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Biology subjects

Becsei, A.

Publications and source records attributed to Becsei, A..

4 recordsLinked to original sources

Calibrating for absolute microbiome abundances without spike-ins

Metagenomics is a widely used approach in microbiome research. However, a major limitation of metagenomic datasets is their compositional nature, which prevents direct quantification of absolute abundances and complicates cross-sample comparisons. Existing strategies for absolute quantification typically require additional experiments or spike-in controls. Here, we introduce the MetaGenome Calibrator (MGCalibrator), a new tool that enables spike-in free, absolute abundance estimation based on routine DNA concentration measurements. We validated the accuracy of absolute abundances obtained with MGCalibrator against qPCR for 5 targets. Our results show a strong correlation with qPCR data, indicating that MGCalibrator enables qPCR-like trend analyses. For Bacteroides dorei, the estimated abundances were highly similar between the two methods (r2 = 0.98, y = 1.00x). For other targets like crAssphage or the bacterial 16S rRNA gene, qPCR values were underrepresented by a factor of 7 or overrepresented by a factor of 4. Benchmarking with synthetic microbiome data demonstrated that our method accurately determines copy numbers in sequencing datasets, and application to whole-cell mock community samples produced expected values based on known extraction biases. In an extraction-bias-free experiment, MGCalibrator accurately quantified genome copy numbers within a twofold range in 98% of cases and determined 16S rRNA gene copies within 1.6-fold or less. Finally, we applied MGCalibrator to track temporal trends in antibiotic resistance genes (ARGs) in wastewater treatment plants in two Dutch provincial capitals. We observed an overall increase in ARGs--such as sul2 in Utrecht and qnrS5 in Houtrust--likely driven by rising bacterial loads. Our findings demonstrate that MGCalibrator provides robust calibration of metagenomic data, paving the way for metagenomics to play a central role in future surveillance by enabling trend analysis across thousands of genetic targets, similar to the capabilities of qPCR for individual genes. The source code and documentation for MGCalibrator are available at github.com/NimroddeWit/MGCalibrator.

microbiology↗

Time-series sewage metagenomics can separate the seasonal, human-derived and environmental microbial communities, holding promise for source-attributed surveillance

Sewage metagenomics has risen to prominence in urban population surveillance of pathogens and antimicrobial resistance (AMR). Unknown species with similarity to known genomes cause database bias in reference-based metagenomics. To improve surveillance, we designed this study to recover sewage genomes and develop a quantification and correlation workflow for these genomes and AMR over time. We used longitudinal sewage sampling in seven treatment plants from five major European cities to explore the utility of catch-all sequencing of these population-level samples. Using metagenomic assembly methods, we recovered 2,332 metagenome-assembled genomes (MAGs) from prokaryotic species, 1,334 of which were previously undescribed. These genomes account for [~]69% of sequenced DNA and provide insight into sewage microbial dynamics. Rotterdam (Netherlands) and Copenhagen (Denmark) showed strong seasonal microbial community shifts, while Bologna, Rome, (Italy) and Budapest (Hungary) had occasional blooms of Pseudomonas-dominated communities, accounting for up to [~]95% of sample DNA. Seasonal shifts and blooms present challenges for effective sewage surveillance. We find that bacteria of known shared origin, like human gut microbiota, form communities, suggesting the potential for source-attributing novel species and their ARGs through network community analysis. This could significantly improve AMR tracking in urban environments.

microbiology↗

Porcine cytomegalovirus detection by nanopore-based metagenomic sequencing in a Hungarian pig farm

The rapid diagnosis of infectious diseases has an essential impact on their control, treatment and recovery. Oxford Nanopore Technologies (ONT) sequencing opens up a new dimension in applying clinical metagenomics. In a large-scale pig farm in Hungary, four fattening and one piglet nasal swab pooled samples were sequenced using ONT for metagenomic analysis. Long reads covering 53.69% of the porcine cytomegalovirus genome were obtained in the piglet sample. The 650 bp long read matching the glycoprotein B gene of the virus is sequentially most similar to Japanese, Chinese and Spanish isolates.

genomics↗

Mobile antimicrobial resistance genes in probiotics

Even though people around the world tend to consume probiotic products for their beneficial health effects on a daily basis, recently, concerns were outlined regarding the uptake and potential intestinal colonisation of the bacteria that they transfer. These bacteria are capable of executing horizontal gene transfer (HGT) which facilitates the movement of various genes, including antimicrobial resistance genes (ARGs), among the donor and recipient bacterial populations. Within our study, 47 shotgun sequencing datasets deriving from various probiotic samples (isolated strains and metagenomes) were bioinformatically analysed. We detected more than 70 ARGs, out of which rpoB mutants conferring resistance to rifampicin, tet(W/N/W) and potentially extended-spectrum beta-lactamase (ESBL) coding TEM-116 were the most common. Numerous ARGs were associated with integrated mobile genetic elements, plasmids or phages promoting the HGT. Our findings raise clinical and public health concerns as the consumption of probiotic products may lead to the transfer of ARGs to human gut bacteria.

genomics↗