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2003
DOI: 10.1099/mic.0.25980-0
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Comparative assessment of virulence traits in Legionella spp.

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Cited by 54 publications
(51 citation statements)
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“…This strategy pruned down the number of bacterial isolates down to 5, of which all of them were Gram negative rods exhibiting both catalase and oxidase activities with hippurate hydrolysis and gelatine liquefaction -a biochemical result suggestive of Legionella spp. Alli et al (2003) have shown before that pore forming activity within the genus Legionella is associated with L. pneumophila and L. spirintensis. It was in view of this that pore forming activity was tested for in all the 5 suspected legionellae isolates by performing haemolysis assay in which sheep red blood cells were used, the result (Figure 1) showed that all exhibited pore forming activity that was very close to that of L. pneumophila AA100 that was used as a positive control.…”
Section: Resultsmentioning
confidence: 99%
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“…This strategy pruned down the number of bacterial isolates down to 5, of which all of them were Gram negative rods exhibiting both catalase and oxidase activities with hippurate hydrolysis and gelatine liquefaction -a biochemical result suggestive of Legionella spp. Alli et al (2003) have shown before that pore forming activity within the genus Legionella is associated with L. pneumophila and L. spirintensis. It was in view of this that pore forming activity was tested for in all the 5 suspected legionellae isolates by performing haemolysis assay in which sheep red blood cells were used, the result (Figure 1) showed that all exhibited pore forming activity that was very close to that of L. pneumophila AA100 that was used as a positive control.…”
Section: Resultsmentioning
confidence: 99%
“…These biochemical tests combined with demonstration of pore forming activity of L. pneumophila helped in narrowing down to L. pneumophila. Pore forming activity has been described as one of the virulence traits of L. pneumophila (Alli et al, 2003) which is best demonstrated by haemolysis assay using sheep red blood cells. Combining this haemolysis assay and the ability to amplify the 0.52 kb portion of the dot/icm region of L. pneumophila helped in the final identification.…”
Section: Discussionmentioning
confidence: 99%
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“…L. pneumophila strain AA100/130b (BAA-74; American Type Culture Collection) and the isogenic mutants dotA, ankB, and complemented ankB mutants were grown as described previously . The L. longbeachae strains and L. micdadei and L. dumoffii strains (Alli et al, 2003) have been previously described. E. coli strain DH5- was used for cloning purposes.…”
Section: Methodsmentioning
confidence: 99%