Strain-level population genomics of C. perfringens reveals eight distinct phylogenetic lineages. a, Mid-point rooted, maximum-likelihood phylogenetic tree of 302 representative C. perfringens strains (derived from a collection of 673 C. perfringens genomes) inferred from 8,506 SNPs (from 858 single-copy core genes), aligned with metadata including genome types, sources, sample hosts, hospitals and lineages assigned using hierBAPS. Black dashed lines, type strain ATCC13124 and several representative strains were labeled in this phylogenetic tree. Branch lengths are indicative of the estimated nucleotide substitution per site (SNPs). MAG, metagenome-assembled genomes (from MGnify study, human gut microbiome-derived C. perfringens genomes only). b, Unrooted phylogenetic tree colored by assigned lineages. c, Pairwise SNP distances among strains located within lineages I (n = 8), II (n = 7), III (n = 11), IV (n = 28), V (n = 57), VI (n = 66), VII (n = 98) and VIII (n = 27) and between lineages. The box in the boxplot represents 50% of the central data, in between the lower and upper quartiles, with a central line representing the median, whereas the whiskers show the most extreme data points. BL, between lineages. d, Proportions of human and animal-derived C. perfringens genomes in each lineage. Credit: Nature Microbiology (2023). DOI: 10.1038/s41564-023-01385-z

Researchers from the Quadram Institute and University of East Anglia have identified what makes some strains of gut bacteria life-threatening in pre-term babies. The findings, now published in the journal Nature Microbiology, will help identify and track dangerous strains and protect vulnerable neonatal babies.

A major threat to neonatal babies with extremely low birth weight is necrotizing enterocolitis (NEC). Rare in full term babies, this microbial infection exploits vulnerabilities destroying gut tissue leading to severe complications. Two out of five cases are fatal.

One that causes especially sudden and is Clostridium perfringens. These are common in the environment and non-disease-causing strains live in healthy human guts.

So what makes certain strains so dangerous in preterm babies?

Prof Lindsay Hall and Dr. Raymond Kiu from the Quadram Institute and UEA led the first major study on C. perfringens genomes from preterm babies, including some babies with necrotizing enterocolitis.

The research team analyzed C. perfringens genomes from the of 70 babies admitted to five UK Neonatal Intensive Care Units (NICUs). Based on genomic similarities, they found one set had a lower capacity to cause disease. This allowed a comparison with the more virulent strains. The less virulent group lacked genes responsible for production of a toxin called PFO and other factors needed for colonization and survival.

This study has begun to construct genomic signatures for C. perfringens associated with healthy preterm babies and those with necrotizing enterocolitis.

Prof Lindsay Hall, from UEA's Norwich Medical School and the Quadram Institute, said, "Exploring genomic signatures from hundreds of Clostridium perfringens genomes has allowed us potentially to discriminate between 'good' bacterial strains that live harmlessly in the preterm gut, and 'bad' ones associated with the devastating and deadly disease necrotizing enterocolitis.

"We hope the findings will help with 'tracking' deadly C. perfringens strains in a very vulnerable group of patients—preterm babies."

Larger studies, across more sites and with more samples may be needed but this research could help identify better ways to control necrotizing enterocolitis.

The team previously worked alongside Prof Paul Clarke and clinical colleagues at the Norfolk and Norwich University Hospital NICU. And they demonstrated the benefits of providing neonatal babies with probiotic supplements.

The enterocolitis gut microbiome of neonatal infants is significantly disrupted, making it susceptible to C. perfringens overgrowth.

Prof Hall said, "Our genomic study gives us more data that we can use in the fight against bacteria that cause disease in babies—where we are harnessing the benefits of another microbial resident, Bifidobacterium, to provide at-risk babies with the best possible start in life."

Dr. Raymond Kiu, from the Quadram Institute, said, "Importantly, this study highlights Whole Genome Sequencing as a powerful tool for identifying new bacterial lineages and determining bacterial virulence factors at strain level which enables us to better understand disease."

More information: Lindsay Hall, Particular genomic and virulence traits associated with preterm infant-derived toxigenic Clostridium perfringens strains, Nature Microbiology (2023). DOI: 10.1038/s41564-023-01385-z. www.nature.com/articles/s41564-023-01385-z

Journal information: Nature Microbiology