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Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities

Psoriasis is a chronic inflammatory skin disease, whose pathogenesis involves dysregulated interplay among immune cells, keratinocytes and environmental triggers, including microbiota. Bacterial and fungal dysbiosis has been recently associated with several chronic immune-mediated diseases including...

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Autores principales: Stehlikova, Zuzana, Kostovcik, Martin, Kostovcikova, Klara, Kverka, Miloslav, Juzlova, Katerina, Rob, Filip, Hercogova, Jana, Bohac, Petr, Pinto, Yishay, Uzan, Atara, Koren, Omry, Tlaskalova-Hogenova, Helena, Jiraskova Zakostelska, Zuzana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437110/
https://www.ncbi.nlm.nih.gov/pubmed/30949136
http://dx.doi.org/10.3389/fmicb.2019.00438
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author Stehlikova, Zuzana
Kostovcik, Martin
Kostovcikova, Klara
Kverka, Miloslav
Juzlova, Katerina
Rob, Filip
Hercogova, Jana
Bohac, Petr
Pinto, Yishay
Uzan, Atara
Koren, Omry
Tlaskalova-Hogenova, Helena
Jiraskova Zakostelska, Zuzana
author_facet Stehlikova, Zuzana
Kostovcik, Martin
Kostovcikova, Klara
Kverka, Miloslav
Juzlova, Katerina
Rob, Filip
Hercogova, Jana
Bohac, Petr
Pinto, Yishay
Uzan, Atara
Koren, Omry
Tlaskalova-Hogenova, Helena
Jiraskova Zakostelska, Zuzana
author_sort Stehlikova, Zuzana
collection PubMed
description Psoriasis is a chronic inflammatory skin disease, whose pathogenesis involves dysregulated interplay among immune cells, keratinocytes and environmental triggers, including microbiota. Bacterial and fungal dysbiosis has been recently associated with several chronic immune-mediated diseases including psoriasis. In this comprehensive study, we investigated how different sampling sites and methods reflect the uncovered skin microbiota composition. After establishing the most suitable approach, we further examined correlations between bacteria and fungi on the psoriatic skin. We compared microbiota composition determined in the same sample by sequencing two distinct hypervariable regions of the 16S rRNA gene. We showed that using the V3V4 region led to higher species richness and evenness than using the V1V2 region. In particular, genera, such as Staphylococcus and Micrococcus were more abundant when using the V3V4 region, while Planococcaceae, on the other hand, were detected only by the V1V2 region. We performed a detailed analysis of skin microbiota composition of psoriatic lesions, unaffected psoriatic skin, and healthy control skin from the back and elbow. Only a few discriminative features were uncovered, mostly specific for the sampling site or method (swab, scraping, or biopsy). Swabs from psoriatic lesions on the back and the elbow were associated with increased abundance of Brevibacterium and Kocuria palustris and Gordonia, respectively. In the same samples from psoriatic lesions, we found a significantly higher abundance of the fungus Malassezia restricta on the back, while Malassezia sympodialis dominated the elbow mycobiota. In psoriatic elbow skin, we found significant correlation between occurrence of Kocuria, Lactobacillus, and Streptococcus with Saccharomyces, which was not observed in healthy skin. For the first time, we showed here a psoriasis-specific correlation between fungal and bacterial species, suggesting a link between competition for niche occupancy and psoriasis. However, it still remains to be elucidated whether observed microbial shift and specific inter-kingdom relationship pattern are of primary etiological significance or secondary to the disease.
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spelling pubmed-64371102019-04-04 Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities Stehlikova, Zuzana Kostovcik, Martin Kostovcikova, Klara Kverka, Miloslav Juzlova, Katerina Rob, Filip Hercogova, Jana Bohac, Petr Pinto, Yishay Uzan, Atara Koren, Omry Tlaskalova-Hogenova, Helena Jiraskova Zakostelska, Zuzana Front Microbiol Microbiology Psoriasis is a chronic inflammatory skin disease, whose pathogenesis involves dysregulated interplay among immune cells, keratinocytes and environmental triggers, including microbiota. Bacterial and fungal dysbiosis has been recently associated with several chronic immune-mediated diseases including psoriasis. In this comprehensive study, we investigated how different sampling sites and methods reflect the uncovered skin microbiota composition. After establishing the most suitable approach, we further examined correlations between bacteria and fungi on the psoriatic skin. We compared microbiota composition determined in the same sample by sequencing two distinct hypervariable regions of the 16S rRNA gene. We showed that using the V3V4 region led to higher species richness and evenness than using the V1V2 region. In particular, genera, such as Staphylococcus and Micrococcus were more abundant when using the V3V4 region, while Planococcaceae, on the other hand, were detected only by the V1V2 region. We performed a detailed analysis of skin microbiota composition of psoriatic lesions, unaffected psoriatic skin, and healthy control skin from the back and elbow. Only a few discriminative features were uncovered, mostly specific for the sampling site or method (swab, scraping, or biopsy). Swabs from psoriatic lesions on the back and the elbow were associated with increased abundance of Brevibacterium and Kocuria palustris and Gordonia, respectively. In the same samples from psoriatic lesions, we found a significantly higher abundance of the fungus Malassezia restricta on the back, while Malassezia sympodialis dominated the elbow mycobiota. In psoriatic elbow skin, we found significant correlation between occurrence of Kocuria, Lactobacillus, and Streptococcus with Saccharomyces, which was not observed in healthy skin. For the first time, we showed here a psoriasis-specific correlation between fungal and bacterial species, suggesting a link between competition for niche occupancy and psoriasis. However, it still remains to be elucidated whether observed microbial shift and specific inter-kingdom relationship pattern are of primary etiological significance or secondary to the disease. Frontiers Media S.A. 2019-03-21 /pmc/articles/PMC6437110/ /pubmed/30949136 http://dx.doi.org/10.3389/fmicb.2019.00438 Text en Copyright © 2019 Stehlikova, Kostovcik, Kostovcikova, Kverka, Juzlova, Rob, Hercogova, Bohac, Pinto, Uzan, Koren, Tlaskalova-Hogenova and Jiraskova Zakostelska. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Stehlikova, Zuzana
Kostovcik, Martin
Kostovcikova, Klara
Kverka, Miloslav
Juzlova, Katerina
Rob, Filip
Hercogova, Jana
Bohac, Petr
Pinto, Yishay
Uzan, Atara
Koren, Omry
Tlaskalova-Hogenova, Helena
Jiraskova Zakostelska, Zuzana
Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities
title Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities
title_full Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities
title_fullStr Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities
title_full_unstemmed Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities
title_short Dysbiosis of Skin Microbiota in Psoriatic Patients: Co-occurrence of Fungal and Bacterial Communities
title_sort dysbiosis of skin microbiota in psoriatic patients: co-occurrence of fungal and bacterial communities
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437110/
https://www.ncbi.nlm.nih.gov/pubmed/30949136
http://dx.doi.org/10.3389/fmicb.2019.00438
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