{"title":"肠道原生动物的细胞外囊泡:宿主-寄生虫通讯的隐藏介质。","authors":"Manouchehr Fadaee, Masoud Lahouty, Fatemeh Ramzi, Fatemeh Alizadeh, Sima Roshanfar, Tohid Kazemi, Adel Spotin, Kareem Hatam-Nahavandi, Ehsan Ahmadpour","doi":"10.1186/s13099-025-00747-8","DOIUrl":null,"url":null,"abstract":"<p><p>Intestinal protozoan parasites, including, Cryptosporidium spp., Giardia duodenalis, Entamoeba histolytica, and Blastocystis sp. pose significant global health challenges, particularly in developing regions with limited access to sanitation and healthcare resources. Extracellular vesicles (EVs) have emerged as critical factors for communication in the complex interplay between intestinal protozoan parasites and their hosts. This review explores the diverse roles of parasite-derived EVs, with a focus on their biogenesis, molecular cargo, and host interactions. Studies show that G. duodenalis EVs disrupt tight junctions in intestinal epithelia and promote Th1 immune responses. Blastocystis sp. EVs modulate cytokine production, increasing IL-6 and TNF-α while reducing IL-10 and IL-4. E. histolytica EVs inhibit immune cell recruitment by downregulating STAT6 signaling and suppressing IL-4 and IL-13. Additionally, Cryptosporidium-infected epithelial cells release EVs enriched in GP60 and CpRom1 proteins that stimulate host immune responses via the TLR4/IKK pathway. Beyond pathogenesis, the specific and stable cargo of parasitic EVs supports their utility as biomarkers and therapeutic agents. Ongoing research into their roles in microbiome modulation and immune regulation may inform future diagnostics and treatments for parasitic infections.</p>","PeriodicalId":12833,"journal":{"name":"Gut Pathogens","volume":"17 1","pages":"69"},"PeriodicalIF":4.0000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12395738/pdf/","citationCount":"0","resultStr":"{\"title\":\"Extracellular vesicles in intestinal protozoa: hidden mediators of host-parasite communication.\",\"authors\":\"Manouchehr Fadaee, Masoud Lahouty, Fatemeh Ramzi, Fatemeh Alizadeh, Sima Roshanfar, Tohid Kazemi, Adel Spotin, Kareem Hatam-Nahavandi, Ehsan Ahmadpour\",\"doi\":\"10.1186/s13099-025-00747-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Intestinal protozoan parasites, including, Cryptosporidium spp., Giardia duodenalis, Entamoeba histolytica, and Blastocystis sp. pose significant global health challenges, particularly in developing regions with limited access to sanitation and healthcare resources. Extracellular vesicles (EVs) have emerged as critical factors for communication in the complex interplay between intestinal protozoan parasites and their hosts. This review explores the diverse roles of parasite-derived EVs, with a focus on their biogenesis, molecular cargo, and host interactions. Studies show that G. duodenalis EVs disrupt tight junctions in intestinal epithelia and promote Th1 immune responses. Blastocystis sp. EVs modulate cytokine production, increasing IL-6 and TNF-α while reducing IL-10 and IL-4. E. histolytica EVs inhibit immune cell recruitment by downregulating STAT6 signaling and suppressing IL-4 and IL-13. Additionally, Cryptosporidium-infected epithelial cells release EVs enriched in GP60 and CpRom1 proteins that stimulate host immune responses via the TLR4/IKK pathway. Beyond pathogenesis, the specific and stable cargo of parasitic EVs supports their utility as biomarkers and therapeutic agents. Ongoing research into their roles in microbiome modulation and immune regulation may inform future diagnostics and treatments for parasitic infections.</p>\",\"PeriodicalId\":12833,\"journal\":{\"name\":\"Gut Pathogens\",\"volume\":\"17 1\",\"pages\":\"69\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12395738/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Gut Pathogens\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s13099-025-00747-8\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gut Pathogens","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13099-025-00747-8","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
Extracellular vesicles in intestinal protozoa: hidden mediators of host-parasite communication.
Intestinal protozoan parasites, including, Cryptosporidium spp., Giardia duodenalis, Entamoeba histolytica, and Blastocystis sp. pose significant global health challenges, particularly in developing regions with limited access to sanitation and healthcare resources. Extracellular vesicles (EVs) have emerged as critical factors for communication in the complex interplay between intestinal protozoan parasites and their hosts. This review explores the diverse roles of parasite-derived EVs, with a focus on their biogenesis, molecular cargo, and host interactions. Studies show that G. duodenalis EVs disrupt tight junctions in intestinal epithelia and promote Th1 immune responses. Blastocystis sp. EVs modulate cytokine production, increasing IL-6 and TNF-α while reducing IL-10 and IL-4. E. histolytica EVs inhibit immune cell recruitment by downregulating STAT6 signaling and suppressing IL-4 and IL-13. Additionally, Cryptosporidium-infected epithelial cells release EVs enriched in GP60 and CpRom1 proteins that stimulate host immune responses via the TLR4/IKK pathway. Beyond pathogenesis, the specific and stable cargo of parasitic EVs supports their utility as biomarkers and therapeutic agents. Ongoing research into their roles in microbiome modulation and immune regulation may inform future diagnostics and treatments for parasitic infections.
Gut PathogensGASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍:
Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology.
Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).