the pseudomonas aeruginosa reference strain pa14 displays increased virulence due to a mutation in lads铜绿假单胞菌参考应变pa14显示由于小伙子的突变增加毒性.pdfVIP
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the pseudomonas aeruginosa reference strain pa14 displays increased virulence due to a mutation in lads铜绿假单胞菌参考应变pa14显示由于小伙子的突变增加毒性
The Pseudomonas aeruginosa Reference Strain PA14
Displays Increased Virulence Due to a Mutation in ladS
Helga Mikkelsen, Rachel McMullan, Alain Filloux*
Division of Cell and Molecular Biology, Department of Life Sciences, Imperial College London, London, United Kingdom
Abstract
Pseudomonas aeruginosa is a pathogen that causes acute and chronic infections in a variety of hosts. The pathogenic
potential of P. aeruginosa is strain-dependent. PA14 is a highly virulent strain that causes disease in a wide range of
organisms, whereas PAO1 is moderately virulent. Although PA14 carries pathogenicity islands that are absent in PAO1, the
presence or absence of specific gene clusters is not predictive of virulence. Here, we show that the virulent strain PA14 has
an acquired mutation in the ladS gene. This mutation has a deleterious impact on biofilm, while it results in elevated type III
secretion system (T3SS) activity and increased cytotoxicity towards mammalian cells. These phenotypes can be reverted by
repairing the ladS mutation on the PA14 genome. The RetS/LadS/GacS signaling cascade is associated with virulence and
the switch between acute and chronic infections. RetS is a sensor that down-regulates biofilm formation and up-regulates
the T3SS. Mutations in retS are acquired in strains isolated from chronically infected cystic fibrosis patients and lead to
hyperbiofilm formation and reduced cytotoxicity. Conversely, the LadS sensor promotes biofilm formation and represses the
T3SS. We conclude that the ladS mutation is partly responsible for the high cytotoxicity of PA14, and our findings
corroborate the central role of RetS and LadS in the switch between acute and chronic infections. Given the extensive use of
the reference strain PA14 in infection and virulence models, the bias cau
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