Identification of prevalence and antibiotic resistance property as a basis for establishing an efficient treatment of bacteria causing mastitis in beef cows https://doi.org/10.12982/VIS.2023.055

Main Article Content

Tran Hoang Diep
Nguyen Trong Ngu

Abstract

The purpose of the study was to examine the occurrence of metritis on reproduction of beef cows. A total of 2,962 cows were examined, and samples were collected from those displaying clinical symptoms of bovine metritis for bacterial analysis. Bacterial species identification was performed using culture and PCR techniques. The findings revealed that bovine metritis affected 5.5% of the reproductive cow population with the presence of Streptococcus spp., Staphylococcus aureus, Escherichia coli, and Salmonella spp. at the rates of 87.7%, 61.1%, 59.9% and 17.3%, respectively. The results also demonstrated that Streptococcus spp. was the most prevalent group, while Salmonella spp. had the lowest prevalence across different breeds and litters. However, in the Limousin crossbred cows, the infection rate of E. coli surpassed that of the other bacteria and a significantly higher infection rate for E. coli was observed in litter 4 and litter ≥6 compared to the others. The disk diffusion method was utilized to assess antibiotic resistance patterns of the isolated bacteria. Among the bacteria, marbofloxacin exhibited the lowest prevalence of antibiotic resistance (16.9%), while doxycycline had the highest prevalence (82.2%). All cows recovered from the disease within 3-5 days of treatment, and all of them resumed estrus in the subsequent reproductive cycle. The pregnancy rate ranged from 66.7% to 80.0% for the first insemination in the next reproductive cycle.

Article Details

How to Cite
Tran Hoang Diep, & Nguyen Trong Ngu. (2023). Identification of prevalence and antibiotic resistance property as a basis for establishing an efficient treatment of bacteria causing mastitis in beef cows: https://doi.org/10.12982/VIS.2023.055. Veterinary Integrative Sciences, 21(3), 783–797. Retrieved from https://he02.tci-thaijo.org/index.php/vis/article/view/263500
Section
Research Articles

References

Abreham, S., Hailu, M., Worku, A., Tsegaye, S., 2017. Antibiotic resistance of aerobic bacteria isolated from uteri of slaughtered cows in and around Addis Ababa, Ethiopia. J. Vet. Sci. Technol. 8(406), 1-5.

Bacha, B., Regassa, F.G., 2010. Subclinical endometritis in Zebu x Friesian crossbred dairy cows: its risk factors, association with subclinical mastitis and effect on reproductive performance. Trop. Anim. Health. Prod. 42, 397-403.

Baishya, S., Das, K., Rahman, H., Borgohain, B., 1998. Antibiogram of bacteria isolated from uterine discharge of repeated cattle. Indian J. Com. Microbiol. Immunol.Infect. Dis. 19, 130-131.

Benko, T., Boldizar, M., Novotny, F., Hura, V., Valocky, I., Dudrikova, K., Petrovic, V., 2015. Incidence of bacterial pathogens in equine uterine swabs, their antibiotic resistance patterns, and selected reproductive indices in English thoroughbred mares during the foal heat cycle. Vet. Med. 60(11), 613-620.

Bicalho, M.L.S., Machado, V.S., Higgins, C.H., Lima, F.S., Bicalho, R.C., 2017. Genetic and functional analysis of the bovine uterine microbiota. Part I: Metritis versus healthy cows. J. Dairy Sci. 100(5), 3850-3862.

Blake, D.P., Humphry, R.W., Scott, K.P., Hillman, K., Fenlon, D.R., Low, J.C., 2003. Influence of tetracycline exposure on tetracycline resistance and the carriage of tetracycline resistance genes within commensal Escherichia coli populations. J.Appl. Microbiol. 94, 1087-1097.

Brakstad, O.G., Aasbakk, K., Maeland, J.A., 1992. Detection of S. aureus by polymerase chain reaction amplification of the nuc gene. J. Clin. Microbiol. 30(7), 1654-1660.

Bromfeld, J.J., Santos, J.E.P., Block, J., Williams, R.S., Sheldon, I.M., 2015. Physiology and endocrinology symposium: Uterine infection: Linking infection and innate immunity with infertility in the high-producing dairy cow. Anim. Sci. J. 93,2021-2033.

BSAC, 2013. BSAC Method for Antimicrobial Susceptibility Testing. Available online:https://bsac.org.uk/wp-content/uploads/2012/02/Version-12-Apr-2013_final.pdf.

CLSI, 2008. Development of in vitro susceptibility testing criteria and quality control parameters; approved guideline, 3rd edition. CLSI document M23-A3. Clinical and Laboratory Standards Institute, Wayne, PA.

CLSI, 2010. Methods for antimicrobial dilution and disk susceptibility testing of infrequently isolated or fastidious bacteria. Approved Guideline, 2nd edition. Clinical Laboratory Standards Instittute, USA.

