Loading…
Phylogeny of hospital acquired MRSA, and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA)
Staphylococcus aureus is emerging as complicated pathogen because of its wide-ranging origin, multiple variants, and compromised antibiotic susceptibilities. Current study was planned to find lineage of hospital acquired methicillin resistant Staphylococcus aureus (HA-MRSA), and its comparative phen...
Saved in:
Published in: | Microbial pathogenesis 2020-12, Vol.149, p.104537-104537, Article 104537 |
---|---|
Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c342t-35b5e16626cd1aa7fca9cd56274bbf9006acd01eee1c8a1f1da2db5e86d5ff2b3 |
---|---|
cites | cdi_FETCH-LOGICAL-c342t-35b5e16626cd1aa7fca9cd56274bbf9006acd01eee1c8a1f1da2db5e86d5ff2b3 |
container_end_page | 104537 |
container_issue | |
container_start_page | 104537 |
container_title | Microbial pathogenesis |
container_volume | 149 |
creator | Rehman, Tayyab ur Aslam, Rizwan Aqib, Amjad Islam Mohsin, Mashkoor Manzoor, Asad Shoaib, Muhammad Naseer, Muhammad Aamir Hasan, Ali Sattar, Huma Fakhar-e-Alam Kulyar, Muhammad Muzammil, Iqra Yao, Wangyuan |
description | Staphylococcus aureus is emerging as complicated pathogen because of its wide-ranging origin, multiple variants, and compromised antibiotic susceptibilities. Current study was planned to find lineage of hospital acquired methicillin resistant Staphylococcus aureus (HA-MRSA), and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA). A total of (n = 200) samples were aseptically collected from wound, nose, and cerebrospinal fluid of patients from metropolitan and rural background hospitals along with on spot filling in of questionnaire. Phylogenetic analysis of HA-MRSA was identified by targeting mecA gene in S. aureus. At optimal tree branch length of 1.91 and evolutionary distance 0.1, high level sequence similarity (97%–99%) was observed with different strains of S. aureus isolated from both human and animal. Non-descriptive statistics at 5% probability found 61% S. aureus, while 43.44% of them were HA-MRSA, 92.62% VRSA, and 42.62% were both MRSA and VRSA. Among assumed risk factors, use of antibiotics, venous catheterization, chronic disease, pre-hospital visits, and ICU admitted patients showed significant association (p |
doi_str_mv | 10.1016/j.micpath.2020.104537 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2446995730</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0882401020309037</els_id><sourcerecordid>2446995730</sourcerecordid><originalsourceid>FETCH-LOGICAL-c342t-35b5e16626cd1aa7fca9cd56274bbf9006acd01eee1c8a1f1da2db5e86d5ff2b3</originalsourceid><addsrcrecordid>eNqFkFGL1DAQgIMouJ7-BCGPJ9g1Sdts-yTHcXoHJ4qnvobZZGpnaZNekq702T9ul713nwaG-T6Yj7G3UmylkPrDYTuSnSD3WyXUaVfV5e4Z20jR6kIq0TxnG9E0qqiEFC_Zq5QOQoi2KtsN-_utX4bwG_3CQ8f7kCbKMHCwjzNFdPzL94er9xy845QTt2GcIEKmI_KpRx_yMpHldiBPNhQ4kcORwipc-B_KPT-CX5nFkucRE6UMPvOHLYc54pz45a9V_-41e9HBkPDN07xgPz_d_Li-Le6_fr67vrovbFmpXJT1vkaptdLWSYBdZ6G1rtZqV-33XSuEBuuERERpG5CddKDcijTa1V2n9uUFuzx7pxgeZ0zZjJQsDgN4DHMyqqp029a7Uqyn9fnUxpBSxM5MkUaIi5HCnKKbg3mKbk7RzTn6yn08c7j-cSSMJllCb9GtNW02LtB_DP8A1EiQpg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2446995730</pqid></control><display><type>article</type><title>Phylogeny of hospital acquired MRSA, and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA)</title><source>Elsevier</source><creator>Rehman, Tayyab ur ; Aslam, Rizwan ; Aqib, Amjad Islam ; Mohsin, Mashkoor ; Manzoor, Asad ; Shoaib, Muhammad ; Naseer, Muhammad Aamir ; Hasan, Ali ; Sattar, Huma ; Fakhar-e-Alam Kulyar, Muhammad ; Muzammil, Iqra ; Yao, Wangyuan</creator><creatorcontrib>Rehman, Tayyab ur ; Aslam, Rizwan ; Aqib, Amjad Islam ; Mohsin, Mashkoor ; Manzoor, Asad ; Shoaib, Muhammad ; Naseer, Muhammad Aamir ; Hasan, Ali ; Sattar, Huma ; Fakhar-e-Alam Kulyar, Muhammad ; Muzammil, Iqra ; Yao, Wangyuan</creatorcontrib><description>Staphylococcus aureus is emerging as complicated pathogen because of its wide-ranging origin, multiple variants, and compromised antibiotic susceptibilities. Current study was planned to find lineage of hospital acquired methicillin resistant Staphylococcus aureus (HA-MRSA), and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA). A total of (n = 200) samples were aseptically collected from wound, nose, and cerebrospinal fluid of patients from metropolitan and rural background hospitals along with on spot filling in of questionnaire. Phylogenetic analysis of HA-MRSA was identified by targeting mecA gene in S. aureus. At optimal tree branch length of 1.91 and evolutionary distance 0.1, high level sequence similarity (97%–99%) was observed with different strains of