Emergence and evolution of antimicrobial resistance genes and mutations in Neisseria gonorrhoeae
Koji Yahara1, Kevin C Ma2, Tatum D Mortimer2
1Antimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan. k-yahara@nih.go.jp.
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.
Insights
Antimicrobial resistance in Neisseria gonorrhoeae is a growing concern. This study reveals how antibiotic use and genetic recombination drive the emergence and spread of drug-resistant gonorrhea strains, particularly those with mosaic penA alleles.
Area of Science:
- Microbiology
- Genetics
- Epidemiology
Background:
- Antimicrobial resistance in Neisseria gonorrhoeae is a significant global health issue.
- Specific strains (ST-7363, ST-1901) exhibit resistance to third-generation cephalosporins due to mosaic penA alleles.
- The origin and spread of these resistant alleles remain largely unknown.
Purpose of the Study:
- To investigate the evolution and emergence of mosaic penA alleles in Neisseria gonorrhoeae.
- To understand the timeline and mechanisms driving the spread of drug-resistant gonorrhea.
- To explore the role of antibiotic use and genetic recombination in resistance development.
Main Methods:
- Whole-genome sequencing of clinical isolates of Neisseria gonorrhoeae from Japan.
- Phylogenetic analysis of over 1000 strains from 35 countries.
- Reconstruction of evolutionary histories for specific sequence types (ST-1901, ST-7363).
Main Results:
- Mosaic penA-34 in ST-1901 likely arose from penA-10 via interspecies and intragenomic recombination.
- ST-7363 rapidly acquired fluoroquinolone resistance through independent mutations after obtaining penA-10.
- Emergence of resistance determinants may be linked to historical antibiotic treatment regimens in Japan.
Conclusions:
- Antibiotic use and Neisseria species recombination are key drivers of drug-resistant gonorrhea.
- Understanding these evolutionary processes is crucial for combating gonorrhea.
- This research highlights the complex interplay of factors contributing to antimicrobial resistance.
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