Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients
Abstract In HIV-1-infected patients, antiretroviral therapy (ART) is a key factor that may impact commensal microbiota and cause the emergence of side effects. However, it is not fully understood how long-term ART regimens have diverse impacts on the microbial compositions over time. Here, we perfor...
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2021
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oai:doaj.org-article:8bb77c505efa44a8bff57079d5c8018d2021-12-02T15:22:58ZImpact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients10.1038/s41598-020-80247-82045-2322https://doaj.org/article/8bb77c505efa44a8bff57079d5c8018d2021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-80247-8https://doaj.org/toc/2045-2322Abstract In HIV-1-infected patients, antiretroviral therapy (ART) is a key factor that may impact commensal microbiota and cause the emergence of side effects. However, it is not fully understood how long-term ART regimens have diverse impacts on the microbial compositions over time. Here, we performed 16S ribosomal RNA gene sequencing of the fecal and salivary microbiomes in patients under different long-term ART. We found that ART, especially conventional nucleotide/nucleoside reverse transcriptase inhibitor (NRTI)-based ART, has remarkable impacts on fecal microbial diversity: decreased α-diversity and increased ß-diversity over time. In contrast, dynamic diversity changes in the salivary microbiome were not observed. Comparative analysis of bacterial genus compositions showed a propensity for Prevotella-enriched and Bacteroides-poor gut microbiotas in patients with ART over time. In addition, we observed a gradual reduction in Bacteroides but drastic increases in Succinivibrio and/or Megasphaera under conventional ART. These results suggest that ART, especially NRTI-based ART, has more suppressive impacts on microbiota composition and diversity in the gut than in the mouth, which potentially causes intestinal dysbiosis in patients. Therefore, NRTI-sparing ART, especially integrase strand transfer inhibitor (INSTI)- and/or non-nucleotide reverse transcriptase inhibitor (NNRTI)-containing regimens, might alleviate the burden of intestinal dysbiosis in HIV-1-infected patients under long-term ART.Mayumi ImahashiHirotaka OdeAyumi KobayashiMichiko NemotoMasakazu MatsudaChieko HashibaAkiko HamanoYoshihiro NakataMikiko MoriKento SekoMasashi NakahataAyumi KogureYasuhito TanakaWataru SugiuraYoshiyuki YokomakuYasumasa IwataniNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-10 (2021) |
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Medicine R Science Q Mayumi Imahashi Hirotaka Ode Ayumi Kobayashi Michiko Nemoto Masakazu Matsuda Chieko Hashiba Akiko Hamano Yoshihiro Nakata Mikiko Mori Kento Seko Masashi Nakahata Ayumi Kogure Yasuhito Tanaka Wataru Sugiura Yoshiyuki Yokomaku Yasumasa Iwatani Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients |
description |
Abstract In HIV-1-infected patients, antiretroviral therapy (ART) is a key factor that may impact commensal microbiota and cause the emergence of side effects. However, it is not fully understood how long-term ART regimens have diverse impacts on the microbial compositions over time. Here, we performed 16S ribosomal RNA gene sequencing of the fecal and salivary microbiomes in patients under different long-term ART. We found that ART, especially conventional nucleotide/nucleoside reverse transcriptase inhibitor (NRTI)-based ART, has remarkable impacts on fecal microbial diversity: decreased α-diversity and increased ß-diversity over time. In contrast, dynamic diversity changes in the salivary microbiome were not observed. Comparative analysis of bacterial genus compositions showed a propensity for Prevotella-enriched and Bacteroides-poor gut microbiotas in patients with ART over time. In addition, we observed a gradual reduction in Bacteroides but drastic increases in Succinivibrio and/or Megasphaera under conventional ART. These results suggest that ART, especially NRTI-based ART, has more suppressive impacts on microbiota composition and diversity in the gut than in the mouth, which potentially causes intestinal dysbiosis in patients. Therefore, NRTI-sparing ART, especially integrase strand transfer inhibitor (INSTI)- and/or non-nucleotide reverse transcriptase inhibitor (NNRTI)-containing regimens, might alleviate the burden of intestinal dysbiosis in HIV-1-infected patients under long-term ART. |
format |
article |
author |
Mayumi Imahashi Hirotaka Ode Ayumi Kobayashi Michiko Nemoto Masakazu Matsuda Chieko Hashiba Akiko Hamano Yoshihiro Nakata Mikiko Mori Kento Seko Masashi Nakahata Ayumi Kogure Yasuhito Tanaka Wataru Sugiura Yoshiyuki Yokomaku Yasumasa Iwatani |
author_facet |
Mayumi Imahashi Hirotaka Ode Ayumi Kobayashi Michiko Nemoto Masakazu Matsuda Chieko Hashiba Akiko Hamano Yoshihiro Nakata Mikiko Mori Kento Seko Masashi Nakahata Ayumi Kogure Yasuhito Tanaka Wataru Sugiura Yoshiyuki Yokomaku Yasumasa Iwatani |
author_sort |
Mayumi Imahashi |
title |
Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients |
title_short |
Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients |
title_full |
Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients |
title_fullStr |
Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients |
title_full_unstemmed |
Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients |
title_sort |
impact of long-term antiretroviral therapy on gut and oral microbiotas in hiv-1-infected patients |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/8bb77c505efa44a8bff57079d5c8018d |
work_keys_str_mv |
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