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High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria

We determined the prevalence and genetic characteristics of methicillin-resistant Staphylococcus aureus (MRSA) isolated from pigs and humans between September 2013 and February 2015 in Kogi State, a central region in Nigeria. A total of 680 nasal swabs were collected and analyzed from pigs (n = 425)...

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Autores principales: Otalu, Otalu Jnr, Kwaga, Jacob K. P., Okolocha, Emmanuel Chukuwdi, Islam, Md Zohorul, Moodley, Arshnee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305073/
https://www.ncbi.nlm.nih.gov/pubmed/30619177
http://dx.doi.org/10.3389/fmicb.2018.03098
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author Otalu, Otalu Jnr
Kwaga, Jacob K. P.
Okolocha, Emmanuel Chukuwdi
Islam, Md Zohorul
Moodley, Arshnee
author_facet Otalu, Otalu Jnr
Kwaga, Jacob K. P.
Okolocha, Emmanuel Chukuwdi
Islam, Md Zohorul
Moodley, Arshnee
author_sort Otalu, Otalu Jnr
collection PubMed
description We determined the prevalence and genetic characteristics of methicillin-resistant Staphylococcus aureus (MRSA) isolated from pigs and humans between September 2013 and February 2015 in Kogi State, a central region in Nigeria. A total of 680 nasal swabs were collected and analyzed from pigs (n = 425) and “pig-contact” humans (n = 55) on 35 farms, and “non-pig-contact” humans (n = 200). MRSA was recovered from 20 (4.7%) pigs on 12 farms and 18 (7.0%) humans. Six (2.4%) of the human isolates were recovered from “pig-contact” humans, of which only three work on farms also harboring MRSA positive pigs. All 38 MRSA were resistant to β-lactams only, belonged to spa type t1603, sequence type (ST) 88, and mecA was associated with a SCCmec IVa element. Four isolates from a pig, a pig-contact human from the same farm, a pig-contact human from a pig farm in a different district, and a non-pig-contact human were subjected to whole genome sequencing (WGS). Core genome SNP analysis revealed high genetic similarity between strains (3–11 SNP differences), despite the temporal (2 year gap) and geographic (165 km) differences between isolates. Furthermore, these Nigerian isolates form a distinct clade when compared to other African MRSA ST88 isolates. All but one porcine strain was positive for scn suggesting a possible human origin and that pigs were either transiently contaminated by humans or result of a very recent human-to-pig transmission event. To our knowledge, this is the first report of genetically confirmed MRSA in pigs in Nigeria, which appear to be a typical CA-MRSA clone present in the human population.
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spelling pubmed-63050732019-01-07 High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria Otalu, Otalu Jnr Kwaga, Jacob K. P. Okolocha, Emmanuel Chukuwdi Islam, Md Zohorul Moodley, Arshnee Front Microbiol Microbiology We determined the prevalence and genetic characteristics of methicillin-resistant Staphylococcus aureus (MRSA) isolated from pigs and humans between September 2013 and February 2015 in Kogi State, a central region in Nigeria. A total of 680 nasal swabs were collected and analyzed from pigs (n = 425) and “pig-contact” humans (n = 55) on 35 farms, and “non-pig-contact” humans (n = 200). MRSA was recovered from 20 (4.7%) pigs on 12 farms and 18 (7.0%) humans. Six (2.4%) of the human isolates were recovered from “pig-contact” humans, of which only three work on farms also harboring MRSA positive pigs. All 38 MRSA were resistant to β-lactams only, belonged to spa type t1603, sequence type (ST) 88, and mecA was associated with a SCCmec IVa element. Four isolates from a pig, a pig-contact human from the same farm, a pig-contact human from a pig farm in a different district, and a non-pig-contact human were subjected to whole genome sequencing (WGS). Core genome SNP analysis revealed high genetic similarity between strains (3–11 SNP differences), despite the temporal (2 year gap) and geographic (165 km) differences between isolates. Furthermore, these Nigerian isolates form a distinct clade when compared to other African MRSA ST88 isolates. All but one porcine strain was positive for scn suggesting a possible human origin and that pigs were either transiently contaminated by humans or result of a very recent human-to-pig transmission event. To our knowledge, this is the first report of genetically confirmed MRSA in pigs in Nigeria, which appear to be a typical CA-MRSA clone present in the human population. Frontiers Media S.A. 2018-12-17 /pmc/articles/PMC6305073/ /pubmed/30619177 http://dx.doi.org/10.3389/fmicb.2018.03098 Text en Copyright © 2018 Otalu, Kwaga, Okolocha, Islam and Moodley. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Otalu, Otalu Jnr
Kwaga, Jacob K. P.
Okolocha, Emmanuel Chukuwdi
Islam, Md Zohorul
Moodley, Arshnee
High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria
title High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria
title_full High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria
title_fullStr High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria
title_full_unstemmed High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria
title_short High Genetic Similarity of MRSA ST88 Isolated From Pigs and Humans in Kogi State, Nigeria
title_sort high genetic similarity of mrsa st88 isolated from pigs and humans in kogi state, nigeria
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305073/
https://www.ncbi.nlm.nih.gov/pubmed/30619177
http://dx.doi.org/10.3389/fmicb.2018.03098
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