Microevolution of serial clinical isolates of Cryptococcus neoformans var. grubii and C. gattii
dc.contributor.author | Chen, Y | |
dc.contributor.author | Farrer, RA | |
dc.contributor.author | Giamberardino, C | |
dc.contributor.author | Sakthikumar, S | |
dc.contributor.author | Jones, A | |
dc.contributor.author | Yang, T | |
dc.contributor.author | Tenor, JL | |
dc.contributor.author | Wagih, O | |
dc.contributor.author | Van Wyk, M | |
dc.contributor.author | Govender, NP | |
dc.contributor.author | Mitchell, TG | |
dc.contributor.author | Litvintseva, AP | |
dc.contributor.author | Cuomo, CA | |
dc.contributor.author | Perfect, JR | |
dc.date.accessioned | 2019-09-23T15:00:02Z | |
dc.date.issued | 2017-03-07 | |
dc.description.abstract | The pathogenic species of Cryptococcus are a major cause of mortality owing to severe infections in immunocompromised as well as immunocompetent individuals. Although antifungal treatment is usually effective, many patients relapse after treatment, and in such cases, comparative analyses of the genomes of incident and relapse isolates may reveal evidence of determinative, microevolutionary changes within the host. Here, we analyzed serial isolates cultured from cerebrospinal fluid specimens of 18 South African patients with recurrent cryptococcal meningitis. The time between collection of the incident isolates and collection of the relapse isolates ranged from 124 days to 290 days, and the analyses revealed that, during this period within the patients, the isolates underwent several genetic and phenotypic changes. Considering the vast genetic diversity of cryptococcal isolates in subSaharan Africa, it was not surprising to find that the relapse isolates had acquired different genetic and correlative phenotypic changes. They exhibited various mechanisms for enhancing virulence, such as growth at 39°C, adaptation to stress, and capsule production; a remarkable amplification of ERG11 at the native and unlinked locus may provide stable resistance to fluconazole. Our data provide a deeper understanding of the microevolution of Cryptococcus species under pressure from antifungal chemotherapy and host immune responses. This investigation clearly suggests a promising strategy to identify novel targets for improved diagnosis, therapy, and prognosis. | en_GB |
dc.description.sponsorship | Wellcome Trust | en_GB |
dc.description.sponsorship | National Institute of Allergy and Infectious Diseases | en_GB |
dc.identifier.citation | Vol. 8: e00166-17 | en_GB |
dc.identifier.doi | 10.1128/mBio.00166-17 | |
dc.identifier.grantnumber | U19 AI110818 | en_GB |
dc.identifier.grantnumber | R01 AI93257 | en_GB |
dc.identifier.grantnumber | R01 AI73896 | en_GB |
dc.identifier.grantnumber | R01 AI025783 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/38869 | |
dc.language.iso | en | en_GB |
dc.publisher | American Society for Microbiology | en_GB |
dc.rights | Copyright © 2017 Chen et al. This is an openaccess article distributed under the terms of the Creative Commons Attribution 4.0 International license | en_GB |
dc.title | Microevolution of serial clinical isolates of Cryptococcus neoformans var. grubii and C. gattii | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2019-09-23T15:00:02Z | |
dc.identifier.issn | 2150-7511 | |
exeter.article-number | ARTN e00166-17 | en_GB |
dc.description | This is the final version. Available from the publisher via the DOI in this record. | en_GB |
dc.identifier.journal | mBio | en_GB |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_GB |
dcterms.dateAccepted | 2017-02-06 | |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2017-03-07 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2019-09-23T14:44:31Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2019-09-23T15:00:11Z | |
refterms.panel | A | en_GB |
refterms.depositException | publishedGoldOA | |
refterms.depositExceptionExplanation | https://doi.org/10.1128/mBio.00166-17 |
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