Exploring the interplay between antiretroviral therapy and the gut-oral microbiome axis in people living with HIV

Author:

Narayanan Aswathy1,Kieri Oscar2,Vesterbacka Jan2,Manoharan Lokeshwaran3,Chen Puran4,Ghorbani Mahin5,Ljunggren Hans-Gustaf4,Chen Margaret Sällberg5,Aleman Soo2,Sönnerborg Anders1,Ray Shilpa1,Nowak Piotr2

Affiliation:

1. Department of Medicine Huddinge, Division of Infectious Diseases, Karolinska Institutet, Stockholm, Sweden

2. Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden

3. National Bioinformatics Infrastructure Sweden (NBIS), SciLifeLab, Department of Laboratory Medicine, Lund University, Lund, Sweden

4. Department of Medicine Huddinge, Center for Infectious Medicine, Karolinska Institutet, Stockholm, Sweden

5. Department of Laboratory Medicine, Division of Pathology, ANA Futura, Karolinska Institutet, Stockholm 141 52 Sweden

Abstract

Abstract Background: The gut and oral microbiome is altered in people living with HIV (PLWH). While antiretroviral treatment (ART) is pivotal in restoring immune function in PLWH, several studies have identified an association between specific antiretrovirals, particularly integrase inhibitors (INSTI), and weight gain. In our study, we have explored the differences in the oral and gut microbiota of PLWH under different ART regimens, and its correlation to Body Mass Index (BMI). Methods: Fecal and salivary samples were collected from PLWH (n=69) and healthy controls (HC, n=80). DNA was extracted for 16S rRNA sequencing on the MiSeq platform. The obtained raw reads were pre-processed, and taxonomy analysis was performed to determine the microbial composition. Additionally, linear discriminant analysis effect size and correlation analyses were used to identify differences in abundant taxa and relationship between microbial abundance and ART regimens, BMI, CD4+T-cell count, CD4/CD8 ratio, and duration of ART. Results: We found that the PLWH had significantly lower richness compared to HC in both the oral and gut environment. Interestingly, the gut microbiome composition of INSTI-treated individuals was enriched with Faecalibacterium and Bifidobacterium, whereas non-nucleotide reverse transcriptase inhibitor (NNRTI) treated individuals were enriched with Gordonibacter, Megasphaera, and Staphylococcus. In the oral microenvironment, Veillonella was significantly more abundant in INSTI-treated individuals and Fusobacterium and Alloprevotella in the NNRTI-treated individuals. Furthermore, Bifidobacterium and Dorea were enriched in gut milieu of PLWH with high BMI. Conclusion: Our study revealed significant shifts in bacterial diversity and composition between HC and PLWH in both the oral and gut environments. Additionally, we also detected specific microbial signatures, which were correlated with different treatment regimens and BMI among the PLWH under successful ART.

Funder

Stiftelsen Läkare mot AIDS Forskningsfond

Karolinska Institutet

Stockholms Läns Landsting

Vetenskapsrådet

Åke Wiberg Stiftelse

Publisher

Research Square Platform LLC

Reference62 articles.

1. UNAIDS, Global AIDS update – 2022

2. WHO publishes New Consolidated HIV guidelines for prevention, treatment, Service Delivery & Monitoring. (n.d.). Retrieved April 6 (2023) from https://www.who.int/news/item/16-07-2021-who-publishes-new-consolidated-hiv-guidelines-for-prevention-treatment-service-delivery-monitoring

3. Impact of long-term antiretroviral therapy on gut and oral microbiotas in HIV-1-infected patients;Imahashi M;Sci Rep,2021

4. The microbiome and HIV persistence: implications for viral remission and cure;Koay WLA;Curr Opin HIV AIDS,2018

5. Nowak P, Troseid M, Avershina E, Barqasho B, Neogi U, Holm K, Hov JR, Noyan K, Vesterbacka J, Svärd J, Rudi K, Sönnerborg A (2015) Gut microbiota diversity predicts immune status in HIV-1 infection. AIDS. ;29(18):2409-18. 10.1097/QAD.0000000000000869. PMID: 26355675

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