Zhou Guilan, Yu Yan, Ge Teng, Tang Chenyu, Zhang Hongbo, He Min
Nanjing Center for Disease Control and Prevention, Nanjing, Jiangsu, China.
Nanjing Municipal Key Laboratory for Public Health Laboratory Technology, Nanjing, Jiangsu, China.
Front Microbiol. 2025 May 14;16:1589971. doi: 10.3389/fmicb.2025.1589971. eCollection 2025.
(), a slow-growing, fastidious Gram-negative bacterium and a leading cause of community-acquired pneumonia globally, remains understudied and underreported across numerous geographical areas in China despite its worldwide significance. This study employed probe capture sequencing for targeted enrichment and direct sequencing of from clinical samples, combined with comparative genomic analyses of contemporary and historical global genomes. Core genome and pan-genome revealed that the genomes were classified into two distinct clades, P1-I and P1-II, each associated with a specific sequence type (ST). Most of the genomes sequenced in this study were identified as P1-I (86.96%, 20/23), contrasting with the previously reported predominance of P1-II in the area. A limited number of single-nucleotide variations were identified in the virulence-associated genes between P1-I and P1-II, leading to amino acid substitutions. The A2063G point mutation in the 23S rRNA gene was detected in all sequenced genomes (23/23), demonstrating a 100% mutation rate. This study provides the first reported application of probe capture methodology for , highlighting the critical importance of sustained surveillance efforts to monitor the evolution and epidemiology of this pathogen.
()是一种生长缓慢、苛求营养的革兰氏阴性细菌,是全球社区获得性肺炎的主要病因,尽管其在全球具有重要意义,但在中国众多地理区域仍未得到充分研究和报告。本研究采用探针捕获测序技术对临床样本中的()进行靶向富集和直接测序,并结合当代和历史全球基因组的比较基因组分析。核心基因组和泛基因组显示,()基因组被分为两个不同的进化枝,P1-I和P1-II,每个进化枝与一种特定的序列类型(ST)相关。本研究中测序的大多数基因组被鉴定为P1-I(86.96%,20/23),这与该地区先前报道的P1-II占主导地位形成对比。在P1-I和P1-II之间的毒力相关基因中鉴定出有限数量的单核苷酸变异,导致氨基酸替换。在所有测序基因组(23/23)中均检测到23S rRNA基因中的A2063G点突变,突变率为100%。本研究首次报道了探针捕获方法在()中的应用,强调了持续监测努力对监测该病原体的进化和流行病学的至关重要性。