SARS‐CoV‐2 infection alters the gut microbiome in diabetes patients: A cross‐sectional study from Bangladesh

Author:

Mannan Adnan12ORCID,Hoque M. Nazmul3ORCID,Noyon Sajjad Hossain12ORCID,Mehedi H. M. Hamidullah4ORCID,Foysal Md Javed5ORCID,Salauddin Asma12ORCID,Islam S. M. Rafiqul12ORCID,Sharmen Farjana12ORCID,Tanni Afroza Akter12ORCID,Siddiki AMAM Zonaed6ORCID,Tay Alfred7,Siddique Md Moradul8,Rahman M. Shaminur9,Galib Syed Md.8,Akter Farhana10ORCID

Affiliation:

1. Department of Genetic Engineering and Biotechnology University of Chittagong Chattogram Bangladesh

2. Next Generation Sequencing, Research and Innovation laboratory Chittagong (NRICh), Biotechnology Research and Innovation Centre (BRIC), Department of Genetic Engineering and Biotechnology University of Chittagong Chattogram Bangladesh

3. Department of Gynecology, Obstetrics and Reproductive Health Bangabandhu Sheikh Mujibur Rahman Agricultural University Gazipur Bangladesh

4. Department of Medicine 250 Bedded General Hospital Chattogram Bangladesh

5. School of Molecular and Life Sciences Curtin University Bentley WA Australia

6. COVID Diagnostic Lab, Department of Pathology and Parasitology Chattogram Veterinary and Animal Sciences University Chattogram Bangladesh

7. Helicobacter Research Laboratory, Marshall Centre for Infectious Disease Research and Training, School of Biomedical Sciences University of Western Australia Perth Western Australia Australia

8. Department of Computer Science and Engineering Jashore University of Science and Technology Jashore Bangladesh

9. Department of Microbiology Jashore University of Science and Technology Jashore Bangladesh

10. Department of Endocrinology Chittagong Medical College Chattogram Bangladesh

Abstract

AbstractPopulations of different South Asian nations including Bangladesh reportedly have a high risk of developing diabetes in recent years. This study aimed to investigate the differences in the gut microbiome of COVID‐19‐positive participants with or without type 2 diabetes mellitus (T2DM) compared with healthy control subjects. Microbiome data of 30 participants with T2DM were compared with 22 age‐, sex‐, and body mass index (BMI)‐matched individuals. Clinical features were recorded while fecal samples were collected aseptically from the participants. Amplicon‐based (16S rRNA) metagenome analyses were employed to explore the dysbiosis of gut microbiota and its correlation with genomic and functional features in COVID‐19 patients with or without T2DM. Comparing the detected bacterial genera across the sample groups, 98 unique genera were identified, of which 9 genera had unique association with COVID‐19 T2DM patients. Among different bacterial groups, Shigella (25%), Bacteroides (23.45%), and Megamonas (15.90%) had higher mean relative abundances in COVID‐19 patients with T2DM. An elevated gut microbiota dysbiosis in T2DM patients with COVID‐19 was observed while some metabolic functional changes correlated with bidirectional microbiome dysbiosis between diabetes and non‐diabetes humans gut were also found. These results further highlight the possible association of COVID‐19 infection that might be linked with alteration of gut microbiome among T2DM patients.

Funder

University of Chittagong

Publisher

Wiley

Subject

Infectious Diseases,Virology

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