2022
DOI: 10.1016/j.mcpro.2022.100233
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New Global Insights on the Regulation of the Biphasic Life Cycle and Virulence Via ClpP-Dependent Proteolysis in Legionella pneumophila

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Cited by 7 publications
(7 citation statements)
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“…They referred to such microbial behavior as a biphasic life cycle. Evidence of a biphasic life cycle has been found in B. bacteriovorus, where significant metabolic changes were observed when comparing predating bacteria with intraperiplasmic bacteria of the same strain ( Herencias et al, 2020 ) and in virulent versus non-virulent L. pneumophila ( Ge et al, 2022 ).…”
Section: Discussionmentioning
confidence: 98%
“…They referred to such microbial behavior as a biphasic life cycle. Evidence of a biphasic life cycle has been found in B. bacteriovorus, where significant metabolic changes were observed when comparing predating bacteria with intraperiplasmic bacteria of the same strain ( Herencias et al, 2020 ) and in virulent versus non-virulent L. pneumophila ( Ge et al, 2022 ).…”
Section: Discussionmentioning
confidence: 98%
“…Table 1 compiles the main regulatory systems described that play an important role in L. pneumophila infection in amoeba and in the biofilm life cycle. Proteomics and transcriptomics studies revealed key metabolic pathways, common to in vivo infection models and in vitro broth cultures, that dictate the phenotypic shift from the replicative to the transmissive phase [ 48 ]. This phenotype transition is coordinated by regulatory systems that control gene expression, such as regulatory proteins (CsrA, RpoS, FliA and FleQ), the LetA/LetS (LetA/S) two-component system ( Legionella transmission activator and sensor, respectively) the stringent response metabolites (RelA, SpoT and ‘ppGpp’) and noncoding/small RNA (nc/sRNA) [ [49] , [50] , [51] , [52] , [53] ].…”
Section: Pneumophila Biphasic Life Cyclementioning
confidence: 99%
“…There are two subclasses of the T4SS, namely the T4SS -A (Lvh) and the T4SS-B (Dot/Icm:(Defect in organelle trafficking/Intracellular multiplication). The Dot/Icm genes encode Dot/Icm secretory system proteins [ 67 ], and are vital for organelle trafficking and intracellular multiplication [ 80 ], while the Lvh secretion system contains genes encoding mobility factors and enzymes [ 81 ]. Furthermore, the Lvh can functionally replace defective Dot/Icm.…”
Section: The Mechanism Of Ldmentioning
confidence: 99%