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Yas KhudhairAl-Ameri, A, Alrufae, M. M. (1401). Phenotypic and Genotypic Identification of Yeast Species Isolated from Diabetic Foot Patients in Al-Najaf Province, Iraq. سامانه مدیریت نشریات علمی, 77(2), 727-731. doi: 10.22092/ari.2022.357104.1975
A Yas KhudhairAl-Ameri; M. M Alrufae. "Phenotypic and Genotypic Identification of Yeast Species Isolated from Diabetic Foot Patients in Al-Najaf Province, Iraq". سامانه مدیریت نشریات علمی, 77, 2, 1401, 727-731. doi: 10.22092/ari.2022.357104.1975
Yas KhudhairAl-Ameri, A, Alrufae, M. M. (1401). 'Phenotypic and Genotypic Identification of Yeast Species Isolated from Diabetic Foot Patients in Al-Najaf Province, Iraq', سامانه مدیریت نشریات علمی, 77(2), pp. 727-731. doi: 10.22092/ari.2022.357104.1975
Yas KhudhairAl-Ameri, A, Alrufae, M. M. Phenotypic and Genotypic Identification of Yeast Species Isolated from Diabetic Foot Patients in Al-Najaf Province, Iraq. سامانه مدیریت نشریات علمی, 1401; 77(2): 727-731. doi: 10.22092/ari.2022.357104.1975

Phenotypic and Genotypic Identification of Yeast Species Isolated from Diabetic Foot Patients in Al-Najaf Province, Iraq

Archives of Razi Institute
مقاله 28، دوره 77، شماره 2، خرداد و تیر 2022، صفحه 727-731    اصل مقاله (529.79 K)
نوع مقاله: Original Articles
شناسه دیجیتال (DOI): 10.22092/ari.2022.357104.1975
نویسندگان
A Yas KhudhairAl-Ameri* 1؛ M. M Alrufae2
1Department of Medical Laboratory Techniques, Faculty of Medical Technologies, Islamic University of Najaf, Najaf, Iraq
2Faculty of Sciences, University of Kufa, Najaf, Iraq
چکیده
Opportunistic yeasts, such as Trichosporon and Candida species (spp.), are reported to cause high rates of morbidity and mortality in immunocompromised and underlying patients. This study was conducted to investigate the phenotypic and genotypic identification of yeast spp. isolated from diabetic patients in Al-Najaf province, Iraq. Samples were collected from the depth of diabetic foot patients’ wounds. They were then cultured on Sabouraud Dextrose Agar (SDA) and incubated at 30°C to 35°C for 5 to 7 days for the growth of yeast spp. The colonies were identified based on their microscopic features. Afterward, these yeast samples were cultured in CHROMagar for the isolation and identification of yeast spp. All collected samples were cultured on the SDA through the use of CHROMagar, which is considered a differential agar since the colonies obtained from Candida intermedia and Trichosporon asahii appear in different colors on this media. The Polymerase Chain Reaction assay was performed to amplify the internal transcribed spacer 1 (ITS1) and Internal transcribed spacer 4 (ITS4) sequences for the identification of the yeast spp. Furthermore, the products were sequenced by the Sanger method and compared to the reference global sequences in the national center for biotechnology information Gene Bank.  The results showed different molecular sizes of the ITS regions of yeast spp. The primer pair was used for the same sample (i.e., ITS1-ITS4) and targeted the ITS regions. Yeast spp. can be considered the most common fungal agent of life-threatening invasive infections in patients with severe immunodeficiency or underlying diseases, and the treatment of these infections requires long stays in the intensive care units.
کلیدواژه‌ها
Candida intermedia؛ Diabetic؛ ITS1-ITS4؛ Trichosporon asahii
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مراجع
  1. Carmona EM, Limper AH. Overview of treatment approaches for fungal infections. Clin Chest Med. 2017;38(3):393-402.
  2. Mohandas V, Ballal M. Distribution of Candida species in different clinical samples and their virulence: biofilm formation, proteinase and phospholipase production: a study on hospitalized patients in southern India. J Glob Infect Dis. 2011;3(1):4.
  3. Nerurkar A, Solanky P, Chavda N, Baria H, Desai B. Isolation of Candida Species in clinical specimens and its virulence factor: The biofilm. Int J Med Sci Public Health. 2012;1(2):97-100
  4. Melo N, Taguchi H, Jorge J, Pedro R, Almeida O, Fukushima K, et al. Oral Candida flora from Brazilian human immunodeficiency virus-infected patients in the highly active antiretroviral therapy era. Mem Inst Oswaldo Cruz. 2004;99(4):425-31.
  5. Chen T-C, Chen Y-H, Tsai J-J, Peng C-F, Lu P-L, Chang K, et al. Epidemiologic analysis and antifungal susceptibility of Candida blood isolates in southern Taiwan. J Microbiol Immunol Infect. 2005;38(3):200-10.
  6. Colombo AL, Padovan ACB, Chaves GM. Current knowledge of Trichosporon spp. and Trichosporonosis. Clin Microbiol Rev. 2011;24(4):682-700.
  1. Devi KM, Mate PH, Singh LN, Devi KR, Devi KS. Disseminated infection with Trichosporon asahii in an immunocompetent patient: a rare case report. J Med Soc. 2015;29(3):174.
  2. Go S-E, Lee K-J, Kim Y, Choi J-K, Kim Y-J, Lee D-G. Catheter-related Trichosporon asahii bloodstream infection in a neutropenic patient with myelodysplastic syndrome. Infect Chemother. 2018;50(2):138-43.
  3. Ebright JR, Fairfax MR, Vazquez JA. Trichosporon asahii, a non-Candida yeast that caused fatal septic shock in a patient without cancer or neutropenia. Clin Infect Dis. 2001;33(5):e28-e30.
  4. White TJ, Bruns T, Lee S, Taylor J. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR protocols: a guide to methods and application. p. 315-22
  5. El-Mashad N, Mahmoud MT, allah El-Shewehy H. Trichosporon identification methods for isolates obtained from different clinical specimens. Afr J Microbiol Res. 2011;5(9):1097-101.
  6. Agrawal V, Bhagwat A, Vishalakshi V, Gode V, Sawant C. Exploring the potential of chromogenic medium for the identification of medically important yeast species other than Candida. Int J Pharm Pharm Sci. 2014;6(3):291-4.
  7. Lu J-J, Lo H-J, Lee C-H, Chen M-J, Lin C-C, Chen Y-Z, et al. The use of MALDI-TOF mass spectrometry to analyze commensal oral yeasts in nursing home residents. Microorganisms. 2021;9(1):142.
  8. Iyampillai T, Michael J, Mathai E, Mathews M. Use of CHROMagar medium in the differentiation of Candida species: is it cost-effective in developing countries? Ann Trop Med Parasitol. 2004;98(3):279-82.
  9. Bellemain E, Carlsen T, Brochmann C, Coissac E, Taberlet P, Kauserud H. ITS as an environmental DNA barcode for fungi: an in silico approach reveals potential PCR biases. BMC Microbiol. 2010;10(1):1-9.
  10. Vu D, Groenewald M, Szoke S, Cardinali G, Eberhardt U, Stielow B, et al. DNA barcoding analysis of more than 9 000 yeast isolates contributes to quantitative thresholds for yeast species and genera delimitation. Stud Mycol. 2016;85:91-105.
 

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