Pools were click here screened for F. tularensis tularensis with a nested PCR reaction targeting the fopA gene as described previously. [14] These primers were chosen for their proven sensitivity and specificity for F. tularensis tularensis, as virtually all D. variabilis on Martha’s Vineyard have been shown to be infected with Francisella endosymbionts. [20] Negative controls were included with every PCR. Ticks from PCR-positive pools were reprocessed individually.
A drop of hemolymph was placed in a tube with 25 ul PBS, boiled and then PXD101 purchase amplified by PCR. PCR was not conducted on individual ticks in years in which the prevalence of PCR positive pools was 1% or less. It was deemed unlikely that multiple ticks within a pool would yield positive results. Therefore,
the estimates and confidence intervals for the prevalence in low years Torin 2 nmr are maximum likelihood estimates calculated using the Pooled Infection Rate V2.0 Excel Add-In http://www.cdc.gov/ncidod/dvbid/westnile/software.htm. Prevalence estimates and confidence intervals from individual tick data were calculated using the web-based calculators at Statpages.net http://statpages.org/confint.html. Test for trend was done using PEPI v4.0. Multiple loci variable number tandem repeat analysis (MLVA) Amplification of VNTR loci was done directly from the hemolymph lysates as described previously [14, 15]. Briefly, PCR was done using a high fidelity Taq polymerase (Picomaxx, Stratagene) and a fluorescently Methane monooxygenase labeled primer (either FAM or HEX). The size of the amplicons was then determined using a capillary sequencer (University of Maine Sequencing Facility, Orono, ME) using GeneMapper software (Applied Biosystems). Each sample contained a DNA ladder for accurate size determination, ABI500 (Applied
Biosystems) or MapMarker1000 (BioVentures, Inc.) depending on the expected size of the fragment. These VNTR loci were shown previously not to amplify the Francisella-like endosymbionts found in our ticks [12] by specifically using them to test whole tick extracts that were determined to be negative for F. tularensis by PCR targeting the fopA gene. Samples with known sizes, such as those derived from the well characterized Live Vaccine Strain (LVS, F. tularensis holarctica) or Schu S4 (F. tularensis tularensis), were included to assess the consistency from run to run. Peak data were analyzed manually using STRand (Veterinary Genetics Lab, University of California) or Peak Scanner Software v1.0 (Applied Biosystems). Our previous work demonstrated that locus Ft-M3 (previously called SSTR9) and Ft-M10 (previously SSTR16) are diverse and informative at our field site [14]. These 2 loci were therefore amplified from all samples. Since that work was done, 25 VNTR loci have been developed for the characterization of Francisella isolates from a global scale [21].