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Systemic Analysis of the mecA Gene Using a Bioinformatics Tool

BACKGROUND: The mecA gene, carried by methicillin-resistant Staphylococcus aureus (MRSA), allows the bacterium to promotes bacterial resistance to antibiotics such as methicillin, penicillin, and other penicillin-like antibiotics. Our objectives are to use a bioinformatics tool to analyze the sequen...

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Autores principales: Tsai, Shin-Yi, Chang, Fu-Chieh, Ma, Kevin Sheng-Kai, Hsu, Cheng-Wei, Tung, Po-Ya, Hung, Yan-Jiun, Chou, Yi-Ting, Kuo, Chien-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631545/
http://dx.doi.org/10.1093/ofid/ofx163.1713
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author Tsai, Shin-Yi
Chang, Fu-Chieh
Ma, Kevin Sheng-Kai
Hsu, Cheng-Wei
Tung, Po-Ya
Hung, Yan-Jiun
Chou, Yi-Ting
Kuo, Chien-Feng
author_facet Tsai, Shin-Yi
Chang, Fu-Chieh
Ma, Kevin Sheng-Kai
Hsu, Cheng-Wei
Tung, Po-Ya
Hung, Yan-Jiun
Chou, Yi-Ting
Kuo, Chien-Feng
author_sort Tsai, Shin-Yi
collection PubMed
description BACKGROUND: The mecA gene, carried by methicillin-resistant Staphylococcus aureus (MRSA), allows the bacterium to promotes bacterial resistance to antibiotics such as methicillin, penicillin, and other penicillin-like antibiotics. Our objectives are to use a bioinformatics tool to analyze the sequence of the mecA gene, which is spread on the SCCmec genetic element, and to investigate the relationship between each mecA gene. METHODS: From 2008 to 2016, we collected 229 MRSA from bacteremia; we extracted DNA from the MRSA and designed specific primers to target mecA using PCR. The primer used are listed in mec A-1(5’-GGGATCATAGCGTCATTATTC-3’) and mec A-2(5’-AACGATTGTGACACGATAGCC-3’). We determined whether the mecA gene was present by using electrophoresis and then sequenced the MRSA samples in which it was present. The POWER tool was employed to analyze the mecA gene and compile a pedigree chart. RESULTS: Using the sequencing data, we created an MRSA database, and the BLAST findings demonstrated that most of the mecA genes were similar, with over 95% identified. The pedigree chart illustrates that there are four groups of mecA genes, and these groups were found to be not differentiated between the sources of the MRSA, whether from communities or hospital association infections. CONCLUSION: Our findings indicate that even though there were four groups with ancestors in the pedigree chart, no significant difference was found between MRSA from community- and hospital-associated infections. We plan to collect more MRSA samples for analysis and investigate the differences between MRSA groups and MRSA from various geographical regions. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-56315452017-11-07 Systemic Analysis of the mecA Gene Using a Bioinformatics Tool Tsai, Shin-Yi Chang, Fu-Chieh Ma, Kevin Sheng-Kai Hsu, Cheng-Wei Tung, Po-Ya Hung, Yan-Jiun Chou, Yi-Ting Kuo, Chien-Feng Open Forum Infect Dis Abstracts BACKGROUND: The mecA gene, carried by methicillin-resistant Staphylococcus aureus (MRSA), allows the bacterium to promotes bacterial resistance to antibiotics such as methicillin, penicillin, and other penicillin-like antibiotics. Our objectives are to use a bioinformatics tool to analyze the sequence of the mecA gene, which is spread on the SCCmec genetic element, and to investigate the relationship between each mecA gene. METHODS: From 2008 to 2016, we collected 229 MRSA from bacteremia; we extracted DNA from the MRSA and designed specific primers to target mecA using PCR. The primer used are listed in mec A-1(5’-GGGATCATAGCGTCATTATTC-3’) and mec A-2(5’-AACGATTGTGACACGATAGCC-3’). We determined whether the mecA gene was present by using electrophoresis and then sequenced the MRSA samples in which it was present. The POWER tool was employed to analyze the mecA gene and compile a pedigree chart. RESULTS: Using the sequencing data, we created an MRSA database, and the BLAST findings demonstrated that most of the mecA genes were similar, with over 95% identified. The pedigree chart illustrates that there are four groups of mecA genes, and these groups were found to be not differentiated between the sources of the MRSA, whether from communities or hospital association infections. CONCLUSION: Our findings indicate that even though there were four groups with ancestors in the pedigree chart, no significant difference was found between MRSA from community- and hospital-associated infections. We plan to collect more MRSA samples for analysis and investigate the differences between MRSA groups and MRSA from various geographical regions. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2017-10-04 /pmc/articles/PMC5631545/ http://dx.doi.org/10.1093/ofid/ofx163.1713 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Tsai, Shin-Yi
Chang, Fu-Chieh
Ma, Kevin Sheng-Kai
Hsu, Cheng-Wei
Tung, Po-Ya
Hung, Yan-Jiun
Chou, Yi-Ting
Kuo, Chien-Feng
Systemic Analysis of the mecA Gene Using a Bioinformatics Tool
title Systemic Analysis of the mecA Gene Using a Bioinformatics Tool
title_full Systemic Analysis of the mecA Gene Using a Bioinformatics Tool
title_fullStr Systemic Analysis of the mecA Gene Using a Bioinformatics Tool
title_full_unstemmed Systemic Analysis of the mecA Gene Using a Bioinformatics Tool
title_short Systemic Analysis of the mecA Gene Using a Bioinformatics Tool
title_sort systemic analysis of the meca gene using a bioinformatics tool
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631545/
http://dx.doi.org/10.1093/ofid/ofx163.1713
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