Fang Yewei, Tao Shuan, Chen Huimin, Xu Yao, Chen Luyan, Liang Wei
Department of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, People's Republic of China.
School of Medicine, Jiangsu University, Zhejiang, People's Republic of China.
Infect Drug Resist. 2023 Aug 23;16:5563-5571. doi: 10.2147/IDR.S423860. eCollection 2023.
The objectives of this study are to determine the differences in clonality, virulence gene (VG) content and phylogenetic group between non extended-spectrum beta-lactamase-producing (non-ESBL-EC) and ESBL-EC isolates from urine.
This study characterized a total of 100 clinical isolates consecutively obtained from the inpatients hospitalized in The First Affiliated Hospital of Ningbo University in China by polymerase-chain reaction (PCR).
Phylogenetic group B2 was found to be the most prevalent in both ESBL-EC and non-ESBL-EC group. Among 100 clinical isolates, the count of acquired virulence genes in group B2 was found to be significantly higher than that in group A, B1, and D ( <0.001). Additionally, the presence of content within virulence genes (the total number of virulence genes detected per isolate) in B2 of non-ESBL-EC and ESBL-EC showed a significant difference (<0.001). ST131 was detected exclusively in ESBL-EC, while ST95 and ST73 were the main sequence types in non-ESBL-EC.
Our study demonstrated the different distribution of MLST, phylogenetic group in ESBL-EC and non-ESBL-EC group. The inverse association between beta-lactamase resistance and VG content performed in this study should get a lot more attention. At the same time, we should also be wary of the appearance of non-ESBL-EC isolates of group B2 harboring more virulence genes which will lead to high pathogenicity.
本研究的目的是确定尿中分离出的非产超广谱β-内酰胺酶(非ESBL-EC)和ESBL-EC菌株在克隆性、毒力基因(VG)含量和系统发育群方面的差异。
本研究通过聚合酶链反应(PCR)对连续从中国宁波大学附属第一医院住院患者中获得的100株临床分离株进行了特征分析。
发现系统发育群B2在ESBL-EC组和非ESBL-EC组中最为普遍。在100株临床分离株中,发现B2组中获得的毒力基因数量显著高于A组、B1组和D组(<0.001)。此外,非ESBL-EC和ESBL-EC的B2组中毒力基因内的含量(每株分离株检测到的毒力基因总数)存在显著差异(<0.001)。ST131仅在ESBL-EC中检测到,而ST95和ST73是非ESBL-EC中的主要序列类型。
我们的研究证明了ESBL-EC组和非ESBL-EC组中多位点序列分型(MLST)、系统发育群的不同分布。本研究中β-内酰胺酶耐药性与VG含量之间的负相关关系应得到更多关注。同时,我们也应警惕携带更多毒力基因的B2组非ESBL-EC分离株的出现,这将导致高致病性。