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dc.contributor.authorTso, Lai Sze
dc.date.accessioned2021-02-03T15:10:17Z
dc.date.available2021-02-03T15:10:17Z
dc.date.issued2020-12-11
dc.date.submitted2020-01
dc.identifier.issn1471-2334
dc.identifier.urihttps://hdl.handle.net/1721.1/129644
dc.description.abstractBackground:Antimicrobial resistance inM. genitaliumis a growing clinical problem. We investigated the mutations associatedwith macrolide and fluoroquinolone resistance, two commonly used medical regimens for treatment in China. Our aim is toanalyze the prevalence and diversity of mutations amongM. genitalium-positive clinical specimens in Guangzhou, south China.Methods:A total of 154 storedM. genitaliumpositive specimens from men and womenattending a STI clinic were testedfor macrolide and fluoroquinolone mutations.M. genitaliumwas detected via TaqMan MGB real-time PCR. Mutationsassociated with macrolide resistance were detected using primers targeting region V of the 23S rRNA gene.Fluoroquinolone resistant mutations were screened via primers targeting topoisomerase IV (parC)andDNAgyrase(gyrA).Results:98.7% (152/154), 95.5% (147/154) and 90.3% (139/154) ofM. genitaliumpositive samples produced sufficientamplicon for detecting resistance mutations in 23S rRNA,gyrAandparCgenes, respectively. 66.4% (101/152), 0.7% (1/147)and 77.7% (108/139) samples manifested mutations in 23S rRNA,gyrAandparCgenes, respectively. A2072G (59/101,58.4%) and S83I (79/108, 73.1%) were highly predominating in 23S rRNA andparCgenes, respectively. Two samples hadamino acid substitutions ingyrA(M95I and A96T, respectively). Two samples had two amino acid substitutions inparC(S83I + D87Y). 48.6% (67/138) of samples harbored both macrolide and fluoroquinolone resistance-associated mutations.The most common combination of mutations was A2072G (23S rRNA) and S83I (parC) (40/67, 59.7%). One sample hadthree amino acid changes in 23S rRNA,gyrAandparCgenes (A2072G + A96T + S83I). Conclusions:The high antimicrobial resistance rate ofM. genitaliumin Guangzhou is a very worrying problem andsuggests that antimicrobial resistance testing and the development of new antibiotic regimens are crucially needed.en_US
dc.description.sponsorshipGuangze Xian (China). Bureau of Science and InformationTechnology (Grant 01704020219)en_US
dc.description.sponsorshipGuangdog Sheng (China). Medical Science andTechnology Foundation (Grants A2017224 and A2018248)en_US
dc.description.sponsorshipLonghua Qu (Shenzhen Shi, China). High Level Project of Medicine (Grant HLPM201907020105)en_US
dc.description.sponsorshipSouthern Medical University (China) (Grant 2019001)en_US
dc.description.sponsorshipResearch Council of Norway (Grant 275002)en_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofhttps://doi.org/10.1186/s12879-020-05659-3en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceBioMed Centralen_US
dc.titleMacrolide and fluoroquinolone associated mutations in Mycoplasma genitalium in a retrospective study of male and female patients seeking care at a STI Clinic in Guangzhou, China, 2016-2018en_US
dc.typeArticleen_US
dc.identifier.citationKe, Wujian et al. “Macrolide and fluoroquinolone associated mutations in Mycoplasma genitalium in a retrospective study of male and female patients seeking care at a STI Clinic in Guangzhou, China, 2016-2018.” BMC infectious diseases, 20 (December 2020): 950 © 2020 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Anthropologyen_US
dc.relation.journalBMC infectious diseasesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-12-13T04:12:45Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.date.submission2020-12-13T04:12:45Z
mit.journal.volume20en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


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