scholarly journals Extra-Chromosomal DNA Sequencing Reveals Episomal Prophages Capable of Impacting Virulence Factor Expression in Staphylococcus aureus

2018 ◽  
Vol 9 ◽  
Author(s):  
Douglas R. Deutsch ◽  
Bryan Utter ◽  
Kathleen J. Verratti ◽  
Heike Sichtig ◽  
Luke J. Tallon ◽  
...  
2019 ◽  
Vol 113 (1) ◽  
pp. 103-122 ◽  
Author(s):  
Heidi A. Crosby ◽  
Nitija Tiwari ◽  
Jakub M. Kwiecinski ◽  
Zhen Xu ◽  
Allison Dykstra ◽  
...  

2007 ◽  
Vol 189 (20) ◽  
pp. 7515-7519 ◽  
Author(s):  
Alexa A. Pragman ◽  
Lisa Herron-Olson ◽  
Laura C. Case ◽  
Sara M. Vetter ◽  
Evan E. Henke ◽  
...  

ABSTRACT The SrrAB system regulates metabolism and virulence factors in Staphylococcus aureus. We sequenced the srrAB loci of 21 isolates and performed a phylogenetic analysis. Vaginal and bovine isolates clustered together, while skin isolates were genetically diverse. Few nucleotide polymorphisms were observed, and most were synonymous. Two strains (N2 and N19) with N-terminal truncations in SrrA displayed defects in growth and abnormally upregulated virulence factor expression under low-oxygen conditions.


2000 ◽  
Vol 182 (11) ◽  
pp. 3197-3203 ◽  
Author(s):  
Peter J. McNamara ◽  
Kathy C. Milligan-Monroe ◽  
Shirin Khalili ◽  
Richard A. Proctor

ABSTRACT A chromosomal insertion of transposon Tn917 partially restores the expression of protease and alpha-toxin activities to PM466, a genetically defined agr-null derivative of the wild-type Staphylococcus aureus strain RN6390. In co-transduction experiments, transposon-encoded erythromycin resistance and a protease- and alpha-toxin-positive phenotype are transferred at high frequency from mutant strains to agr-null strains ofS. aureus. Southern analysis of chromosomal DNA and sequence analysis of DNA flanking the Tn917 insertion site in mutant strains revealed that the transposon interrupted a 498-bp open reading frame (ORF). Similarity searches using a conceptual translation of the ORF identified a region of homology to the known staphylococcal global regulators AgrA and SarA. To verify that the mutant allele conferred the observed phenotype, a wild-type allele of the mutant gene was introduced into the genome of a mutant strain by homologous recombination. The resulting isolates had a restoredagr-null phenotype. Virulence factor gene expression in mutant, restored mutant, and wild-type strains was quantified by measuring alpha-toxin activity in culture supernatant fluids and by Northern analysis of the alpha-toxin transcript. We named this ORFrot (for repressor of toxins) (GenBank accession no.AF189239 ) because of the activity associated withrot::Tn917 mutant strains.


PLoS ONE ◽  
2015 ◽  
Vol 10 (2) ◽  
pp. e0116945 ◽  
Author(s):  
Wouter Rozemeijer ◽  
Pamela Fink ◽  
Eduardo Rojas ◽  
C. Hal Jones ◽  
Danka Pavliakova ◽  
...  

2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Mark E. Hart ◽  
Morgan J. Hart ◽  
Anna J. Roop

Hyaluronidases degrade hyaluronic acid, a major polysaccharide of the extracellular matrix of tissues, and are considered important for virulence in a number of Gram-positive and -negative bacteria. The purpose of the present study was to determine the prevalence of hyaluronidase among clinical strains ofStaphylococcus aureusand among otherStaphylococcusspecies. Spent media and chromosomal DNA were assessed for hyaluronidase activity and the absence or presence of a hyaluronidase gene (hysA) by Southern analysis, respectively. AllS. aureusstrains examined exhibited at least one hybridizing band (half of the strains exhibited two or more hybridizing bands) when probed forhysAand all but three of these strains produced hyaluronidase. In contrast, none of the type strains of 19 other species exhibited either hyaluronidase activity or hybridizing bands when probed forhysA. These data support the hypothesis that among members of theStaphylococcusgenus only strains ofS. aureuspossess the enzyme hyaluronidase. This would suggest that hyaluronidase represents yet another potential virulence factor employed byS. aureusto cause disease and may represent a diagnostically important characteristic for distinguishingS. aureusfrom other members of this genus.


BMC Genomics ◽  
2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Vijay Aswani ◽  
Fares Najar ◽  
Madhulatha Pantrangi ◽  
Bob Mau ◽  
William R. Schwan ◽  
...  

Microbiology ◽  
2005 ◽  
Vol 151 (6) ◽  
pp. 1789-1800 ◽  
Author(s):  
Niamh Harraghy ◽  
Jan Kormanec ◽  
Christiane Wolz ◽  
Dagmar Homerova ◽  
Christiane Goerke ◽  
...  

Eap and Emp are two Staphylococcus aureus adhesins initially described as extracellular matrix binding proteins. Eap has since emerged as being important in adherence to and invasion of eukaryotic cells, as well as being described as an immunomodulator and virulence factor in chronic infections. This paper describes the mapping of the transcription start point of the eap and emp promoters. Moreover, using reporter-gene assays and real-time PCR in defined regulatory mutants, environmental conditions and global regulators affecting expression of eap and emp were investigated. Marked differences were found in expression of eap and emp between strain Newman and the 8325 derivatives SH1000 and 8325-4. Moreover, both genes were repressed in the presence of glucose. Analysis of expression of both genes in various regulatory mutants revealed that sarA and agr were involved in their regulation, but the data suggested that there were additional regulators of both genes. In a sae mutant, expression of both genes was severely repressed. sae expression was also reduced in the presence of glucose, suggesting that repression of eap and emp in glucose-containing medium may, in part, be a consequence of a decrease in expression of sae.


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