Multiplex size marker (YEAST PLEX) for rapid and accurate identification of pathogenic yeasts

被引:10
作者
Aboutalebian, Shima [1 ,2 ]
Mahmoudi, Shahram [3 ]
Charsizadeh, Arezoo [4 ]
Nikmanesh, Bahram [5 ]
Hosseini, Mahnaz [2 ]
Mirhendi, Hossein [1 ,2 ]
机构
[1] Isfahan Univ Med Sci, Sch Med, Dept Med Parasitol & Mycol, Esfahan, Iran
[2] Isfahan Univ Med Sci, Mycol Reference Lab, Res Core Facil Lab, Esfahan, Iran
[3] Iran Univ Med Sci, Sch Med, Dept Parasitol & Mycol, Tehran, Iran
[4] Univ Tehran Med Sci, Immunol Asthma & Allergy Res Inst, Tehran, Iran
[5] Univ Tehran Med Sci, Sch Allied Med Sci, Dept Med Lab Sci, Tehran, Iran
关键词
Candida; identification; multiplex PCR; yeasts; INTERNAL TRANSCRIBED SPACER; SEQUENCE-ANALYSIS; CANDIDA-ALBICANS; BLOOD; REGION; INFECTIONS; GENE;
D O I
10.1002/jcla.24370
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background Multiple yeast species can cause human disease, involving superficial to deep-seated infections. Treatment of these infections depends on the accurate identification of causative agents; however, reliable methods are not available in many laboratories, especially not in resource-limited settings. Here, a new multiplex assay for rapid and low-cost identification of pathogenic yeasts is described. Methods A two-step multiplex assay named YEAST PLEX that comprises of four tubes and identifies 17 clinically important common to rare yeasts was designed and evaluated. The set also provides PCR amplicon of unidentified species for direct sequencing. The specificity of YEAST PLEX was tested using 28 reference strains belonging to 17 species and 101 DNA samples of clinically important non-target bacteria, parasites, and fungi as well as human genomic DNA. The method was further analyzed using 203 previously identified and 89 unknown clinical yeast isolates. Moreover, the method was tested for its ability to identify mixed yeast colonies by using 18 mixed suspensions of two or three species. Results YEAST PLEX was able to identify all the target species without any non-specific PCR products. When compared to PCR-sequencing/MALDI-TOF, the results of YEAST PLEX were in 100% agreement. Regarding the 89 unknown clinical isolates, random isolates were selected and subjected to PCR-sequencing. The results of sequencing were in agreement with those of YEAST PLEX. Furthermore, this method was able to correctly identify all yeasts in mixed suspensions. Conclusion YEAST PLEX is an accurate, low-cost, and rapid method for identification of yeasts, with applicability, especially in developing countries.
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页数:9
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