Emerging epidemic of the Africa-type plasmid in penicillinase-producing Neisseria gonorrhoeae in Guangdong, China, 2013-2022.

IF 8.4 2区 医学 Q1 IMMUNOLOGY
Emerging Microbes & Infections Pub Date : 2025-12-01 Epub Date: 2024-12-26 DOI:10.1080/22221751.2024.2440489
Xiao-Lin Qin, Yang Chen, Xing-Zhong Wu, Wen-Tao Chen, Yao-Hua Xue, Jin-Mei Huang, San-Mei Tang, Yin-Yuan Lan, Zhan-Qin Feng, Han Zhou, Zi-Yan Zhang, Qing-Xian Zhan, Kui Cheng, He-Ping Zheng
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引用次数: 0

Abstract

The prevalence of penicillinase-producing Neisseria gonorrhoeae (PPNG) is a crucial public health concern because of its resistance to penicillin and cephalosporins. From 2013 to 2022, a total of 1748 N. gonorrhoeae isolates from Guangdong, China, were examined for their antibiotic susceptibility and molecular epidemiological characteristics. PPNG prevalence increased markedly from 37.25% to 63.87%. This increase was accompanied by a shift in predominant plasmid types carried by PPNG isolates: the rate of PPNG isolates carrying the Africa-type plasmid increased from 18.42% to 91.55%, whereas the rate of isolates carrying the Asia-type plasmid decreased from 81.58% to 7.58%. The prevalence of blaTEM-135, which is linked to cephalosporin resistance, declined from 52.63% to 4.37%, whereas that of blaTEM-1 increased from 47.37% to 86.88%, and new blaTEM variants emerged (10.99% by 2022). Most blaTEM-1 (88.26%) and new blaTEM alleles (83.70%) were associated with the Africa-type plasmid, whereas 86.79% of blaTEM-135 alleles were linked to the Asia-type plasmid. Resistance to ceftriaxone was higher in the Asia-type group (11.67%) than in the Africa-type, Toronto/Rio-type and non-PPNG groups. Genotyping identified diverse sequence types (STs) among PPNGs, in which MLST ST7363, NG-STAR ST2477, NG-MAST ST17748, and NG STAR CC1124 were predominant. This study underscores the rising prevalence of PPNG in Guangdong driven by clonal expansion and changing plasmid dynamics, affecting cephalosporin resistance and highlighting the need for continued surveillance and research into effective treatment strategies.

2013-2022年广东产青霉酶淋病奈瑟菌非洲型质粒新发流行
由于产青霉素酶淋病奈瑟菌(PPNG)对青霉素和头孢菌素类药物产生耐药性,因此它的流行是一个重要的公共卫生问题。从2013年到2022年,研究人员对中国广东的1748株淋病奈瑟菌分离株进行了抗生素敏感性和分子流行病学特征检测。PPNG的流行率从37.25%显著上升至63.87%。与此同时,PPNG 分离物携带的主要质粒类型也发生了变化:携带非洲型质粒的 PPNG 分离物比例从 18.42% 上升到 91.55%,而携带亚洲型质粒的分离物比例则从 81.58% 下降到 7.58%。与头孢菌素耐药性有关的 blaTEM-135 的流行率从 52.63% 下降到 4.37%,而 blaTEM-1 的流行率则从 47.37% 上升到 86.88%,并且出现了新的 blaTEM 变种(到 2022 年占 10.99%)。大多数 blaTEM-1 等位基因(88.26%)和新的 blaTEM 等位基因(83.70%)与非洲型质粒有关,而 86.79% 的 blaTEM-135 等位基因与亚洲型质粒有关。亚洲型组对头孢曲松的耐药性(11.67%)高于非洲型、多伦多/里奥型和非巴布亚新几内亚组。基因分型在 PPNG 中发现了不同的序列类型(ST),其中以 MLST ST7363、NG-STAR ST2477、NG-MAST ST17748 和 NG STAR CC1124 为主。这项研究强调,在克隆扩增和质粒动态变化的驱动下,PPNG 在广东的流行率不断上升,影响了头孢菌素的耐药性,突出了持续监测和研究有效治疗策略的必要性。
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来源期刊
Emerging Microbes & Infections
Emerging Microbes & Infections IMMUNOLOGY-MICROBIOLOGY
CiteScore
26.20
自引率
2.30%
发文量
276
审稿时长
20 weeks
期刊介绍: Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses. The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries. This journal addresses topics of critical biological and clinical importance, including but not limited to: - Epidemic surveillance - Clinical manifestations - Diagnosis and management - Cellular and molecular pathogenesis - Innate and acquired immune responses between emerging microbes and their hosts - Drug discovery - Vaccine development research Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.
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