ISSN: 2536-7099
Model: Open Access/Peer Reviewed
DOI: 10.31248/JASVM
Start Year: 2016
Email: jasvm@integrityresjournals.org
https://doi.org/10.31248/JASVM2021.255 | Article Number: C5E63A7B2 | Vol.7 (1) - February 2022
Received Date: 17 February 2021 | Accepted Date: 15 March 2021 | Published Date: 28 February 2022
Authors: Kenneth Nnamdi ANUEYIAGU* , Ebere Roseann AGUSI , Benshak John AUDU and Lagi Chrysantus ACHI
Keywords: phylogeny, Antibiogram, β-lactamases, California Mastitis Test, ESBL, zoonosis.
The study was conducted to determine the genetic characteristics, antibiotic susceptibility, and genetic relatedness of blaTEM-type and blaCTX-M-type ESBLs producing coliforms from ruminants suffering mastitis. In a cross sectional study, a total of 1052 milk samples were collected aseptically from ruminants across Plateau State, Nigeria. Bacterial culture and biotyping were performed according to standard guidelines. Phenotypic assay for ESBL production was carried out using the Brilliance ESBL Chromogenic Culture Medium (Oxoid, UK). Conventional PCR was used for amplification and detection of blaCTX-M, blaSHV, blaTEM genes as described previously. Sequencing reactions were also performed in the Master Cycler pro 384 (Eppendorf) using the ABI BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems), following the protocols supplied by the manufacturer. Sequences obtained were aligned with sequences deposited in the GenBank using the Basic Local Alignment Search Tool (BLAST) and phylogentic analysis performed MEGA software version 10.1.8. Coliforms isolated from milk samples included Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Enterobacter aerogenes, and Serratia marcescens. 677 coliforms were isolated from the 1052 milk samples across Plateau State, where Escherichia coli had the highest prevalence of 44% while Serratia marcescens had the least with 1.8%. Plateau South had the highest prevalence of 82.3%, followed by Plateau North and Plateau Central with 72.9% and 20.5% prevalence respectively. E. aerogenes recorded the highest resistance (85.71%) against Gentamycin, followed by Serratia marcescens with an 81.82% resistance against Gentamycin. The blaCTX-M was more frequently isolated than blaTEM having 24.39 and 12.19% prevalence respectively. The high-level of phylodiversity observed among ruminants means that there is transfer coliform harboring the blaCTX-M and blaTEM genes which might have been transmitted from clones of varying origins. The relatedness of the genes among organisms in different animals from diverse geographical locations demand a quick intervention that would reduce mortality and morbidity of animals and zoonotic transmissions. Sustained hygienic standards of livestock housing, milking procedures and processes, culling of chronically affected livestock, regular laboratory screening of pastoralists for infections can serve as good interventions.
Abdellah, C., Fouzia, R. F., Abdelkader, C., Rachida, S. B., & Mouloud, Z. (2009). Prevalence and antimicrobial susceptibility of Salmonella isolates from chicken carcasses and giblets in Meknés, Morocco. African Journal of Microbiology Research, 3(5), 215-219. | ||||
Ali, T, Ur Rahman, S., Zhang, L., Shahid, M., Zhang S., Liu, G., Gao, J., & Han B. (2016). ESBL-producing Escherichia coli from cows suffering mastitis in China contain clinical class 1 integrons with CTX-M linked to ISCR1. Frontiers in Microbiology, 7, Article 1931. Crossref |
||||
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990). Basic local alignment search tool. Journal of Molecular Biology, 215(3), 403-410. Crossref |
||||
Balows, A., Hausier, W. J., Hermann, K. L., Isengeng, J. D., & Shadomy, J. H. (1991). Manual of Clinical Microbiology, 5th Edition. American Society of Microbiology, Washington D.C. | ||||
Cantón, R., González-Alba, J. M., & Galán, J. C. (2012). CTX-M enzymes: Origin and diffusion. Frontiers in Microbiology, 3, Article 110. Crossref |
||||
CDC (2007). Methicillin-resistant Staphylococcus aureus (MRSA) in healthcare settings. Centers for Disease Control and Prevention Infection Control in Healthcare. Link |
||||
Chen, H., Shu, W., Chang, X., Chen, J. A., Guo, Y., & Tan, Y. (2010). The profile of antibiotics resistance and integrons of extended-spectrum beta-lactamase producing thermotolerant coliforms isolated from the Yangtze River basin in Chongqing. Environmental Pollution, 158(7), 2459-2464. Crossref |
