Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus

ABSTRACT Systemic lupus erythematosus (SLE) is the prototypical systemic autoimmune disease in humans and is characterized by the presence of hyperactive immune cells and aberrant antibody responses to nuclear and cytoplasmic antigens, including characteristic anti–double-stranded DNA antibodies. We...

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Autores principales: Arancha Hevia, Christian Milani, Patricia López, Adriana Cuervo, Silvia Arboleya, Sabrina Duranti, Francesca Turroni, Sonia González, Ana Suárez, Miguel Gueimonde, Marco Ventura, Borja Sánchez, Abelardo Margolles
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Publicado: American Society for Microbiology 2014
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spelling oai:doaj.org-article:0d47767074f34d26b887e4a9f3961c692021-11-15T15:45:54ZIntestinal Dysbiosis Associated with Systemic Lupus Erythematosus10.1128/mBio.01548-142150-7511https://doaj.org/article/0d47767074f34d26b887e4a9f3961c692014-10-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01548-14https://doaj.org/toc/2150-7511ABSTRACT Systemic lupus erythematosus (SLE) is the prototypical systemic autoimmune disease in humans and is characterized by the presence of hyperactive immune cells and aberrant antibody responses to nuclear and cytoplasmic antigens, including characteristic anti–double-stranded DNA antibodies. We performed a cross-sectional study in order to determine if an SLE-associated gut dysbiosis exists in patients without active disease. A group of 20 SLE patients in remission, for which there was strict inclusion and exclusion criteria, was recruited, and we used an optimized Ion Torrent 16S rRNA gene-based analysis protocol to decipher the fecal microbial profiles of these patients and compare them with those of 20 age- and sex-matched healthy control subjects. We found diversity to be comparable based on Shannon’s index. However, we saw a significantly lower Firmicutes/Bacteroidetes ratio in SLE individuals (median ratio, 1.97) than in healthy subjects (median ratio, 4.86; P < 0.002). A lower Firmicutes/Bacteroidetes ratio in SLE individuals was corroborated by quantitative PCR analysis. Notably, a decrease of some Firmicutes families was also detected. This dysbiosis is reflected, based on in silico functional inference, in an overrepresentation of oxidative phosphorylation and glycan utilization pathways in SLE patient microbiota. IMPORTANCE Growing evidence suggests that the gut microbiota might impact symptoms and progression of some autoimmune diseases. However, how and why this microbial community influences SLE remains to be elucidated. This is the first report describing an SLE-associated intestinal dysbiosis, and it contributes to the understanding of the interplay between the intestinal microbiota and the host in autoimmune disorders.Arancha HeviaChristian MilaniPatricia LópezAdriana CuervoSilvia ArboleyaSabrina DurantiFrancesca TurroniSonia GonzálezAna SuárezMiguel GueimondeMarco VenturaBorja SánchezAbelardo MargollesAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 5, Iss 5 (2014)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Arancha Hevia
Christian Milani
Patricia López
Adriana Cuervo
Silvia Arboleya
Sabrina Duranti
Francesca Turroni
Sonia González
Ana Suárez
Miguel Gueimonde
Marco Ventura
Borja Sánchez
Abelardo Margolles
Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus
description ABSTRACT Systemic lupus erythematosus (SLE) is the prototypical systemic autoimmune disease in humans and is characterized by the presence of hyperactive immune cells and aberrant antibody responses to nuclear and cytoplasmic antigens, including characteristic anti–double-stranded DNA antibodies. We performed a cross-sectional study in order to determine if an SLE-associated gut dysbiosis exists in patients without active disease. A group of 20 SLE patients in remission, for which there was strict inclusion and exclusion criteria, was recruited, and we used an optimized Ion Torrent 16S rRNA gene-based analysis protocol to decipher the fecal microbial profiles of these patients and compare them with those of 20 age- and sex-matched healthy control subjects. We found diversity to be comparable based on Shannon’s index. However, we saw a significantly lower Firmicutes/Bacteroidetes ratio in SLE individuals (median ratio, 1.97) than in healthy subjects (median ratio, 4.86; P < 0.002). A lower Firmicutes/Bacteroidetes ratio in SLE individuals was corroborated by quantitative PCR analysis. Notably, a decrease of some Firmicutes families was also detected. This dysbiosis is reflected, based on in silico functional inference, in an overrepresentation of oxidative phosphorylation and glycan utilization pathways in SLE patient microbiota. IMPORTANCE Growing evidence suggests that the gut microbiota might impact symptoms and progression of some autoimmune diseases. However, how and why this microbial community influences SLE remains to be elucidated. This is the first report describing an SLE-associated intestinal dysbiosis, and it contributes to the understanding of the interplay between the intestinal microbiota and the host in autoimmune disorders.
format article
author Arancha Hevia
Christian Milani
Patricia López
Adriana Cuervo
Silvia Arboleya
Sabrina Duranti
Francesca Turroni
Sonia González
Ana Suárez
Miguel Gueimonde
Marco Ventura
Borja Sánchez
Abelardo Margolles
author_facet Arancha Hevia
Christian Milani
Patricia López
Adriana Cuervo
Silvia Arboleya
Sabrina Duranti
Francesca Turroni
Sonia González
Ana Suárez
Miguel Gueimonde
Marco Ventura
Borja Sánchez
Abelardo Margolles
author_sort Arancha Hevia
title Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus
title_short Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus
title_full Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus
title_fullStr Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus
title_full_unstemmed Intestinal Dysbiosis Associated with Systemic Lupus Erythematosus
title_sort intestinal dysbiosis associated with systemic lupus erythematosus
publisher American Society for Microbiology
publishDate 2014
url https://doaj.org/article/0d47767074f34d26b887e4a9f3961c69
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