The phage Φ13-encoded transcriptional regulator Ltr controls phage assembly in Staphylococcus aureus
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Temperate phages play a central role in evolution and pathogenicity of Staphylococcus aureus . Sa3int phages, in particular, contribute highly human-specific virulence factors that promote immune evasion and survival within the host. The reversible excision of these phages which occurs without phage production and bacterial lysis allows the simultaneous expression of phage virulence genes and the hlb gene where they usually integrate. However, the regulatory mechanisms controlling phage assembly and the cross-talk with host factors remain poorly understood. In this study, we analyzed the regulatory mechanism controlling late gene transcription in Sa3int phage Φ13. We identified a functional promoter, P 23, located upstream of the late phage genes that control DNA processing and packaging, capsid assembly, bacterial lysis and immune evasion. SAOUHSC_02200 , the gene located upstream of P 23 , encodes for a late transcriptional regulator (Ltr). Mutating the P 23 TATA-box or the ltr gene abolished P 23 activity and formation of mature intact phage particles, thus confirming the role of Ltr in regulating P 23 activity. Four direct repeats upstream of the P 23 transcriptional start site were identified as potential Ltr binding sites. RT-qPCR analysis confirmed that Ltr-dependent P 23 activation is essential for expression of late genes and the subsequent propagation of Φ13. Furthermore, comparative analysis of P 23 activity and ltr expression in different host strain backgrounds revealed strain-specific differences that appear to depend on the alternative sigma factor SigB and its downstream effector SpoVG. These findings establish Ltr as the major regulator of late gene expression in Φ13 and reveal bacterial host factors that control successful phage assembly, and bacterial lysis.
Importance
The dynamic integration and excision of highly prevalent Sa3int phages in Staphylococcus aureus is considered a regulatory switch that enables bacterial adaptation to specific niches. These phages carry several human-specific virulence genes and integrate into the hlb virulence gene. It was assumed that they undergo a mechanism termed ’active lysogeny’, which allows the phages to be excised reversibly without phage production or bacterial lysis. Here, we have identified a new phage-encoded ’late transcriptional regulator’ (Ltr) that controls the expression of all late phage genes and thus phage assembly and lysis. We found that Ltr activity is regulated by the alternative sigma factor B and its downstream effector SpoVG. Restriction of SpoVG, and consequently phage assembly, likely contributes to the maintenance of Sa3int phages, even under phage-inducing conditions. This may be relevant in certain infectious conditions where both the phage-encoded virulence genes and the gene that is usually interrupted by the phage are required for infectivity.
