Abstract

Intestinal microorganisms play a crucial role in health and disease. The disruption of host–microbiota homeostasis has been reported to occur not only during disease development but also as a result of medication. Familial Mediterranean fever (FMF) is an inflammatory genetic disease characterized by elevated systemic reactivity against the commensal gut microbiota and high levels of Candida albicans in the gut. This study’s major objective was to investigate the effects of commercial probiotic Narine on the relative abundance of gut bacteria (specifically, enterobacteria, lactobacilli, Staphylococcus aureus, and enterococci) of C. albicans carrier and non-carrier FMF patients in remission. Our main finding indicates that the probiotic reduces numbers of C. albicans and abundance of enterobacteria in male and female patients of C. albicans carriers and non-carriers. It has pivotal effect on Enterococcus faecalis: increase in male non-carriers and decrease in female ones regardless of C. albicans status. No effect was seen for Lactobacillus and S. aureus. Our data suggest that M694V/V726A pyrin inflammasome mutations leading to FMF disease may contribute to gender-specific differences in microbial community structure in FMF patients. The study’s secondary objective was to elucidate the gender-specific differences in the gut’s microbial community of FMF patients. The tendency was detected for higher counts of enterobacteria in female FMF subjects. However, the small number of patients of these groups preclude from conclusive statements, pointing at the need for additional investigations with appropriate for statistical analysis groups of subjects involved in the study.

Highlights

  • Candida albicans is an opportunistic pathogen, which often exists as a harmless human commensal microorganism [1]

  • This study examined the effect of L. acidophilus INMIA 9602 Er 317/402, isolated from the commercial probiotic formulation used by Armenian familial Mediterranean fever (FMF) patients, on the relative abundance of gut enteric bacteria, lactobacilli, S. aureus, and E. faecalis in C. albicans-carrier FMF patients with the MEFV pyrin inflammasome mutation M694V/V726A, which is the prevalent pattern in the Armenian cohort

  • Despite the prevalence of men among Armenian FMF patients [16, 26] and the indication of possible associations between C. albicans infections and gender [27], our investigations showed that the number of C. albicans-carrier male FMF patients did not differ from the number of female carriers

Read more

Summary

Introduction

Candida albicans is an opportunistic pathogen, which often exists as a harmless human commensal microorganism [1]. Cooperative interaction of C. albicans and Escherichia coli increased the probability of fungal urinary tract infections due to increased E. coli-induced adhesion of C. albicans to the bladder mucosa [4]. Another possibly synergistic interaction was shown between Staphylococcus aureus and C. albicans [5]. The disruption of inflammasomes, intracellular protein complexes with an important role in the sensing of intracellular pathogen- and danger-associated molecular patterns, can lead to susceptibility to infection, gut auto-inflammation, and tumorigenesis [6,7,8]. Klebsiella pneumoniae and P. mirabilis were found to be associated with colitis in animals using the T-bet−/− × Rag2−/− ulcerative colitis model [9]

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.