Evidence map›Paper›PMID 42430114›Full record

ArticleInfection2026

Rapid expansion of penA allele 60.001-containing endemic ceftriaxone-resistant gonococcal ST8123 lineage in Hangzhou, China.

Xia Sun, Ying Fu, Feng Zhao, Xu'ai Lin, Yan Chen, Stijn van der Veen

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Article in Infection, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Xia SunDepartment of Infectious Diseases of the Second Affiliated Hospital of Zhejiang University School of Medicine, Zhejiang University-University of Edinburgh Institute, School of Medicine, Zhejiang University, Hangzhou, China.
Ying FuDepartment of Clinical Laboratory, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Feng ZhaoDepartment of Clinical Laboratory, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Xu'ai LinDepartment of Microbiology, School of Medicine, Zhejiang University, Haining, China.
Yan ChenDepartment of Infectious Diseases, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Stijn van der VeenDepartment of Infectious Diseases of the Second Affiliated Hospital of Zhejiang University School of Medicine, Zhejiang University-University of Edinburgh Institute, School of Medicine, Zhejiang University, Hangzhou, China. stijnvanderveen@zju.edu.cn.ORCID https://orcid.org/0000-0002-8176-391X

Funding

National Natural Science Foundation of China 82572622, 82272382, 82150610507, 82072320Natural Science Foundation of Zhejiang Province LZ24H190001
6 · The paper itself

Abstract

purposeEmergence of ceftriaxone-resistant Neisseria gonorrhoeae strains expressing penA allele 60.001 poses a major threat to the efficacy of ceftriaxone-based therapies. This study in Hangzhou, China, investigated the molecular epidemiology and antimicrobial susceptibility of 479 N. gonorrhoeae isolates collected from 2019 to 2025 to track the evolution of this resistance.

methodsAntimicrobial susceptibility of N. gonorrhoeae isolates was determined by agar dilution method. Sequence types were identified by multi-locus sequence typing (MLST). Whole-genome sequencing and phylogenetic analysis were performed on high-level ceftriaxone-resistant isolates.

resultsWhile overall ceftriaxone resistance fluctuated, a significant and alarming resurgence of high-level resistance (MIC ≥ 0.5 mg/L) was observed in 2024 (35%) and 2025 (19%), which was primarily driven by the expansion of strains harboring penA allele 60.001. Genetic characterization revealed a critical epidemiological shift: whereas early penA allele 60.001 isolates (2019-2021) were linked to the internationally disseminated FC428 clone (MLST ST1903), subsequent years witnessed the complete displacement of this clone by successful endemic lineages. From 2022 onwards, the resistant isolates belonged predominantly to ST8123 and, to a lesser extent, ST7365. Whole-genome sequencing and core-genome phylogenetic analysis confirmed that ST8123 forms a genetically distinct clade from ST1903, demonstrating that local, highly prevalent strains have acquired penA allele 60.001 and are now responsible for propagating this critical resistance determinant.

conclusionThe rapid clonal expansion of ceftriaxone-resistant endemic lineages in China underscores an urgent need for enhanced global surveillance and a re-evaluation of current empirical therapy guidelines to mitigate the impending threat of untreatable gonorrhea.

Indexed as

CeftriaxoneFC428Multidrug-resistanceNeisseria gonorrhoeaepenA 60.001ST8123

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.