Abstract:Exfoliative toxin A (ETA) causes staphylococcal scalded-skin syndrome in children. The gene for ETA was believed to be coded by the chromosomal DNA. We isolated temperate phages from an ETA-producing strain, ZM, using a restriction minus strain, 1039, as an indicator. One of the prophages, designated revealed that phage (1)-ZM-1 carries the structural gene for ETA.
“…Genomic analyses revealed that the ETA gene is chromosomally located, whereas the ETB gene is carried on plasmids [8,10]. Furthermore, the eta gene is encoded in the genomic sequence of a temperate phage, and phage infection converts ETA non-producing strains into ETA producers [11,12]. ETA and ETB comprise 242 and 246 amino acids, respectively, and share approximately 40% amino acid homology [8].…”
“…Genomic analyses revealed that the ETA gene is chromosomally located, whereas the ETB gene is carried on plasmids [8,10]. Furthermore, the eta gene is encoded in the genomic sequence of a temperate phage, and phage infection converts ETA non-producing strains into ETA producers [11,12]. ETA and ETB comprise 242 and 246 amino acids, respectively, and share approximately 40% amino acid homology [8].…”
“…Three distinct ETs, ETA, ETB, and ETD, which are proteins of 27-30 kDa, have been identified in S. aureus. The genes for these ETs, eta, etb, and etd, have been identified on mobile genetic elements, e.g., a bacteriophage for eta, a plasmid for etb, and a pathogenicity island for etd, indicating that S. aureus strains might have increased or changed their pathogenic potential by acquiring virulent determinants [13][14][15].…”
“…Yoshizawa et al [31] described, for the first time, a temperate phage that carried the structural gene for ETA from an ETA-producing strain of S. aureus. Yamaguchi et al [32] also isolated a phage (φ ETA) that encodes an ETA from S. aureus, isolated from a human impetigo patient, and determined the complete nucleotide sequence of the φ ETA genome.…”
Bacteriophages play an important role in the pathogenicity of Staphylococcus aureus (S. aureus) either by carrying accessory virulence factors or several superantigens. Despite their importance, there are not many studies showing the actual distribution of the virulence genes carried by the prophages obtained from the clinically isolated Staphylococcus. In this study, we investigated prophages obtained from methicillin-resistant S. aureus (MRSA) strains isolated from hospital-and community-associated (HA-CA) infections for the virulence factors. In the study, 43 phages isolated from 48 MRSA were investigated for carrying toxin genes including the sak, eta, lukF-PV, sea, selp, sek, seg, seq chp, and scn virulence genes using polymerase chain reaction (PCR) and Southern blot. Restriction fragment length polymorphism was used to analyze phage genomes to investigate the relationship between the phage profiles and the toxin genes' presence. MRSA strains isolated from HA infections tended to have higher prophage presence than the MRSA strains obtained from the CA infections (97% and 67%, respectively). The study showed that all the phages with the exception of one phage contained one or more virulence genes in their genomes with different combinations. The most common toxin genes found were sea (83%) followed by sek (77%) and seq (64%). The study indicates that prophages encode a significant proportion of MRSA virulence factors.
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