The BK polyomavirus (BKV) is widespread in the general population. In transplant recipients, the patients' weakened immune response may encourage reactivation of latent infection, leading to BKV-related diseases. Rapid and quantitative detection might help to delineate viral reactivation patterns and could thus play an important role in their clinical management. In our study we developed an "in-house" quantitative real-time PCR to detect BKV DNA. The effectiveness of this assay was evaluated by a retrospective analysis of 118 plasma specimens from 22 bone marrow transplant (BMT) recipients and 107 samples from immunocompetent subjects. Eight (36.3%) of the 22 bone marrow transplant recipients tested positive for BKV. The viral load varied from specimen to specimen (10 to 10(5) copies/ml). BKV related disease like hemorrhagic cystitis (HC) was diagnosed in three patients. Specimens from the control group all tested negative. Our results showed the high sensitivity of the real-time PCR, allowing accurate and reproducible measuring of the viral load in order to identify patients at risk for BKV-related diseases. With due caution in interpreting threshold values, the real-time PCR could provide a rapid, sensitive and specific tool for detecting BKV and distinguishing latent and active infection.

Marchetti, S., Graffeo, R., Siddu, A., Santangelo, R., Ciotti, M., Picardi, A., Favalli, C., Fadda, G., Cattani, P., BK virus DNA detection by real-time polymerase chain reaction in clinical specimens., <<NEW MICROBIOLOGICA>>, 2007; 30 (2): 119-126 [http://hdl.handle.net/10807/15065]

BK virus DNA detection by real-time polymerase chain reaction in clinical specimens.

Marchetti, Simona;Graffeo, Rosalia;Siddu, Alessia;Santangelo, Rosaria;Fadda, Giovanni;Cattani, Paola
2007

Abstract

The BK polyomavirus (BKV) is widespread in the general population. In transplant recipients, the patients' weakened immune response may encourage reactivation of latent infection, leading to BKV-related diseases. Rapid and quantitative detection might help to delineate viral reactivation patterns and could thus play an important role in their clinical management. In our study we developed an "in-house" quantitative real-time PCR to detect BKV DNA. The effectiveness of this assay was evaluated by a retrospective analysis of 118 plasma specimens from 22 bone marrow transplant (BMT) recipients and 107 samples from immunocompetent subjects. Eight (36.3%) of the 22 bone marrow transplant recipients tested positive for BKV. The viral load varied from specimen to specimen (10 to 10(5) copies/ml). BKV related disease like hemorrhagic cystitis (HC) was diagnosed in three patients. Specimens from the control group all tested negative. Our results showed the high sensitivity of the real-time PCR, allowing accurate and reproducible measuring of the viral load in order to identify patients at risk for BKV-related diseases. With due caution in interpreting threshold values, the real-time PCR could provide a rapid, sensitive and specific tool for detecting BKV and distinguishing latent and active infection.
Inglese
Marchetti, S., Graffeo, R., Siddu, A., Santangelo, R., Ciotti, M., Picardi, A., Favalli, C., Fadda, G., Cattani, P., BK virus DNA detection by real-time polymerase chain reaction in clinical specimens., <<NEW MICROBIOLOGICA>>, 2007; 30 (2): 119-126 [http://hdl.handle.net/10807/15065]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/15065
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