A portion of
the XT midgut contents were also placed in culture.
Standard PCR and RT - PCR for ospA, ospC and flaB were also performed with either SCID mouse tissues or
XT midguts using primers described elsewhere [35].
Not exact matches
Given that our wild type B. burgdorferi acquired by xenodiagnostic ticks retain the ability to express ospC (also shown by RT - PCR in Fig 4), we can not rule out the possibility that a tick
midgut - adapted phenotype, in the absence of salivation and feeding, contributed to the failure of the B. burgdorferi acquired from
XT to infect SCID mice.
Panel A = positive control for IFA using B. burgdorferi culture; Panel B =
XT from animal IH11 (treated); Panel C =
XT from animal IK14 (treated); Panel D =
XT from animal IL09 (treated); Panel E = positive control for DFA using
midgut smear of tick that was capillary tube - fed B. burgdorferi; Panel F =
XT from animal IP55 (untreated); Panel G =
XT culture pellet from animal IP55 (untreated); Panel H =
XT culture pellet from animal IK14 (treated).
In addition to staining the
midgut contents with FITC - labeled polyclonal anti-Borrelia species antibody, we washed and re-stained this set and stained the second set of xenodiagnostic tick (
XT) samples with an anti-OspA monoclonal antibody (CB10, obtained from J. Benach [41]-RRB-, followed by anti-mouse IgG - Alexa 488 (Molecular Probes).