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. Author manuscript; available in PMC: 2018 Apr 11.
Published in final edited form as: J Med Entomol. 2012 Nov;49(6):1485–1494. doi: 10.1603/me11291

Table 2.

Detection of R. typhi and R. felis DNA in flea DNA samples

Location, flea species No. of flea pools tested (total fleas) No. of positive pools (%) Minimum infection rate (%)a


R. typhi R. felis Dual positive R. typhi R. felis
Orange County
Ctenocephalides felis 727 (1405) 7 (0.9) 428 (58.9) 22 (3.0) 2.1 32
Pulex irritans 55 (109) 4 (7.3) 9 (16.4) 0 3.7 8.3
Echidnophaga gallinacea 2 (2) 0 0 0 0 0
Diamanus montanus 3 (4) 0 2 (66.7) 0 0 50
Leptosylla segnis 1 (1) 0 0 0 0 0
Los Angeles County
Ctenocephalides felis 1,146 (2144) 18 (1.6) 454 (39.6) 10 (0.9) 1.3 21.6
Pulex irritans 3 (3) 0 1 (33.3) 0 0 33.3
Xenopsylla cheopis 4 (5) 0 2 (50.0) 0 0 40
Echidnophaga gallinacea 9 (17) 0 4 (44.4) 1 (11.1) 5.9 29.4
a

Minimum infection rate: no. of PCR positive flea pools/total no. of fleas tested. Assumes that each PCR positive pool contains DNA of at least one flea infected with either R. typhi or R. felis, respectively.