4.6 Article

Clinical Molecular and Genomic Epidemiology of Morganella morganii in China

Journal

FRONTIERS IN MICROBIOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.744291

Keywords

Morganella morganii; molecular epidemiology; bla(OXA-181); genomic island; bla(IMP-1)

Categories

Funding

  1. National Natural Science Foundation of China [81772249, 81871703]
  2. Guangdong Science and Technology Program [2019A030317003]

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The study revealed that a clade of M. morganii is prone to acquiring resistance genes, leading to an increasing number of multidrug resistant strains with a variety of mobile genetic elements (MGEs), including two newly discovered ones in the species. This highlights the potential for M. morganii to pose a more extensive and challenging antimicrobial resistance issue.
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 beta-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-1 beta 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.

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