Issue 4, 2016

Transcriptional changes are involved in phenotype switching in Streptococcus equi subspecies equi

Abstract

Phenotypic heterogeneity within a population of bacteria, through genetic or transcriptional variation, enables survival and persistence in challenging and changing environments. We report here that a recent clinical isolate of S. equi, strain 1691 (Se1691), yielded a mixture of reduced capsule and mucoid colonies on primary isolation when grown on colistin-oxolinic acid blood agar (COBA) streptococcal selective plates. Passaging colonies of Se1691, with a reduced capsule phenotype maintained this mixed phenotype. In contrast, passaging mucoid colonies fixed the mucoid phenotype, suggesting adaptive genetic or transcriptional changes in response to growth on artificial media. However, despite obvious phenotypic and transcriptional differences, there were no apparent differences in the genome sequences of Se1691 recovered from colonies with a mucoid or reduced capsule phenotype. We identified 105 differentially transcribed genes in the transcriptomes of reduced capsule and mucoid colonies. The reduced capsule phenotype was associated with a significant reduction in transcription of the has locus (SEQ_0269 Q = 0.0015, SEQ_0270 Q = 0.0015, SEQ_0271 Q = 0.0285) and the amount of hyaluronic acid on the surface of S. equi recovered from non-mucoid colonies (P = 0.017). Significant differences in the transcription of 21 surface and secreted proteins were also observed. Our data show that changes in the bacterial transcriptome are linked to the mixed colony phenotype of Se1691.

Graphical abstract: Transcriptional changes are involved in phenotype switching in Streptococcus equi subspecies equi

Supplementary files

Article information

Article type
Paper
Submitted
13 Nov 2015
Accepted
03 Feb 2016
First published
03 Feb 2016

Mol. BioSyst., 2016,12, 1194-1200

Author version available

Transcriptional changes are involved in phenotype switching in Streptococcus equi subspecies equi

K. F. Steward, C. Robinson and A. S. Waller, Mol. BioSyst., 2016, 12, 1194 DOI: 10.1039/C5MB00780A

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