CLSI, 2016. Performance standards for antimicrobial susceptibility testing m100s, 26th edition. Clinical Laboratory Standards Instittute, USA.

Dong, V.V., 2016. Investigate some factors affecting conception in dairy cows in Tien Giang (Thesis Master of Veterinary Medicine). Nong Lam University, Ho Chi Minh.

Donofrio, G., Ravanetti, L., Cavirani, S., Herath, S., Capocefalo, A., Sheldon, I.M., 2008. Bacterial infection of endometrial stromal cells influences bovine herpesvirus 4 immediate early gene activation: a new insight into bacterial and viral interaction for uterine disease. Reproduction. 136, 361-366.

Drillich, M., Beetz, O., Pfutzner, A., Sabin, M., Sabin, H.J., Kutzner, P., Nattermann, H.,Heuwieser, W., 2001. Evaluation of systemic antibiotictreatment of toxic puerperal metritis in dairy cows. J. Dairy Sci. 84, 2010-2017.

Duong, C.V., 2011. Research on determining some reproductive indicators, obstetric diseases and testing the treatment of metritis on dairy cows in some localities in Nghe An province (Master Thesis of Agriculture). Hanoi Agricultural University, Ha Noi.

El-Khadrawy, H., Wahid, M., Zaabal, M., Emtenan, M., 2015. Strategies for diagnosis and treatment of uterine infection in bovines. Glob. Vet. 15, 98-105.

EUCAST, 2017. Breakpoint tables for interpretation of MICs and zone diameters. Version 7.1. European Committee on Antimicrobial Susceptibility Testing, Sweden.

Ghanem, M.E., Tezuka, E., Devkota, B., Izaike, Y., Osawa, T., 2014. Persistence of uterine bacterial infection, and its associations with endometritis and ovarian function in postpartum dairy cows. J. Reprod. Dev. 61(1), 54-60.

Gilbert, R.O., 2011. The effect of endometritis on the establishment of pregnancy in cattle.Reprod. Fertil. Dev. 24, 252-257.

Gurunathan, S., 2015. Biologically synthesized silver nanoparticles enhances antibiotic activity against Gram-negative bacteria. J. Ind. Eng. Chem. 29, 217-226.

Hansen, P.J., 2013. Physiology and endocrinology symposium: maternal immunological adjustments to pregnancy and parturition in ruminants and possible implications for postpartum uterine health: is there a prepartum-postpartum nexus?. J. Anim Sci. 91,

-1649.

Huszenicza, G.M., Fodor, M., Gags, M., Kucsar, M.J., Dohmen, W., Varmos, M., Porkolas,L., Kegel, T., Bartyik, J., Lohuis, J.C.M., Janos, S., 1999. Uterine bacteriology, resumption of cyclic ovarianactivity and fertility in postpartum cows kept inlargescale dairy herd. Reprod. Domest. Anim. 34, 237-245.

Irmler, S., Schafer, H., Beisert, B., Rauhut, D., Berthoud, H., 2009. Identication and characterization of a strain-dependent cystathionine β/γ - lyase in Lactobacillus casei potentially involved in cysteine biosynthesis. FEMS Microbiol. Lett. 295, 67-76.

Jorgensen, H.J., Pfaller, A.H., Carroll, C.K., Landry, L.M., Funke, G., Richter, S.S., Warnock, W.D., 2015. Manual of Clinical Microbiology, 11th edition. ASM Press, Washington,D.C.Kateete, P.D., Kimani, C.N., Katabazi, F.A., Okeng, A., Okee, M.S., Nanteza, A., Joloba,

M.L., Najjuka, F.C., 2010. Identification of S. aureus: Dnase and Mannitol salt agar improve the efficiency of the tube coagulase test. Ann. Clin. Microbiol. 9, 23.

Kien, P.T., 2012. Study on the current status of metritis in dairy cows raised in the Red River Delta and test preventive measures (Master's Thesis in Agriculture). Hanoi University of Agriculture, Ha Noi city, Viet Nam.

Kirby-Bauer, 1996. Antimicrobial sensitivity testing by agar diffusion method. J. Clin. Pathol.44, 493.

LeBlanc, S.J., 2008. Postpartum uterine disease and dairy herd reproductive performance: a review. Vet. J. 176, 102-114.

Lohuis, J.A.C.M., Dohmen, M.J.W., Nagy, P., Huszenicza, C., Ague, D., 1994. Bacteriological andclinical findings in cows with subacute/chronic endometritis. Proc. of the 6th Intern. EAVPT, Edinburgh, pp. 7-11.

Madhumeet, S., Pravesh, K., 2018. Isolation and antimicrobial susceptibility of bacteria from dairy cows with sub-clinical endometritis. Haryana Veterinarian. 57(1), 103-105.

