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      Detection oftoxoplasma gondiiparasitemia by polymerase chain reaction in perorally infected mice

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      Parasite

      EDP Sciences

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          Abstract

          Sequential blood samples collected from mice infected perorally with an avirulent strain of T. gondii were analysed for parasite DNA by a polymerase chain reaction method (PCR). Two pairs of primers specific for gene B1 and the repetitive DNA sequence TGR1E were used for DNA amplification. Amplified products were detected by means of electrophoresis with ethidium bromide staining. Parasitemia was also determined by cell culture. Parasitemia was never detected by the tissue culture method, whereas parasite DNA was continuously detected with PCR from day 2 to day 21. These results confirm the high sensitivity of PCR for T. gondii DNA in blood, and show that circulating DNA is present for long periods in mice following primary infection.

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          Author and article information

          Journal
          Parasite
          Parasite
          EDP Sciences
          1252-607X
          1776-1042
          June 1995
          September 2014
          : 2
          : 2
          : 181-184
          Article
          10.1051/parasite/1995022181
          7582378
          © 1995

          This work is licensed under a Creative Commons Attribution 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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          Self URI (journal page): http://www.parasite-journal.org/

          Parasitology, Life sciences

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