Measurement of Proteinase Enzyme Produced in Candida Species Isolated from Oral Candidiasis in Cancer Patients Receiving Chemotherapy at the Hospitals of Tonekabon and Ramsar, Iran

Document Type : Original article

Authors

1 M.Sc. Islamic Azad University of Tonekabon Branch, Tonekabon, Iran.

2 PhD, Department of Medical Mycology, Faculty of Medical Sciences, Islamic Azad University of Tonekabon Branch, Tonekabon, Iran

3 MD, Department of Oncology and Adult Cancer, Faculty of Medical Sciences, Islamic Azad University of Tonekabon Branch, Tonekabon, Iran

Abstract

Abstract
Introduction:
Candidiasis is a common fungal infection caused by various Candida species. Theproduction of extracellular enzymes, like proteinase, as a pathogenic factor plays a significant role inyeast adherence andpenetration to the host. Regarding this, the present study was conducted toevaluate the production of proteinase enzyme in cancer patients with oral candidiasis.
Materials and Methods: A total of 20 oral swab specimens were collected from cancerous and noncancerous patients with oral candidiasis referring to the Oncology Center of Ramsar and Tonekabonhospitals, Iran, in 2014-2015. The samples obtained from the cancerous and non-cancerous patientswere assigned into the case and control groups, respectively. These specimens were cultured inSabouraud dextrose agar containing chloramphenicol. The yeast isolates were identified by means ofphenotypic method. The evaluation of proteinase enzyme activity was accomplished on a specificmedium. The diameter of the halo formed around each colony was also measured to determine therate of enzyme production.
Results: Out of the 20 samples, 19 (95%) and 6 (30%) Candida species were isolated from the caseand controlgroups, respectively. Candida albicans and Candida glabrata had the prevalence of 16(84%) and 3 (16%), respectively. In the control group, all isolated yeasts were identified as Candidaalbicans. The mean diameter of the halo around the yeast cells producing proteinase enzyme incancer patients with oral candidiasis was 2.21 mm in comparison to the non-cancerous group.
Conclusion: Proteinase enzyme production as an important virulence factor leading to oralcandidiasis was significantly higher in the cancer patients than that in the non -cancer ones

Keywords


1.         Akpan A, Morgan R. Oral candidiasis. Postgraduate medical journal. 2002;78(922):455-9.
2.         Meurman J, Siikala E, Richardson M, Rautemaa R. Non-Candida albicans Candida yeasts of the oral cavity. Communicating current research and educational topics and trends in applied microbiology. 2007;1(1):719-31.
3.         Al-Abeid HM, Abu-Elteen KH, Elkarmi AZ, Hamad MA. Isolation and characterization of Candida spp. in Jordanian cancer patients: prevalence, pathogenic determinants, and antifungal sensitivity. Jpn J Infect Dis. 2004;57(6):279-84.
4.         Calamari S-E, Bojanich M-A, Barembaum S-R, Berdicevski N, Azcurra A-I. Antifungal and post-antifungal effects of chlorhexidine, fluconazole, chitosan and its combinations on Candida albicans. Med Oral Patol Oral Cir Bucal. 2011;16(1):E23-E8.
5.         Sun J, Qi C, Lafleur MD, Qi Q-g. Fluconazole susceptibility and genotypic heterogeneity of oral Candida albicans colonies from the patients with cancer receiving chemotherapy in China. International journal of oral science. 2009;1(3):156.
6.         Widmer F, Wright LC, Obando D, Handke R, Ganendren R, Ellis DH, et al. Hexadecylphosphocholine (miltefosine) has broad-spectrum fungicidal activity and is efficacious in a mouse model of cryptococcosis. Antimicrobial agents and chemotherapy. 2006;50(2):414-21.
7.         Cronin UP, Wilkinson MG. Monitoring growth phase-related changes in phosphatidylcholine-specific phospholipase C production, adhesion properties and physiology of Bacillus cereus vegetative cells. Journal of industrial microbiology & biotechnology. 2008;35(12):1695-703.
8.         Mandujano-González V, Villa-Tanaca L, Anducho-Reyes MA, Mercado-Flores Y. Secreted fungal aspartic proteases: A review. Revista Iberoamericana de Micología. 2016 33(2):76-82.
9.         Parra-Ortega B, Hernández-Rodríguez C, Villa-Tanaca L. Evolution of GPI-Aspartyl Proteinases (Yapsines) of Candida spp: INTECH Open Access Publisher; 2011, 257pp.
10.       Richardson MD, Warnock DW. Fungal infection: diagnosis and management: John Wiley & Sons; 2012, 476 pp.
11.       Galan-Ladero M, Blanco M, Sacristán B, Fernández-Calderón M, Pérez-Giraldo C, Gomez-Garcia A. Enzymatic activities of Candida tropicalis isolated from hospitalized patients. Medical mycology. 2010;48(1):207-10.
12.       Bhat V, Sharma S, Shetty V, Shastry C, Rao V. Extracellular enzymes of Candida albicans and their role in development of denture stomatitis-a review. JIADS. 2011;2(1):26-30.
13.       de Cássia Mardegan R, Foglio MA, Gonçalves RB, Höfling JF. Candida albicans proteinases. Brazilian Journal of Oral Sciences. 2015;5(16):944-52.
14.       Cutler JE. Putative virulence factors of Candida albicans. Annual Reviews in Microbiology. 1991;45(1):187-218.
15.       Sachin C, Ruchi K, Santosh S. In vitro evaluation of proteinase, phospholipase and haemolysin activities of Candida species isolated from clinical specimens. International journal of Medicine and Biomedical research. 2012;1(2):153-7.
16.       Oliveira SKR, Anjos DCVd, Gonçalves LHB, Ferro TAF, Monteiro SG, Figueiredo PdMS, et al. Prevalence and production of enzymes by Candida isolates from vaginal secretion samples. Rev Patol Trop. 2013;42:161-76.
17.       Deepa K, Jeevitha T, Michael A. In vitro evaluation of virulence factors of Candida species isolated from oral cavity. Journal of Microbiology and Antimicrobials. 2015;7(3):28-32.
18.       Sacristán B, Blanco M, Galan-Ladero M, Blanco J, Perez-Giraldo C, Gómez-García A. Aspartyl proteinase, phospholipase, hemolytic activities and biofilm production of Candida albicans isolated from bronchial aspirates of ICU patients. Medical mycology. 2011;49(1):94-7.
19.       Kantarcioǧlu AS, Yücel A. Phospholipase and protease activities in clinical Candida isolates with reference to the sources of strains. Mycoses. 2002;45(56):160-5.
20.       Tsang C, Chu F, Leung W, Jin L, Samaranayake L, Siu S. Phospholipase, proteinase and haemolytic activities of Candida albicans isolated from oral cavities of patients with type 2 diabetes mellitus. Journal of medical microbiology. 2007;56(10):1393-8.