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Results for “Siphonaptera”

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PubMed1989

Activity of insecticides against the preemerged adult cat flea in the cocoon (Siphonaptera: Pulicidae).

The activity of insecticides against the adult cat flea, Ctenocephalides felis (Bouché), inside the cocoon (preemerged) was determined by spraying the cocoons directly and observing subsequent emergence of adults over the next 14 d. Direct sprays of 0.5% trimethacarb wettable powder (WP) and chlorpyrifos emulsifiable concentrate (EC) and WP provided greater than 70% kill. The order of activity against the preemerged adult exposed to direct sprays was organophosphates greater than carbamates greater than pyrethroids. In general, pyrethroids and proprietary aerosols failed to kill preemerged adults. Even though most sprays did not kill preemerged adults, they stimulated adult emergence from cocoons. Preemerged adults placed in the nap of carpet were not killed by chlorpyrifos, diazinon, or propetamphos sprays; the carpet protected them effectively.

Animals↗
PubMed1989

Use of DNA hybridizations probes for detection of the plague bacillus (Yersinia pestis) in fleas (Siphonaptera: Pulicidae and Ceratophyllidae).

The detection of active plaque in nature relies primarily on demonstration of the etiologic agent of the disease. Yersinia pestis, in the flea vectors and susceptible mammalian hosts. A live animal assay is currently used for identification of a Y. pestis virulence antigen that is not expressed in the flea. We have found that DNA hybridization probes specific for Y. pestis, used in very simple sample preparation schemes, allow detection of Y. pestis in three species of fleas as well as tissues of experimentally infected mice at minimum concentrations of 1 x 10(6) bacilli/ml. We detected Y. pestis in 22 of 90 (24%) experimentally infected Xenopsylla cheopis (Rothschild), 13 of 25 (52%) Thrassis bacchi (Rothschild), and 9 of 25 (36%) Diamanus montanus (Baker), but no hybridization signals were observed from fleas that had fed on normal mice. The probe technique indicated infection in 9 of 10 potentially infected liver and spleen samples and none of the 5 control samples. Our techniques permit definitive diagnosis in 48 h.

Animals↗