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Moura de Sousa, J. A.

Publications and source records attributed to Moura de Sousa, J. A..

2 recordsLinked to original sources

Phage inducible chromosomal minimalist island (PICMI), a family of satellites of marine virulent phages

Phage satellites are genetic elements that hijack the phage machinery for their own dissemination. However, only few phage satellites have been characterized, and mechanisms by which they influence microbial evolution in nature are unclear. Here we identify a new family of satellites, the Phage Inducible Chromosomal Minimalist Island (PICMI), which is broadly distributed in the marine bacteria Vibrionaceae. PICMI is characterized by reduced gene content, does not encode genes for capsid remodeling and packages its DNA as a concatemer. PICMI is integrated in the bacterial host genome at the end of the fis regulator and encodes three core proteins necessary for excision and replication. PICMI is dependent on virulent phage particles to spread to other bacteria and confers host protection from other competitive phages, without interfering with its helper phage. The discovery of PICMI strongly suggests that phages, including virulent ones, play important roles for mobility of phage defense elements.

microbiology↗

Modular prophage interactions driven by capsule serotype select for capsule loss under phage predation

Klebsiella species are able to colonize a wide range of environments and include worrisome nosocomial pathogens. Here, we sought to determine the abundance and infectivity of prophages of Klebsiella to understand how the interactions between induced prophages and bacteria affect population dynamics and evolution. We identified many prophages in the species, placing these taxa among the top 5% of the most polylysogenic bacteria. We selected 35 representative strains of the Klebsiella pneumoniae species complex to establish a network of induced phage-bacteria interactions. This revealed that many prophages are able to enter the lytic cycle, and subsequently kill or lysogenize closely-related Klebsiella strains. Although 60% of the tested strains could produce phages that infect at least one other strain, the interaction network of all pairwise cross-infections is very sparse and mostly organized in modules corresponding to the strains capsule serotypes. Accordingly, capsule mutants remain uninfected showing that the capsule is a key factor for successful infections. Surprisingly, experiments in which bacteria are predated by their own prophages result in accelerated loss of the capsule. Our results show that phage infectiousness defines interaction modules between small subsets of phages and bacteria in function of capsule serotype. This limits the role of prophages as competitive weapons because they can infect very few strains of the species complex. This should also restrict phage-driven gene flow across the species. Finally, the accelerated loss of the capsule in bacteria being predated by their own phages, suggests that phages drive serotype switch in nature.

microbiology↗