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de Souza, G.

Publications and source records attributed to de Souza, G..

2 recordsLinked to original sources

Identification of antibiotic resistance genes in fecal microbiota selected donors during the establishment of a biobank in the south of Brazil

Fecal microbiota transplantation (FMT) is an effective therapy for recurrent Clostridioides difficile infection and is increasingly explored for other dysbiosis-related disorders. However, its implementation as a regulated therapeutic strategy still requires robust donor screening, biosafety frameworks, and standardized processing workflows. Here, we describe the establishment of the first fecal microbiota biobank in the south of Brazil and evaluate the incorporation of metagenomic sequencing as a complementary layer of donor safety assessment. A structured donor selection pipeline based on international guidelines was implemented, integrating clinical screening, biochemical and serological testing, and microbiological analyses. Of 100 screened candidates, only four donors met all eligibility criteria and were included in the biobank, highlighting the stringency of the selection process. Shotgun metagenomic sequencing revealed a diverse resistome across all donors, including a shared core set of resistance-related genes alongside marked interindividual variability. Dominant antibiotic resistance genes included tetracycline-associated determinants, as well as ermF, CfxA-type {beta}-lactamases, and aminoglycoside-modifying enzymes, each linked to specific gut taxa. Notably, the relatively high abundance of tetW and ermF in Bacteroides fragilis suggests that this dominant commensal species may act as a reservoir for tetracycline and multidrug resistance determinants within the intestinal microbiota. Rather than serving as exclusion criteria, such determinants highlight the importance of integrating functional genomic profiling into donor characterization. Overall, this study provides a framework for microbiota biobank implementation and supports the use of metagenomics as a complementary strategy to improve biosafety and functional assessment in FMT.

microbiology↗

Discrimination between Mycobacterium tuberculosis and Mycobacterium bovis using Fourier Transform Infrared Spectroscopy

Zoonotic tuberculosis (TB) caused by Mycobacterium bovis (Mb) is a neglected disease that hinders efforts to eradicate human tuberculosis. Developing a rapid, high-throughput diagnostic test to distinguish Mb from Mycobacterium tuberculosis (Mtb) isolates could enhance global zoonotic TB diagnostics and surveillance. This study aimed to evaluate the ability of Fourier Transform Infrared Spectroscopy (FT-IRS), using the IR Biotyper(R) system, to differentiate clinical isolates of Mb and Mtb. Two bacterial inactivation protocols-- paraformaldehyde and boiling--were tested using Mtb and BCG strains grown in liquid culture. While both methods allowed FT-IRS analysis, boiling was preferred due to its ease of use and efficiency in biomass recovery. Subsequently, Mtb and Mb isolates were analyzed using FT-IRS, and the resulting spectra were used to construct a sample classifier employing machine learning algorithms. Linear Discriminant Analysis (LDA) and a UPGMA dendrogram demonstrated clear separations between Mtb and Mb ecotypes. Additionally, a classifier built and internally validated using artificial neural networks achieved 99% accuracy in distinguishing Mb and Mtb. Further FT-IRS analysis of few available Mycobacterium africanum (Maf) strains demonstrated its capacity to differentiate Maf from Mtb and Mb, expanding its utility in regions where Maf is endemic. This is the first study to apply FT-IRS to distinguish tuberculous mycobacteria. FT-IRS proved to be a highly effective, rapid, and accurate diagnostic tool for differentiating Mb and Mtb strains, with promising applications for other tuberculous mycobacteria such as Maf. IMPORTANCEZoonotic tuberculosis (TB) caused by Mycobacterium bovis (Mb) remains a major threat due to its clinical similarity to human TB, higher rates of extrapulmonary cases, and resistance to pyrazinamide, complicating treatment. Current diagnostic methods used to differentiate M. tuberculosis (Mtb) from Mb and are limited by costs, resource needs, and technical complexity. We developed a method based on Fourier Transform Infrared Spectroscopy (FT-IRS) to differentiate Mb and Mtb clinical isolates with high accuracy. This diagnostic assay offers advantages over traditional molecular techniques by eliminating the need for DNA extraction, requiring less technical expertise, and providing fast, accurate differentiation of Mtb and Mb strains. This innovative approach can improve global diagnostics and surveillance of zoonotic TB.

microbiology↗