||||
CLSI (2014). Standards for antimicrobial disk susceptibility tests. Approved standard. In: Ninth edition Document M2-A9. Clinical and Laboratory Standards Institute, Wayne, PA. | ||||
Contreras, G. A., & Rodríguez, J. M. (2011). Mastitis: comparative etiology and epidemiology. Journal of Mammary Gland Biology and Neoplasia, 16(4), 339-356. Crossref |
||||
Dahmen, S., Métayer, V., Gay, E., Madec, J. Y., & Haenni, M. (2013). Characterization of extended-spectrum beta-lactamase (ESBL)-carrying plasmids and clones of Enterobacteriaceae causing cattle mastitis in France. Veterinary Microbiology, 162(2-4), 793-799. Crossref |
||||
Datta N., and Kontomichalou P. (1965). Penicillinase synthesis controlled by infectious R factor in Enterobacteriaceae. Nature 208: 239-244 Crossref |
||||
David, R. C. (2011). Staining and interpretation of smears. Laboratory Studies in Applied Microbiology. Rice University, USA. Pp. 74-78. | ||||
Enoch, D. A., Brown, F., Sismey, A. W., Mlangeni, D. A., Curran, M. D., Karas, J. A., Cone, D. B., Aliyu, S. H., Dhanji, H., Doumith, M., & Maharjan, S. (2012). Epidemiology of extended-spectrum beta-lactamase-producing Enterobacteriaceae in a UK district hospital; an observational study. Journal of Hospital Infection, 81(4), 270-277. Crossref |
||||
Ezeanya, C. C., Agbakoba, N. R., Ejike, C. E., & Okwelogu, S. I. (2017). Evaluation of a chromogenic medium for the detection of ESBL with comparison to Double Disk Synergy Test. British Journal of Medicine & Medical Research, 21(12), 1-11, Article no. BJMMR.33259. Crossref |
||||
Falagas, M. E., & Karageorgopoulos, D. E. (2009). Extended-spectrum beta-lactamase-producing organisms. Journal of Hospital Infection, 73(4),345-54. Crossref |
||||
Fladberg, Ø. A., Jørgensen, S. B., & Aamot, H. V. (2017). Genotypic characterization of gentamicin and cephalosporin resistant Escherichia coli isolates from blood cultures in a Norwegian university hospital 2011-2015. Antimicrobial Resistance & Infection Control, 6, Article number 121. Crossref |
||||
Garedew, L., Berhanu, A., Mengesha, D., & Tsegay, G. (2012). Identification of gram-negative bacteria from critical control points of raw and pasteurized cow milk consumed at Gondar town and its suburbs, Ethiopia. BMC public health, 12, Article number 950. Crossref |
||||
Geser, N., Stephan, R., & Hächler, H. (2012). Occurrence and characteristics of extended-spectrum β-lactamase (ESBL) producing Enterobacteriaceae in food producing animals, minced meat and raw milk. BMC Veterinary Research, 8, Article number 21. Crossref |
||||
Ghuysen J. M. (1991). Serine β-Lactamases and penicillin binding proteins. Annual Review of Microbiology 45, 37-67. Crossref |
||||
Harada, K., Nakai, Y., & Kataoka, Y. (2012). Mechanisms of resistance to cephalosporin and emergence of O25b‐ST131 clone harboring CTX‐M‐27 β‐lactamase in extraintestinal pathogenic Escherichia coli from dogs and cats in Japan. Microbiology and Immunology, 56(7), 480-485. Crossref |
||||
Horton, R. A., Randall, L. P., Snary, E. L., Cockrem, H., Lotz, S., Wearing, H., Duncan, D., Rabie, A., McLaren, I., Watson, E., & Coldham, N. G. (2011). Fecal carriage and shedding density of CTX-M extended-spectrum β-lactamase-producing Escherichia coli in cattle, chickens, and pigs: implications for environmental contamination and food production. Applied and Environmental Microbiology, 77(11), 3715-3719. Crossref |
||||
Jena, J., Debata, N. K., Sahoo, R. K., Gaur, M., & Subudhi, E. (2017). Genetic diversity study of various β-lactamase-producing multidrug-resistant Escherichia coli isolates from a tertiary care hospital using ERIC-PCR. Indian Journal of Medical Research, 146(Suppl.), S23-S29. Crossref |
||||
Kibret, M., & Abera, B. (2011). Antimicrobial susceptibility patterns of E. coli from clinical sources in northeast Ethiopia. African Health Sciences, 11(Special Issue 1), 540-545. Crossref |
||||
Kiratisin, P., Apisarnthanarak, A., Laesripa, C., & Saifon, P. (2008). Molecular characterization and epidemiology of extended-spectrum-β-lactamase-producing Escherichia coli and Klebsiella pneumoniae isolates causing health care-associated infection in Thailand, where the CTX-M family is endemic. Antimicrobial Agents and Chemotherapy, 52(8), 2818-2824. Crossref |
