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Clinical Molecular and Genomic Epidemiology of Morganella morganii in China

Objectives: Ongoing acquisition of antimicrobial resistance genes has made Morganella morganii a new clinical treatment challenge. Understanding the molecular epidemiology of M. morganii will contribute to clinical treatment and prevention. Methods: We undertook a 6-year clinical molecular epidemiol...

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Detalles Bibliográficos
Autores principales: Xiang, Guoxiu, Lan, Kai, Cai, Yimei, Liao, Kang, Zhao, Mei, Tao, Jia, Ma, Yi, Zeng, Jianming, Zhang, Weizheng, Wu, Zhongwen, Yu, Xuegao, Liu, Yuyang, Lu, Yang, Xu, Caixia, Chen, Liang, Tang, Yi-Wei, Chen, Cha, Jia, Wei, Huang, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507844/
https://www.ncbi.nlm.nih.gov/pubmed/34650543
http://dx.doi.org/10.3389/fmicb.2021.744291
Descripción
Sumario:Objectives: Ongoing acquisition of antimicrobial resistance genes has made Morganella morganii a new clinical treatment challenge. Understanding the molecular epidemiology of M. morganii will contribute to clinical treatment and prevention. Methods: We undertook a 6-year clinical molecular epidemiological investigation of M. morganii from three tertiary hospitals in China since 2014. Antimicrobial susceptibility testing was performed using a VITEK-2 system. All isolates were screened for β-lactam and plasmid-mediated quinolone resistance genes by PCR. Isolates carrying carbapenem-resistant genes were subjected to whole-genome sequencing (WGS). The variation and evolution of these mobile genetic elements (MGEs) were then systematically analyzed. Results: Among all M. morganii isolates (n = 335), forty (11.9%) were recognized as multidrug resistant strains. qnrD1, aac(6′)-Ib-cr, bla(TEM–104), and bla(CTX–M–162) were the top four most prevalent resistance genes. Notably, phylogenomic and population structure analysis suggested clade 1 (rhierBAPS SC3 and SC5) associated with multiple resistance genes seemed to be widely spread. WGS showed a bla(OXA–181)-carrying IncX3 plasmid and a Proteus genomic island 2 variant carrying bla(CTX–M–3), aac(6′)-Ib-cr coexisted in the same multidrug resistant strain zy_m28. Additionally, a bla(IMP–1)-carrying IncP-1β type plasmid was found in the strain nx_m63. Conclusion: This study indicates a clade of M. morganii is prone to acquire resistance genes, and multidrug resistant M. morganii are increasing by harboring a variety of MGEs including two newly discovered ones in the species. We should be vigilant that M. morganii may bring more extensive and challenging antimicrobial resistance issue.