A method for the detection and quantification of Candida albicans in biological samples (blood, urine and serum) was developed with the use of Real-Time PCR utilizing CaMP65-specific primers. Two different systems were used for the detection in the LightCycler platform (Roche): the SYBR green fluorescent dye with melting peak analysis and the 5′nuclease fluorescent-probe detection. The amplification was highly specific for C. albicans, providing no cross-reaction on genomic DNA extracted from other Candida species or Aspergillus. The sensitivity in simulated biological samples was especially high (1 genome) when applied to sera and urine, and in blood samples the limit of detection was higher by ten-fold. Finally, the real-time PCR was employed in order to detect and quantify C. albicans in the sera from patients with invasive candidiasis. © 2006 Elsevier Ltd. All rights reserved.
Use of 65 kDa mannoprotein gene primers in Real Time PCR identification of Candida albicans in biological samples / Arancia, S; Carattoli, A; LA VALLE, Roberto; Cassone, PIETRO ANGELO; De Bernardis, F.. - In: MOLECULAR AND CELLULAR PROBES. - ISSN 0890-8508. - 20:5(2006), pp. 263-268. [10.1016/j.mcp.2006.01.006]
Use of 65 kDa mannoprotein gene primers in Real Time PCR identification of Candida albicans in biological samples
Carattoli A;LA VALLE, ROBERTO;CASSONE, PIETRO ANGELO;De Bernardis F.
2006
Abstract
A method for the detection and quantification of Candida albicans in biological samples (blood, urine and serum) was developed with the use of Real-Time PCR utilizing CaMP65-specific primers. Two different systems were used for the detection in the LightCycler platform (Roche): the SYBR green fluorescent dye with melting peak analysis and the 5′nuclease fluorescent-probe detection. The amplification was highly specific for C. albicans, providing no cross-reaction on genomic DNA extracted from other Candida species or Aspergillus. The sensitivity in simulated biological samples was especially high (1 genome) when applied to sera and urine, and in blood samples the limit of detection was higher by ten-fold. Finally, the real-time PCR was employed in order to detect and quantify C. albicans in the sera from patients with invasive candidiasis. © 2006 Elsevier Ltd. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
