Microbial Prevalence and Antimicrobial Sensitivity in Dairy Animals Suffering From Purulent Vaginal Discharge
DOI:
https://doi.org/10.48165/ijar.2022.43.2.4Keywords:
Bovine, uterine infection, microbiological study, culture sensitivity testAbstract
Uterine infection can be diagnosed by taking a swab from fornix vagina or directly from cervix and can be used for cytology and microbiological evaluation. In this study, vaginal swabs for culture and sensitivity test were obtained from 20 buffaloes and two cows which were shedding purulent pus discharge from their reproductive tract. The most isolated microorganism was Escherichia coli which were detected in 17 animals, followed by Staphylococcus spp. and Streptococcus spp. which was detected in 15 and 14 animals, respectively. Klebsiella spp and Baccilus spp. were diagnosed in two animals whereas; Psuedomonas spp. and Candida spp. were also diagnosed in one animal. Regarding sensitivity tests, the most efficient antibiotics were Gentamicin 54.5% (12/22) followed by Ciprofloxacin 50% (11/22), Enrofloxacin 45% (10/22), Neomycin 45% (10/22), Amikacin 45% (10/22), Cefoperazone 36% (8/22), Levofloxacin 31% (7/22), Norfloxacin 27% (6/22), Chloramphenicol 27% (6/22) and Cephalexin 22.7% (5/22). Likewise, the most resistant antibiotics in descending order were Streptomycin 95.4% (21/22), Penicillin and Cloxacillin 90.9% (20/22), Amoxicilin, Moxifloxacin and Ampicillin 86% (19/22), Oxytetracycline and Ceftriaxone 81.8% (18/22), Cephalexin 72.7% (16/22), Levofloxacillin 68% (15/22), Carbenicillin, Chloramphenicol, Kanamycin and Cefoperazone 63.6% (14/22), Tobramycin, Neomycin and Enrofloxacin 54.5% (12/22), Amikacin and Ciprofloxacin 50% (11/22), Cephotaxime 45.5 (10/22), Norfloxacin and Gentamycin 40.9% (9/22), Clindamycin and Septran 22.7% (5/22), Amoxiclav and Erythromycin 18 % (4/22). The present study concluded that the most prevalent microorganisms isolated from uterine discharge, were found to be resistant to beta-lactam antimicrobials as well, the study highlighted the significance of performing microbiological analyses as well as sensitivity tests prior to applying an antimicrobial therapy.
References
Ahmadi, M.R., Nazifi, S. and Ghaisari, H.R. (2006). Comparative cervical cytology and conception rate in postpartum dairy cows. Vet. Arhiv., 76(4), 323-332.
Brooks, G.F., Butel J.S., Jawetz, E., Morse, S.A., Melnick, J.L. and Adelberg, E.A. (2001). Medical microbiology. 22nd ed. USA. Appleton and Lange Publishers.
Chandrakar, D., Tiwari, R.P., Awasthi, M.K. and Hirpurkar, S.D. (2002). Microbial profile their antibiogram pattern in cervico-uterine contents and conception rate following treatment in repeat breeder crossbred cows. Indian J. Anim. Reprod., 23, 148-150.
Foldi, J., Kulksar, M., Pecsi, A. and Lohuis, J.A.C.M. (2006). Bacterial complications of postpartum uterine involution in cattle. Anim. Reprod. Sci., 96, 265-281.
Getahun, K., Kelay, B., Bekana, M. and Lobago, F. (2008). Bovine mastitis and antibiotic resistance patterns in Selalle small holder dairy farms, central Ethiopia. Trop. Anim. Health Prod., 40: 261-68.
Gilbert, R.O. (2011). The effect of endometritis on the establishment of pregnancy in cattle. Reprod. Fertil. Dev., 24, 252-257.
Jadon, R.S., Dhaliwal, G.S. and Jand, S.K. (2005). Prevalence of aerobic and anaerobic bacteria during peripartum period in normal and dystocia affected buffaloes. Anim. Reprod. Sci., 88, 215-224.
Kaczmarowski, M., Malinowski E. and Markiewicz, H. (2004). Influence of various treatments on bacteriological findings in cows with puerperal endometritis. Pol. J. Vet. Sci., 7(3), 171-174.
LeBlanc, S.J., Lissemore, K.D., Kelton, D.F., Duffield, T.F. and Leslie, K.E. (2006). Major advances in disease prevention in dairy cattle. J. Dairy Sci., 89(4): 1267-1279.
Momtaz, H., Rahimi, E. and Tajbakhsh, E. (2010). Detection of some virulence factors in Staphylococcus aureus isolated from clinical and subclinical bovine mastitis in Iran. Afr. J. Biotech., 9(25): 3753-3758.
Mshelia, G.D., Okpaje, G., Voltaire Y.A.C. and Egwu, G.O. (2014). Comparative studies on genital infections and antimicrobial susceptibility patterns of isolates from camels (Camelus dromedarius) and cows (Bos indicus) in Maiduguri, North-eastern Nigeria. Springer plus 3: 91.
Patel, P.P., Panchal, M.T., Kalyani, I.H. and Kavani F.S. (2009). Antibiotic sensitivity spectrum of bacterial isolates from cervico vaginal mucus of postpartum rural buffaloes. Intas Polivet., 10(1): 29-31.
Risco, C.A., Youngquist, R.S. and Shore, M.D. (2007). Postpartum uterine infection. In: Youngquist RS, Threfall WR, editors. Current therapy in Large Animal Theriogenology. USA: Saunders Elseviers.
Sadig, N.B.M. (2010). Identification of aerobic bacteria isolated from vagina of cross-bred dairy cows during early postpartum. M.Sc. Thesis, Khartoum, North Sudan.
Sheldon, I.M. and Dobson, H. (2004). Postpartum uterine health in cattle. Anim. Reprod. Sci., 82-83: 295-306.
Sheldon, I.M., Lewis, G.S., LeBlanc, S. and Gilbert, R.O. (2006). Defining postpartum uterine disease in cattle. Theriogenology., 65: 1516-1530.
Sheldon, I.M., Williams, E.J., Miller, A.N.A., Nash, D.M. and Herath, S. (2008). Uterine diseases in cattle after parturition. Vet. J., 176: 115-121.
Takamtha, A., Phanaratkitti, V., Adirekkiet, O., Panyapornwitaya, V., Boonyayatra, S., and Kraeusukol, K. (2013). Prevalence of isolated bacteria from clinical endometritis uterine and antimicrobial susceptibility in postpartum dairy cows. Chiang Mai Vet. J., 11(3): 237-245.