S. aureus isolated from both human and animal. Non-descriptive statistics at 5% probability found 61% S. aureus, while 43.44% of them were HA-MRSA, 92.62% VRSA, and 42.62% were both MRSA and VRSA. Among assumed risk factors, use of antibiotics, venous catheterization, chronic disease, pre-hospital visits, and ICU admitted patients showed significant association (p<0.05) with pathogen. HA-MRSA was 37.50%, 80%, and 37.50% sensitive to chloramphenicol, gentamicin, and oxacillin, respectively. While <50% of VRSA were sensitive against oxacillin, enoxacin, and chloramphenicol. A significant difference (p<0.05) of percentage responses of MRSA and VRSA at resistant, intermediate, and sensitive cadre against all antibiotics except chloramphenicol was obvious in this study. The Current study concluded higher prevalence of MRSA & VRSA, significant association of risk factors, limiting antibiotic susceptibility profile, and genetic transfer at animal-human interface which suggests further studies cum preventive strategies to be planned.
•S. aureus is emerging as complicated pathogen due to its wide-ranging origin.•High prevalence of MRSA, VRSA in hospital patients on base of mecA gene.•Trimethoprim-sulphamethoxazole, oxytetracycline, gentamicin showed higher efficacacy.•Clade (3650727_4_P; S. aureus_P10_Human) shared a common ancestor from same geographical location.</description><identifier>ISSN: 0882-4010</identifier><identifier>EISSN: 1096-1208</identifier><identifier>DOI: 10.1016/j.micpath.2020.104537</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Antibiotic susceptibility assay ; Epidemiology ; HA-MRSA ; Phylogeny ; Risk factors ; VRSA</subject><ispartof>Microbial pathogenesis, 2020-12, Vol.149, p.104537-104537, Article 104537</ispartof><rights>2020 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-35b5e16626cd1aa7fca9cd56274bbf9006acd01eee1c8a1f1da2db5e86d5ff2b3</citedby><cites>FETCH-LOGICAL-c342t-35b5e16626cd1aa7fca9cd56274bbf9006acd01eee1c8a1f1da2db5e86d5ff2b3</cites><orcidid>0000-0003-2446-4080 ; 0000-0001-5574-5630</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Rehman, Tayyab ur</creatorcontrib><creatorcontrib>Aslam, Rizwan</creatorcontrib><creatorcontrib>Aqib, Amjad Islam</creatorcontrib><creatorcontrib>Mohsin, Mashkoor</creatorcontrib><creatorcontrib>Manzoor, Asad</creatorcontrib><creatorcontrib>Shoaib, Muhammad</creatorcontrib><creatorcontrib>Naseer, Muhammad Aamir</creatorcontrib><creatorcontrib>Hasan, Ali</creatorcontrib><creatorcontrib>Sattar, Huma</creatorcontrib><creatorcontrib>Fakhar-e-Alam Kulyar, Muhammad</creatorcontrib><creatorcontrib>Muzammil, Iqra</creatorcontrib><creatorcontrib>Yao, Wangyuan</creatorcontrib><title>Phylogeny of hospital acquired MRSA, and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA)</title><title>Microbial pathogenesis</title><description>Staphylococcus aureus is emerging as complicated pathogen because of its wide-ranging origin, multiple variants, and compromised antibiotic susceptibilities. Current study was planned to find lineage of hospital acquired methicillin resistant Staphylococcus aureus (HA-MRSA), and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA). A total of (n = 200) samples were aseptically collected from wound, nose, and cerebrospinal fluid of patients from metropolitan and rural background hospitals along with on spot filling in of questionnaire. Phylogenetic analysis of HA-MRSA was identified by targeting mecA gene in S. aureus. At optimal tree branch length of 1.91 and evolutionary distance 0.1, high level sequence similarity (97%–99%) was observed with different strains of S. aureus isolated from both human and animal. Non-descriptive statistics at 5% probability found 61% S. aureus, while 43.44% of them were HA-MRSA, 92.62% VRSA, and 42.62% were both MRSA and VRSA. Among assumed risk factors, use of antibiotics, venous catheterization, chronic disease, pre-hospital visits, and ICU admitted patients showed significant association (p<0.05) with pathogen. HA-MRSA was 37.50%, 80%, and 37.50% sensitive to chloramphenicol, gentamicin, and oxacillin, respectively. While <50% of VRSA were sensitive against oxacillin, enoxacin, and chloramphenicol. A significant difference (p<0.05) of percentage responses of MRSA and VRSA at resistant, intermediate, and sensitive cadre against all antibiotics except chloramphenicol was obvious in this study. The Current study concluded higher prevalence of MRSA & VRSA, significant association of risk factors, limiting antibiotic susceptibility profile, and genetic transfer at animal-human interface which suggests further studies cum preventive strategies to be planned.
