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1.
Am J Trop Med Hyg ; 77(3): 562-6, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17827380

RESUMO

Although body louse is a well-known vector of trench fever, the growth kinetics of Bartonella quintana in body lice has not been fully understood. We performed a quantitative analysis of bacterial multiplication rate. B. quintana started proliferation in body lice 4 days after ingestion and was constantly excreted in the feces for at least 3 weeks. The number of bacteria in feces reached the maximum 10(7)/louse per day on Day 15. The doubling time of B. quintana estimated from logistic regression formula was 21.3 hours. Scanning electron microscopy showed the presence of bacterial masses in feces. Immunofluorescent study using specific monoclonal antibody confirmed identification of B. quintana. Such an explosive multiplication rate and active excretion of B. quintana from the body lice could be related to epidemics of trench fever in developed countries.


Assuntos
Bartonella quintana/fisiologia , Pediculus/microbiologia , Animais , Bartonella quintana/ultraestrutura , Fezes/microbiologia , Fatores de Tempo
2.
Appl Environ Microbiol ; 72(11): 7349-52, 2006 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16950915

RESUMO

The symbiotic bacteria associated with the stomach disc, a large aggregate of bacteriocytes on the ventral side of the midgut, of human body and head lice were characterized. Molecular phylogenetic analysis of 16S rRNA gene sequences showed that the symbionts formed a distinct and well-defined clade in the Gammaproteobacteria. The sequences exhibited AT-biased nucleotide composition and accelerated molecular evolution. In situ hybridization revealed that in nymphs and adult males, the symbiont was localized in the stomach disc, while in adult females, the symbiont was not in the stomach disc but in the lateral oviducts and the posterior pole of the oocytes due to female-specific symbiont migration. We propose the designation "Candidatus Riesia pediculicola" for the louse symbionts.


Assuntos
Gammaproteobacteria/classificação , Gammaproteobacteria/isolamento & purificação , Pediculus/microbiologia , Estômago/microbiologia , Simbiose , Animais , DNA Bacteriano/análise , Feminino , Gammaproteobacteria/genética , Gammaproteobacteria/crescimento & desenvolvimento , Humanos , Hibridização In Situ , Masculino , Dados de Sequência Molecular , Ninfa , Pediculus/crescimento & desenvolvimento , Filogenia , RNA Ribossômico 16S/genética , Análise de Sequência de DNA
3.
J Med Entomol ; 40(4): 468-74, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-14680113

RESUMO

The problem of pyrethroid-resistance in head lice, Pediculus humanus capitis (De Geer), is growing worldwide, and an insensitive sodium channel is suspected as the major mechanism of this resistance. We sequenced an open reading frame (ORF) encoding for the para-orthologous sodium channel from an insecticide-susceptible strain of the body louse, Pediculus humanus humanus (L.), based on conserved peptide sequences and a known partial gene sequence. Phenothrin-susceptible and -resistant head louse colonies from Japanese were individually analyzed for point mutations of the sodium channel cDNA; susceptible head and body lice differed in double homozygous synonymous substitutions. The resistant head lice shared 23 base substitutions homozygously, in which four resulted in amino acid substitutions: D11E in the N-terminal inner-membrane segment; M850T in the outer-membrane loop between segments four and five of domain II; T952I and L955 F in the trans-membrane segment five of domain II. The latter two substitutions coincided with those of pyrethroid-resistant head lice in the U.S. and U.K. (Lee et al. 2000), within the available published information on the peptide sequences. The potential mechanisms of head louse pyrethroid-resistance are discussed based on the four structural changes of the target molecule.


Assuntos
Resistência a Medicamentos/genética , Inseticidas/toxicidade , Pediculus/genética , Piretrinas/toxicidade , Canais de Sódio/genética , Sequência de Aminoácidos , Animais , Humanos , Dados de Sequência Molecular , Reação em Cadeia da Polimerase/métodos , RNA Mensageiro/genética , Mapeamento por Restrição , Alinhamento de Sequência , Homologia de Sequência de Aminoácidos , Canais de Sódio/química
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