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Reduced vancomycin susceptibility in porcine ST9 MRSA isolates

Porcine strains of livestock-associated methicillin resistant Staphylococcus aureus (LA-MRSA) have been recognized in many countries and have been shown to be able to cause human infection. Resistance to non-beta lactam antibiotics has been reported but non-susceptibility to vancomycin, which is kno...

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Autores principales: Kwok, Gabriella M. L., O'Donoghue, Margaret M., Doddangoudar, Vijaya C., Ho, Jeff, Boost, Maureen V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829576/
https://www.ncbi.nlm.nih.gov/pubmed/24298270
http://dx.doi.org/10.3389/fmicb.2013.00316
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author Kwok, Gabriella M. L.
O'Donoghue, Margaret M.
Doddangoudar, Vijaya C.
Ho, Jeff
Boost, Maureen V.
author_facet Kwok, Gabriella M. L.
O'Donoghue, Margaret M.
Doddangoudar, Vijaya C.
Ho, Jeff
Boost, Maureen V.
author_sort Kwok, Gabriella M. L.
collection PubMed
description Porcine strains of livestock-associated methicillin resistant Staphylococcus aureus (LA-MRSA) have been recognized in many countries and have been shown to be able to cause human infection. Resistance to non-beta lactam antibiotics has been reported but non-susceptibility to vancomycin, which is known to occur in human MRSA, has so far not been observed in LA-MRSA. Such resistance is typically fairly low level involving changes in the cell wall thickness. The development of resistance is usually preceded by presence of a sub-population having an increased MIC, which is selected for by exposure to vancomycin. This study investigated vancomycin susceptibility of one hundred porcine MRSA isolates using three MIC methods including spiral gradient endpoint (SGE) technique which allows visualization of more resistant sub-populations. SGE revealed 16 strains with an MIC above 2.0 mg/L, of which 14 were determined to have MIC 4 mg/L by agar dilution (AD). SGE revealed a further two isolates with MIC < 2 mg/L had a sub-population >2 mg/L. In addition, trailing endpoints not reaching resistance were present in 26 isolates with MIC < 2 mg/L. Sequencing of the genes of the VraSR/GraSR two component systems of ten of the resistant strains for comparison with susceptible strains revealed changes, including the presence of stop codons, in vraS and graR, but these were not consistent in all isolates. Other genetic changes may contribute to vancomycin non-susceptibility and require investigation. As failure to respond to treatment has been reported in clinical isolates with MIC > 1.5 mg/L, the presence of vancomycin non-susceptibility in porcine isolates is of concern and further monitoring of LA-MRSA is essential.
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spelling pubmed-38295762013-12-02 Reduced vancomycin susceptibility in porcine ST9 MRSA isolates Kwok, Gabriella M. L. O'Donoghue, Margaret M. Doddangoudar, Vijaya C. Ho, Jeff Boost, Maureen V. Front Microbiol Microbiology Porcine strains of livestock-associated methicillin resistant Staphylococcus aureus (LA-MRSA) have been recognized in many countries and have been shown to be able to cause human infection. Resistance to non-beta lactam antibiotics has been reported but non-susceptibility to vancomycin, which is known to occur in human MRSA, has so far not been observed in LA-MRSA. Such resistance is typically fairly low level involving changes in the cell wall thickness. The development of resistance is usually preceded by presence of a sub-population having an increased MIC, which is selected for by exposure to vancomycin. This study investigated vancomycin susceptibility of one hundred porcine MRSA isolates using three MIC methods including spiral gradient endpoint (SGE) technique which allows visualization of more resistant sub-populations. SGE revealed 16 strains with an MIC above 2.0 mg/L, of which 14 were determined to have MIC 4 mg/L by agar dilution (AD). SGE revealed a further two isolates with MIC < 2 mg/L had a sub-population >2 mg/L. In addition, trailing endpoints not reaching resistance were present in 26 isolates with MIC < 2 mg/L. Sequencing of the genes of the VraSR/GraSR two component systems of ten of the resistant strains for comparison with susceptible strains revealed changes, including the presence of stop codons, in vraS and graR, but these were not consistent in all isolates. Other genetic changes may contribute to vancomycin non-susceptibility and require investigation. As failure to respond to treatment has been reported in clinical isolates with MIC > 1.5 mg/L, the presence of vancomycin non-susceptibility in porcine isolates is of concern and further monitoring of LA-MRSA is essential. Frontiers Media S.A. 2013-10-25 /pmc/articles/PMC3829576/ /pubmed/24298270 http://dx.doi.org/10.3389/fmicb.2013.00316 Text en Copyright © 2013 Kwok, O'Donoghue, Doddangoudar, Ho and Boost. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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
Kwok, Gabriella M. L.
O'Donoghue, Margaret M.
Doddangoudar, Vijaya C.
Ho, Jeff
Boost, Maureen V.
Reduced vancomycin susceptibility in porcine ST9 MRSA isolates
title Reduced vancomycin susceptibility in porcine ST9 MRSA isolates
title_full Reduced vancomycin susceptibility in porcine ST9 MRSA isolates
title_fullStr Reduced vancomycin susceptibility in porcine ST9 MRSA isolates
title_full_unstemmed Reduced vancomycin susceptibility in porcine ST9 MRSA isolates
title_short Reduced vancomycin susceptibility in porcine ST9 MRSA isolates
title_sort reduced vancomycin susceptibility in porcine st9 mrsa isolates
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829576/
https://www.ncbi.nlm.nih.gov/pubmed/24298270
http://dx.doi.org/10.3389/fmicb.2013.00316
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