In-vitro evaluation of virulence markers and antifungal resistance of clinical Candida albicans strains isolated from Karachi, Pakistan

被引:6
作者
Jabeen, Gul [1 ,2 ]
Naz, Sehar Afshan [1 ]
Rangel, Drauzio E. N. [3 ]
Jabeen, Nusrat [2 ]
Shafique, Maryam [1 ]
Yasmeen, Kousar [4 ]
机构
[1] Fed Urdu Univ Arts Sci & Technol, Dept Microbiol, Lab Appl Microbiol & Clin Mycol, Karachi 75300, Pakistan
[2] Univ Karachi, Dept Microbiol, Karachi, Pakistan
[3] Univ Tecnol Fed Parana, BR-85660000 Dois Vizinhos, Parana, Brazil
[4] Fed Urdu Univ Arts Sci & Technol, Dept Chem, Karachi 75300, Pakistan
关键词
Candidiasis; Candida albicans; Virulence factors; Hydrolytic enzymes; Antifungal resistance; BIOFILM FORMATION; INVASIVE CANDIDIASIS; EPIDEMIOLOGY; SUSCEPTIBILITY; PATHOGENICITY; COAGULASE; INFECTIONS; PREVALENCE;
D O I
10.1016/j.funbio.2023.04.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Candidiasis is a significant fungal infection with high mortality and morbidity rates worldwide. Candida albicans is the most dominant species responsible for causing different manifestations of candidiasis. Certain virulence traits as well as its resistance to antifungal drugs contribute to the pathogenesis of this yeast. This study was designed to determine the production of some virulence factors, such as biofilm formation and extracellular hydrolytic enzymes (esterase, coagulase, gelatinase, and catalase) by this fungus, as well as its antifungal resistance profile. A total of 304 clinical C. albicans isolates obtained from different clinical specimens were identified by a conventional diagnostic protocol. The antifungal sus-ceptibility of C. albicans strains was determined by disk diffusion technique against commercially available antifungal disks, such as nystatin 50 & mu;g, amphotericin B 100 unit, fluconazole 25 & mu;g, itraco-nazole 10 & mu;g, ketoconazole 10 & mu;g, and voriconazole 1 & mu;g. The assessment of biofilm formation was determined by the tube staining assay and spectrophotometry. Gelatinase, coagulase, catalase, and esterase enzyme production was also detected using standard techniques. A total of 66.1% (201/304) and 28.9% (88/304) of C. albicans strains were susceptible-dose dependent (SDD) to nystatin and itraconazole, respectively. Among the antifungal drugs, C. albicans strains showed high resistance to ketoconazole 24.7% (75/304); however, no statistically significant relationship between the clinical origin of C. albicans isolates and antifungal drug resistance pattern was detected. For virulence factors, the majority of the C. albicans strains actively produced biofilm and all hydrolytic enzymes. Biofilm formation was demonstrated by 88% (267/304) of the strains with a quantitative mean value 0.1762 (SD & PLUSMN; 0.08293). However, 100% (304/304) of isolates produced catalase enzyme, 69% (211/304) produced coagulase, 66% (197/304) produced gelatinase, and 52% (157/304) produced esterase enzyme. A significant relationship between the source of specimens and biofilm formation by C. albicans was observed; nevertheless, there was no significant relationship between different sources of C. albicans strains and the production of different enzymatic virulence factors. The study found that C. albicans strains have excellent potential to produce virulence markers and resistance to antifungals, which necessitates surveillance of these opportunistic pathogens to minimize the chances of severe invasive infections.& COPY; 2023 British Mycological Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1241 / 1249
页数:9
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