Quantitative competitive PCR as a technique for exploring flea - Yersina pestis dynamics

We used a quantitative competitive polymerase chain reaction assay to quant ify Yersinia pestis loads in fleas and bacteremia levels in mice that were used as sources of infectious blood meals for feeding the fleas. Xenopsylla cheopis, the Oriental rat flea, achieved higher infection rates, developed greater bacterial loads, and became infectious more rapidly than Oropsylla montana, a ground squirrel flea. Both flea species required about 10(6) Y. pestis cells per flea to be able to transmit to mice. Most fleas that achi eved these levels, however, were incapable of transmitting. Our results sug gest that at the time of flea feeding, host blood must contain greater than or equal to 10(6) bacteria/ml to result in detectable Y. pestis infections in these fleas, and greater than or equal to 10(7) bacteria/mL to cause in fection levels sufficient for both species to eventually become capable of transmitting Y. pestis to uninfected mice. Yersinia pestis colonies primari ly developed in the midguts of O. montana, whereas infections in X. cheopis often developed simultaneously in the proventriculus and the midgut. These findings were visually confirmed by infecting fleas with a strain of Y. pe stis that had been transformed with the green fluorescent protein gene.