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Journal of Clinical Microbiology, November 2001, p. 4145-4148, Vol. 39, No. 11
Division of Vector-Borne Infectious Diseases,
National Center for Infectious Diseases, Centers for Disease
Control and Prevention, U.S. Public Health Service, Fort Collins,
Colorado 80522
Received 2 April 2001/Returned for modification 29 July
2001/Accepted 20 August 2001
Quantitative real-time PCR was used to assay spirochetes
in feeding ticks. Spirochetes in tick midguts increased sixfold, from
998 per tick before attachment to 5,884 at 48 h of attachment. Spirochetes in tick salivary glands increased >17-fold, from 1.2 per
salivary gland pair before feeding to 20.8 at 72 h postattachment. The period of the most rapid increase in the number of spirochetes in
the salivary glands occurred from 48 to 60 h postattachment; this
time period coincides with the maximal increase in transmission risk
during nymphal tick feeding.
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.11.4145-4148.2001
Use of Quantitative PCR To Measure Density of
Borrelia burgdorferi in the Midgut and
Salivary Glands of Feeding Tick Vectors
*
Corresponding author. Mailing address: CDC/DVBID, P.O.
Box 2087, Fort Collins, CO 80522. Phone: (970) 221-6408. Fax: (970) 221-6476. E-mail: JPiesman{at}cdc.gov.
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