Cargando…

Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae

BACKGROUND: 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 detecte...

Descripción completa

Detalles Bibliográficos
Autores principales: Yahara, Koji, Ma, Kevin C., Mortimer, Tatum D., Shimuta, Ken, Nakayama, Shu-ichi, Hirabayashi, Aki, Suzuki, Masato, Jinnai, Michio, Ohya, Hitomi, Kuroki, Toshiro, Watanabe, Yuko, Yasuda, Mitsuru, Deguchi, Takashi, Eldholm, Vegard, Harrison, Odile B., Maiden, Martin C. J., Grad, Yonatan H., Ohnishi, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008663/
https://www.ncbi.nlm.nih.gov/pubmed/33785063
http://dx.doi.org/10.1186/s13073-021-00860-8
_version_ 1783672731507621888
author Yahara, Koji
Ma, Kevin C.
Mortimer, Tatum D.
Shimuta, Ken
Nakayama, Shu-ichi
Hirabayashi, Aki
Suzuki, Masato
Jinnai, Michio
Ohya, Hitomi
Kuroki, Toshiro
Watanabe, Yuko
Yasuda, Mitsuru
Deguchi, Takashi
Eldholm, Vegard
Harrison, Odile B.
Maiden, Martin C. J.
Grad, Yonatan H.
Ohnishi, Makoto
author_facet Yahara, Koji
Ma, Kevin C.
Mortimer, Tatum D.
Shimuta, Ken
Nakayama, Shu-ichi
Hirabayashi, Aki
Suzuki, Masato
Jinnai, Michio
Ohya, Hitomi
Kuroki, Toshiro
Watanabe, Yuko
Yasuda, Mitsuru
Deguchi, Takashi
Eldholm, Vegard
Harrison, Odile B.
Maiden, Martin C. J.
Grad, Yonatan H.
Ohnishi, Makoto
author_sort Yahara, Koji
collection PubMed
description BACKGROUND: 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-7363 N. 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 mosaic penA-34) and ST-7363 (harboring mosaic penA-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 Neisseria species, 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 within Neisseria species intersect in driving the emergence and spread of drug-resistant gonorrhea. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-021-00860-8.
format Online
Article
Text
id pubmed-8008663
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-80086632021-03-31 Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae Yahara, Koji Ma, Kevin C. Mortimer, Tatum D. Shimuta, Ken Nakayama, Shu-ichi Hirabayashi, Aki Suzuki, Masato Jinnai, Michio Ohya, Hitomi Kuroki, Toshiro Watanabe, Yuko Yasuda, Mitsuru Deguchi, Takashi Eldholm, Vegard Harrison, Odile B. Maiden, Martin C. J. Grad, Yonatan H. Ohnishi, Makoto Genome Med Research BACKGROUND: 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-7363 N. 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 mosaic penA-34) and ST-7363 (harboring mosaic penA-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 Neisseria species, 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 within Neisseria species intersect in driving the emergence and spread of drug-resistant gonorrhea. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-021-00860-8. BioMed Central 2021-03-30 /pmc/articles/PMC8008663/ /pubmed/33785063 http://dx.doi.org/10.1186/s13073-021-00860-8 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yahara, Koji
Ma, Kevin C.
Mortimer, Tatum D.
Shimuta, Ken
Nakayama, Shu-ichi
Hirabayashi, Aki
Suzuki, Masato
Jinnai, Michio
Ohya, Hitomi
Kuroki, Toshiro
Watanabe, Yuko
Yasuda, Mitsuru
Deguchi, Takashi
Eldholm, Vegard
Harrison, Odile B.
Maiden, Martin C. J.
Grad, Yonatan H.
Ohnishi, Makoto
Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
title Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
title_full Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
title_fullStr Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
title_full_unstemmed Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
title_short Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
title_sort emergence and evolution of antimicrobial resistance genes and mutations in neisseria gonorrhoeae
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008663/
https://www.ncbi.nlm.nih.gov/pubmed/33785063
http://dx.doi.org/10.1186/s13073-021-00860-8
work_keys_str_mv AT yaharakoji emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT makevinc emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT mortimertatumd emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT shimutaken emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT nakayamashuichi emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT hirabayashiaki emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT suzukimasato emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT jinnaimichio emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT ohyahitomi emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT kurokitoshiro emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT watanabeyuko emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT yasudamitsuru emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT deguchitakashi emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT eldholmvegard emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT harrisonodileb emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT maidenmartincj emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT gradyonatanh emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae
AT ohnishimakoto emergenceandevolutionofantimicrobialresistancegenesandmutationsinneisseriagonorrhoeae