» Articles » PMID: 30941104

Genetic Modification of Closely Related Species

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2019 Apr 4
PMID 30941104
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Species from the genus are among the most important human fungal pathogens. Several of them are frequent commensals of the human microbiota but are also able to cause a variety of opportunistic infections, especially when the human host becomes immunocompromised. By far, most of the research to understand the molecular underpinnings of the pathogenesis of these species has focused on , the most virulent member of the genus. However, epidemiological data indicates that related species are also clinically important. Here, we describe the generation of a set of strains and plasmids to genetically modify and , the two pathogenic species most closely related to is an ideal model to understand pathogenesis since it is the closest species to but considerably less virulent. On the other hand, is ranked among the four most common causes of infections by species. Given that and are obligate diploids with no known conventional sexual cycle, we generated strains that are auxotrophic for at least two amino acids which allows the tandem deletion of both alleles of a gene by complementing the two auxotrophies. The strains were generated in two different genetic backgrounds for each species - one for which the genomic sequence is available and a second clinically important one. In addition, we have adapted plasmids developed to delete genes and epitope/fluorophore tag proteins in so that they can be employed in . The tools generated here allow for efficient genetic modification of and , and thus facilitate the study of the molecular basis of pathogenesis in these medically relevant fungi.

Citing Articles

Genetic modification of , a non-pathogenic CTG species, reveals function.

Chavez-Tinoco M, Garcia-Ortega L, Mancera E Microbiology (Reading). 2024; 170(3).

PMID: 38456839 PMC: 10999747. DOI: 10.1099/mic.0.001447.


The hyphal-specific toxin candidalysin promotes fungal gut commensalism.

Liang S, Sircaik S, Dainis J, Kakade P, Penumutchu S, McDonough L Nature. 2024; 627(8004):620-627.

PMID: 38448595 PMC: 11230112. DOI: 10.1038/s41586-024-07142-4.


Development of engineered Candida tropicalis strain for efficient corncob-based xylitol-ethanol biorefinery.

Singh A, Deeba F, Kumar M, Kumari S, Wani S, Paul T Microb Cell Fact. 2023; 22(1):201.

PMID: 37803395 PMC: 10557352. DOI: 10.1186/s12934-023-02190-3.


Split-marker-mediated genome editing improves homologous recombination frequency in the CTG clade yeast Candida intermedia.

Peri K, Faria-Oliveira F, Larsson A, Plovie A, Papon N, Geijer C FEMS Yeast Res. 2023; 23.

PMID: 36893808 PMC: 10035504. DOI: 10.1093/femsyr/foad016.


Convergent and divergent roles of the glucose-responsive kinase SNF4 in .

Ke C, Lew S, Hsieh Y, Chang S, Lin C Virulence. 2023; 14(1):2175914.

PMID: 36745535 PMC: 9928470. DOI: 10.1080/21505594.2023.2175914.


References
1.
Porman A, Hirakawa M, Jones S, Wang N, Bennett R . MTL-independent phenotypic switching in Candida tropicalis and a dual role for Wor1 in regulating switching and filamentation. PLoS Genet. 2013; 9(3):e1003369. PMC: 3605238. DOI: 10.1371/journal.pgen.1003369. View

2.
Basso Jr L, Bartiss A, Mao Y, Gast C, Coelho P, Snyder M . Transformation of Candida albicans with a synthetic hygromycin B resistance gene. Yeast. 2010; 27(12):1039-48. PMC: 4243612. DOI: 10.1002/yea.1813. View

3.
Anderson M, Porman A, Wang N, Mancera E, Huang D, Cuomo C . A Multistate Toggle Switch Defines Fungal Cell Fates and Is Regulated by Synergistic Genetic Cues. PLoS Genet. 2016; 12(10):e1006353. PMC: 5053522. DOI: 10.1371/journal.pgen.1006353. View

4.
Sears D, Schwartz B . Candida auris: An emerging multidrug-resistant pathogen. Int J Infect Dis. 2017; 63:95-98. DOI: 10.1016/j.ijid.2017.08.017. View

5.
Staib P, Moran G, Sullivan D, Coleman D, Morschhauser J . Isogenic strain construction and gene targeting in Candida dubliniensis. J Bacteriol. 2001; 183(9):2859-65. PMC: 99503. DOI: 10.1128/JB.183.9.2859-2865.2001. View