It is suggested that JAsa55 has lytic activity against selected MDR S. aureus strains and may be further evaluated as a candidate component for phage-based control strategies in milk.
Abstract
Staphylococcus aureus (S. aureus) is a prominent foodborne pathogen that frequently causes food poisoning by contaminating various foods, particularly dairy products, and poses severe threats to food safety and public health. The increasing prevalence of multidrug-resistant S. aureus strains has further limited the efficacy of conventional interventions. In this study, we isolated and characterized a novel lytic phage JAsa55 using an MDR S. aureus strain as host. Transmission electron microscopy showed that JAsa55 possesses an icosahedral head and a long non-contractile tail, consistent with a siphovirus-like morphology. Notably, JAsa55 retained detectable activity after exposure to 4-60°C and remained active under pH 3.0-11.0. One-step growth analysis indicated a latent period (15 min) and an estimated burst size (∼500 PFU/cell) based on the first rise phase. Genome annotation did not identify obvious integrase genes, known virulence factors, or antimicrobial-resistance genes. In artificially contaminated milk, phage JAsa55 reduced S. aureus populations by up to ∼1.6 log CFU/mL at 4°C and ∼3.3 log CFU/mL at 25°C within 24 h. These findings suggest that JAsa55 has lytic activity against selected MDR S. aureus strains and may be further evaluated as a candidate component for phage-based control strategies in milk.
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Staphylococcus aureus
poses a significant threat to food safety, driving the search for effective antibacterial agents. This study investigated the antibacterial and anti-virulence properties of the ethanolic extract of
Etlingera pavieana
rhizome (EE) against
S. aureus
. EE exhibited bactericidal activity with...
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The SKS1-KO Saccharomyces cerevisiae showed effective antibacterial activity against common clinical pathogenic bacteria in vitro, which has been confirmed through the determination of the minimum inhibitory concentration (MIC), growth curve analysis, inhibitory spectrum analysis and co-culture experiments.
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