancassola R, Poirier P, Chermette R (1999) Role of Cryptosporidium parvum as a pathogen in neonatal diarrhoea com-plex in suckling and dairy calves in France. Vet Parasitol 85: 245-257.
Ng J, Yang R, McCarthy S, Gordon C, Hijjawi N, Ryan U (2011) Molecular characterization of Cryptosporidium and Giardia in pre-weaned calves in Western Australia and New South Wales. Vet Parasitol 176: 145-150.
O’Handley RM (2007) Cryptosporidium parvum infection in cattle: are current perceptions accurate? Trends Parasitol 23: 477-480.
Paul S, Chandra D, Ray DD, Tewari AK, Rao JR, Banerjee PS, Baidya S, Raina OK (2008) Prevalence and molecular characterization of bovine Cryptosporidium isolates in India. Vet Parasitol 153: 143-146.
Pedraza-Díaz S, Amar C, Nichols GL, McLauchlin J (2001) Nested polymerase chain reaction for amplification of the Cryptosporidium oo-cyst wall protein gene. Emerg Infect Dis 7: 49-56.
Pilarczyk B, Kołodziejczyk L, Zaja̧czkowska K, Kuźna Grygıel W, Balıcka-Ramısz A, Tomza-Marcınıak A, Pılarczyk R(2009) Prevalence of Eimeria and Crypto- sporidium sp. protozoa in polish cows and in cows imported from the Netherlands as in-calf heifers. Bull Vet Inst Pulawy 53: 637-640.
Ralston BJ, McAllister TA, Olson ME (2003) Prevalence and infection pattern of naturally acquired giardiasis and cryptosporidiosis in range beef calves and their dams. Vet Parasitol 114: 113-122.
Robertson L, Gjerde B, Hansen EF, Stachurska-Hagen T (2009) A water contamination incident in Oslo, Norway during October 2007; a basis for discussion of boil-water notices and the potential for post-treatment contamination of drinking water supplies. J Water Health 7: 55-56.
Rzezutka A, Kaupke A (2013) Occurrence and molecular identification of Cryptosporidium species isolated from cattle in Poland. Vet Parasi-tol 196: 301-306.
Santín M, Trout JM, Xiao L, Zhou L, Greiner E, Fayer R (2004) Prevalence and age-related variation of Cryptosporidium species and geno-types in dairy calves. Vet Parasitol 122: 103-117.
Şahal M, Terzi OS, Ceylan E, Kara E (2018) Calf Diarrhea and Prevention Methods. Lalahan Hay. Araşt. Enst. Derg 58: 41-49.
Sevinc F, Irmak K, Sevinc M (2003) The prevalence of Cryptosporidium parvum infection in the diarrhoiec and non- diarrhoeic calves. Rev Med Vet 154: 357-361.
Silverlås C (2010) Cryptosporidium infection in dairy cattle. Doctoral Thesis. Swedish University of Agricultural Sciences, Uppsala.
Şimsek AT, İnci A, Yıldırım A, Çiloğlu A, Bişkin Z, Düzlü Ö (2012) Detection of Cryptosporidiosis in Diarrhoeic Neonatal Calves in Nevşehir District by Real Time PCR and Nested PCR Techniques. Erciyes Üni Vet Fak Derg 9: 79-87.
Singh BB, Sharma R, Kumar H, Banga HS, Signh Aulakh R, Gill JPS, Sharma JK (2006) Prevalence of Cryptospori- dium parvum infection in Punjab (India) and its association with diarrhea in neonatal dairy calves. Vet Parasitol 140: 162-165.
Spano F, Putignani L, McLauchlin J, Casemore DP, Crisanti A (1997) PCR-RFLP analysis of the Cryptosporidium oocyst wall protein (COWP) gene discriminates between C. wrairi and C. parvum, and between C. parvum isolates of human and animal origin. FEMS Microbiol Lett 150: 209-217.
Taniuchi M, Verweij JJ, Noor Z, Sobuz SU, Van Lieshout L, Petri Jr WA, Haque R, Houpt ER (2011) High throughput multiplex PCR and probe-based detection with luminex beads for seven intestinal parasites. Am J Trop Med Hyg 84: 332-337.
Thompson HP, Dooley JSG, Kenny J, McCoy M, Lowery JC, Moore JE, Xiao L (2007) Genotypes and subtypes of Cryptosporidium spp. in neonatal calves in Northern Ireland. Parasitol Res 100: 619-624.
Thompson RCA (2004) The zoonotic significance and molecular epidemiology of Giardia and giardiasis. Vet Parasitol 126: 15-35.
Torsein M, Lindberg A, Sandgren CH, Waller KP, Törnquist M, Svensson C (2011) Risk factors for calf mortality in large Swedish dairy herds. Prev Vet Med 99: 136-147.
Trotz-Williams LA, Jarvie BD, Martin SW, Leslie KE, Peregrine SA (2005) Prevalence of Cryptosporidium parvum infection in southwestern Ontario and its association with diarrhea in neonatal dairy calves. Can Vet J 46: 349-351.
Turgay N, Unver-Yolasiǧmaz A, Oyur T, Bardak-Özcem S, Töz S (2012) Monthly distribution of intestinal parasites detected in a part of western Turkey between May 2009-April 2010-results of acid fast and modified trichrome staining methods. Turkiye Parazitol Derg 36: 71-74.
Xiao L, Feng Y (2008) Zoonotic cryptosporidiosis. FEMS Immunol Med Microbiol 52: 309-323.
Go to article

Authors and Affiliations

M. Karakavuk
1 2
H. Can
3
M. Döşkaya
1
T. Karakavuk
1
S. Erkunt-Alak
3
A.E. Köseoğlu
3
A. Gül
4
C. Ün
3
Y. Gürüz
1
A. Değirmenci-Döşkaya
1

  1. Ege University Faculty of Medicine, Department of Parasitology, Bornova, İzmir, Turkey
  2. Ege University, Ödemiş Vocational School, Veterinary technology programs, Ödemiş, Izmir, Turkey
  3. Ege University Faculty of Science, Department of Biology, Molecular Biology Section, Bornova, İzmir, Turkey
  4. Ege University Faculty of Engineering, Department of Bioengineering, Bornova, İzmir, Turkey

This page uses 'cookies'. Learn more