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Infect Immun, August 1998, p. 3783-3787, Vol. 66, No. 8
Division of Parasitology,
Received 3 March 1998/Returned for modification 24 April
1998/Accepted 11 May 1998
Detection and analysis of pathogens by PCR plays an important role
in infectious disease research. The value of these studies would be
diminished if nuclear material from dead parasites were found to remain
in circulation for extended periods and thus result in positive
amplification. This possibility was tested in experimental rodent
malaria infections. Blood samples were obtained from infected mice
during and following drug or immune clearance of Plasmodium chabaudi chabaudi parasitemias. Detection of parasite DNA by a sensitive Plasmodium-specific PCR amplification assay was
associated with the presence of viable parasites, as detected by
subinoculation. No parasite DNA could be detected by PCR 48 h
after the injection of killed parasites into mice. Nuclear material
from parasites removed by drug or immune responses is rapidly cleared
from the circulation and does not contribute significantly to
amplification. Thus, results from PCR analysis of malaria-infected
blood accurately reflect the presence of live parasites.
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Only Viable Parasites Are Detected by PCR following
Clearance of Rodent Malarial Infections by Drug Treatment or
Immune Responses
*
Corresponding author. Mailing address: Department of
Infection and Tropical Medicine, Imperial College School of Medicine, Lister Unit, Northwick Park Hospital, Harrow, Middlesex HA1 3UJ, United
Kingdom. Phone: (44) (181) 869 3507. Fax: (44) (181) 869 3504. E-mail: g.snounou{at}ic.ac.uk.
Infect Immun, August 1998, p. 3783-3787, Vol. 66, No. 8
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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