Abstract

Common Variable Immunodeficiency (CVID) is the most frequent symptomatic immune disorder characterized by reduced serum immunoglobulins. Patients often suffer from infectious and serious non-infectious complications which impact their life tremendously. The monogenic cause has been revealed in a minority of patients so far, indicating the role of multiple genes and environmental factors in CVID etiology. Using 16S and ITS rRNA amplicon sequencing, we analyzed the bacterial and fungal gut microbiota, respectively, in a group of 55 participants constituting of CVID patients and matched healthy controls including 16 case-control pairs living in the same household, to explore possible associations between gut microbiota composition and disease phenotype. We revealed less diverse and significantly altered bacterial but not fungal gut microbiota in CVID patients, which additionally appeared to be associated with a more severe disease phenotype. The factor of sharing the same household impacted both bacterial and fungal microbiome data significantly, although not as strongly as CVID diagnosis in bacterial assessment. Overall, our results suggest that gut bacterial microbiota is altered in CVID patients and may be one of the missing environmental drivers contributing to some of the symptoms and disease severity. Paired samples serving as controls will provide a better resolution between disease-related dysbiosis and other environmental confounders in future studies.

Highlights

  • Common Variable Immunodeficiency (CVID) is the most frequent symptomatic immune disorder, estimated to affect 1 in 25,000 people worldwide, the prevalence can vary across different countries [1, 2]

  • We even detected Anaerotruncus and Eggerthella genera to be significantly increased in CVID, which was opposite to their results

  • We reveal the strong impact of sharing the same household on bacterial and fungal microbiome data, weaker than that of CVID diagnosis in bacterial assessment

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Summary

Introduction

Common Variable Immunodeficiency (CVID) is the most frequent symptomatic immune disorder, estimated to affect 1 in 25,000 people worldwide, the prevalence can vary across different countries [1, 2]. CVID includes clinically and genetically heterogeneous disorders characterized by reduced serum immunoglobulins IgG, IgA, and inconstantly IgM. As a result of a defect in antibody production, most patients suffer from severe, recurrent infections, mainly of the respiratory and gastrointestinal tract, and have impaired vaccine responses [3, 4]. These often manifest as autoimmune complications or inflammatory conditions. The monogenic cause was revealed in

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