Identification of proteins involved in the adhesionof Candida species to different medical devices
Microbial Pathogenesis, ISSN: 0882-4010, Vol: 107, Page: 293-303
2017
- 24Citations
- 47Captures
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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.
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Metrics Details
- Citations24
- Citation Indexes24
- 24
- CrossRef14
- Captures47
- Readers47
- 47
Article Description
Adhesion is the first step for Candida species to form biofilms on medical devices implanted in the human host. Both the physicochemical nature of the biomaterial and cell wall proteins (CWP) of the pathogen play a determinant role in the process. While it is true that some CWP have been identified in vitro, little is known about the CWP of pathogenic species of Candida involved in adhesion. On this background, we considered it important to investigate the potential role of CWP of C. albicans, C. glabrata, C. krusei and C. parapsilosis in adhesion to different medical devices. Our results indicate that the four species strongly adher to polyvinyl chloride (PVC) devices, followed by polyurethane and finally by silicone. It was interesting to identify fructose-bisphosphate aldolase (Fba1) and enolase 1 (Eno1) as the CWP involved in adhesion of C. albicans, C. glabrata and C. krusei to PVC devices whereas phosphoglycerate kinase (Pgk) and Eno1 allow C. parapsilosis to adher to silicone-made implants. Results presented here suggest that these CWP participate in the initial event of adhesion and are probably followed by other proteins that covalently bind to the biomaterial thus providing conditions for biofilm formation and eventually the onset of infection.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0882401017301092; http://dx.doi.org/10.1016/j.micpath.2017.04.009; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85017324913&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/28396240; https://linkinghub.elsevier.com/retrieve/pii/S0882401017301092; https://dx.doi.org/10.1016/j.micpath.2017.04.009
Elsevier BV
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