bioRxiv Science⌕ Search

bioRxiv · 10.1101/2024.04.15.589521

Development and Implementation of a Core Genome Multilocus Sequence Typing (cgMLST) scheme for Haemophilus influenzae

Abstract

2.Haemophilus influenzae is part of the human nasopharyngeal microbiota and a pathogen causing invasive disease. The extensive genetic diversity observed in H. influenzae necessitates discriminatory analytical approaches to evaluate its population structure. This study developed a core genome MLST (cgMLST) scheme for H. influenzae using pangenome analysis tools and validated the cgMLST scheme using datasets consisting of complete reference genomes (N=14) and high-quality draft H. influenzae genomes (N=2,297). The draft genome dataset was divided into a development (N=921) and a validation dataset (N=1,376). The development dataset was used to identify potential core genes with the validation dataset used to refine the final core gene list to ensure the reliability of the proposed cgMLST scheme. Functional classifications were made for all resulting core genes. Phylogenetic analyses were performed using both allelic profiles and nucleotide sequence alignments of the core genome to test congruence, as assessed by Spearmans correlation and Ordinary Least Square linear regression tests. Preliminary analyses using the development dataset identified 1,067 core genes, which were refined to 1,037 with the validation dataset. More than 70% of core genes were predicted to encode proteins essential for metabolism or genetic information processing. Phylogenetic and statistical analyses indicated that the core genome allelic profile accurately represented phylogenetic relatedness among the isolates (R2 = 0.945). We used this cgMLST scheme to define a high-resolution population structure for H. influenzae, which enhances the genomic analysis of this clinically relevant human pathogen. 3. Impact statementDiscriminating H. influenzae variants and evaluating population structure has been challenging and largely unstandardised. To address this, we have developed a cgMLST scheme for H. influenzae. Since an accurate typing approach relies on precise reflection of the underlying population structure, we explored various methods to define the scheme. The core genes included in this scheme were predicted to encode functions in essential biological pathways, such as metabolism and genetic information processing, and could be reliably assembled from short-read sequence data. Single-linkage clustering, based on core genome allelic profiles, showed high congruence to genealogy reconstructed by Maximum-Likelihood (ML) methods from the core genome nucleotide alignment. The cgMLST scheme v1 enables rapid and accurate depiction of high-resolution H. influenzae population structure, and making this scheme accessible via the PubMLST database, ensures that microbiology reference laboratories and public health authorities worldwide can use it for genomic surveillance. 4. Data summaryThe H. influenzae cgMLST scheme is accessible via https://pubmlst.org/organisms/haemophilus-influenzae. The list of isolate IDs available publicly from pubmlst.org is provided in Supplementary File 1. The pipeline for cgMLST scheme development and validation is published at https://www.protocols.io/private/EF6DB7FE429311EEB8630A58A9FEAC02. All in-house R and Python scripts for data processing and analysis are available from https://gitfront.io/r/user-4399403/ZHt8DArALHcY/cgmlst-hinf/.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Krisna, M. A., Jolley, K. A., Monteith, W., Boubour, A., Hamers, R. L., Brueggemann, A. B., Harrison, O. B., Maiden, M. C. J.. 2024-04-16. Development and Implementation of a Core Genome Multilocus Sequence Typing (cgMLST) scheme for Haemophilus influenzae. https://doi.org/10.1101/2024.04.15.589521

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

KEEP EXPLORING

Related preprints

Contig-Resolved Genetic Context of Antimicrobial Resistome in Sediments of Two Contrasting Wastewater-Impacted Rivers

