Candida albicans VPS4 is required for secretion of aspartyl proteases and in vivo virulence
Mycopathologia, ISSN: 0301-486X, Vol: 167, Issue: 2, Page: 55-63
2009
- 28Citations
- 24Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations28
- Citation Indexes28
- 28
- CrossRef17
- Captures24
- Readers24
- 24
Article Description
Candida albicans secretes aspartyl proteases (Saps) during infection. Although Saps are secretory proteins, little is known about the intracellular trafficking and secretion of these proteins. We previously cloned and analyzed the C. albicans pre-vacuolar protein sorting gene VPS4, and demonstrated that extracellular Sap2p is absent in the culture supernatants of the vps4Δ null mutant. We therefore investigated the role of the C. albicans pre-vacuolar secretion pathway in the trafficking of Sap4-6p and in vivo virulence. The C. albicans vps4Δ mutant failed to produce extracellular Sap4-6p. Next, when tested in a mouse model of disseminated candidiasis, the vps4Δ mutant was greatly attenuated in virulence. Histopathological analysis indicated that infection with the vps4Δ mutant did not cause renal microabscess formation, in contrast to the wild-type strain. Our results imply that VPS4 is required for extracellular secretion of Sap4-6p, and that C. albicans requires an intact pre-vacuolar secretory pathway for wild-type virulence in vivo. © 2008 Springer Science+Business Media B.V.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=58349106843&origin=inward; http://dx.doi.org/10.1007/s11046-008-9155-7; http://www.ncbi.nlm.nih.gov/pubmed/18814053; http://link.springer.com/10.1007/s11046-008-9155-7; https://dx.doi.org/10.1007/s11046-008-9155-7; https://link.springer.com/article/10.1007/s11046-008-9155-7; http://www.springerlink.com/index/10.1007/s11046-008-9155-7; http://www.springerlink.com/index/pdf/10.1007/s11046-008-9155-7
Springer Science and Business Media LLC
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