Amanda M. Brandow, Samantha N. Atkinson, Zulmary Manjarres, Vanessa L. Ehlers, McKenna L. Pratt, Iti Mehta, Sruthi Mudunuri, Aishwarya Kappagantu, Stephanie I. Shiers, Khadijah Mazhar, Mackenzie A. Simms, Sahar Alhendi, Anagha Sheshadri, Anna M. Cervantes, Jeffrey C. Reese, Diana Tavares-Ferreira, Ishwarya Sankaranarayanan, Mandee K. Schaub, Tyler B. Waltz, Michael Hayward, Katelyn E. Sadler
{"title":"肠道微生物群和代谢物驱动小鼠慢性镰状细胞病疼痛","authors":"Amanda M. Brandow, Samantha N. Atkinson, Zulmary Manjarres, Vanessa L. Ehlers, McKenna L. Pratt, Iti Mehta, Sruthi Mudunuri, Aishwarya Kappagantu, Stephanie I. Shiers, Khadijah Mazhar, Mackenzie A. Simms, Sahar Alhendi, Anagha Sheshadri, Anna M. Cervantes, Jeffrey C. Reese, Diana Tavares-Ferreira, Ishwarya Sankaranarayanan, Mandee K. Schaub, Tyler B. Waltz, Michael Hayward, Katelyn E. Sadler","doi":"10.1016/j.chom.2025.08.012","DOIUrl":null,"url":null,"abstract":"Individuals with sickle cell disease (SCD) suffer from debilitating chronic pain that does not have a clear etiology. Recent 16S ribosomal RNA gene sequencing studies revealed gut dysbiosis in individuals with SCD. It is unclear, however, whether these intestinal microbial changes contribute to chronic SCD pain. Using transgenic SCD mice, we determined that chronic SCD pain is alleviated following fecal microbiota transplantation from healthy controls, specifically by increasing the relative abundance of probiotic <em>Akkermansia muciniphila</em>. Reciprocally, transplantation of the SCD gut microbiome induced persistent pain in wild-type recipients via bilirubin-vagus nerve TRPM2 signaling. Biospecimens from individuals with SCD and spatial transcriptomic analysis of human nodose ganglia tissue identified additional bacterial species and neuronally expressed transcripts that should be explored as novel SCD analgesic targets.","PeriodicalId":9693,"journal":{"name":"Cell host & microbe","volume":"35 1","pages":""},"PeriodicalIF":18.7000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gut microbiota and metabolites drive chronic sickle cell disease pain in mice\",\"authors\":\"Amanda M. Brandow, Samantha N. Atkinson, Zulmary Manjarres, Vanessa L. Ehlers, McKenna L. Pratt, Iti Mehta, Sruthi Mudunuri, Aishwarya Kappagantu, Stephanie I. Shiers, Khadijah Mazhar, Mackenzie A. Simms, Sahar Alhendi, Anagha Sheshadri, Anna M. Cervantes, Jeffrey C. Reese, Diana Tavares-Ferreira, Ishwarya Sankaranarayanan, Mandee K. Schaub, Tyler B. Waltz, Michael Hayward, Katelyn E. Sadler\",\"doi\":\"10.1016/j.chom.2025.08.012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Individuals with sickle cell disease (SCD) suffer from debilitating chronic pain that does not have a clear etiology. Recent 16S ribosomal RNA gene sequencing studies revealed gut dysbiosis in individuals with SCD. It is unclear, however, whether these intestinal microbial changes contribute to chronic SCD pain. Using transgenic SCD mice, we determined that chronic SCD pain is alleviated following fecal microbiota transplantation from healthy controls, specifically by increasing the relative abundance of probiotic <em>Akkermansia muciniphila</em>. Reciprocally, transplantation of the SCD gut microbiome induced persistent pain in wild-type recipients via bilirubin-vagus nerve TRPM2 signaling. Biospecimens from individuals with SCD and spatial transcriptomic analysis of human nodose ganglia tissue identified additional bacterial species and neuronally expressed transcripts that should be explored as novel SCD analgesic targets.\",\"PeriodicalId\":9693,\"journal\":{\"name\":\"Cell host & microbe\",\"volume\":\"35 1\",\"pages\":\"\"},\"PeriodicalIF\":18.7000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell host & microbe\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.chom.2025.08.012\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell host & microbe","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.chom.2025.08.012","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Gut microbiota and metabolites drive chronic sickle cell disease pain in mice
Individuals with sickle cell disease (SCD) suffer from debilitating chronic pain that does not have a clear etiology. Recent 16S ribosomal RNA gene sequencing studies revealed gut dysbiosis in individuals with SCD. It is unclear, however, whether these intestinal microbial changes contribute to chronic SCD pain. Using transgenic SCD mice, we determined that chronic SCD pain is alleviated following fecal microbiota transplantation from healthy controls, specifically by increasing the relative abundance of probiotic Akkermansia muciniphila. Reciprocally, transplantation of the SCD gut microbiome induced persistent pain in wild-type recipients via bilirubin-vagus nerve TRPM2 signaling. Biospecimens from individuals with SCD and spatial transcriptomic analysis of human nodose ganglia tissue identified additional bacterial species and neuronally expressed transcripts that should be explored as novel SCD analgesic targets.
期刊介绍:
Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.