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Gut and Respiratory Microbiota Landscapes in IgA Nephropathy: a Cross-sectional Study

Overview
Journal Ren Fail
Publisher Informa Healthcare
Date 2024 Sep 9
PMID 39248406
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Abstract

Background: IgA nephropathy (IgAN) is intimately linked to mucosal immune responses, with nasopharyngeal and intestinal lymphoid tissues being crucial for its abnormal mucosal immunity. The specific pathogenic bacteria in these sites associated with IgAN, however, remain elusive. Our study employs 16S rRNA sequencing and machine learning (ML) approaches to identify specific pathogenic bacteria in these locations and to investigate common pathogens that may exacerbate IgAN.

Methods: In this cross-sectional analysis, we collected pharyngeal swabs and stool specimens from IgAN patients and healthy controls. We applied 16SrRNA sequencing to identify differential microbial populations. ML algorithms were then used to classify IgAN based on these microbial differences. Spearman correlation analysis was employed to link key bacteria with clinical parameters.

Results: We observed a reduced microbial diversity in IgAN patients compared to healthy controls. In the gut microbiota of IgAN patients, increases in , and , and decreases in , , , and were notable. In the respiratory microbiota, increases in , , , and , and decreases in , , and were observed. Post-immunosuppressive therapy, and levels were significantly reduced in the gut, while and levels decreased in the respiratory tract. and appeared to influence IgAN through dual immune loci, with abundance correlating with IgAN severity.

Conclusions: This study revealing that changes in flora structure could provide important pathological insights for identifying therapeutic targets, and ML could facilitate noninvasive diagnostic methods for IgAN.

Citing Articles

The evolving understanding of systemic mechanisms in organ-specific IgA nephropathy: a focus on gut-kidney crosstalk.

Wang X, Zhou X, Qiao X, Falchi M, Liu J, Zhang H Theranostics. 2025; 15(2):656-681.

PMID: 39744688 PMC: 11671385. DOI: 10.7150/thno.104631.

References
1.
Currie E, Coburn B, Porfilio E, Lam P, Rojas O, Novak J . Immunoglobulin A nephropathy is characterized by anticommensal humoral immune responses. JCI Insight. 2022; 7(5). PMC: 8983137. DOI: 10.1172/jci.insight.141289. View

2.
Endo Y, Kanbayashi H, Hara M . Experimental immunoglobulin A nephropathy induced by gram-negative bacteria. Nephron. 1993; 65(2):196-205. DOI: 10.1159/000187474. View

3.
Liang Y, Lee M, Zhou A, Khanthaphixay B, Hwang D, Yoon J . eXtreme gradient boosting-based classification of bacterial mixtures in water and milk using wireless microscopic imaging of quorum sensing peptide-conjugated particles. Biosens Bioelectron. 2023; 227:115144. PMC: 10066731. DOI: 10.1016/j.bios.2023.115144. View

4.
Valkenborg D, Rousseau A, Geubbelmans M, Burzykowski T . Support vector machines. Am J Orthod Dentofacial Orthop. 2023; 164(5):754-757. DOI: 10.1016/j.ajodo.2023.08.003. View

5.
Rogers M, Aronoff D . The influence of non-steroidal anti-inflammatory drugs on the gut microbiome. Clin Microbiol Infect. 2015; 22(2):178.e1-178.e9. PMC: 4754147. DOI: 10.1016/j.cmi.2015.10.003. View