The Role of hlb-Converting Bacteriophages in Staphylococcus aureus Host Adaption

Abstract

As an opportunistic pathogen of humans and animals, <i>Staphylococcus aureus</i> asymptomatically colonizes the nasal cavity but is also a leading cause of life-threatening acute and chronic infections. The evolution of <i>S. aureus</i> resulting from short- and long-term adaptation to diverse hosts is tightly associated with mobile genetic elements<i>. S. aureus</i> strains can carry up to four temperate phages, many of which possess accessory genes encoding staphylococcal virulence factors. More than 90% of human nasal isolates of <i>S. aureus</i> have been shown to carry Sa3int phages, whereas invasive <i>S. aureus</i> isolates tend to lose these phages. Sa3int phages integrate as prophages into the bacterial <i>hlb</i> gene, disrupting the expression of the sphingomyelinase Hlb, an important virulence factor under specific infection conditions. Virulence factors encoded by genes carried by Sa3int phages include staphylokinase, enterotoxins, chemotaxis-inhibitory protein, and staphylococcal complement inhibitor, all of which are highly human specific and probably essential for bacterial survival in the human host. The transmission of <i>S. aureus</i> from humans to animals is strongly correlated with the loss of Sa3int phages, whereas phages are regained once a strain is transmitted from animals to humans. Thus, both the insertion and excision of prophages may confer a fitness advantage to this bacterium<i>.</i> There is also growing evidence that Sa3int phages may perform “active lysogeny,” a process during which prophages are temporally excised from the chromosome without forming intact phage particles. The molecular mechanisms controlling the peculiar life cycle of Sa3int phages remain largely unclear. Nevertheless, their regulation is likely fine-tuned to ensure bacterial survival within different hosts.