RESUMO
Listeria monocytogenes strain 10403S harbors two phage elements in its chromosome; one produces infective virions and the other tailocins. It was previously demonstrated that induction of the two elements is coordinated, as they are regulated by the same anti-repressor. In this study, we identified AriS as another phage regulator that controls the two elements, bearing the capacity to inhibit their lytic induction under SOS conditions. AriS is a two-domain protein that possesses two distinct activities, one regulating the genes of its encoding phage and the other downregulating the bacterial SOS response. While the first activity associates with the AriS N-terminal AntA/AntB domain, the second associates with its C-terminal ANT/KilAC domain. The ANT/KilAC domain is conserved in many AriS-like proteins of listerial and non-listerial prophages, suggesting that temperate phages acquired such dual-function regulators to align their response with the other phage elements that cohabit the genome.
Assuntos
Bacteriófagos , Listeria monocytogenes , Bacteriófagos/genética , Listeria monocytogenes/genética , Lisogenia , Prófagos/genética , Resposta SOS em GenéticaRESUMO
Some Listeria monocytogenes (Lm) strains harbor a prophage within the comK gene, which renders it inactive. During Lm infection of macrophage cells, the prophage turns into a molecular switch, promoting comK gene expression and therefore Lm intracellular growth. During this process, the prophage does not produce infective phages or cause bacterial lysis, suggesting it has acquired an adaptive behavior suited to the pathogenic lifestyle of its host. In this study, we demonstrate that this non-classical phage behavior, named active lysogeny, relies on a transcriptional response that is specific to the intracellular niche. While the prophage undergoes lytic induction, the process is arrested midway, preventing the transcription of the late genes. Further, we demonstrate key phage factors, such as LlgA transcription regulator and a DNA replicase, that support the phage adaptive behavior. This study provides molecular insights into the adaptation of phages to their pathogenic hosts, uncovering unusual cooperative interactions.
Assuntos
Proteínas de Bactérias/genética , Listeria monocytogenes/metabolismo , Lisogenia/fisiologia , Fatores de Transcrição/genética , Animais , Proteínas de Bactérias/metabolismo , Bacteriófagos/genética , Feminino , Listeriose/metabolismo , Camundongos , Camundongos Endogâmicos C57BL , Prófagos/genética , Fatores de Transcrição/metabolismo , Ativação Viral/fisiologiaRESUMO
Bacterial pathogens often carry multiple prophages and other phage-derived elements within their genome, some of which can produce viral particles in response to stress. Listeria monocytogenes 10403S harbors two phage elements in its chromosome, both of which can trigger bacterial lysis under stress: an active prophage (Ï10403S) that promotes the virulence of its host and can produce infective virions, and a locus encoding phage tail-like bacteriocins. Here, we show that the two phage elements are co-regulated, with the bacteriocin locus controlling the induction of the prophage and thus its activity as a virulence-associated molecular switch. More specifically, a metalloprotease encoded in the bacteriocin locus is upregulated in response to stress and acts as an anti-repressor for CI-like repressors encoded in each phage element. Our results provide molecular insight into the phenomenon of polylysogeny and its intricate adaptation to complex environments.
Assuntos
Bacteriófagos/imunologia , Cromossomos Bacterianos/imunologia , Listeria monocytogenes/imunologia , Prófagos/imunologia , Sequência de Aminoácidos , Bacteriocinas/genética , Bacteriocinas/imunologia , Bacteriólise/imunologia , Bacteriófagos/genética , Bacteriófagos/fisiologia , Cromossomos Bacterianos/genética , Cromossomos Bacterianos/virologia , Genoma Bacteriano/genética , Genoma Bacteriano/imunologia , Genoma Viral/genética , Genoma Viral/imunologia , Interações Hospedeiro-Patógeno/imunologia , Listeria monocytogenes/genética , Listeria monocytogenes/virologia , Lisogenia/genética , Lisogenia/imunologia , Metaloproteases/genética , Metaloproteases/imunologia , Prófagos/genética , Prófagos/fisiologia , Homologia de Sequência de Aminoácidos , Ativação Viral/genética , Ativação Viral/imunologiaRESUMO
Bacteriophages are ubiquitous and affect most facets of life, from evolution of bacteria, through ecology and global biochemical cycling to human health. The interactions between phages and bacteria often lead to biological novelty and an important milestone in this process is the ability of phages to regulate their host's behavior. In this review article, we will focus on newly reported cases that demonstrate how temperate phages regulate bacterial gene expression and behavior in a variety of bacterial species, pathogenic and environmental. This regulation is mediated by diverse mechanisms such as transcription factors, sRNAs, DNA rearrangements, and even controlled bacterial lysis. The outcome is mutualistic relationships that enable adaptively enhanced communal phage-host fitness under specific conditions.
