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- Title
Characterization of Three Porcine Acinetobacter towneri Strains Co-Harboring tet (X3) and bla <sub>OXA-58</sub>.
- Authors
Ma, Jiangang; Wang, Juan; Feng, Jie; Liu, Yingqiu; Yang, Baowei; Li, Ruichao; Bai, Li; He, Tao; Wang, Xinglong; Yang, Zengqi
- Abstract
Tigecycline is the antibiotic of last resort for the treatment of extensively drug-resistant bacterial infections, mainly those of multidrug-resistant Gram-negative bacteria. The plasmid-mediated tet (X3) gene has recently been described in various pathogens that are resistant to tigecycline. We report three tigecycline-resistant Acinetobacter towneri strains isolated from porcine faeces in China, which all contained the tet (X3)-harboring plasmids. A broth microdilution method was used to examine the antimicrobial susceptibility of the isolates, and S1-Nuclease digestion pulsed-field gel electrophoresis (S1-PFGE) was used to characterize their plasmid profiles. The whole-genome sequences of the isolates were determined with the Nanopore PromethION platform. The sequence analysis indicated that the strains were A. towneri. They showed resistance to multiple antibiotics, and all the resistance genes were located on plasmids. The three tet (X3)-harboring plasmids had a similar backbone structure, and all contained bla OXA-58 with various insertion elements (IS). IS CR2 is considered an important factor in tet (X3) mobilization. In addition to IS CR2 , we demonstrate that IS 26 generates a circular intermediate containing the tet (X3) gene, which could increase the dissemination risk. To our knowledge, this is the first report of tet (X3)- and bla OXA-58-harboring plasmids in A. towneri. Because the IS 26 is frequently found in front of tet (X3), research should be directed toward the action of IS 26 in the spread of tet (X3).
- Subjects
CHINA; PLASMIDS; PULSED-field gel electrophoresis; ACINETOBACTER; NUCLEOTIDE sequencing; DRUG resistance in bacteria; TIGECYCLINE
- Publication
Frontiers in Cellular & Infection Microbiology, 2020, Vol 10, pN.PAG
- ISSN
2235-2988
- Publication type
Article
- DOI
10.3389/fcimb.2020.586507