Parvovirus B19 infection is associated with anemia and spontaneous abortion
s. While many qualitative assays are available, a few molecular-based quant
itative methods have been described. This study reports the development and
optimization of a quantitative direct-probe method for the detection of Pa
rvovirus B19 DNA. Different concentrations of RNA probes were used to ident
ify the optimal conditions for hybridizing to the target DNA. Detection of
DNA was linear between concentrations of 2 ng/ml to 200 pg/ml. Because this
method requires no enzymatic amplification, it is not susceptible to ampli
fier contamination or enzymatic inhibitors, and it can be applied to serum
samples or paraffin-embedded tissue. (C) 2000 Wiley-Liss, Inc.