<i>Candidiasis</i> and Mechanisms of Antifungal Resistance

<i>Candidiasis</i> can be present as a cutaneous, mucosal or deep-seated organ infection, which is caused by more than 20 types of <i>Candida</i> sp., with <i>C. albicans</i> being the most common. These are pathogenic yeast and are usually present in the normal m...

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Main Authors: Somanon Bhattacharya (Author), Sutthichai Sae-Tia (Author), Bettina C. Fries (Author)
Format: Book
Published: MDPI AG, 2020-06-01T00:00:00Z.
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100 1 0 |a Somanon Bhattacharya  |e author 
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700 1 0 |a Bettina C. Fries  |e author 
245 0 0 |a <i>Candidiasis</i> and Mechanisms of Antifungal Resistance 
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520 |a <i>Candidiasis</i> can be present as a cutaneous, mucosal or deep-seated organ infection, which is caused by more than 20 types of <i>Candida</i> sp., with <i>C. albicans</i> being the most common. These are pathogenic yeast and are usually present in the normal microbiome. High-risk individuals are patients of human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS), organ transplant, and diabetes. During infection, pathogens can adhere to complement receptors and various extracellular matrix proteins in the oral and vaginal cavity. Oral and vaginal <i>Candidiasis</i> results from the overgrowth of <i>Candida</i> sp. in the hosts, causing penetration of the oral and vaginal tissues. Symptoms include white patches in the mouth, tongue, throat, and itchiness or burning of genitalia. Diagnosis involves visual examination, microscopic analysis, or culturing. These infections are treated with a variety of antifungals that target different biosynthetic pathways of the pathogen. For example, echinochandins target cell wall biosynthesis, while allylamines, azoles, and morpholines target ergosterol biosynthesis, and 5-Flucytosine (5FC) targets nucleic acid biosynthesis. Azoles are commonly used in therapeutics, however, because of its fungistatic nature, <i>Candida</i> sp. evolve azole resistance. Besides azoles, <i>Candida</i> sp. also acquire resistance to polyenes, echinochandins, and 5FC. This review discusses, in detail, the drug resistance mechanisms adapted by <i>Candida</i> sp. 
546 |a EN 
690 |a candidiasis 
690 |a antifungal resistance 
690 |a azole resistance 
690 |a efflux pump 
690 |a ergosterol biosynthesis 
690 |a echinochandin resistance 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
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786 0 |n Antibiotics, Vol 9, Iss 6, p 312 (2020) 
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787 0 |n https://doaj.org/toc/2079-6382 
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