Mari Ishida , Takao Irie , Ryusei Tanaka , Haruhiko Maruyama , Ayako Yoshida
{"title":"转录组分析揭示了鼠圆线虫组织迁移幼虫基因表达的变化。","authors":"Mari Ishida , Takao Irie , Ryusei Tanaka , Haruhiko Maruyama , Ayako Yoshida","doi":"10.1016/j.meegid.2025.105839","DOIUrl":null,"url":null,"abstract":"<div><div><em>Strongyloides ratti</em> is an intestinal nematode commonly found in rats. Unlike other <em>Strongyloides</em> species, the tissue-migrating third-stage larvae in <em>S. ratti</em> follow a unique route of invasion via the nasofrontal region before reaching the gut. Despite its importance in host invasion, the transcriptomic profile of this larval stage has not been characterized. In this study, we performed RNA sequencing (RNA-seq) to examine gene expression in head-derived tissue-migrating third-stage larvae (hL3) and infective third-stage larvae (iL3) of the <em>S. ratti</em> Tokyo strain. hL3 were collected from rat heads at 30 h post-infection. Differential expression analysis revealed 664 upregulated genes in hL3. Functional annotation showed enrichment of genes encoding astacin metalloproteases and sperm-coating protein/Tpx-1/Ag5/PR-1/Sc7 (SCP/TAPS) protein families—both associated with tissue invasion and immune modulation. Quantitative RT-PCR was used to validate selected differentially expressed genes. Seven hL3-specific astacin genes were identified, of which six belonged to the M12A group. One hL3-specific astacin gene showed domain similarity to strongylastacin, a known tissue-penetration protein. Two SCP/TAPS genes were unique to hL3 and were absent from parasitic females, suggesting distinct roles in larval migration. By contrast, G protein-coupled receptor genes, particularly those related to chemosensory functions, were not upregulated in hL3, indicating that these pathways may be less important during this stage. These results provide the first transcriptomic profile of hL3 in <em>S. ratti</em>, and identify potential molecular mechanisms driving larval migration and immune evasion during host infection.</div></div>","PeriodicalId":54986,"journal":{"name":"Infection Genetics and Evolution","volume":"135 ","pages":"Article 105839"},"PeriodicalIF":2.6000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transcriptome analysis reveals the gene expression changes in Strongyloides ratti tissue-migrating larvae\",\"authors\":\"Mari Ishida , Takao Irie , Ryusei Tanaka , Haruhiko Maruyama , Ayako Yoshida\",\"doi\":\"10.1016/j.meegid.2025.105839\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Strongyloides ratti</em> is an intestinal nematode commonly found in rats. Unlike other <em>Strongyloides</em> species, the tissue-migrating third-stage larvae in <em>S. ratti</em> follow a unique route of invasion via the nasofrontal region before reaching the gut. Despite its importance in host invasion, the transcriptomic profile of this larval stage has not been characterized. In this study, we performed RNA sequencing (RNA-seq) to examine gene expression in head-derived tissue-migrating third-stage larvae (hL3) and infective third-stage larvae (iL3) of the <em>S. ratti</em> Tokyo strain. hL3 were collected from rat heads at 30 h post-infection. Differential expression analysis revealed 664 upregulated genes in hL3. Functional annotation showed enrichment of genes encoding astacin metalloproteases and sperm-coating protein/Tpx-1/Ag5/PR-1/Sc7 (SCP/TAPS) protein families—both associated with tissue invasion and immune modulation. Quantitative RT-PCR was used to validate selected differentially expressed genes. Seven hL3-specific astacin genes were identified, of which six belonged to the M12A group. One hL3-specific astacin gene showed domain similarity to strongylastacin, a known tissue-penetration protein. Two SCP/TAPS genes were unique to hL3 and were absent from parasitic females, suggesting distinct roles in larval migration. By contrast, G protein-coupled receptor genes, particularly those related to chemosensory functions, were not upregulated in hL3, indicating that these pathways may be less important during this stage. These results provide the first transcriptomic profile of hL3 in <em>S. ratti</em>, and identify potential molecular mechanisms driving larval migration and immune evasion during host infection.</div></div>\",\"PeriodicalId\":54986,\"journal\":{\"name\":\"Infection Genetics and Evolution\",\"volume\":\"135 \",\"pages\":\"Article 105839\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-10-08\",\"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/S1567134825001285\",\"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/S1567134825001285","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Transcriptome analysis reveals the gene expression changes in Strongyloides ratti tissue-migrating larvae
Strongyloides ratti is an intestinal nematode commonly found in rats. Unlike other Strongyloides species, the tissue-migrating third-stage larvae in S. ratti follow a unique route of invasion via the nasofrontal region before reaching the gut. Despite its importance in host invasion, the transcriptomic profile of this larval stage has not been characterized. In this study, we performed RNA sequencing (RNA-seq) to examine gene expression in head-derived tissue-migrating third-stage larvae (hL3) and infective third-stage larvae (iL3) of the S. ratti Tokyo strain. hL3 were collected from rat heads at 30 h post-infection. Differential expression analysis revealed 664 upregulated genes in hL3. Functional annotation showed enrichment of genes encoding astacin metalloproteases and sperm-coating protein/Tpx-1/Ag5/PR-1/Sc7 (SCP/TAPS) protein families—both associated with tissue invasion and immune modulation. Quantitative RT-PCR was used to validate selected differentially expressed genes. Seven hL3-specific astacin genes were identified, of which six belonged to the M12A group. One hL3-specific astacin gene showed domain similarity to strongylastacin, a known tissue-penetration protein. Two SCP/TAPS genes were unique to hL3 and were absent from parasitic females, suggesting distinct roles in larval migration. By contrast, G protein-coupled receptor genes, particularly those related to chemosensory functions, were not upregulated in hL3, indicating that these pathways may be less important during this stage. These results provide the first transcriptomic profile of hL3 in S. ratti, and identify potential molecular mechanisms driving larval migration and immune evasion during host infection.
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 .