An in silico analysis of acquired antimicrobial resistance genes in Aeromonas plasmids

被引:18
作者
Nwaiwu, Ogueri [1 ]
Aduba, Chiugo Claret [2 ]
机构
[1] Univ Nottingham, Sch Biosci, Sutton Bonington Campus, Nottingham, England
[2] Univ Nigeria, Dept Sci Lab Technol, Nsukka, Nigeria
来源
AIMS MICROBIOLOGY | 2020年 / 6卷 / 01期
关键词
Aeromonas; acquired antimicrobial resistance; plasmids; GC content; multiple antimicrobial resistance; predicted multidrug resistance; Colistin; ANTIBIOTIC-RESISTANCE; BETA-LACTAMASE; EFFLUX PUMPS; HYDROPHILA; SPP; DETERMINANTS; INTEGRONS; FISH; IDENTIFICATION; AAC(6')-IB-CR;
D O I
10.3934/microbiol.2020005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sequences of 105 Aeromonas species plasmids were probed for acquired anti-microbial resistance (AMR) genes using a bioinformatics approach. The plasmids showed no positive linear correlation between size and GC content and up to 55 acquired AMR genes were found in 39 (37%) plasmids after in silico screening for resistance against 15 antibiotic drug classes. Overall, potential multiple antibiotic resistance (p-MAR) index ranged from 0.07 to 0.53. Up to 18 plasmids were predicted to mediate multiple drug resistance (MDR). Plasmids pS121-1a (A. salmonicida), pWCX23_1 (A. hydrophila) and pASP-a58 (A. veronii) harboured 18, 15 and 14 AMR genes respectively. The five most occurring drug classes for which AMR genes were detected were aminoglycosides (27%), followed by beta-lactams (17%), sulphonamides (13%), fluoroquinolones (13%), and phenicols (10%). The most prevalent genes were a sulphonamide resistant gene Sul1, the gene aac (6')-Ib-cr (aminoglycoside 6'-N-acetyl transferase type Ib-cr) resistant to aminoglycosides and the blaKPC-2 gene, which encodes carbapenemase-production. Plasmid acquisition of AMR genes was mainly inter-genus rather than intra-genus. Eighteen plasmids showed template or host genes acquired from Pseudomonas monteilii, Salmonella enterica or Escherichia coli. The most occurring antimicrobial resistance determinants (ARDs) were beta-lactamase, followed by aminoglycosides acetyl-transferases, and then efflux pumps. Screening of new isolates in vitro and in vivo is required to ascertain the level of phenotypic expression of colistin and other acquired AMR genes detected.
引用
收藏
页码:75 / 91
页数:17
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