Yu Jing, Ding Yanzi, Zhang Xue, Tai Shuhong, Zhang Chengwen, Liu Cailin, Yuan Enwu, Duan Yitao
Department of Laboratory Medicine, the Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, People's Republic of China.
Zhengzhou Key Laboratory for in vitro Diagnosis of Hypertensive Disorders of Pregnancy, Zhengzhou, Henan, 450052, People's Republic of China.
Infect Drug Resist. 2024 Sep 13;17:3945-3953. doi: 10.2147/IDR.S478304. eCollection 2024.
Understanding the horizontal transfer of resistance genes, such as , is pivotal in developing strategies to control the spread of resistance. In this study, we isolated two bacterial strains, (designated GYB01) and (designated GYB02), from a single patient. The aim of our research is to explore the biological characteristics of these strains and to investigate the interspecies horizontal transfer of .
Strain identification and antimicrobial susceptibility testing were conducted using the Vitek 2 system. Both GYB01 and GYB02 were sequenced with the Illumina HiSeq platform. Bioinformatics analysis tools, including multilocus sequence typing, PlasmidFinder, ResFinder, and others, were utilized to analyze the strains. Additionally, conjugation assays and infection assays were employed to assess the strains.
The isolates exhibited similar antimicrobial resistance profiles and both harbored the gene within the IncFIA plasmids (pGYB01-2, 165.8 kb and pGYB02-2, 211.6 kb, respectively). These plasmids (pGYB01-2 and pGYB02-2) shared over 99% homology, suggesting a common ancestral origin. Conjugation experiments confirmed the transferability of the carrying IncFIA plasmids among . GYB02 possessed an gene cluster, exhibited high virulence, and tested positive in the string test.
Our findings provide direct evidence of potential in vivo interspecies transfer of a multidrug-resistant plasmid, thus enriching our understanding of the mechanisms driving multidrug resistance (MDR) and aiding in the formulation of containment and treatment strategies.
了解耐药基因的水平转移,如[具体基因名称未给出],对于制定控制耐药性传播的策略至关重要。在本研究中,我们从一名患者身上分离出两株细菌菌株,[菌株名称1未给出](命名为GYB01)和[菌株名称2未给出](命名为GYB02)。我们研究的目的是探索这些菌株的生物学特性,并研究[具体基因名称未给出]的种间水平转移。
使用Vitek 2系统进行菌株鉴定和抗菌药物敏感性测试。GYB01和GYB02均采用Illumina HiSeq平台进行测序。利用包括多位点序列分型、质粒查找器、耐药基因查找器等在内的生物信息学分析工具对菌株进行分析。此外,采用接合试验和[感染试验名称未给出]感染试验对菌株进行评估。
分离株表现出相似的抗菌耐药谱,并且在IncFIA质粒(分别为pGYB01 - 2,165.8 kb和pGYB02 - 2,211.6 kb)中均携带[具体基因名称未给出]基因。这些质粒(pGYB01 - 2和pGYB02 - 2)具有超过99%的同源性,表明它们有共同的祖先起源。接合实验证实了携带IncFIA质粒的[具体基因名称未给出]在[相关物种未给出]之间具有可转移性。GYB02拥有一个[基因簇名称未给出]基因簇,表现出高毒力,并且在串珠试验中呈阳性。
我们的研究结果提供了多药耐药质粒在体内潜在种间转移的直接证据,从而丰富了我们对驱动多药耐药(MDR)机制的理解,并有助于制定遏制和治疗策略。