Improved transformation efficiency of group A Streptococcus by inactivation of a type I restriction modification system
Open Access
- 29 April 2021
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 16 (4) , e0248201
Abstract
Streptococcus pyogenes or group A Streptococcus (GAS) is a leading cause of bacterial pharyngitis, skin and soft tissue infections, life-threatening invasive infections, and the post-infectious autoimmune syndromes of acute rheumatic fever and post-streptococcal glomerulonephritis. Genetic manipulation of this important pathogen is complicated by resistance of the organism to genetic transformation. Very low transformation efficiency is attributed to recognition and degradation of introduced foreign DNA by a type I restriction-modification system encoded by the hsdRSM locus. DNA sequence analysis of this locus in ten GAS strains that had been previously transformed with an unrelated plasmid revealed that six of the ten harbored a spontaneous mutation in hsdR, S, or M. The mutations were all different, and at least five of the six were predicted to result in loss of function of the respective hsd gene product. The unexpected occurrence of such mutations in previously transformed isolates suggested that the process of transformation selects for spontaneous inactivating mutations in the Hsd system. We investigated the possibility of exploiting the increased transformability of hsd mutants by constructing a deletion mutation in hsdM in GAS strain 854, a clinical isolate representative of the globally dominant M1T1 clonal group. Mutant strain 854ΔhsdM exhibited a 5-fold increase in electrotransformation efficiency compared to the wild type parent strain and no obvious change in growth or off-target gene expression. We conclude that genetic transformation of GAS selects for spontaneous mutants in the hsdRSM restriction modification system. We propose that use of a defined hsdM mutant as a parent strain for genetic manipulation of GAS will enhance transformation efficiency and reduce the likelihood of selecting spontaneous hsd mutants with uncharacterized genotypes.Keywords
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Funding Information
- National Institutes of Health (AI029952)
This publication has 22 references indexed in Scilit:
- Evolutionary pathway to increased virulence and epidemic group A Streptococcus disease derived from 3,615 genome sequencesProceedings of the National Academy of Sciences, 2014
- Overcoming restriction as a barrier to DNA transformation in Caldicellulosiruptor species results in efficient marker replacementBiotechnology for Biofuels, 2013
- Vitamin D and the Human Antimicrobial Peptide LL-37 Enhance Group AStreptococcusResistance to Killing by Human CellsmBio, 2012
- Fast gapped-read alignment with Bowtie 2Nature Methods, 2012
- Signal Transduction through CsrRS Confers an Invasive Phenotype in Group A StreptococcusPLOS Pathogens, 2011
- PerR Confers Phagocytic Killing Resistance and Allows Pharyngeal Colonization by Group A StreptococcusPLOS Pathogens, 2008
- Sau1: a Novel Lineage-Specific Type I Restriction-Modification System That Blocks Horizontal Gene Transfer into Staphylococcus aureus and between S. aureus Isolates of Different LineagesJournal of Bacteriology, 2006
- UCSF Chimera—A visualization system for exploratory research and analysisJournal of Computational Chemistry, 2004
- Molecular analysis of the role of the group A streptococcal cysteine protease, hyaluronic acid capsule, and M protein in a murine model of human invasive soft-tissue infection.Journal of Clinical Investigation, 1998
- An M protein with a single C repeat prevents phagocytosis of Streptococcus pyogenes: use of a temperature‐sensitive shuttle vector to deliver homologous sequences to the chromosome of S. pyogenesMolecular Microbiology, 1993