Global epidemiology of antimicrobial resistance in commensal Neisseria species: A systematic review

IF 4.5 3区 医学 Q1 MICROBIOLOGY
Thibaut Vanbaelen , Christophe Van Dijck , Jolein Laumen , Natalia Gonzalez , Irith De Baetselier , Sheeba S. Manoharan-Basil , Tessa De Block , Chris Kenyon
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引用次数: 10

Abstract

Background

Commensal Neisseria species (spp). represent an important reservoir of antimicrobial resistance genes for pathogenic Neisseria spp. In this systematic review, we aimed to assess the antimicrobial susceptibility of commensal Neisseria spp. and how this has evolved over time. We also aimed to assess if commensal Neisseria spp. showed intrinsic resistance to four antimicrobials - penicillin, azithromycin, ceftriaxone and ciprofloxacin.

Methods

Pubmed and Google Scholar were searched following the PRISMA guidelines. Articles reporting MICs of commensal Neisseria spp. were included according to inclusion/exclusion criteria, and the quality of the articles was assessed using a pre-designed tool. Individual and summary measures of penicillin, azithromycin, ceftriaxone and ciprofloxacin MICs were collected. Additional data was sought to perform a comparison between the MICs of pathogenic and commensal Neisseria spp.

Results

A total of 15 studies met our criteria.We found no evidence of intrinsic AMR in commensal Neisseria spp. We did find evidence of an increasing trend in MICs of commensal Neisseria spp. over time for all antimicrobials assessed. These findings were similar in various countries. Eight additional studies were included to compare pathogenic and commensal Neisseria spp.

Conclusion

The MICs of commensal Neisseria spp. appear to be increasing in multiple countries. Surveillance of MICs in commensals could be used as an early warning system for antimicrobial resistance emergence in pathogens. Our findings underline the need for antibiotic stewardship interventions, particularly in populations with high antimicrobial consumption.

共生奈瑟菌耐药性的全球流行病学:系统综述
共生奈瑟菌种(种)。在这篇系统综述中,我们旨在评估共生奈瑟菌的抗菌敏感性以及这种敏感性是如何随着时间的推移而演变的。我们还旨在评估共生奈瑟菌是否对青霉素、阿奇霉素、头孢曲松和环丙沙星四种抗菌素表现出内在耐药性。方法按照PRISMA指南对spubmed和Google Scholar进行检索。根据纳入/排除标准纳入报道共生奈瑟菌属mic的文章,并使用预先设计的工具评估文章的质量。收集青霉素、阿奇霉素、头孢曲松和环丙沙星mic单项和汇总指标。对致病性和共生性奈瑟菌的mic进行比较。结果共有15项研究符合我们的标准。我们没有发现共生奈瑟氏菌固有抗菌素耐药性的证据,但我们确实发现,随着时间的推移,所有被评估的抗菌素中共生奈瑟氏菌的mic呈上升趋势。这些发现在不同的国家都是相似的。结论共生奈瑟菌的mic值在多个国家呈上升趋势。共生菌中MICs监测可作为病原菌耐药性出现的早期预警系统。我们的研究结果强调了抗生素管理干预措施的必要性,特别是在抗菌素消费量高的人群中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.70
自引率
0.00%
发文量
18
审稿时长
45 days
期刊介绍: Pathogen genome sequencing projects have provided a wealth of data that need to be set in context to pathogenicity and the outcome of infections. In addition, the interplay between a pathogen and its host cell has become increasingly important to understand and interfere with diseases caused by microbial pathogens. IJMM meets these needs by focussing on genome and proteome analyses, studies dealing with the molecular mechanisms of pathogenicity and the evolution of pathogenic agents, the interactions between pathogens and host cells ("cellular microbiology"), and molecular epidemiology. To help the reader keeping up with the rapidly evolving new findings in the field of medical microbiology, IJMM publishes original articles, case studies and topical, state-of-the-art mini-reviews in a well balanced fashion. All articles are strictly peer-reviewed. Important topics are reinforced by 2 special issues per year dedicated to a particular theme. Finally, at irregular intervals, current opinions on recent or future developments in medical microbiology are presented in an editorial section.
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