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Molecular epidemiology and molecular mechanisms of antimicrobial resistance in Neisseria gonorrhoeae in China: Implications for disease control.

机译:中国淋病奈瑟菌的分子流行病学和耐药机制的分子机制:对疾病控制的启示。

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摘要

Gonorrhea, caused by the human pathogen Neisseria gonorrhoeae, is a severe public health problem worldwide with more than 82 million new infections each year. N. gonorrhoeae is transmitted by sexual contact and primarily causes urogenital mucosal infections in men and women. Left untreated, this infection may cause severe complications, especially in females. Eye infections of the newborn can occur. Gonorrhea infections enhance HIV transmission. The highly prevalent antibiotic resistance and the emergence of new drug resistances render treatment of the infections increasingly difficult. Close monitoring of antimicrobial susceptibility of this pathogen is crucial, and enhanced knowledge of molecular mechanisms of gonococcal antimicrobial resistance is urgently needed. There are no vaccines available against N. gonorrhoeae. Control of gonorrhea relies on comprehensive strategies which can be better formulated by understanding, at molecular levels, how N. gonorrhoeae is transmitted in communities.;My research aimed to illustrate the severe burden of antimicrobial resistance in N. gonorrhoeae temporally and geographically in China and to reveal the molecular mechanisms of antibiotic resistance particularly the development of reduced susceptibility to ceftriaxone in N. gonorrhoeae isolates. To determine specific strain distributions, N. gonorrhoeae isolates were characterized using molecular typing methods such as a modified porB-based typing scheme and the N. gonorrhoeae Multi-Antigen Typing (NG-MAST) method, compared to traditional epidemiological approaches. The ultimate goal was to provide information for better formulating disease control strategies for gonorrhea.;In this research, male patients with gonorrhea and their sex partners were recruited in Shanghai (2005 and 2008) and in Urumchi (2007-2008), China. Epidemiological information pertaining to sexual contacts was collected. N. gonorrhoeae isolates were investigated for their antimicrobial susceptibility. Molecular mechanisms of antimicrobial resistance were explored by analysis of potential resistant determinants (gyrA, parC, porB, mtrR, ponA and penA). The molecular data were combined with bioinformatic analysis and traditional epidemiological data.;High percentages of N. gonorrhoeae isolates (11% - 19% in Shanghai, 4.5% in Urumchi) exhibited reduced susceptibility to ceftriaxone (MICs = 0.125-0.25 mg/L), the first line drug recommended for the treatment of gonorrhea in China. The majority of isolates (>98%) were susceptible to spectinomycin, an alternative regimen for gonorrhea treatment; however, the proportion of isolates having intermediate levels of susceptibility increased from 1.9% in 2005 to 9.9% in 2008. The majority of isolates tested were resistant to penicillin (80% - 93%), tetracycline (56% - 65%) and ciprofloxacin (98% - 100%). Plasmid-mediated resistance in N. gonorrhoeae isolates were highly prevalent (51% - 79%) in Shanghai and Urumchi.;Analysis of 60 