Genomic island type IV secretion system and transposons in genomic islands involved in antimicrobial resistance in Trueperella pyogenes

• Published in: Veterinary microbiology 2020-03, Vol.242, p.108602-108602, Article 108602
• Main Authors: Dong, Wen-Long, Xu, Qi-Jun, Atiah, Luke Atiewin, Odah, Kokou Ayefounin, Gao, Yun-Hang, Kong, Ling-Cong, Ma, Hong-Xia
• Format: Article
• Language: English
• Subjects: Amikacin; Antimicrobial agents; Antimicrobial resistance; Azithromycin; Cefazolin; Ciprofloxacin; Comparative analysis; Drug resistance; Enrofloxacin; Erythromycin; Florfenicol; Gene transfer; Genes; Genomes; Genomic island; Genomic islands; Gentamicin; Horizontal transfer; Multidrug resistance; Opportunist infection; Secretion; Sequence analysis; T. pyogenes; T4SS; Transposon; Transposons; Trueperella pyogenes
• ISSN: 0378-1135; 1873-2542
• DOI: 10.1016/j.vetmic.2020.108602

•The GI-type T4SSs located on a genomic islands were found in Trueperella pyogenes for the first time.•The insertion sequences IS6100 and IS1634 were found in Trueperella pyogenes for the first time.•Two copies of erm(X) and two IS1634 elements located in TP4-GI8 may have formed a composite transposon. Trueperella pyogenes (T. pyogenes) is a well-known opportunistic pathogen of many animal species. It can cause a variety of suppurative infections. The objective of this research was to get insight into the gene context and the location of the antimicrobial resistance determinants in the two multi-resistant T. pyogenes isolates TP3 and TP4. Comparative analysis of key factors leading to antimicrobial resistance was performed. Both isolates were resistant to erythromycin, azithromycin and tetracycline, and susceptible to ciprofloxacin, enrofloxacin, cefazolin and florfenicol. In addition, TP4 was resistant to amikacin and gentamicin. Whole-genome analyses revealed that both TP3 and TP4 contained two different genomic islands (TP3-GI1, TP3-GI5, TP4-GI5 and TP4-GI8) involved in multi-drug resistance. There is a common region in TP3-GI1 and TP4-GI5, containing the tetracycline resistance gene tet(W) and a series of genes involved in type IV secretion systems. Several genes located on TP3-GI5 and TP4-GI8 are highly homologous. Tetracycline-resistance gene tet(33) was potentially acquired by horizontal gene transfer via IS6100 located on 57,936 bp TP3-GI5. The macrolide resistance gene erm(X) was located near the end of the TP3-GI5. The sequence analysis of TP4-GI8 showed that two copies of erm(X) and two IS1634 elements located in the same orientation may have formed a composite transposon. GI-type T4SS, transposons and multiple resistance genes located on GIs play a key role in multiple drug resistance of TP3 and TP4.