Frontiers in microbiology · 2026
Recurrent gene conversions and subcluster-specific variants are associated with Mycobacterium tuberculosis adaptation to intensive host pressure: a comparative genomic study.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Lin Tianyu, Chen Kun, Chen Zhenchun, Jin Yurou, Chen Weizhen
Аннотация
BACKGROUND: Long-read sequencing has revealed complex variations, such as gene conversions in immunologically critical PE/PPE gene families, yet their role in Mycobacterium tuberculosis host adaptation remains unclear.
METHODS: We performed a comparative genomic analysis across a gradient of host-imposed selective pressure: chronic within-host infection, latent household transmission, and a 21-year clonal outbreak in Bern, Switzerland.
RESULTS: We observed a constrained accumulation of mutational events across distinct epidemiological settings, with rates ranging from 0.36 to 0.81 events per genome per year. Under minimal host-imposed selection, the pathogen accumulated only small-scale variants (i.e., SNPs and indels). During the outbreak, however, the genetic diversity landscape shifted toward larger-scale variants, including recurrent gene conversions and structural variations. Notably, an early PPE19-to-PPE18 conversion emerged in the ancestral strain and was maintained across the entire lineage. In contrast, 86% of variants were transient singletons, with only a small proportion persisting under selection.
CONCLUSION: These findings suggest a framework in which M. tuberculosis maintains genomic stability through purifying selection, while retaining the capacity to generate adaptive diversity through large-scale genetic rearrangements in immunologically relevant genomic features under intensified host pressure.
METHODS: We performed a comparative genomic analysis across a gradient of host-imposed selective pressure: chronic within-host infection, latent household transmission, and a 21-year clonal outbreak in Bern, Switzerland.
RESULTS: We observed a constrained accumulation of mutational events across distinct epidemiological settings, with rates ranging from 0.36 to 0.81 events per genome per year. Under minimal host-imposed selection, the pathogen accumulated only small-scale variants (i.e., SNPs and indels). During the outbreak, however, the genetic diversity landscape shifted toward larger-scale variants, including recurrent gene conversions and structural variations. Notably, an early PPE19-to-PPE18 conversion emerged in the ancestral strain and was maintained across the entire lineage. In contrast, 86% of variants were transient singletons, with only a small proportion persisting under selection.
CONCLUSION: These findings suggest a framework in which M. tuberculosis maintains genomic stability through purifying selection, while retaining the capacity to generate adaptive diversity through large-scale genetic rearrangements in immunologically relevant genomic features under intensified host pressure.