4.6 Article

Association among biofilm formation, virulence gene expression, and antibiotic resistance in Proteus mirabilis isolates from diarrhetic animals in Northeast China

Journal

BMC VETERINARY RESEARCH
Volume 16, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12917-020-02372-w

Keywords

Proteus mirabilis; Animal; Diarrhea; Biofilm; Virulence gene; Antibiotic resistance; Pathogenicity

Funding

  1. Academic Backbone Project of Northeast Agricultural University [17XG10]
  2. National Natural Science Foundation of China [31672532]
  3. SIPT Program [201910224139]

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BackgroundThe aim of this study was to investigate the association among biofilm formation, virulence gene expression, and antibiotic resistance in P. mirabilis isolates collected from diarrhetic animals (n=176) in northeast China between September 2014 and October 2016.ResultsApproximately 92.05% of the isolates were biofilm producers, whereas 7.95% of the isolates were non-producers. The prevalence of virulence genes in the biofilm producer group was significantly higher than that in the non-producer group. Biofilm production was significantly associated with the expression of ureC, zapA, rsmA, hmpA, mrpA, atfA, and pmfA (P<0.05). The results of drug susceptibility tests revealed that approximately 76.7% of the isolates were multidrug-resistant (MDR) and extensively drug-resistant (XDR). Biofilm production was significantly associated with resistance to doxycycline, tetracycline, sulfamethoxazole, kanamycin, and cephalothin (P<0.05). Although the pathogenicity of the biofilm producers was stronger than that of the non-producers, the biofilm-forming ability of the isolates was not significantly associated with morbidity and mortality in mice (P>0.05).ConclusionOur findings suggested that a high level of multidrug resistance in P. mirabilis isolates obtained from diarrhetic animals in northeast China. The results of this study indicated that the positive rates of the genes expressed by biofilm-producing P. mirabilis isolates were significantly higher than those expressed by non-producing isolates.

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