Search bioRxiv⌕ Search

bioRxiv · 10.1101/2022.09.19.508624

Antimicrobial Susceptibility Profiles of Bacteria Isolated from The Ozama River in Santo Domingo, Dominican Republic

Abstract

The dissemination of antimicrobial-resistant bacteria in environmental waters is an emerging concern in medical and industrial settings. In the present study, our research team analyzed superficial water samples from 3 different collection sites along the Ozama River, the most important river in the Dominican metropolitan area. Seventy-six isolates were obtained from culture media previously enriched with cefotaxime and imipenem and subsequently identified by MALDI-ToF. Our isolates spanned 12 genera of bacteria; over 30% were of clinical relevance, and 43% exhibited a phenotype classified as multi-drug resistance. The most frequent species identified as Stenotrophomonas maltophilia (n = 33), an emerging nosocomial pathogen. This study constitutes part of the initiative to understand the profiles of the perils of multi-drug resistance in metropolitan areas of the Dominican Republic: a nation with poor antibiotic use regulation. IMPORTANCENearly two billion people are sourcing their water from low-quality reservoirs world-wide. These reservoirs consist of contaminated waters with anthropogenic pollutants such as antibiotics, disinfectants, and other substances used to treat water in societies with scarce resources and unregulated industries. Furthermore, the exposure of these antibiotics to potable water reservoirs promotes the increase of clinically relevant bacteria with antibiotic-resistance capabilities, becoming a public health crisis. Therefore, treating patients with infectious diseases and providing prophylactic measures against infection-associated conditions (such as post-surgical recovery) has become progressively more difficult. Based on this evidence frame, it is of considerable importance to analyze the bacterial profiles of rivers that fall prey to anthropogenic contamination, as these investigations on antibiotic resistance will, of course, benefit the life of humans.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bonnellly, R., Cavalcante, A. L. Q., del Rosario Zorrilla, C., Calderon, V. V., Duarte, A., Barauna, R. A., Juca Ramos, R. T., Rodriguez, Y., Rodriguez de Francisco, L. E., Maroto, L. O., Perdomo, O. P., Franco, E. F.. 2022-09-22. Antimicrobial Susceptibility Profiles of Bacteria Isolated from The Ozama River in Santo Domingo, Dominican Republic. https://doi.org/10.1101/2022.09.19.508624

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↗