{"title":"基于pe-ppe基因家族的结核分枝杆菌L2.1全球遗传多样性","authors":"Olabisi Flora Davies-Bolorunduro , Bharkbhoom Jaemsai , Wuthiwat Ruangchai , Thanakron Noppanamas , Manon Boonbangyang , Prasit Palittapongarnpim","doi":"10.1016/j.meegid.2025.105802","DOIUrl":null,"url":null,"abstract":"<div><div>There are four major lineages of <em>Mycobacterium tuberculosis</em> (Mtb) whose geographic ranges vary considerably. Mtb lineage 2 (L2) or the East Asia lineage is particularly common in East and Southeast Asia, and also reported worldwide. Most L2 isolates belong to a sublineage L2.2 while L2.1 is more restricted to the Southern part of East Asia. It was reported that the L2.1 isolates in Thailand usually resisted isoniazid, rifampin and fluoroquinolones, <em>i.e.</em>, being pre-XDR strains. It is, therefore, of particular public health concern. Our previous study in a limited number of available complete genomes of L2.1 suggested unique structural variations of some <em>pe-ppe</em> genes. The gene family plays roles in immune evasion and host-pathogen interactions and, hence, is integral to the bacterium's virulence. Here we examine the identified structural variations of the <em>pe-ppe</em> gene family among all 180 L2.1 samples from eight countries, whose WGS data with high-quality are available in GenBank. We identified the deletion of the <em>esxR-esxS</em> gene segment in 26 L2.1 genomes, 19 of which, primarily restricted to Vietnam, Thailand, and China, belonged to a single clade. Additionally, we confirmed the deletions of four <em>pe-ppe</em> genes, <em>wag22, ppe38, ppe50</em> and <em>ppe66</em>, in all L2.1 samples. These genetic deletions may contribute to the virulence, pathogenesis, and evolutionary dynamics of the L2.1 strains, with significant implications for understanding the molecular mechanisms underlying the persistence and spread of this lineage.</div></div>","PeriodicalId":54986,"journal":{"name":"Infection Genetics and Evolution","volume":"134 ","pages":"Article 105802"},"PeriodicalIF":2.6000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Global genetic diversity of Mycobacterium tuberculosis L2.1 based on pe-ppe gene family\",\"authors\":\"Olabisi Flora Davies-Bolorunduro , Bharkbhoom Jaemsai , Wuthiwat Ruangchai , Thanakron Noppanamas , Manon Boonbangyang , Prasit Palittapongarnpim\",\"doi\":\"10.1016/j.meegid.2025.105802\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>There are four major lineages of <em>Mycobacterium tuberculosis</em> (Mtb) whose geographic ranges vary considerably. Mtb lineage 2 (L2) or the East Asia lineage is particularly common in East and Southeast Asia, and also reported worldwide. Most L2 isolates belong to a sublineage L2.2 while L2.1 is more restricted to the Southern part of East Asia. It was reported that the L2.1 isolates in Thailand usually resisted isoniazid, rifampin and fluoroquinolones, <em>i.e.</em>, being pre-XDR strains. It is, therefore, of particular public health concern. Our previous study in a limited number of available complete genomes of L2.1 suggested unique structural variations of some <em>pe-ppe</em> genes. The gene family plays roles in immune evasion and host-pathogen interactions and, hence, is integral to the bacterium's virulence. Here we examine the identified structural variations of the <em>pe-ppe</em> gene family among all 180 L2.1 samples from eight countries, whose WGS data with high-quality are available in GenBank. We identified the deletion of the <em>esxR-esxS</em> gene segment in 26 L2.1 genomes, 19 of which, primarily restricted to Vietnam, Thailand, and China, belonged to a single clade. Additionally, we confirmed the deletions of four <em>pe-ppe</em> genes, <em>wag22, ppe38, ppe50</em> and <em>ppe66</em>, in all L2.1 samples. These genetic deletions may contribute to the virulence, pathogenesis, and evolutionary dynamics of the L2.1 strains, with significant implications for understanding the molecular mechanisms underlying the persistence and spread of this lineage.</div></div>\",\"PeriodicalId\":54986,\"journal\":{\"name\":\"Infection Genetics and Evolution\",\"volume\":\"134 \",\"pages\":\"Article 105802\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Infection Genetics and Evolution\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1567134825000917\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection Genetics and Evolution","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1567134825000917","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Global genetic diversity of Mycobacterium tuberculosis L2.1 based on pe-ppe gene family
There are four major lineages of Mycobacterium tuberculosis (Mtb) whose geographic ranges vary considerably. Mtb lineage 2 (L2) or the East Asia lineage is particularly common in East and Southeast Asia, and also reported worldwide. Most L2 isolates belong to a sublineage L2.2 while L2.1 is more restricted to the Southern part of East Asia. It was reported that the L2.1 isolates in Thailand usually resisted isoniazid, rifampin and fluoroquinolones, i.e., being pre-XDR strains. It is, therefore, of particular public health concern. Our previous study in a limited number of available complete genomes of L2.1 suggested unique structural variations of some pe-ppe genes. The gene family plays roles in immune evasion and host-pathogen interactions and, hence, is integral to the bacterium's virulence. Here we examine the identified structural variations of the pe-ppe gene family among all 180 L2.1 samples from eight countries, whose WGS data with high-quality are available in GenBank. We identified the deletion of the esxR-esxS gene segment in 26 L2.1 genomes, 19 of which, primarily restricted to Vietnam, Thailand, and China, belonged to a single clade. Additionally, we confirmed the deletions of four pe-ppe genes, wag22, ppe38, ppe50 and ppe66, in all L2.1 samples. These genetic deletions may contribute to the virulence, pathogenesis, and evolutionary dynamics of the L2.1 strains, with significant implications for understanding the molecular mechanisms underlying the persistence and spread of this lineage.
期刊介绍:
(aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID)
Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance.
However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors.
Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases.
Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .