Search bioRxiv⌕ Search

bioRxiv · 10.1101/2024.01.29.577889

Association of Blastocystis and Gut Microbiota in Type 2 Diabetic Mellitus Patients and Non-Diabetic Individuals.

Abstract

The influence of anaerobic protozoan Blastocystis on human gut health is not well understood. While Blastocystis species frequently inhabit the gut, their clinical importance and ecological function remain ambiguous. A study on Blastocystis was carried out enrolling a total of 203 participants including T2DM patients and non-diabetic individuals to evaluate the prevalence of Blastocystis and its association in gut microbiota. Blastocystis subtypes were identified by PCR and faecal microbiome was accessed by targeting V4 region of the bacterial 16S ribosomal gene. The prevalence of Blastocystis in T2DM was 25.49% and 17.82% in non-diabetic individuals with the most prevalent subtype on total population was ST3, followed by ST1 and ST2. The composition of gut microbiota was significantly different between Blastocystis-positive and Blastocystis-negative individuals. Blastocystis carriage was positively associated with higher alpha diversity in T2DM patients and non-diabetic individuals. Interestingly, at the phylum level, the T2DM group had an obvious increase of Bacteroidetes and a marked increase of Actinobacteria with the present of Blastocystis. The findings suggested that the presence of Blastocystis was linked to increased diversity and richness in the gut bacterial composition, signifying at a potentially beneficial association between Blastocystis and the gut microbiota. Author SummaryType 2 Diabetes Mellitus Patients (T2DM), a prevalent global disease, affects a significant portion of the population across the world. Thus, there is need to better understanding on Blastocystis infection among T2DM that could lead to the alteration toward gut health. We evaluated the association between Blastocystis and gut microbiota, where involving two groups; T2DM patients and non-Diabetic individuals. The research revealed a higher Blastocystis in T2DM patients compared to non-diabetic individuals, emphasizing on assumption toward its pathogenicity. However, amplicon-based sequencing of 16S rRNA genes indicates that Blastocystis carriers exhibit increased gut microbiota diversity. Our result suggested that, Blastocystis highlighted its potential role as a component of a balanced microbiota. Notably, optimal alteration in Actinobacteria and Bacteroidetes may contribute to the several gut health. Hence, the study could prompt for further exploration regarding of Blastocystis subtypes and gut microbiota specifically in T2DM to propose for more precise assessment of Blastocystis and gut microbial diversity.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Mohd Shaari, N. S., Wan Sulaiman, W. S., Omar, M. R., Umaisara, N. A., Lee, I. L., Tengku Ahmad Basri, T. S. A., Abdullah, N. S.. 2024-01-31. Association of Blastocystis and Gut Microbiota in Type 2 Diabetic Mellitus Patients and Non-Diabetic Individuals.. https://doi.org/10.1101/2024.01.29.577889

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

A population-scale landscape of the subgingival microbiome reveals divergent routes to periodontal dysbiosis

Periodontitis is an archetypical mucosal inflammatory disease in which microbiome dysbiosis at the tooth-epithelial interface interacts with host genetic and behavioral risk factors to drive immune-mediated tissue destruction. Although subgingival microbiome compositional shifts are thought to parallel disease severity, microbiome variation at the population-level and its relationship to periodontal clinical phenotypes and disease-modifying factors remain poorly defined. Here, we use unsupervised manifold learning to map the compositional landscape of the subgingival microbiome in 1,355 adults spanning periodontal health to severe periodontitis. We identified eight latent microbiome states organized along a branching continuum from eubiosis to dysbiosis. An intermediate microbial configuration marked ecological destabilization and bifurcation into two distinct periodontitis-associated dysbiotic trajectories, distinguished by links to gingival inflammation and smoking. Although the microbiome trajectories broadly tracked periodontal destruction, a minority of individuals showed discordant microbiome-clinical phenotypes, with some individuals with periodontitis retaining otherwise eubiotic microbiomes enriched for low-abundance pathobionts, while some cases of health or mild disease had highly dysbiotic communities, suggesting distinct host susceptibility. Together, these findings define a population-scale ecological landscape of the subgingival microbiome, reveal divergent trajectories to periodontal dysbiosis, and highlight heterogeneity in the relationship between microbial community structure and clinical disease expression.

microbiology↗

The iron-binding siderophore enterobactin is required for the response of multi-drug resistant Klebsiella pneumoniae to zinc limitation

To persist during infection Klebsiella pneumoniae must overcome nutrient iron and zinc limitation imposed by the host immune system through a process called nutritional immunity. Secreted small molecule siderophores are a major virulence determinant of Klebsiella pneumoniae pathogenesis and are presumed to overcome nutritional immunity by binding iron for bacterial acquisition. In this work, we set out to identify how a multi-drug resistant K. pneumoniae grows in zinc limited environments. Using unbiased transcriptomics, proteomics, and an arrayed transposon screen, we identified that synthesis and uptake of the siderophore enterobactin is required to allow for growth in low zinc conditions. Iron-specific chelators did not replicate this phenotype and addition of supplemental iron through heme in growth media could not complement severe growth defects of enterobactin mutant K. pneumoniae experiencing zinc limitation. Finally, zinc starvation induced enterobactin production independent of the canonical zinc uptake regulator (Zur) transcription factor suggesting an unidentified regulatory mechanism by which Gram-negative pathogens may respond to zinc stress. Together, these studies expand the role of enterobactin beyond iron regulation and highlight a previously unreported link between iron and zinc homeostasis in Klebsiella pneumoniae.

microbiology↗

A microbiota-derived protease links phage susceptibility to host epithelial responses

Bacteriophages are major ecological drivers of gut microbial ecology, yet whether bacterial mechanisms that determine phage susceptibility have consequences for the mammalian host remains poorly understood. Here, we identify dipeptidyl peptidase 11 (Dpp11a), the predominant active serine protease of the prevalent gut commensal Phocaeicola vulgatus, as an unexpected bacterial defence factor. Dpp11a protects against environmental proteases and confers resistance to bacteriophage infection. Metatranscriptomic analyses further reveal increased expression of both dpp11a and P. vulgatus-associated phage transcripts in ulcerative colitis stool samples, indicating that both components of this interaction are transcriptionally active in disease-associated human microbiomes. Using the microfluidic gut-on-a-chip co-culture model HuMiX, we show that the absence of Dpp11 is accompanied by altered epithelial tight-junction remodelling during phage-bacterial infection. Together, our findings reveal that the consequences of bacterial phage defence can extend beyond phage-bacterium interactions to the mammalian epithelium.

microbiology↗