clinical isolates revealed that reduced susceptibility to ceftriaxone is mediated by porB1b allele and is associated with specific mutations in penicillin binding protein 2 and in the DNA binding and dimerization domains of MtrR. Penicillin binding protein 1 is not involved in reduced susceptibility to ceftriaxone. Although mutation patterns in quinolone resistant determinant regions (QRDRs) varied, the majority of ciprofloxacin resistant isolates had double mutations in GyrA (S91F and D95G/A/N) and most isolates also carried a S87R/N mutation in ParC. The presence of mutations in the QRDR of ParC is correlated with elevated ciprofloxacin MICs.;A modified porB-based molecular typing scheme was developed and involved ∼82% of the DNA sequence of gonococcal porB. This typing method proved to have high discriminatory ability (index of discrimination = 0.93 -- 0.96), and was cost effective and easy to perform as compared to the NG-MAST analysis. Using the modified porB-based typing method, N. gonorrhoeae isolates were reliably differentiated, and transmission clusters were identified. Molecular epidemiology using the porB-based method confirmed direct sexual connections and identified sexual networks otherwise unrevealed by the patient self-reporting or traditional case-tracing methods.;Key words: Neisseria gonorrhoeae, antimicrobial susceptibility/resistance, molecular determinants of antimicrobial resistance, molecular epidemiology, molecular typing, strain transmission, sexual networks.
机译:淋病是由人类病原体淋病奈瑟氏球菌引起的,是世界范围内的严重公共卫生问题,每年新增感染超过8200万。淋病奈瑟氏球菌是通过性接触传播的,主要引起男性和女性泌尿生殖道粘膜感染。如果不及时治疗,这种感染可能会导致严重的并发症,尤其是女性。新生儿可能会发生眼部感染。淋病感染会增加艾滋病毒的传播。高度普遍的抗生素抗性和新药物抗性的出现使得感染的治疗越来越困难。密切监测该病原体的抗菌敏感性至关重要,因此迫切需要增强对淋球菌抗菌素耐药性分子机制的认识。没有针对淋病奈瑟氏球菌的疫苗。控制淋病依赖于综合策略,可以通过在分子水平上了解淋病奈瑟菌在社区中的传播方式来更好地制定。我的研究旨在阐明中国淋病奈瑟菌在时间和地理上的严重负担。以揭示抗生素抗性的分子机制,特别是淋病奈瑟氏球菌分离物中对头孢曲松敏感性降低的发展。为了确定特定的菌株分布,与传统的流行病学方法相比,使用分子分型方法(例如基于porB的改良分型方案)和淋病奈瑟氏球菌多抗原分型(NG-MAST)法对淋病奈瑟氏球菌分离株进行了表征。最终目的是提供信息,以更好地制定淋病的疾病控制策略。在本研究中,招募了上海(2005年和2008年)和乌鲁木齐(2007-2008年)的男性淋病患者及其性伴侣。收集了有关性接触的流行病学信息。研究了淋病奈瑟氏球菌分离株的抗菌敏感性。通过分析潜在的耐药决定簇(gyrA,parC,porB,mtrR,ponA和penA),探索了抗菌药物耐药的分子机制。分子数据与生物信息学分析和传统流行病学数据相结合;高比例淋病奈瑟氏球菌(上海占11%-19%,乌鲁木齐占4.5%)对头孢曲松的敏感性降低(MICs = 0.125-0.25 mg / L) ,是中国治疗淋病的一线药物。多数分离株(> 98%)易受壮观霉素的感染,这是淋病的另一种治疗方案。然而,具有中等敏感性的分离株的比例从2005年的1.9%增加到2008年的9.9%。测试的大多数分离株对青霉素(80%-93%),四环素(56%-65%)和环丙沙星耐药(98%-100%)。在上海和乌鲁木齐,淋病奈瑟氏球菌分离株的质粒介导的耐药率很高(51%-79%);对60株临床分离株的分析表明,对头孢曲松的敏感性降低是由porB1b等位基因介导的,并且与青霉素结合的特定突变有关蛋白2和MtrR的DNA结合和二聚结构域中。青霉素结合蛋白1不参与降低对头孢曲松的敏感性。尽管喹诺酮抗性决定簇区域(QRDRs)中的突变模式各不相同,但大多数环丙沙星抗性分离株在GyrA中具有双突变(S91F和D95G / A / N),大多数分离株在ParC中也带有S87R / N突变。 ParC QRDR中突变的存在与环丙沙星MIC的升高有关。开发了一种基于porB的改良分子分型方案,涉及了约82%的淋球菌porB DNA序列。事实证明,这种分类方法具有很高的区分能力(区分指数= 0.93-0.96),并且与NG-MAST分析相比,具有成本效益且易于执行。使用改良的基于porB的分型方法,淋病奈瑟氏球菌分离株得到了可靠的区分,并鉴定了传播簇。使用基于porB的方法进行的分子流行病学证实了直接的性关系,并确定了患者自我报告或传统的病例追踪方法未发现的性关系。关键词:淋病奈瑟菌,抗菌药敏感性/耐药性,抗菌素耐药性的分子决定因素,分子流行病学,分子分型,菌株传播,性网络。

著录项

  • 作者

    Liao, Mingmin.;

  • 作者单位

    The University of Saskatchewan (Canada).;

  • 授予单位 The University of Saskatchewan (Canada).;
  • 学科 Microbiology.;Epidemiology.;Public health.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 243 p.
  • 总页数 243
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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