Literature DB >> 35506689

The Role of Glycoside Hydrolases in S. gordonii and C. albicans Interactions.

Zhiyan Zhou1,2, Biao Ren1, Jiyao Li1,2, Xuedong Zhou1,2, Xin Xu1,2, Yuan Zhou3.   

Abstract

Candida albicans can coaggregate with Streptococcus gordonii and cocolonize in the oral cavity. Saliva provides a vital microenvironment for close interactions of oral microorganisms. However, the level of fermentable carbohydrates in saliva is not sufficient to support the growth of multiple species. Glycoside hydrolases (GHs) that hydrolyze glycoproteins are critical for S. gordonii growth in low-fermentable-carbohydrate environments such as saliva. However, whether GHs are involved in the cross-kingdom interactions between C. albicans and S. gordonii under such conditions remains unknown. In this study, C. albicans and S. gordonii were cocultured in heart infusion broth with a low level of fermentable carbohydrate. Planktonic growth, biofilm formation, cell aggregation, and GH activities of monocultures and cocultures were examined. The results revealed that the planktonic growth of cocultured S. gordonii in a low-carbohydrate environment was elevated, while that of cocultured C. albicans was reduced. The biomass of S. gordonii in dual-species biofilms was higher than that of monocultures, while that of cocultured C. albicans was decreased. GH activity was observed in S. gordonii, and elevated activity of GHs was detected in S. gordonii-C. albicans cocultures, with elevated expression of GH-related genes of S. gordonii. By screening a mutant library of C. albicans, we identified a tec1Δ/Δ mutant strain that showed reduced ability to promote the growth and GH activities of S. gordonii compared with the wild-type strain. Altogether, the findings of this study demonstrate the involvement of GHs in the cross-kingdom metabolic interactions between C. albicans and S. gordonii in an environment with low level of fermentable carbohydrates. IMPORTANCE Cross-kingdom interactions between Candida albicans and oral streptococci such as Streptococcus gordonii have been reported. However, their interactions in a low-fermentable-carbohydrate environment like saliva is not clear. The current study revealed glycoside hydrolase-related cross-kingdom communications between S. gordonii and C. albicans under the low-fermentable-carbohydrate condition. We demonstrate that C. albicans can promote the growth and metabolic activities of S. gordonii by elevating the activities of cell-wall-anchored glycoside hydrolases of S. gordonii. C. albicans gene TEC1 is critical for this cross-kingdom metabolic communication.

Entities:  

Keywords:  Candida albicans; Streptococcus gordonii; TEC1 protein; biofilms; glycoside hydrolases; microbial interactions

Mesh:

Substances:

Year:  2022        PMID: 35506689      PMCID: PMC9128511          DOI: 10.1128/aem.00116-22

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   5.005


  101 in total

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Journal:  Microbiology       Date:  2000-01       Impact factor: 2.777

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Journal:  Mol Microbiol       Date:  2003-02       Impact factor: 3.501

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Journal:  Mol Cell Biol       Date:  2001-10       Impact factor: 4.272

5.  Genome-wide transcriptional profiling and enrichment mapping reveal divergent and conserved roles of Sko1 in the Candida albicans osmotic stress response.

Authors:  Dawn H Marotta; Andre Nantel; Leonid Sukala; Jennifer R Teubl; Jason M Rauceo
Journal:  Genomics       Date:  2013-06-15       Impact factor: 5.736

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Authors:  S M Saporito-Irwin; C E Birse; P S Sypherd; W A Fonzi
Journal:  Mol Cell Biol       Date:  1995-02       Impact factor: 4.272

7.  The Rbf1, Hfl1 and Dbp4 of Candida albicans regulate common as well as transcription factor-specific mitochondrial and other cell activities.

Authors:  Kasra Khamooshi; Patricia Sikorski; Nuo Sun; Richard Calderone; Dongmei Li
Journal:  BMC Genomics       Date:  2014-01-22       Impact factor: 3.969

8.  Candida albicans induces mucosal bacterial dysbiosis that promotes invasive infection.

Authors:  Martinna Bertolini; Amit Ranjan; Angela Thompson; Patricia I Diaz; Takanori Sobue; Kendra Maas; Anna Dongari-Bagtzoglou
Journal:  PLoS Pathog       Date:  2019-04-22       Impact factor: 7.464

9.  The carbohydrate-active enzymes database (CAZy) in 2013.

Authors:  Vincent Lombard; Hemalatha Golaconda Ramulu; Elodie Drula; Pedro M Coutinho; Bernard Henrissat
Journal:  Nucleic Acids Res       Date:  2013-11-21       Impact factor: 16.971

10.  Selective BET bromodomain inhibition as an antifungal therapeutic strategy.

Authors:  Flore Mietton; Elena Ferri; Morgane Champleboux; Ninon Zala; Danièle Maubon; Yingsheng Zhou; Mike Harbut; Didier Spittler; Cécile Garnaud; Marie Courçon; Murielle Chauvel; Christophe d'Enfert; Boris A Kashemirov; Mitchell Hull; Muriel Cornet; Charles E McKenna; Jérôme Govin; Carlo Petosa
Journal:  Nat Commun       Date:  2017-05-18       Impact factor: 14.919

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