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dc.contributor.authorYahara, Koji
dc.contributor.authorMa, Kevin C.
dc.contributor.authorShimuta, Ken
dc.contributor.authorNakayama, Shu-ichi
dc.contributor.authorHirabayashi, Aki
dc.contributor.authorSuzuki, Masato
dc.contributor.authorJinnai, Michio
dc.contributor.authorOhya, Hitomi
dc.contributor.authorKuroki, Toshiro
dc.contributor.authorWatanabe, Yuko
dc.contributor.authorYasuda, Mitsuru
dc.contributor.authorDeguchi, Takashi
dc.contributor.authorEldholm, Vegard
dc.contributor.authorHarrison, Odile B.
dc.contributor.authorMaiden, Martin C.J.
dc.contributor.authorGrad, Yonatan H.
dc.contributor.authorOhnishi, Makoto
dc.date.accessioned2021-08-31T10:55:01Z
dc.date.available2021-08-31T10:55:01Z
dc.date.created2021-08-10T12:42:06Z
dc.date.issued2021
dc.identifier.issn1756-994X
dc.identifier.urihttps://hdl.handle.net/11250/2771922
dc.description.abstractBackground: Antimicrobial resistance in Neisseria gonorrhoeae is a global health concern. Strains from two internationally circulating sequence types, ST-7363 and ST-1901, have acquired resistance to third-generation cephalosporins, mainly due to mosaic penA alleles. These two STs were first detected in Japan; however, the timeline, mechanism, and process of emergence and spread of these mosaic penA alleles to other countries remain unknown. Methods: We studied the evolution of penA alleles by obtaining the complete genomes from three Japanese ST-1901 clinical isolates harboring mosaic penA allele 34 (penA-34) dating from 2005 and generating a phylogenetic representation of 1075 strains sampled from 35 countries. We also sequenced the genomes of 103 Japanese ST-7363N. gonorrhoeae isolates from 1996 to 2005 and reconstructed a phylogeny including 88 previously sequenced genomes. Results: Based on an estimate of the time-of-emergence of ST-1901 (harboring mosaicpenA-34) and ST-7363(harboring mosaicpenA-10), and >300 additional genome sequences of Japanese strains representing multiple STs isolated in 1996–2015, we suggest that penA-34 in ST-1901 was generated from penA-10 via recombination with another Neisseriaspecies, followed by recombination with a gonococcal strain harboring wildtype penA-1. Following the acquisition of penA-10 in ST-7363, a dominant sub-lineage rapidly acquired fluoroquinolone resistance mutations at GyrA 95 and ParC 87-88, by independent mutations rather than horizontal gene transfer. Data in the literature suggest that the emergence of these resistance determinants may reflect selection from the standard treatment regimens in Japan at that time. Conclusions: Our findings highlight how antibiotic use and recombination across and withinNeisseriaspeciesintersect in driving the emergence and spread of drug-resistant gonorrhea. Keywords: Recombination, Horizontal gene transfer, Genomic epidemiology, Antimicrobial resistance, Phylogeny,Surveillance, Evolution,Neisseria gonorrhoeae
dc.language.isoeng
dc.titleEmergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.volume13
dc.source.journalGenome Medicine
dc.source.issue51
dc.identifier.doi10.1186/s13073-021-00860-8
dc.identifier.cristin1925014
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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