Cargando…
A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients
Lyme disease is the most common vector-borne disease in the United States, with an estimated incidence of 300,000 infections annually. Antibiotic intervention cures Lyme disease in the majority of cases; however, 10 to 20% of patients develop posttreatment Lyme disease syndrome (PTLDS), a debilitati...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527730/ https://www.ncbi.nlm.nih.gov/pubmed/32994327 http://dx.doi.org/10.1128/mBio.02310-20 |
_version_ | 1783589119311478784 |
---|---|
author | Morrissette, Madeleine Pitt, Norman González, Antonio Strandwitz, Philip Caboni, Mariaelena Rebman, Alison W. Knight, Rob D’Onofrio, Anthony Aucott, John N. Soloski, Mark J. Lewis, Kim |
author_facet | Morrissette, Madeleine Pitt, Norman González, Antonio Strandwitz, Philip Caboni, Mariaelena Rebman, Alison W. Knight, Rob D’Onofrio, Anthony Aucott, John N. Soloski, Mark J. Lewis, Kim |
author_sort | Morrissette, Madeleine |
collection | PubMed |
description | Lyme disease is the most common vector-borne disease in the United States, with an estimated incidence of 300,000 infections annually. Antibiotic intervention cures Lyme disease in the majority of cases; however, 10 to 20% of patients develop posttreatment Lyme disease syndrome (PTLDS), a debilitating condition characterized by chronic fatigue, pain, and cognitive difficulties. The underlying mechanism responsible for PTLDS symptoms, as well as a reliable diagnostic tool, has remained elusive. We reasoned that the gut microbiome may play an important role in PTLDS given that the symptoms overlap considerably with conditions in which a dysbiotic microbiome has been observed, including mood, cognition, and autoimmune disorders. Analysis of sequencing data from a rigorously curated cohort of patients with PTLDS revealed a gut microbiome signature distinct from that of healthy control subjects, as well as from that of intensive care unit (ICU) patients. Notably, microbiome sequencing data alone were indicative of PTLDS, which presents a potential, novel diagnostic tool for PTLDS. |
format | Online Article Text |
id | pubmed-7527730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-75277302020-10-19 A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients Morrissette, Madeleine Pitt, Norman González, Antonio Strandwitz, Philip Caboni, Mariaelena Rebman, Alison W. Knight, Rob D’Onofrio, Anthony Aucott, John N. Soloski, Mark J. Lewis, Kim mBio Research Article Lyme disease is the most common vector-borne disease in the United States, with an estimated incidence of 300,000 infections annually. Antibiotic intervention cures Lyme disease in the majority of cases; however, 10 to 20% of patients develop posttreatment Lyme disease syndrome (PTLDS), a debilitating condition characterized by chronic fatigue, pain, and cognitive difficulties. The underlying mechanism responsible for PTLDS symptoms, as well as a reliable diagnostic tool, has remained elusive. We reasoned that the gut microbiome may play an important role in PTLDS given that the symptoms overlap considerably with conditions in which a dysbiotic microbiome has been observed, including mood, cognition, and autoimmune disorders. Analysis of sequencing data from a rigorously curated cohort of patients with PTLDS revealed a gut microbiome signature distinct from that of healthy control subjects, as well as from that of intensive care unit (ICU) patients. Notably, microbiome sequencing data alone were indicative of PTLDS, which presents a potential, novel diagnostic tool for PTLDS. American Society for Microbiology 2020-09-29 /pmc/articles/PMC7527730/ /pubmed/32994327 http://dx.doi.org/10.1128/mBio.02310-20 Text en Copyright © 2020 Morrissette et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Morrissette, Madeleine Pitt, Norman González, Antonio Strandwitz, Philip Caboni, Mariaelena Rebman, Alison W. Knight, Rob D’Onofrio, Anthony Aucott, John N. Soloski, Mark J. Lewis, Kim A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients |
title | A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients |
title_full | A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients |
title_fullStr | A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients |
title_full_unstemmed | A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients |
title_short | A Distinct Microbiome Signature in Posttreatment Lyme Disease Patients |
title_sort | distinct microbiome signature in posttreatment lyme disease patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527730/ https://www.ncbi.nlm.nih.gov/pubmed/32994327 http://dx.doi.org/10.1128/mBio.02310-20 |
work_keys_str_mv | AT morrissettemadeleine adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT pittnorman adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT gonzalezantonio adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT strandwitzphilip adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT cabonimariaelena adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT rebmanalisonw adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT knightrob adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT donofrioanthony adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT aucottjohnn adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT soloskimarkj adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT lewiskim adistinctmicrobiomesignatureinposttreatmentlymediseasepatients AT morrissettemadeleine distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT pittnorman distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT gonzalezantonio distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT strandwitzphilip distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT cabonimariaelena distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT rebmanalisonw distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT knightrob distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT donofrioanthony distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT aucottjohnn distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT soloskimarkj distinctmicrobiomesignatureinposttreatmentlymediseasepatients AT lewiskim distinctmicrobiomesignatureinposttreatmentlymediseasepatients |