Medico-legal Update, January-March 2021, Vol. 21, No. 1 703 Antibiofilm Activity of Nystatin, Aspirin and EDTA Against Candida albicans Isolated from Iraqi Women with Vulvovaginitis Noor Naser Raheem1, Kais Kassim Ghaima2* 1Research Scholar, M Sc Student, Kamal Al-Samarrai Hospital, Ministry of Health, Baghdad, Iraq, 2Assistant Professor, Institute of Genetic Engineering and Biotechnology for Postgraduate Studies, University of Baghdad, Baghdad, Iraq Abstract The vulvovaginitis candidiasis is often associated with biofilm formation byCandida albicans and using of antifungal agents against C. albicans biofilms is urgently needed. Microtiter plate assay using crystal violet was used for detection the ability of Candida albicans to form biofilm and the microtiter broth dilution method was used for determination the minimum inhibitory concentrations (MICs). Out of 42 Candida albicans isolated from vulvovaginitis, 37 (88%) can produce biofilm at the varying degrees. Twenty-eight (75.7%) isolates could form a strong biofilm. The results of minimum inhibitory concentrations (MICs) of Nystatin, Aspirin and EDTA (Ethylenediaminetetraacetic acid) against 28 C. albicans isolates which formed the strong biofilm, revealed that range of concentrations of Nystatin were (6.25-100 µg/ml), while the MICs of aspirin and EDTA were more than 1000 µg/ml. It was obvious that the Nystatin had the inhibitory activity at the concentrations 6.25 and 12.5 µg/ml. The highest antibiofilm activity by Nystatin were demonstrated at the subinhibitory concentration 50 μg/ml with biofilm eradication percent (75.80%), while the lowest antifungal effect (2.86-10.70%) was at very low concentrations (3.125-6.25 μg/ml). Also, there was an obvious biofilm eradication of Aspirin and EDTA at the concentrations 500 and 1000 μg/ml but the effect of aspirin at the concentration 1000 μg/ml (70.51%) is more than EDTA (60.12%) in contrast with the concentration 500 μg/ml, it was found that the effect of EDTA (51.29%) is more than aspirin (34.25%). In conclusion, the present study highlights the role of Aspirin and EDTA as antibiofilm agents when used with Nystatin which have the ability to inhibit the growth of C. albicans in patients with vulvovaginitis. Keywords: Nystatin, Aspirin, EDTA, C. albicans, Biofilm, Vulvovaginitis. Introduction dimorphism and the ability to adhere and form biofilm on medical device and/or the host mucosal epithelium, Vulvovaginal candidiasis (VVC) is considered enhance the pathogenicity of C. albicans(2). Vulvovaginal as the main infection caused by Candida albicans. candidiasis defined as a disorder characterized by Numerous virulence determinants and escalating signs and symptoms of vaginal inflammation when the resistance to antifungal therapy have contributed to Candida species are found and is an ever living problem its pathogenicity(1). Some virulence factors such as affecting 70–75% of women of reproductive age at least once during their life(3). The evolution of drug resistance of Candida species to conventional antifungal agents Corresponding Author: has been a major medical challenge worldwide; attempt Kais Kassim Ghaima to use the potential antifungal agents with appropriate Assistant Professor, Institute of Genetic Engineering therapy efficacy and minimum effects is considerably and Biotechnology for Postgraduate Studies, growing(4). The mechanism underlying development University of Baghdad, Baghdad, Iraq of antifungal resistance of C. albicans are complex e-mail: [email protected] and involve multiple pathways and genes. Further, 704 Medico-legal Update, January-March 2021, Vol. 21, No. 1 these mechanisms continue to change and evolve and μg/ml). Wells without Nystatin, Aspirin and EDTA challenging the medical clinic (5). The widespread use of were used as a positive control while those without antibiotics, frequent use of indwelling medical devices, Candida were considered as negative controls. After and a trend towards increased patient immunosuppression 24 hours incubation at 37°C, the wells were visually has resulted in a creation of opportunity for clinically inspected for the growth. The MIC was considered as important Candida to form biofilms and there is growing the lowest concentration of Nystatin, Aspirin and EDTA evidence of the importance of Candida biofilms in that inhibits the Yeast growth(8). clinical problems (6). Therefore the aim of this study is investigate the biofilm formation of C. albicans isolates Antibiofilm activity of Nystatin, Aspirin and as the causative agent of vulvovaginitis in Iraqi women, EDTA: This test was performed on four strains that also using of some compounds such as Aspirin and showed strong biofilm formation ability in the biofilm EDTA as antifungal agents against the high antifungal production assay. The effect of different concentrations resistant isolates. of Nystatin (3.125-100 μg/ml), while Aspirin and EDTA (31.25-1000 μg/ml) to inhibit the ability of C. albicans Materials and Method cells to form a biofilm was assessed using the TCP method adopted by Khodavandi et al. (2011) (9). Nearly, Candida albicans isolates: In this study, a total 100 μl of 0.5 McFarland yeast cultures was dispensed of 42 C. albicans clinical strains were collected from into each well of 96-well polystyrene microtiter plates in women patients with vulvovaginitis from three hospitals the presence of 100 μl of the antibiofilm agent at different in Baghdad, Iraq, during the period from September to concentrations, and plates were incubated at 37°C for 48 December 2019. All strains were previously identified hours. Antimicrobial agent free wells served as positive by API Candida system (bioMérieux, France) and controls for the biofilm growth. After incubation, the confirmed using VITEK 2 compact system (bioMérieux, medium and non-adherent cells were removed and wells France). were washed three times with sterile PBS. The plates were air dried and then the dye was resolubilized with Quantitative biofilm production assay: The Colonies from all isolates of fresh C. albicans cultures absolute ethanol. The OD of each well was measured (48 hours) were grown at 37°C in Sabouraud dextrose at 570 nm using ELISA reader (BioTek, Korea). Each broth medium for 24 hours. Biofilm formation was tested assay was performed in triplicates. by adding 100 μl of this standardized cell suspension Statistical Analysis: The Statistical Analysis to wells of microtiter plates that contained 100 μl of System- SAS (2012) (10) program was used to detect fresh Sabouraud dextrose broth media and incubating the effect of difference factors in study percentage. Chi- them at 37°C for 48 hours. Thereafter, the medium was square test was used to significant compare between removed and planktonic cells were removed by washing percentage (0.05 and 0.01 probability). Least significant the biofilms in phosphate buffered saline. After staining difference LSD test (Analysis of Variation-ANOVA) plates with 2% crystal violet for 20 m, excess stain was was used to significant compare between means in this removed using water. The plates were air dried and study. then the dye was resolubilized with absolute ethanol. The optical density (OD) of each well was measured at Results and Discussion 570 nm using Enzyme-Linked Immunosorbent Assay (ELISA) reader (BioTek, Korea). Optical density cut-off Biofilm formation: Out of 42 Candida albicans value (ODc) was calculated using the equation: average isolates, 37 (88%) can produce biofilm at the varying OD of negative control + (3*SD of negative control) (7). degrees. Twenty-eight (75.7%) isolates could form a strong biofilm, while 6 isolates were the moderate Minimum inhibitory concentration of Nystatin, producer, and only 3 isolates were weak biofilm formers. Aspirin and EDTA: Nearly, 100 μl (0.5 McFarland) of Also it was found that five isolates don’t have the ability the C. albicans culture was inoculated into each well of to formation the biofilm (table 1). Microtiter plate assay a 96-well microtiter plate containing 100 μl Nystatin, using crystal violet was used for detection the ability of Aspirin and EDTA at different concentrations (0.39–200 Candida albicans to form biofilm (figure 1). Medico-legal Update, January-March 2021, Vol. 21, No. 1 705 Table 1. Distribution of biofilm formation ability among Candida albicans isolates. Biofilm formation Candida albicans Weak Moderate Strong Negative Total no of Isolate = 42 3 6 28 5 % 7.14% 14.29% 66.67% 11.90% 2 Chi-Square (χ ­­­­­) 12.073 ** ** (P≤0.01). Figure 1. Biofilm formation detection ofCandida albicans isolates by microtiter plate assay. This study revealed that the most of Candida biofilm formers were 12/22 (54.5%). In a previous albicans isolated from Iraqi women patients with study, it was found the Candida biofilms have important vulvovaginitis formed a strong biofilm. Many studies clinical implications since the biofilm associated with demonstrated the ability of Candida albicans clinical Candida or Gardnerella genital infections may act as a isolates to form heterogeneous biofilms. The presence of chlamydial reservoir contributing to the transmission of these communities in vulvovaginitis may explain why C. Chlamydia trachomatis in the population, alongside its albicans infections remain unresponsive to therapy, and dissemination in the female upper genital tract (15). The there was a relationship between biofilm formation and biofilm formation is very important virulence factor in antifungal resistance among Candida isolates (11, 12). The C. albicans, where this species expresses hyphal-specific study of Shreif et al. (2019) (13) in Egypt which included adhesins and regulators required for adhesion. Also, one hundred Candida albicans isolates from patients the morphological dimorphism in Candida albicans with nosocomial infections revealed that the biofilm supports noticeable phagocyte escape mechanism (16). capacity was identified by the microplate method in 58% of C. albicans and the optical density was intense The present study investigated the role of some in 20 isolates, moderate in 21 isolates and mild in 17 compounds as antibiofilm agents against the biofilm isolates. The local study of Mohammed et al. (2017) (14) formation in C.