River sediments harbor diverse antimicrobial resistance (AMR) determinants; however, gene abundance alone provides limited insight into their genomic context, mobility potential, and associated bacterial hosts. This study employed an assembly- and read-mapping metagenomic framework to surface-sediment metagenomes (40.78 Gb clean data) from two contrasting wastewater-impacted Indian rivers, Adyar (Chennai) and Musi (Hyderabad), retaining sample-, contig- and open reading frame level provenance. ARG-carrying contigs (ACCs; n = 2,402) were annotated for mobile genetic elements (MGEs), biocide/metal resistance genes (BMRGs), virulence factor genes (VFGs), nitrogen-cycling genes (NCycGs), and putative host taxonomy. The resistomes exhibited substantial diversity (264 ARG subtypes) and spatial heterogeneity, with subtype richness in the Adyar (up to 171 subtypes) than in the Musi, where richness progressively declined downstream. Rank IV determinants dominated ARG abundance (77.82%), whereas Rank I determinants accounted for only 9.89%. MGEs were detected on just 3.12% (75/2,402) of ACCs, predominantly comprising plasmid-like contigs and proximal ARG-MGE associations. Co-occurrence with BMRGs was observed on 386 ACCs, whereas VFGs were uncommon (26 ACCs) and primarily represented dual-annotated efflux and envelope-integrity determinants rather than independent virulence loci. NCyc annotations were sparse (12 ACCs), with no evidence of complete nitrification or denitrification pathways. Taxonomic classification resolved 217 ACCs to the species level, with no matches to curated human pathogenic bacteria. Only two Acinetobacter-assigned ACCs exhibited both genus-level pathogenicity and mobility evidence. These findings highlight the importance of integrating mobility and host-taxonomic information to distinguish baseline environmental resistance from potential priorities for AMR surveillance.

genomics↗

Time-resolved single-cell screening reveals the dynamic regulatory architecture of human cardiogenesis

Congenital heart disease (CHD) originates during early embryogenesis, yet when disease genes act cannot be determined from existing data. Human fetal heart atlases lack critical time points, and perturbation screens that systematically assess gene function currently profile at most a few time points. Here we combined single-cell CRISPR screening of 400 disease-relevant genes in cardioids, sampled daily over seven developmental days (~975,000 cells), with a matched multiome atlas. Perturbation phenotypes were strongly dependent on developmental stage. Perturbations that reshaped cell-fate allocation or gene expression were enriched for CHD-linked genes, and most acted already during progenitor stages. Timing was largely independent of the target gene's own expression, marking instead when a cell state became functionally dependent on it, and some effects persisted after expression declined. Consensus gene regulatory networks integrating perturbation and multiome data recovered stage-specific regulators and nominated HOXB2 and HOXB3 as candidate cardiac regulators. Many perturbations converged on shared downstream programmes, which were reorganised through differentiation. Effects correlated in progenitors were maintained in differentiated cells, split into distinct programmes, converged with other perturbations or disappeared entirely, indicating that gene function is highly context dependent. Beyond advancing our understanding of the developmental regulatory logic underlying CHD, our work provides a resource for developing context-dependent models for in silico prediction of perturbation effects.

genomics↗

A Y-specific translocated gsdf copy is a candidate master sex-determining gene in common dab (Limanda limanda)

Sex-determining systems in flatfishes are highly diverse, and even closely related species can differ in both sex-determining loci and heterogametic systems. In common dab (Limanda limanda), the genetic basis of sex determination has not yet been established. Here, we investigated sex determination using pooled whole-genome sequencing combined with long-read genome sequencing of females and males from Iceland and Norway. Genome-wide allele-frequency analyses identified sex-associated regions consistent with male heterogamety (XX/XY), with the strongest signal on chromosome 16. Comparison of the existing reference assembly, which represents an X haplotype at this locus, with a haplotype-resolved male PacBio HiFi assembly revealed a [~]21.5 kb Y-specific insertion on chromosome 16. The insertion showed complete coverage in male pools but little or no coverage in female pools from either population. It contained a translocated genomic segment including a copy of gonadal soma-derived factor (gsdf) and a predicted gene of unknown function. Comparative genomic analyses were consistent with this segment originating from an autosomal gsdf-containing region on chromosome 1. Given the recurrent recruitment of gsdf as a sex-determining factor in teleosts, we designate the Y-linked copy gsdfY and identify it as the strongest candidate for the master sex-determining gene in common dab. Additional broad sex-associated differentiation on chromosome 19 was restricted to the Icelandic samples and may reflect population-specific expansion of the sex-linked region, although its structural basis remains unresolved. Together, these findings provide the first genomic characterization of sex determination in common dab and demonstrate how gene duplication and translocation can contribute to the evolution of novel sex-determining systems in flatfishes.

genomics↗