Candida tropicalis Isolates from Mexican Republic Exhibit High Susceptibility to Bleomycin and Variable Susceptibility to Hydrogen Peroxide

被引:2
作者
Gomez-Casanova, Natalia [1 ]
Bellido, Alberto [1 ]
Espinosa-Texis, Alejandra [2 ]
Cueva, Rosario [1 ]
Ciudad, Toni [1 ]
Larriba, German [1 ]
机构
[1] Univ Extremadura, Fac Ciencias, Dept Ciencias Biomed, Badajoz 06011, Spain
[2] Benemerita Univ Autonoma Puebla, Inst Ciencias, Ctr Invest Ciencias Microbiol, Lab Micol, Puebla, Mexico
关键词
Candida tropicalis; DNA-damaging agents; bleomycin; hydrogen peroxide; DOUBLE-STRAND BREAKS; ALBICANS; EPIDEMIOLOGY; GROWTH; DAMAGE;
D O I
10.1089/mdr.2017.0253
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Candida sp. are found as part of the commensal flora in humans but can cause invasive candidiasis in patients with severe underlying disease, especially cancer patients. These patients are frequently subjected to nonsurgical anticancer treatments such as ionizing radiation and anticancer drugs, which kill proliferating human cells by damaging DNA but also affect the microbiota of the patient. C. tropicalis, an emerging fungal pathogen, is associated with high mortality rates of cancer patients especially in tropical regions. In this study, we have investigated the in vitro susceptibility of 38 C. tropicalis clinical isolates from several Mexican hospitals to chronic treatments with several DNA damaging agents, including oxidizing compounds and anticancer drugs. C. tropicalis isolates displayed a high variability in their susceptibility to hydrogen peroxide (H2O2) while showing a high susceptibility to bleomycin (BLM), an anticancer drug that causes double-strand breaks in DNA. This contrasted with the moderate-to-high resistance exhibited by several C. albicans laboratory strains. At least for the C. tropicalis reference strain MYA3404, this susceptibility was hardly modified by the presence of serum. Our results open the possibility of using susceptibility to BLM to differentiate between C. tropicalis and C. albicans; however, analysis of a larger number of isolates is required. The use of BLM for prevention of C. tropicalis infections in neutropenic patients with cancer should be also evaluated. Finally, the variable susceptibility to H2O2 might be due to allelic variation of the histone acetyl-transferase complex which modulates the induction kinetics of H2O2-induced genes in C. tropicalis.
引用
收藏
页码:1031 / 1039
页数:9
相关论文
共 26 条
[1]  
Alvarez Gasca M A, 1998, Rev Latinoam Microbiol, V40, P15
[2]   Candida tropicalis in human disease [J].
Chai, Louis Yi Ann ;
Denning, David W. ;
Warn, Peter .
CRITICAL REVIEWS IN MICROBIOLOGY, 2010, 36 (04) :282-298
[3]   Mechanistic studies on bleomycin-mediated DNA damage: multiple binding modes can result in double-stranded DNA cleavage [J].
Chen, Jingyang ;
Ghorai, Manas K. ;
Kenney, Grace ;
Stubbe, JoAnne .
NUCLEIC ACIDS RESEARCH, 2008, 36 (11) :3781-3790
[4]   Bleomycins: Towards better therapeutics [J].
Chen, JY ;
Stubbe, J .
NATURE REVIEWS CANCER, 2005, 5 (02) :102-112
[5]   Base Damage Immediately Upstream from Double-Strand Break Ends is a More Severe Impediment to Nonhomologous End Joining than Blocked 3′-Termini [J].
Datta, Kamal ;
Purkayastha, Shubhadeep ;
Neumann, Ronald D. ;
Pastwa, Elzbieta ;
Winters, Thomas A. .
RADIATION RESEARCH, 2011, 175 (01) :97-112
[6]  
EVANS EGV, 1974, SABOURAUDIA, V12, P112
[7]   Role of the homologous recombination genes RAD51 and RAD59 in the resistance of Candida albicans to UV light, radiomimetic and anti-tumor compounds and oxidizing agents [J].
Garcia-Prieto, Fatima ;
Gomez-Raja, Jonathan ;
Andaluz, Encarnacion ;
Calderone, Richard ;
Larriba, German .
FUNGAL GENETICS AND BIOLOGY, 2010, 47 (05) :433-445
[8]   ISOLATION OF THE CANDIDA-ALBICANS GENE FOR OROTIDINE-5'-PHOSPHATE DECARBOXYLASE BY COMPLEMENTATION OF S-CEREVISIAE URA3 AND ESCHERICHIA-COLI PYRF MUTATIONS [J].
GILLUM, AM ;
TSAY, EYH ;
KIRSCH, DR .
MOLECULAR & GENERAL GENETICS, 1984, 198 (01) :179-182
[9]   Bleomycin therapy of experimental disseminated candidiasis in mice [J].
Graybill, JR ;
Bocanegra, R ;
Fothergill, A ;
Rinaldi, MG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (03) :816-818
[10]  
HENNER WD, 1983, J BIOL CHEM, V258, P5198