•S. aureus is emerging as complicated pathogen due to its wide-ranging origin.•High prevalence of MRSA, VRSA in hospital patients on base of mecA gene.•Trimethoprim-sulphamethoxazole, oxytetracycline, gentamicin showed higher efficacacy.•Clade (3650727_4_P; S. aureus_P10_Human) shared a common ancestor from same geographical location.</description><subject>Antibiotic susceptibility assay</subject><subject>Epidemiology</subject><subject>HA-MRSA</subject><subject>Phylogeny</subject><subject>Risk factors</subject><subject>VRSA</subject><issn>0882-4010</issn><issn>1096-1208</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkFGL1DAQgIMouJ7-BCGPJ9g1Sdts-yTHcXoHJ4qnvobZZGpnaZNekq702T9ul713nwaG-T6Yj7G3UmylkPrDYTuSnSD3WyXUaVfV5e4Z20jR6kIq0TxnG9E0qqiEFC_Zq5QOQoi2KtsN-_utX4bwG_3CQ8f7kCbKMHCwjzNFdPzL94er9xy845QTt2GcIEKmI_KpRx_yMpHldiBPNhQ4kcORwipc-B_KPT-CX5nFkucRE6UMPvOHLYc54pz45a9V_-41e9HBkPDN07xgPz_d_Li-Le6_fr67vrovbFmpXJT1vkaptdLWSYBdZ6G1rtZqV-33XSuEBuuERERpG5CddKDcijTa1V2n9uUFuzx7pxgeZ0zZjJQsDgN4DHMyqqp029a7Uqyn9fnUxpBSxM5MkUaIi5HCnKKbg3mKbk7RzTn6yn08c7j-cSSMJllCb9GtNW02LtB_DP8A1EiQpg</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Rehman, Tayyab ur</creator><creator>Aslam, Rizwan</creator><creator>Aqib, Amjad Islam</creator><creator>Mohsin, Mashkoor</creator><creator>Manzoor, Asad</creator><creator>Shoaib, Muhammad</creator><creator>Naseer, Muhammad Aamir</creator><creator>Hasan, Ali</creator><creator>Sattar, Huma</creator><creator>Fakhar-e-Alam Kulyar, Muhammad</creator><creator>Muzammil, Iqra</creator><creator>Yao, Wangyuan</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2446-4080</orcidid><orcidid>https://orcid.org/0000-0001-5574-5630</orcidid></search><sort><creationdate>202012</creationdate><title>Phylogeny of hospital acquired MRSA, and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA)</title><author>Rehman, Tayyab ur ; Aslam, Rizwan ; Aqib, Amjad Islam ; Mohsin, Mashkoor ; Manzoor, Asad ; Shoaib, Muhammad ; Naseer, Muhammad Aamir ; Hasan, Ali ; Sattar, Huma ; Fakhar-e-Alam Kulyar, Muhammad ; Muzammil, Iqra ; Yao, Wangyuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-35b5e16626cd1aa7fca9cd56274bbf9006acd01eee1c8a1f1da2db5e86d5ff2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antibiotic susceptibility assay</topic><topic>Epidemiology</topic><topic>HA-MRSA</topic><topic>Phylogeny</topic><topic>Risk factors</topic><topic>VRSA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rehman, Tayyab ur</creatorcontrib><creatorcontrib>Aslam, Rizwan</creatorcontrib><creatorcontrib>Aqib, Amjad Islam</creatorcontrib><creatorcontrib>Mohsin, Mashkoor</creatorcontrib><creatorcontrib>Manzoor, Asad</creatorcontrib><creatorcontrib>Shoaib, Muhammad</creatorcontrib><creatorcontrib>Naseer, Muhammad Aamir</creatorcontrib><creatorcontrib>Hasan, Ali</creatorcontrib><creatorcontrib>Sattar, Huma</creatorcontrib><creatorcontrib>Fakhar-e-Alam Kulyar, Muhammad</creatorcontrib><creatorcontrib>Muzammil, Iqra</creatorcontrib><creatorcontrib>Yao, Wangyuan</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Microbial pathogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rehman, Tayyab ur</au><au>Aslam, Rizwan</au><au>Aqib, Amjad Islam</au><au>Mohsin, Mashkoor</au><au>Manzoor, Asad</au><au>Shoaib, Muhammad</au><au>Naseer, Muhammad Aamir</au><au>Hasan, Ali</au><au>Sattar, Huma</au><au>Fakhar-e-Alam Kulyar, Muhammad</au><au>Muzammil, Iqra</au><au>Yao, Wangyuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phylogeny of hospital acquired MRSA, and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA)</atitle><jtitle>Microbial pathogenesis</jtitle><date>2020-12</date><risdate>2020</risdate><volume>149</volume><spage>104537</spage><epage>104537</epage><pages>104537-104537</pages><artnum>104537</artnum><issn>0882-4010</issn><eissn>1096-1208</eissn><abstract>Staphylococcus