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A prophage and two ICESa2603-family integrative and conjugative elements (ICEs) carrying optrA in Streptococcus suis.
Shang, Yanhong; Li, Dexi; Hao, Wenbo; Schwarz, Stefan; Shan, Xinxin; Liu, Bianzhi; Zhang, Su-Mei; Li, Xin-Sheng; Du, Xiang-Dang.
Afiliación
  • Shang Y; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
  • Li D; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
  • Hao W; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
  • Schwarz S; Institute of Microbiology and Epizootics, Centre for Infection Medicine, Department of Veterinary Medicine, Freie Universität Berlin, Berlin, Germany.
  • Shan X; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
  • Liu B; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
  • Zhang SM; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
  • Li XS; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
  • Du XD; College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, P. R. China.
J Antimicrob Chemother ; 74(10): 2876-2879, 2019 10 01.
Article en En | MEDLINE | ID: mdl-31314095
OBJECTIVES: To investigate the presence and transfer of the oxazolidinone/phenicol resistance gene optrA and identify the genetic elements involved in the horizontal transfer of the optrA gene in Streptococcus suis. METHODS: A total of 237 S. suis isolates were screened for the presence of the optrA gene by PCR. Whole-genome DNA of three optrA-positive strains was completely sequenced using the Illumina MiSeq and Pacbio RSII platforms. MICs were determined by broth microdilution. Transferability of the optrA gene in S. suis was investigated by conjugation. The presence of circular intermediates was examined by inverse PCR. RESULTS: The optrA gene was present in 11.8% (28/237) of the S. suis strains. In three strains, the optrA gene was flanked by two copies of IS1216 elements in the same orientation, located either on a prophage or on ICESa2603-family integrative and conjugative elements (ICEs), including one tandem ICE. In one isolate, the optrA-carrying ICE transferred with a frequency of 2.1 × 10-8. After the transfer, the transconjugant displayed elevated MICs of the respective antimicrobial agents. Inverse PCRs revealed that circular intermediates of different sizes were formed in the three optrA-carrying strains, containing one copy of the IS1216E element and the optrA gene alone or in combination with other resistance genes. CONCLUSIONS: A prophage and two ICESa2603-family ICEs (including one tandem ICE) associated with the optrA gene were identified in S. suis. The association of the optrA gene with the IS1216E elements and its location on either a prophage or ICEs will aid its horizontal transfer.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Streptococcus suis / Secuencias Repetitivas Esparcidas / Farmacorresistencia Bacteriana / Profagos Límite: Animals Idioma: En Revista: J Antimicrob Chemother Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Streptococcus suis / Secuencias Repetitivas Esparcidas / Farmacorresistencia Bacteriana / Profagos Límite: Animals Idioma: En Revista: J Antimicrob Chemother Año: 2019 Tipo del documento: Article