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Table 2 Mutations in episodes with phenotypic changes

From: Genomic exploration of sequential clinical isolates reveals a distinctive molecular signature of persistent Staphylococcus aureus bacteraemia

Patient code

Gene

Type

Mutation

Product

Category

Significance

P_03

ptsG

del

G306fs (stop at residue 341/682)

PTS system glucose-specific EIICBA component

Carbohydrate transport and metabolism

Three-component glucose transporter with phosphorylation activity [73]. ptsG deletion associated to resistance to glycosylated bacteriocins [74]

P_03

rpoB

snp

R503H

DNA-directed RNA polymerase subunit beta

Transcription

R503H associated with VISA phenotype in vitro. No rifampicin resistance [52]

P_03

rplV

complex

AIN95GR

50S ribosomal protein L22

Translation, ribosomal structure and biogenesis

Association with slow growth in in vitro selected VISA harbouring rpoB A621E [53]

P_03

rplD

del

KG68del

50S ribosomal protein L4

Translation, ribosomal structure and biogenesis

Mutations at positions 68 and 69 associated with linezolid resistance [75] and macrolide resistance [76]

P_05

stp

snp

N137D

Serine/threonine phosphatase stp

Signal transduction mechanisms

VISA phenotype in clinical strains; confirmed by mutagenesis [54, 55]

P_30

–

del

HVC139R

hypothetical protein

Function unknown

 

P_30

ywlC

snp

A60D

Threonylcarbamoyl-AMP synthase

Translation, ribosomal structure and biogenesis

Required for the attachment of a threonylcarbamoyl group to ANN-decoding tRNA [56]

  1. PTS phosphotransferase system, VISA vancomycin-intermediate Staphylococcus aureus, AMP adenosine monophosphate