aureus is emerging as complicated pathogen because of its wide-ranging origin, multiple variants, and compromised antibiotic susceptibilities. Current study was planned to find lineage of hospital acquired methicillin resistant Staphylococcus aureus (HA-MRSA), and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA). A total of (n = 200) samples were aseptically collected from wound, nose, and cerebrospinal fluid of patients from metropolitan and rural background hospitals along with on spot filling in of questionnaire. Phylogenetic analysis of HA-MRSA was identified by targeting mecA gene in S. aureus. At optimal tree branch length of 1.91 and evolutionary distance 0.1, high level sequence similarity (97%–99%) was observed with different strains of S. aureus isolated from both human and animal. Non-descriptive statistics at 5% probability found 61% S. aureus, while 43.44% of them were HA-MRSA, 92.62% VRSA, and 42.62% were both MRSA and VRSA. Among assumed risk factors, use of antibiotics, venous catheterization, chronic disease, pre-hospital visits, and ICU admitted patients showed significant association (p<0.05) with pathogen. HA-MRSA was 37.50%, 80%, and 37.50% sensitive to chloramphenicol, gentamicin, and oxacillin, respectively. While <50% of VRSA were sensitive against oxacillin, enoxacin, and chloramphenicol. A significant difference (p<0.05) of percentage responses of MRSA and VRSA at resistant, intermediate, and sensitive cadre against all antibiotics except chloramphenicol was obvious in this study. The Current study concluded higher prevalence of MRSA & VRSA, significant association of risk factors, limiting antibiotic susceptibility profile, and genetic transfer at animal-human interface which suggests further studies cum preventive strategies to be planned.
•S. aureus is emerging as complicated pathogen due to its wide-ranging origin.•High prevalence of MRSA, VRSA in hospital patients on base of mecA gene.•Trimethoprim-sulphamethoxazole, oxytetracycline, gentamicin showed higher efficacacy.•Clade (3650727_4_P; S. aureus_P10_Human) shared a common ancestor from same geographical location.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.micpath.2020.104537</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2446-4080</orcidid><orcidid>https://orcid.org/0000-0001-5574-5630</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0882-4010 |
ispartof | Microbial pathogenesis, 2020-12, Vol.149, p.104537-104537, Article 104537 |
issn | 0882-4010 1096-1208 |
language | eng |
recordid | cdi_proquest_miscellaneous_2446995730 |
source | Elsevier |
subjects | Antibiotic susceptibility assay Epidemiology HA-MRSA Phylogeny Risk factors VRSA |
title | Phylogeny of hospital acquired MRSA, and its comparative phenotypic clinico-epidemiology with vancomycin resistant S. aureus (VRSA) |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T01%3A27%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Phylogeny%20of%20hospital%20acquired%20MRSA,%20and%20its%20comparative%20phenotypic%20clinico-epidemiology%20with%20vancomycin%20resistant%20S.%20aureus%20(VRSA)&rft.jtitle=Microbial%20pathogenesis&rft.au=Rehman,%20Tayyab%20ur&rft.date=2020-12&rft.volume=149&rft.spage=104537&rft.epage=104537&rft.pages=104537-104537&rft.artnum=104537&rft.issn=0882-4010&rft.eissn=1096-1208&rft_id=info:doi/10.1016/j.micpath.2020.104537&rft_dat=%3Cproquest_cross%3E2446995730%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c342t-35b5e16626cd1aa7fca9cd56274bbf9006acd01eee1c8a1f1da2db5e86d5ff2b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2446995730&rft_id=info:pmid/&rfr_iscdi=true |