||||
Klibi, A., Jouini, A., Boubaker El Andolsi, R., Kmiha, S., Ben Hamda, C., Ghedira, K., Hamrouni, S., Ghram, A., & Maaroufi, A. (2019). Epidemiology of β-lactamase-producing staphylococci and gram negative bacteria as cause of clinical Bovine mastitis in Tunisia. BioMed Research International, Volume 2019, Article ID 2165316, 9 pages. Crossref |
||||
Madec, J. Y., Lazizzera, C., Châtre, P., Meunier, D., Martin, S., Lepage, G., Ménard, M. F., Lebreton, P., & Rambaud, T. (2008). Prevalence of fecal carriage of acquired expanded-spectrum cephalosporin resistance in Enterobacteriaceae strains from cattle in France. Journal of Clinical Microbiology, 46(4), 1566-1567. Crossref |
||||
Madec, J. Y., Poirel, L., Saras, E., Gourguechon, A., Girlich, D., Nordmann, P., & Haenni, M. (2012). Non-ST131 Escherichia coli from cattle harbouring human-like bla CTX-M-15-carrying plasmids. Journal of Antimicrobial Chemotherapy, 67(3), 578-581. Crossref |
||||
Mbuk, E. U., Kwaga, J. K. P., Bale, J. O. O., Boro, L. A., & Umoh, J. U. (2016). Coliform organisms associated with milk of cows with mastitis and their sensitivity to commonly available antibiotics in Kaduna State, Nigeria. Journal of Veterinary Medicine and Animal Health, 8(12), 228-236. Crossref |
||||
Müller, E. E., Grabow, W. O. K., & Ehlers, M. M. (2003). Immunomagnetic separation of Escherichia coli O157: H7 from environmental and wastewater in South Africa. Water South Africa, 29(4), 427-432. Crossref |
||||
Overdevest, I., Willemsen, I., Rijnsburger, M., Eustace, A., Xu, L., Hawkey, P., Heck, M., Savelkoul, P., Vandenbroucke-Grauls, C., van der Zwaluw, K., & Kluytmans, J. (2011). Extended-spectrum β-lactamase genes of Escherichia coli in chicken meat and humans, The Netherlands. Emerging Infectious Diseases, 17(7), 1216-1222. Crossref |
||||
Reuland, E. A., Overdevest, I. T. M. A., Al Naiemi, N., Kalpoe, J. S., Rijnsburger, M. C., Raadsen, S. A., Ligtenberg-Burgman, I., van der Zwaluw, K. W., Heck, M., Savelkoul, P. H. M. & Kluytmans, J. A. J. W. (2013). High prevalence of ESBL-producing Enterobacteriaceae carriage in Dutch community patients with gastrointestinal complaints. Clinical Microbiology and Infection, 19(6), 542-549. Crossref |
||||
Salman, A. M. A., & Hamad, I. M. (2011). Enumeration and identification of coliform bacteria from raw milk in Khartoum State, Sudan. Journal of Cell and Animal Biology, 5(7), 121-128. | ||||
Sawant, A. A., Sordillo, L. M., & Jayarao, B. M. (2005). A survey on antibiotic usage in dairy herds in Pennsylvania. Journal of Dairy Science, 88(8), 2991-2999. Crossref |
||||
Schmid, A., Hörmansdorfer, S., Messelhäusser, U., Käsbohrer, A., Sauter-Louis, C., & Mansfeld, R. (2013). Prevalence of extended-spectrum β-lactamase-producing Escherichia coli on Bavarian dairy and beef cattle farms. Applied and Environmental Microbiology, 79(9), 3027-3032. Crossref |
||||
Tekiner, I. H., & Özpınar, H. (2016). Occurrence and characteristics of extended spectrum beta-lactamases-producing Enterobacteriaceae from foods of animal origin. Brazilian Journal of Microbiology, 47(2), 444-451. Crossref |
||||
Tiwari, J. G., Babra, C., Tiwari, H., Williams, V., De Wet, S., Gibson, J., Paxman, A., Morgan, E., Costantino, P., Sunagar, R., & Mukkur, T. (2013). Trends in therapeutic and prevention strategies for management of bovine mastitis: an overview. Journal of Vaccines & Vaccination, 4(1), Article number 176. Crossref |
||||
Villegas, M. V., Correa, A., Perez, F., Zuluaga, T., Radice, M., Gutkind, G., Casellas J. M., Ayala, J., Lolans, K., & Quinn, J. P. (2004). CTX-M-12 _-Lactamase in a Klebsiella pneumoniae Clinical Isolate in Colombia. Antimicrobial Agents and Chemotherapy, 48(2), 629-631. Crossref |
||||
Yu, Z. N., Wang, J., Ho, H., Wang, Y. T., Huang, S. N., & Han, R. W. (2019). Prevalence, antimicrobial-resistance phenotypes and genotypes of Escherichia coli isolated from raw milk samples from mastitis cases in four regions of China. Journal of Global Antimicrobial Resistance, 22, 94-101 Crossref |
||||
Zeryehun, T., & Abera, G. (2017). Prevalence and bacterial isolates of mastitis in dairy farms in selected districts of Eastern Harrarghe Zone, Eastern Ethiopia. Journal of Veterinary Medicine, Volume 2017, Article ID 6498618, 7 pages. Crossref |
||||
http://blast.ncbi.nlm.nih.gov/Blast.cgi. | ||||
http://www.megasoftware.net. |