Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia

Methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a problem in veterinary medicine and is no longer considered as a mere nosocomial pathogen. We studied the occurrence of MRSA in veterinary personnel, cats and dogs and the environmental premises in University Veterinary Hospital (UVH...

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Main Authors: Erkihun Aklilu, Zunita, Z., Latifah Hassan, Chen Hui Cheng
Format: Indexed Article
Published: 2012
Online Access:http://discol.umk.edu.my/id/eprint/7464/
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0043329
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spelling my.umk.eprints.74642022-05-23T10:00:23Z http://discol.umk.edu.my/id/eprint/7464/ Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia Erkihun Aklilu Zunita, Z. Latifah Hassan Chen Hui Cheng Methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a problem in veterinary medicine and is no longer considered as a mere nosocomial pathogen. We studied the occurrence of MRSA in veterinary personnel, cats and dogs and the environmental premises in University Veterinary Hospital (UVH). We found the prevalence of MRSA as follows: UVH 2/28 (7.1%) staff, 8/100 (8%) of the pets [5/50 (10%) of the dogs and 3/50 (6%) of the cats)], and 9/28 (4.5%) of the environmental samples. Antibiotic sensitivity tests (AST) show multi-resistance characteristics of the MRSA and the minimum inhibitory concentration (MIC) values for the isolates ranged from 1.5 µg to >256 µg/ml. Molecular typing by using multi-locus sequence typing (MLST), staphylococcal protein A typing (spa typing) and pulsed-field gel electrophoresis (PFGE) was conducted and the results from MLST indicated that an isolate from a veterinary personnel (PG21), typed as ST1241 belonged to the same clonal complex (CC) as the two isolates from two dogs (DG16 and DG20), both being typed as ST59. The PFGE results revealed that the two isolates from two veterinary personnel, PG21 and PG16 belonged to closely related MRSA strains with isolates from dog (DG36) and from environmental surface (EV100) respectively. The fact that PFGE revealed close similarity between isolates from humans, a dog and environmental surfaces indicates the possibility for either of them to be the source of MRSA and the potential routes and risks of spread. 2012 Indexed Article NonPeerReviewed Erkihun Aklilu and Zunita, Z. and Latifah Hassan and Chen Hui Cheng (2012) Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia. PLOS ONE Journal, 7 (8). ISSN 1932-6203 http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0043329
institution Universiti Malaysia Kelantan
building Perpustakaan Universiti Malaysia Kelantan
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Kelantan
content_source UMK Institutional Repository
url_provider http://umkeprints.umk.edu.my/
description Methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a problem in veterinary medicine and is no longer considered as a mere nosocomial pathogen. We studied the occurrence of MRSA in veterinary personnel, cats and dogs and the environmental premises in University Veterinary Hospital (UVH). We found the prevalence of MRSA as follows: UVH 2/28 (7.1%) staff, 8/100 (8%) of the pets [5/50 (10%) of the dogs and 3/50 (6%) of the cats)], and 9/28 (4.5%) of the environmental samples. Antibiotic sensitivity tests (AST) show multi-resistance characteristics of the MRSA and the minimum inhibitory concentration (MIC) values for the isolates ranged from 1.5 µg to >256 µg/ml. Molecular typing by using multi-locus sequence typing (MLST), staphylococcal protein A typing (spa typing) and pulsed-field gel electrophoresis (PFGE) was conducted and the results from MLST indicated that an isolate from a veterinary personnel (PG21), typed as ST1241 belonged to the same clonal complex (CC) as the two isolates from two dogs (DG16 and DG20), both being typed as ST59. The PFGE results revealed that the two isolates from two veterinary personnel, PG21 and PG16 belonged to closely related MRSA strains with isolates from dog (DG36) and from environmental surface (EV100) respectively. The fact that PFGE revealed close similarity between isolates from humans, a dog and environmental surfaces indicates the possibility for either of them to be the source of MRSA and the potential routes and risks of spread.
format Indexed Article
author Erkihun Aklilu
Zunita, Z.
Latifah Hassan
Chen Hui Cheng
spellingShingle Erkihun Aklilu
Zunita, Z.
Latifah Hassan
Chen Hui Cheng
Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia
author_facet Erkihun Aklilu
Zunita, Z.
Latifah Hassan
Chen Hui Cheng
author_sort Erkihun Aklilu
title Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia
title_short Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia
title_full Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia
title_fullStr Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia
title_full_unstemmed Molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia
title_sort molecular relatedness of methicillin-resistant s. aureus isolates from staff, environment and pets at university veterinary hospital in malaysia
publishDate 2012
url http://discol.umk.edu.my/id/eprint/7464/
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0043329
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