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利用全基因组测序分析乌鲁木齐不同谱系中 的毒力因子分布以及毒力基因突变对治疗结果的影响。

Analyzing the distribution of virulence factors of and the impact of virulence gene mutations on treatment outcomes in different lineages using whole-genome sequencing in Urumqi.

作者信息

Yang Jiandong, Lu Yaoqin, Chen Yanggui, Wang Yida, Wang Chao, Wang Kai

机构信息

School of Public Health, Xinjiang Medical University, Urumqi, People's Republic of China.

Department for Tuberculosis Control and Prevention, Urumqi Center for Disease Control and Prevention, Urumqi, People's Republic of China.

出版信息

Virulence. 2025 Dec;16(1):2552875. doi: 10.1080/21505594.2025.2552875. Epub 2025 Sep 16.

Abstract

This study centers on Urumqi, utilizing whole-genome sequencing and comparative genomics, we explored virulence factor mutations in different lineages and their impact on tuberculosis patient prognosis. We utilized routine national drug resistance surveillance data from Urumqi, gathering demographic, epidemiological, and clinical data of patients with tuberculosis between 1 January 2017 to 31 December 2021. Whole-genome sequencing was employed, followed by bioinformatics analysis using various methods and statistical models. A total of 457 patients with tuberculosis were analyzed. Through whole-genome sequencing and bioinformatics analysis, we categorized these strains into three lineages: Lineage2 (347), Lineage3 (37), and Lineage4 (73), identifying 71 virulence factor mutations. The mutation rates of virulence factors in exhibited polarization. Significant differences in virulence factor mutation rates were observed among different lineages (all values  < 0.05). Additionally, mutations in espE, fadE29, and mbtI genes among Lineage2 patients were considered as risk factors influencing treatment outcomes (all values < 0.05), with odds ratios of 13.6200 (1.7285-107.3201), 7.1262 (1.3294-38.1997), and 14.8340 (1.1577-190.0784), respectively. Varied virulence factor mutations and virulence factor-related gene mutations exist across different lineages. Mutations in the espE, fadE29, and mbtI genes are risk factors that significantly affect the treatment outcome of Lineage2 patients. This finding serves as a reference for investigating the future evolutionary direction, transmissibility, drug resistance, and pathogenicity of virulence factors in regions with diverse lineages and frequent population movements.

摘要

本研究以乌鲁木齐为中心,利用全基因组测序和比较基因组学,探索不同谱系中的毒力因子突变及其对结核病患者预后的影响。我们利用了乌鲁木齐的国家常规耐药监测数据,收集了2017年1月1日至2021年12月31日期间结核病患者的人口统计学、流行病学和临床数据。采用全基因组测序,随后使用各种方法和统计模型进行生物信息学分析。共分析了457例结核病患者。通过全基因组测序和生物信息学分析,我们将这些菌株分为三个谱系:谱系2(347株)、谱系3(37株)和谱系4(73株),鉴定出71个毒力因子突变。毒力因子的突变率呈现两极分化。不同谱系之间毒力因子突变率存在显著差异(所有P值<0.05)。此外,谱系2患者中espE、fadE29和mbtI基因的突变被认为是影响治疗结果的危险因素(所有P值<0.05),比值比分别为13.6200(1.7285 - 107.3201)、7.1262(1.3294 - 38.1997)和14.8340(1.1577 - 190.0784)。不同谱系存在不同的毒力因子突变和与毒力因子相关的基因突变。espE、fadE29和mbtI基因的突变是显著影响谱系2患者治疗结果的危险因素。这一发现为调查不同谱系且人口流动频繁地区结核菌毒力因子的未来进化方向、传播性、耐药性和致病性提供了参考。

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