Characterization of the CRISPR1-Cas array and its subtyping potential in Enterococcus faecalis from Malaysia

TL;DR

This study characterizes the CRISPR1-Cas system in Enterococcus faecalis from Malaysia and shows its potential for strain typing and surveillance.

Contribution

The study introduces novel primers for CRISPR1-cas and demonstrates its subtyping potential in E. faecalis.

Findings

Half of the isolates carried the CRISPR1-cas9 locus, and CRISPR1 arrays were amplified in 12 out of 13 isolates with the cas9 gene.

CRISPR1-cas differs from CRISPR2 in spacer identities and terminal repeat sequences, despite similar array lengths and repeats.

Combined CRISPR1-cas and CRISPR2 typing offers discriminatory power comparable to MLST at lower sequencing costs.

Abstract

Enterococcus faecalis is a gram-positive bacterium and a common cause of hospital-associated infections. Three major CRISPR loci have been discovered in this species, namely, CRISPR1-cas, CRISPR2 and CRISPR3-cas. We developed novel primers which target the CRISPR1-cas loci in E. faecalis and tested these primers on 26 E. faecalis isolates isolated from diverse settings from Segamat, Malaysia. Half of the isolates were found to carry the CRISPR1-cas9 locus, and the CRISPR1 array was successfully amplified in 12 out of 13 isolates that contained the cas9 gene. Characterization of the CRISPR array shows that CRISPR1-cas shares similar array length and typical repeat sequences with CRISPR2 but differs significantly in terms of spacer identities and terminal repeat (TR) sequences. Most CRISPR spacers encode for chromosomal DNA sequences. Genotype characterization based on ancestral spacer (AS) and TR sequences indicates that E. faecalis with the same CRISPR1-AS genotype do not always harbour the same CRISPR2-AS genotypes and vice versa. A combined CRISPR1-cas and CRISPR2 typing offers comparable discriminatory power to MLST, suggesting its potential to be used in short-term strain identification and epidemiological surveillance at a lower sequencing cost. Our study provides a genetic reference for future studies in Southeast Asia.

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