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Characterization of florfenicol resistance genes in the coagulase-negative Staphylococcus (CoNS) isolates and genomic features of a multidrug-resistant Staphylococcus lentus strain H29

Authors
  • Wu, Chongyang1, 2, 3
  • Zhang, Xueya1, 2
  • Liang, Jialei2
  • Li, Qiaoling1, 2
  • Lin, Hailong1, 2
  • Lin, Chaoqin2
  • Liu, Hongmao2
  • Zhou, Danying1
  • Lu, Wei1
  • Sun, Zhewei1
  • Lin, Xi1
  • Zhang, Hailin2
  • Li, Kewei1
  • Xu, Teng4
  • Bao, Qiyu1
  • Lu, Junwan1
  • 1 Wenzhou Medical University, Chashan University Town, Wenzhou, Zhejiang, 325035, China , Wenzhou (China)
  • 2 Wenzhou Medical University, Wenzhou, Zhejiang, 325027, China , Wenzhou (China)
  • 3 Sichuan University, Chengdu, Sichuan, 610041, China , Chengdu (China)
  • 4 Baotou Central Hospital, Baotou, 014040, China , Baotou (China)
Type
Published Article
Journal
Antimicrobial Resistance & Infection Control
Publisher
BioMed Central
Publication Date
Jan 07, 2021
Volume
10
Issue
1
Identifiers
DOI: 10.1186/s13756-020-00869-5
Source
Springer Nature
Keywords
License
Green

Abstract

BackgroundWith the wide use of florfenicol to prevent and treat the bacterial infection of domestic animals, the emergence of the florfenicol resistance bacteria is increasingly serious. It is very important to elucidate the molecular mechanism of the bacteria’s resistance to florfenicol.MethodsThe minimum inhibitory concentration (MIC) levels were determined by the agar dilution method, and polymerase chain reaction was conducted to analyze the distribution of florfenicol resistance genes in 39 CoNS strains isolated from poultry and livestock animals and seafood. The whole genome sequence of one multidrug resistant strain, Staphylococcus lentus H29, was characterized, and comparative genomics analysis of the resistance gene-related sequences was also performed.ResultsAs a result, the isolates from the animals showed a higher resistance rate (23/28, 82.1%) and much higher MIC levels to florfenicol than those from seafood. Twenty-seven animal isolates carried 37 florfenicol resistance genes (including 26 fexA, 6 cfr and 5 fexB genes) with one carrying a cfr gene, 16 each harboring a fexA gene, 5 with both a fexA gene and a fexB gene and the other 5 with both a fexA gene and a cfr gene. On the other hand, all 11 isolates from seafood were sensitive to florfenicol, and only 3 carried a fexA gene each. The whole genome sequence of S. lentus H29 was composed of a chromosome and two plasmids (pH29-46, pH29-26) and harbored 11 resistance genes, including 6 genes [cfr, fexA, ant(6)-Ia, aacA-aphD, mecA and mph(C)] encoded on the chromosome, 4 genes [cfr, fexA, aacA-aphD and tcaA] on pH29-46 and 1 gene (fosD) on pH29-26. We found that the S. lentus H29 genome carried two identical copies of the gene arrays of radC-tnpABC-hp-fexA (5671 bp) and IS256-cfr (2690 bp), of which one copy of the two gene arrays was encoded on plasmid pH29-46, while the other was encoded on the chromosome.ConclusionsThe current study revealed the wide distribution of florfenicol resistance genes (cfr, fexA and fexB) in animal bacteria, and to the best of our knowledge, this is the first report that one S. lentus strain carried two identical copies of florfenicol resistance-related gene arrays.

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