Peng Yao, Wang Yanting, Kang Xingxing, Cai Xunchao
Department of Gastroenterology and Hepatology, Shenzhen University General Hospital, Shenzhen University, Shenzhen, 518055, China.
Department of Biochemical Pharmacy, School of Pharmacy, Naval Medical University, Shanghai, 200433, China.
Heliyon. 2024 Aug 28;10(17):e37114. doi: 10.1016/j.heliyon.2024.e37114. eCollection 2024 Sep 15.
are known as opportunistic human pathogens that can cause a variety of infections. is a novel species associated with appendicitis, whereas their genomic characteristics and virulence potential remain understudied. This study aims to compare the genomic features of to that of the close species, and to assess its virulence-factor encoding capacity as an emerging pathogen.
Genomes similar to that of . HZ0627 were retrieved from the PATRIC-v3.6.10 web-server using the implanted Similar Genome Finder tool. Average nucleotide identity (ANI) between HZ0627 and the retrieved genomes was calculated using FastANI-v1.33. Core-genome sequences were extracted using Roary-v3.13.0, and core-genomic tree was constructed using FastTree-v2.1.11. Virulence-factor encoding capacity was predicted using PathoFact-v1.0.
Two previously unclassified sp. strains were reclassified as . Strains phylogenomically close to were clustered into five species, three of which were previously categorized under biogroup 3. Remarkably, genomosp. 6 was identified as the closest species to , exhibiting ANI values ranging from 94.45 % to 94.95 % against HZ0627. Genome annotation revealed shared genomic features and antimicrobial resistance (AMR) genes between and its phylogenetic neighbors. Additionally, is hypothesized to share infection mechanisms with genomosp. 6, as evidenced by the encoding of numerous virulence factors implicated in cell lysis and membrane pore-formation in the genome of both species.
This study provides genomic insights of sp. nov. and its taxonomic relatives, shedding light on their evolutionary relationships, pathogenic mechanisms, and AMR profiles. The findings are significant for the development of targeted therapeutic interventions against infections caused by this emerging pathogen.
已知作为机会性人类病原体可引起多种感染。是一种与阑尾炎相关的新物种,但其基因组特征和毒力潜力仍未得到充分研究。本研究旨在比较与相近物种的基因组特征,并评估其作为新兴病原体的毒力因子编码能力。
使用植入的相似基因组查找工具从PATRIC-v3.6.10网络服务器检索与HZ0627相似的基因组。使用FastANI-v1.33计算HZ0627与检索到的基因组之间的平均核苷酸同一性(ANI)。使用Roary-v3.13.0提取核心基因组序列,并使用FastTree-v2.1.11构建核心基因组树。使用PathoFact-v1.0预测毒力因子编码能力。
两个先前未分类的菌株被重新分类为。系统发育上与相近的菌株聚为五个物种,其中三个先前归类于生物群3。值得注意的是,基因组种6被确定为与最接近的物种,与HZ0627的ANI值范围为94.45%至94.95%。基因组注释揭示了与其系统发育邻域之间共享的基因组特征和抗菌耐药性(AMR)基因。此外,假设与基因组种6共享感染机制,这在两个物种的基因组中编码的许多参与细胞裂解和膜孔形成的毒力因子中得到证明。
本研究提供了新物种及其分类学亲属的基因组见解,揭示了它们的进化关系、致病机制和AMR概况。这些发现对于开发针对这种新兴病原体引起的感染的靶向治疗干预措施具有重要意义。