UNIGE document Scientific Article
previous document  unige:7543  next document
add to browser collection

Transcriptomic and functional analysis of an autolysis-deficient, teicoplanin-resistant derivative of methicillin-resistant Staphylococcus aureus

Huggler, Elzbieta
Majcherczyk, Paul
show hidden authors show all authors [1 - 11]
Published in Antimicrobial agents and chemotherapy. 2006, vol. 50, no. 9, p. 3048-3061
Abstract The molecular basis of glycopeptide-intermediate S. aureus (GISA) isolates is not well defined though frequently involves phenotypes such as thickened cell walls and decreased autolysis. We have exploited an isogenic pair of teicoplanin-susceptible (strain MRGR3) and teicoplanin-resistant (strain 14-4) methicillin-resistant S. aureus strains for detailed transcriptomic profiling and analysis of altered autolytic properties. Strain 14-4 displayed markedly deficient Triton X-100-triggered autolysis compared to its teicoplanin-susceptible parent, although microarray analysis paradoxically did not reveal significant reductions in expression levels of major autolytic genes atl, lytM, and lytN, except for sle1, which showed a slight decrease. The most important paradox was a more-than-twofold increase in expression of the cidABC operon in 14-4 compared to MRGR3, which was correlated with decreased expression of autolysis negative regulators lytSR and lrgAB. In contrast, the autolysis-deficient phenotype of 14-4 was correlated with both increased expression of negative autolysis regulators (arlRS, mgrA, and sarA) and decreased expression of positive regulators (agr RNAII and RNAIII). Quantitative bacteriolytic assays and zymographic analysis of concentrated culture supernatants showed a striking reduction in Atl-derived, extracellular bacteriolytic hydrolase activities in 14-4 compared to MRGR3. This observed difference was independent of the source of cell wall substrate (MRGR3 or 14-4) used for analysis. Collectively, our results suggest that altered autolytic properties in 14-4 are apparently not driven by significant changes in the transcription of key autolytic effectors. Instead, our analysis points to alternate regulatory mechanisms that impact autolysis effectors which may include changes in posttranscriptional processing or export.
Keywords Bacteriolysis/geneticsCell Wall/geneticsExtracellular Fluid/enzymologyHumansHydrolases/metabolismMethicillin ResistanceOctoxynolOligonucleotide Array Sequence AnalysisPeptide Hydrolases/biosynthesis/genetics/metabolismStaphylococcus aureus/drug effects/genetics/isolation & purification/ physiologyTeicoplanin/ pharmacologyTranscription, Genetic
PMID: 16940101
Full text
(ISO format)
RENZONI, Adriana Maria et al. Transcriptomic and functional analysis of an autolysis-deficient, teicoplanin-resistant derivative of methicillin-resistant Staphylococcus aureus. In: Antimicrobial agents and chemotherapy, 2006, vol. 50, n° 9, p. 3048-3061. doi: 10.1128/AAC.00113-06 https://archive-ouverte.unige.ch/unige:7543

522 hits

0 download


Deposited on : 2010-06-21

Export document
Format :
Citation style :