@article {125,
	title = {Controlled study of malathion and d-phenothrin lotions for Pediculus humanus var capitis infested schoolchildren},
	journal = {Lancet},
	volume = {344},
	year = {1994},
	month = {1994},
	pages = {1724 - 1727},
	abstract = {Anecdotal reports have suggested that reduced efficacy of pediculicides against Pediculus humanus capitis could be related to resistance to treatments. Ovicidal and pediculicidal activities of 0.5\% malathion and 0.3\% d-phenothrin lotions were tested in an experimental model of P humanus capitis grown on rabbits to ensure that the two treatments were pharmacologically equipotent. We then did a randomised controlled trial in which the lotions were administered to 193 P humanus capitis-infested schoolchildren (malathion, 95; d-phenothrin, 98). Success rate was defined as the absence of both live lice and viable nits. Before treatment, live lice were collected and subjected to a pediculicidal test. Pharmacological tests showed 100\% killing of the rabbit-grown nits and lice after exposure to both pediculicides. On day 1 of the controlled trial, the success rate was 92\% in the malathion group (95\% CI, 0.86-0.97) and 40\% in the d-phenothrin group (0.30-0.49) (p < 0.0001); on day 7, it was 95\% in the malathion group (0.90-0.99) and 39\% in the d-phenothrin group (0.29-0.48, p < 0.0001). Malathion was also significantly more active in the pediculicidal tests compared to d-phenothrin and control. These results suggest an acquired resistance to d-phenothrin in the schoolchildren tested, since all other conditions of the administration of insecticides were standardised.},
	keywords = {animals, child, Comparative Study, humans, Insecticide Resistance, Lice Infestations/drug therapy, malathion, Pediculus, Pyrethrum, Rabbit, Research Support, Non-U.S. Gov{\textquoteright}t, scalp dermatoses},
	url = {http://www.phthiraptera.info/Publications/45219.pdf},
	author = {Chosidow,Olivier and Chastang,C. and Brue,C. and Bouvet,E. and Izri,M. and Monteny,N. and Bastuji-Garin,S. and Rousset,J. J. and Revuz,J.}
}
@article {91,
	title = {Isoenzymes of human lice: Pediculus humanus and P. capitis},
	journal = {Medical and Veterinary Entomology},
	volume = {14},
	year = {2000},
	note = {LR: 20041117; JID: 8708682; 0 (Isoenzymes); EC 3.1. (Esterases); EC 5.4.2.2 (Phosphoglucomutase); ppublish},
	month = {2000},
	pages = {419 - 425},
	address = {England},
	abstract = {Human lice (Phthiraptera: Pediculidae) from Africa, America and Europe were electrophoresed for 28 enzymes, with special interest in metabolic factors likely to be involved with insecticide resistance. Zymogram profiles of the body louse (Pediculus humanus L. from France and U.S.A.) and the head louse (P. capitis DeGeer from France, Madagascar, Mali \& Senegal) were compared. Only esterase two enzymes, phosphoglucomutase (Pgm) and 3 (Est-3), showed electrophoretic variation. In our starch gel electrophoresis conditions, P. humanus showed three electromorphs of Pgm migrating anodally 6, 11 and 16 mm (designated alleles a, b, c, respectively). Of the putative Pgm alleles, b and c occurred in all samples of both species of lice, whereas allele a was found only in P. humanus lab strain from U.S.A. Esterase 3 had four electromorphs migrating 23, 26, 30 and 35 mm (designated alleles a, b, c and d). Among putative Est alleles, a was found only in P. capitis from Bamako (all 14 specimens aa homozygotes), allele d was found only in P. capitis from Dakar (39\% frequency), whereas Est-3 alleles b and c showed apparently balanced polymorphism in all samples of both P. humanus and P. capitis except that from Bamako. Despite the limited amount of isoenzyme variation detected (only 2/31 polymorphic loci), divergences of Est-3 and Pgm among Pediculus populations may be relevant to their biosystematics and resistance.},
	keywords = {animals, electrophoresis, France, humans, Isoenzymes/chemistry, Madagascar, Mali, Pediculus, polymorphism, Research Support, Non-U.S. Gov{\textquoteright}t, Senegal, U.S.A.},
	isbn = {0269-283X},
	author = {Amevigbe,M. D. and Ferrer,A. and Champorie,S. and Monteny,N. and Deunff,J. and Richard-Lenoble,D.}
}
