Institut Pasteur de Madagascar, Antananarivo, Madagascar.
Institut Pasteur de Madagascar, Antananarivo, Madagascar.
J Glob Antimicrob Resist. 2020 Mar;20:178-182. doi: 10.1016/j.jgar.2019.07.013. Epub 2019 Jul 17.
A molecular analysis was performed of two Providencia rettgeri (P. rettgeri) strains (Pr 297 and Pr 269) collected in 2007 and 2009 from wound swabs of patients admitted to the intensive care units at Joseph Ravoangy Andrianavalona hospital and the Military Hospital in Antananarivo, Madagascar.
The two P. rettgeri isolates were subjected to susceptibility testing. Whole genome sequencing was performed to characterise the antibiotic resistance genes, genomic islands and mobilomes (integrons, plasmids and insertion sequences).
All isolates were found to be multidrug-resistant. Antibiotic-resistant genes described were amongst eight different classes of antimicrobial agents. Thirty insertion sequences and twelve genomic islands were predicted in each genome. Class 1 and class 2 integrons were found in both genomes, with gene cassette regions encompassing arr-2 - cmlA5 - bla - ant (3")-Ia and dfrA1 - sat2 - ant (3")-Ia - orfX, respectively. IncA/C2, ColM and ColE1-like plasmids were described harbouring bla, qnrD and aac(6')-Ib-cr4 genes, respectively. Phylogenetic analysis showed that Pr 297 and Pr 269 isolates were genetically identical and clustered with P. rettgeri strains described in the USA and Spain.
It is believed that this is the first molecular characterisation of wound infection pathogens from Madagascan patients and the first description of P. rettgeri co-producing CMY-30, OXA-10 and AAC(6')-Ib-cr4 enzymes. The diversity of the resistance determinants and mobile genetic elements was probably due to extensive horizontal gene transfer events, highlighting the need to conduct further molecular monitoring studies to understand the genomic plasticity of resistant bacteria in Madagascan hospitals.
对 2007 年和 2009 年从马达加斯加约瑟夫·拉沃安雅尼纳瓦罗亚医院和塔那那利佛军事医院重症监护病房患者的伤口拭子中收集的两株普罗威登斯菌(P. rettgeri)菌株(Pr 297 和 Pr 269)进行分子分析。
对两株 P. rettgeri 分离株进行药敏试验。进行全基因组测序以鉴定抗生素耐药基因、基因组岛和移动元件(整合子、质粒和插入序列)。
所有分离株均被发现为多药耐药。描述的抗生素耐药基因属于 8 种不同类别的抗菌药物。在每个基因组中预测到 30 个插入序列和 12 个基因组岛。两个基因组中均发现了 1 类和 2 类整合子,基因盒区分别包含 arr-2 - cmlA5 - bla - ant(3")-Ia 和 dfrA1 - sat2 - ant(3")-Ia - orfX。描述了携带 bla、qnrD 和 aac(6')-Ib-cr4 基因的 IncA/C2、ColM 和 ColE1 样质粒。系统发育分析表明,Pr 297 和 Pr 269 分离株在遗传上是相同的,与美国和西班牙描述的 P. rettgeri 菌株聚类。
据信,这是首次对来自马达加斯加患者的伤口感染病原体进行分子特征分析,也是首次描述同时产生 CMY-30、OXA-10 和 AAC(6')-Ib-cr4 酶的 P. rettgeri。耐药决定因素和移动遗传元件的多样性可能是由于广泛的水平基因转移事件,这突出表明需要进一步进行分子监测研究,以了解马达加斯加医院中耐药菌的基因组可塑性。