Klebsiella pneumoniae genomes
75 sequence types. No evidence of patient-to-patient transmission in a 15-month hospital surveillance study.
Microbial Genomics →Microbial genomics · Aotearoa New Zealand
I use bacterial genomics to resolve transmission, determine how antimicrobial resistance is moving, and define what the evidence supports.

75 sequence types. No evidence of patient-to-patient transmission in a 15-month hospital surveillance study.
Microbial Genomics →Global plasmid context used to resolve how mobile colistin resistance reached and persisted in New Zealand.
IJAA →Two decades of AK3 evolution reconstructed alongside the mobile elements acquired and lost through time.
Microbial Genomics →Four connected problems: transmission, mobile resistance, bacterial evolution, and the methods used to infer them.
High-resolution genomes can confirm transmission, rule it out, or expose a reservoir routine surveillance did not see.
Genomic surveillance →Plasmids and other mobile elements can move resistance across bacterial backgrounds that look unrelated on the chromosome.
Mobile resistance →Phylogenomics connects bacterial relationships to the genomic changes that accompany emergence, persistence and expansion.
Phylogenomics →Focused software makes fragile analytical steps explicit, reproducible and testable.
Research software →Results that changed the interpretation of transmission, resistance or bacterial evolution.
Rapid local sequencing identified Klebsiella variicola, linked four neonatal cases, and placed sink isolates in the same genomic cluster.
Read the study →Chromosome, plasmid backbone and resistance gene context were analysed together to reconstruct a carbapenem-resistant E. coli ST131 outbreak.
Read the study →Genomic epidemiology revealed geographical clustering within multidrug-resistant ST131 associated with bacteraemia in Wales.
Read the study →Nanopore sequencing resolved plasmid-encoded carbapenem resistance dynamics and linked resistance to its genomic reservoirs.
Read the study →Precise excision of coordinate-labelled genomic sites from transposed NEXUS matrices, with deterministic provenance and SHA-256 checksums.
# remove reference-defined regions $ nexcise input.nex regions.tsv \ --output filtered.nex \ --report report.json # deterministic output # checksums + counts + warnings
Collaborate
I work across clinical microbiology, infection prevention, reference laboratories, bioinformatics and public-health surveillance.
Current interests: outbreak reconstruction · complete bacterial genomes · nanopore sequencing · phylogenomics · reproducible methods.