bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.01.30.635773

Conjugative Plasmids Rarely Confer Antibiotic Resistance or Virulence

Abstract

Plasmids are autonomous DNA molecules that can replicate independently and transfer horizontally between bacterial cells. They play a key role in disseminating adaptive traits, such as antimicrobial resistance and virulence. Understanding plasmid mobility and its association with these traits is crucial to microbial ecology, public health and genomic surveillance. Several databases have been developed to catalogue plasmids assembled from bacterial isolates and metagenomic samples. However, differences in database construction and curation can introduce biases that affect subsequent analyses. In this study, we compare three distinct plasmid genome datasets -- the NCBI Reference Sequence Database (RefSeq), the Integrated Microbial Genomes & Microbiomes system (IMG/PR) from bacterial isolates (I) and microbiomes (M) -- to assess the influence of data origin on inferences about plasmid mobility types, antimicrobial resistance genes (ARGs), virulence genes (VGs) and host taxonomy. Our analysis reveals that plasmids assembled from metagenomes tend to be smaller than those assembled from isolates. RefSeq plasmids are enriched in conjugative plasmids (pCONJ) and display a higher frequency of ARGs and VGs. In contrast, regardless of whether they originate from isolates or metagenomes, IMG/PR plasmids are enriched in mobilizable plasmids (pMOB). Furthermore, ARGs are more frequently associated with highly mobile plasmids, particularly pCONJ. These findings highlight the importance of database selection in studies of plasmid epidemiology, functional potential and mobility. Standardised curation practices and cross-database comparisons are essential to ensure robust and reproducible insights into plasmid-mediated gene flow. ImportancePlasmids are DNA molecules that can replicate and transfer between bacteria, thereby helping to spread genes that enable bacteria to survive and adapt in different environments. This gene exchange plays a significant part in bacterial evolution. Researchers study these processes using plasmid databases, but the way these databases are constructed can influence the conclusions that are drawn. In this study, we found that key traits, such as those involved in antibiotic resistance and the ability to cause disease, are more often linked to plasmids with greater mobility, particularly in databases containing more clinical samples. However, our results demonstrate that the choice of dataset can significantly impact our understanding of the dissemination of critical genes among bacteria. These findings are valuable for tracking and controlling antibiotic resistance and disease, and highlight the need for carefully constructed, representative databases to support accurate research into how bacteria share genes.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Domingues, C. P. F., Rebelo, J. S., Dionisio, F., Nogueira, T. I.. 2025-01-30. Conjugative Plasmids Rarely Confer Antibiotic Resistance or Virulence. https://doi.org/10.1101/2025.01.30.635773

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

KEEP EXPLORING

Related preprints

Chromosome-level, haplotype-resolved genome assembly of the tanniferous forage legume big trefoil (Lotus pedunculatus Cav.) using CiFi

Big trefoil (Lotus pedunculatus Cav.) is a perennial forage legume that thrives on acidic, low-fertility soils and produces condensed tannins that reduce enteric methanogenesis in ruminants. Despite this agronomic potential, genomic resources for the species remain scarce, and the existing haploid assembly does not resolve the two haplotypes of this outcrossing diploid species. Here we present a haplotype-resolved, chromosome-level reference genome for L. pedunculatus genotype Lusitano29 -- the first plant genome assembled using CiFi, a long-read chromosome conformation capture method. We combined PacBio HiFi long reads with CiFi concatemers produced from DpnII and HindIII libraries; in silico digestion and combinatorial pairing of the resulting monomers yielded 790.3 M and 10.3 M pseudo-paired contacts, respectively, enabling scaffolding and manual curation to chromosome level. The 991.1 Mb assembly resolves two phased haplotypes of 500 and 491 Mb, with 96.6% of the sequence anchored in twelve pseudo-chromosomes (six per haplotype). Telomeric repeats were detected at 19 of 24 pseudo-chromosome ends, and no structural errors were detected (scaffold N50 73.8 Mb; consensus QV 64.7; k-mer completeness 99.4%; genome-mode BUSCO completeness 97.0%; CRAQ S-AQI 100.0). Annotation supported by PacBio Iso-Seq full-length transcripts predicted 38,069 and 36,484 protein-coding genes in haplotypes 1 and 2, respectively (protein-mode BUSCO completeness 96.5%), indicating a high completeness of annotated genes. This genome assembly provides a foundation for allele-aware trait dissection of proanthocyanidin biosynthesis, comparative genomics in Lotus, and population genomics and genomics-assisted breeding in L. pedunculatus.

genomics↗

Bramble: projection of spliced genomic alignments into transcriptomic space for improved transcript quantification

Accurate transcript abundance estimation is central to many transcriptomic studies. Many current quantification methods rely on reads mapped directly to the transcriptome, but transcriptome alignment can misassign reads from unannotated transcripts to annotated isoforms, leading to biased abundance estimates. We introduce Bramble, a method that projects spliced genomic alignments into transcriptomic coordinates to produce alignments compatible with downstream transcript quantification tools. Across simulated short- and long-read RNA-seq datasets and multiple levels of reference annotation completeness, incorporating Bramble into quantification pipelines consistently improved accuracy and reduced error. These results suggest that genome-derived transcriptomic alignments can improve transcript quantification by preserving compatible alignments to annotated transcripts while filtering alignments likely originating from unannotated transcripts.

genomics↗

PRDM9-mediated meiotic hotspot specification is constrained in humans despite extensive sequence diversity

PRDM9 specifies meiotic recombination hotspots through a rapidly evolving C2H2 zinc-finger (ZNF) coding minisatellite that determines DNA-binding specificity. Although this minisatellite harbors extraordinary allelic diversity in humans, the functional consequences of most naturally occurring variants remain unknown. Here we functionally characterize 80 human PRDM9 alleles using genome-wide chromatin profiling. Despite extensive sequence diversity within the ZNF array, most alleles function indistinguishably from common A and C hotspot-specifying alleles, revealing that human PRDM9 function is more constrained than its sequence diversity predicts. In contrast, rare and infertility-associated variants occupy two functional extremes: either abundant and novel DNA binding specificity or minimal DNA binding, suggesting that both gain- and loss-of-function alleles may disrupt symmetric hotspot specification during meiosis, thus representing a plausible contributor to human infertility. Together, our findings define the functional landscape of human PRDM9 variation and provide a framework for interpreting the impact of newly discovered PRDM9 alleles.

genomics↗