Moges, N., Regassa, F., Yilma, T., Unakal, C.G., 2013. Isolation and antimicrobial susceptibility of bacteria from dairy cows with clinical endometritis. J. Reprod.Infertil. 4(1), 04-08.

Moriarty, E.M., Sinton, L.W., Mackenzie, M.L., Karki, N., Wood, D.R., 2008. A survey of enteric bacteria and protozoans in fresh bovine faeces on New Zealand dairy farms.J. Appl. Microbiol. 105(6), 2015-2025.

Nha, G.T., Anh, N.H., 2008. Situation of obstetric diseases in reproductive cows in Duy Xuyen district, Quang Nam province and remedial measures. Hue. Univ. J. Sci. 46,2008.

Noakes, D.E., Till, D., Smith, G.R., 1989. Bovine uterine flora post partum: a comparison of swabbing and biopsy. Vet. Rec. 124, 563-564.

Pangprasit, N., Srithanasuwan, A., Suriyasathaporn, W., Chaisri, W., 2020. Antibacterial properties of lauric acid in combination with organic acids against major pathogens causing dairy mastitis. Vet. Integr. Sci. 19(1), 37-44.

Phengvongsone, X., Thamrongyoswittayakul, C., Sukon, P., Aimsaard, J., Mektrirat, R.,2022. Antibacterial effect of ethanolic Morus alba Linn. leaf extract against mastitiscausing Escherichia coli and S. aureus in vitro. Vet. Integr. Sci. 20(3), 517-529.

Sheldon, I.M., Dobson, H., 2004. Postpartum uterine health in cattle. Anim. Reprod. Sci. 82-83, 295-306.

Sheldon, I.M., Lewis, G., LeBlanc, S., Gilbert, R., 2006. Defining postpartum uterine disease in dairy cattle. Theriogenology. 65(8), 1516-1530.

Sheldon, I.M., Nookes, D.E., Rycroft, A.N., Dobson, H.E., 2002. Influence of uterine bacterial contamination after parturition on ovarian dominant follicle selection and follicle growth and function in cattle. Reproduction. 123, 837-845.

Singh, K.P., Singh, B., Singh, S.V., Singh, J.P., Singh, P., Singh, H.N., 2014. Comparative evaluation of anti-microbials in treatment and improving conception rate in endometritic crossbred cows. Intas. Polivet. 15(1), 79-82.

Smith, B.I., Risco, C.A., 2002. Predisposing factors and potential causes of postpartum metritis in dairy cattle. Comp. Cont. Vet. Ed. 24, 74-80.

Soumet, C., Ermel, G., Fach, P., Colin, P., 1994. Evaluation of different DNA extraction procedures for the detection of Salmonella from chicken products by polymerase chain reaction. J. Appl. Microbiol. 19, 294-298.

Tien, L.T., 2006. Study on transformation of some clinical, non-clinical, bacteriological and experimental treatment of metritis in dairy cows (Master Thesis of Veterinary Medicine). Hanoi Agricultural University, Ha Noi City, Vietnam.

Vietnam Ministry of Health, 2018. A report on antibiotic usage and antibiotic resistance in fifteen Vietnamese hospitals from 2008-2009. Vietnamese Ministry of Health in partnership with the Global Cooperation Project on Antibiotic Resistance (GARP Vietnam) and the Oxford University Clinical Research Unit, Ho Chi Minh.

Wagener, K., Grunert, T., Prunner, I., Ehling-Schulz, M., Drillich, M., 2014. Dynamics of uterine infections with Escherichia coli, Streptococcus uberis and Trueperella pyogenes in post-partum dairy cows and their association with clinical endometritis.Vet. J. 202, 527-532.

Williams, E.J., Fischer, D.P., Pfeiffer, D.U., England, G.C., Noakes, D.E., Dobson, H.,Sheldon, I.M., 2005. Clinical evaluation of postpartum vaginal mucus reflects uterine bacterial infection and the immune response in cattle. Theriogenology. 63,102-117.

Yah, C.S., Simate, G.S., 2015. Nanoparticles as potential new generation broad spectrum antimicrobial agents. DARU J. Pharm. Sci. 23, 1-14.

Yang, LM., Wang, Y.H., Peng, Y., Min, J.T., Hang, S.Q., Zhu, W.Y., 2016. Genomic characterization and antimicrobial susceptibility of bovine intrauterine Escherichia coli and its relationship with postpartum uterine infections. J. Integr. Agr. 15(6),1345-1354.

Yoshihiko, S., Tetsuo, M., Toshie, K. Hiroshi, N., 2000. Salmonella virchow infection in an infant transmitted by household dogs. J. Vet. Med. Sci. 62(7), 767-769.

Zahraei, S.T., Mahzounieh, M. Saeedzadeh, A., 2005. Dectection of InvA gene in isolated Salmonella from broilers by PCR method. Int. J. Poult. Sci. 4(8), 557-559.