The effect of hygromycin B quality towards candida albicans susceptibility

Candida albicans is a medically important opportunistic pathogen that can be found in oral cavity. It is greatly associates in mono- and polymicrobial biofilms development with other oral microorganisms. However, aberrant ploidy number and unusual codon usage in C. albicans complicate its genetic ed...

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Bibliographic Details
Main Authors: Engku Nasrullah Satiman, Engku Anis Fariha, Kaderi, Mohd Arifin, Ramzi, Ahmad Bazli, Arzmi, Mohd Hafiz
Format: Conference or Workshop Item
Language:English
Published: 2021
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Online Access:http://irep.iium.edu.my/93970/1/93970_complete.pdf
http://irep.iium.edu.my/93970/
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Institution: Universiti Islam Antarabangsa Malaysia
Language: English
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Summary:Candida albicans is a medically important opportunistic pathogen that can be found in oral cavity. It is greatly associates in mono- and polymicrobial biofilms development with other oral microorganisms. However, aberrant ploidy number and unusual codon usage in C. albicans complicate its genetic editing process. Hygromycin B is an antifungal that is useful for a selective marker in C. albicans genetic transformation. Specialised codon-optimized hygromycin resistance gene (CaHygB) derived from plasmid pYM70 enables C. albicans transformants to grow on a selective plate containing hygromycin B. The objective of the study is to determine the effect of hygromycin B quality in the detection of C. albicans gene transformation with the hypothesis that the performance of two different qualities is similar during the selection of C. albicans transformants on YPD-hygromycin B agar plate. C. albicans ATCC MYA-4901 was revived and grown on YPD agar for 48 hours at 37°C. Meanwhile, glycerol stock of E. coli carrying pYM70 was revived on LB-ampicillin agar at 37°C for overnight. Plasmid pYM70 was later extracted and used in the subsequent transformation of C. albicans. The competent cell of C. albicans was prepared using the modified lithium-acetate method. Plasmid pYM70 was transformed into the competent cells of C. albicans using the electroporation method. The transformed cells were sub-cultured on YPD agar containing 600 μg/ml hygromycin B from two brands. The growth of transformants was observed after three to four days of incubation at 37°C in a dark environment. Our study showed a successful transformation of C. albicans with pYM70, which exhibited resistance towards both hygromycin B (Gb and Bb). However, wild-type and empty competent cells (negative controls) exhibited resistance towards hygromycin B Bb. In conclusion, different qualities of hygromycin B affect the susceptibility of C. albicans which may lead to a false result during C. albicans transformation.