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1.
Infect Genet Evol ; 8(3): 381-5, 2008 May.
Artigo em Inglês | MEDLINE | ID: mdl-18304894

RESUMO

Ten microsatellites were isolated and characterized from a partial genomic library of Rhodnius prolixus, the principal Chagas disease vector in Venezuela, Colombia and Central America. These polymorphic molecular markers could be particularly useful in Chagas disease control initiatives. A wider applicability of the primer-pairs isolated was shown, from 6 to 10 loci being amplifiable in five out of the ten Rhodnius species tested, namely R. domesticus, R. nasutus, R. neglectus, R. neivai and R. robustus. Interestingly, all the loci were amplified in the latter. These markers may be of interest to trace the colonization of human dwellings from triatomine sylvatic populations in order to better define epidemiological risk patterns.


Assuntos
Doença de Chagas/parasitologia , Repetições de Microssatélites , Rhodnius/genética , Animais , Vetores de Doenças , Biblioteca Gênica , Geografia , Reação em Cadeia da Polimerase/métodos , Rhodnius/parasitologia , Especificidade da Espécie
2.
Genetics ; 128(2): 393-403, 1991 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-1649072

RESUMO

The mitochondrial genome of honeybees is characterized by the presence of a long intergenic sequence located between the COI and COII genes. In addition, the length of this sequence varies between and within subspecies. Four length categories (200, 250, 450 and 650 bp) have been found in 63 sampled colonies. Analysis of the sequence of the largest type reveals the existence of two units: P (54 bp, 100% A + T) and Q (196 bp, 93.4% A + T). The lengths encountered in the sample are explained by the following combinations: Q, PQ, PQQ and PQQQ. According to similarities in primary and secondary structures, the sequence Q has been divided into three parts: Q1 (similar to the 3' end of the COI gene), Q2 (similar to the neighboring tRNA(leu) gene) and Q3 (highly similar to the P sequence). These relationships led us to hypothesize that these sequences, which do not have any counterpart in Drosophila yakuba mitochondrial DNA (mtDNA), arose by tandem duplication. The usual location of length variation in mtDNA control regions prompted us to examine the hypothesis that this COI-COII intergenic region might contain an origin of replication. High A + T content, stability profile, hairpin and cloverleaf putative secondary structures are all in favor of this hypothesis.


Assuntos
Abelhas/genética , DNA Mitocondrial/genética , Complexo IV da Cadeia de Transporte de Elétrons/genética , Sequência de Aminoácidos , Animais , Composição de Bases , Sequência de Bases , Abelhas/enzimologia , Evolução Biológica , Clonagem Molecular , Replicação do DNA , Complexo IV da Cadeia de Transporte de Elétrons/metabolismo , Variação Genética , Dados de Sequência Molecular , Conformação de Ácido Nucleico , Sequências Repetitivas de Ácido Nucleico , Mapeamento por Restrição , Especificidade da Espécie
3.
Genetics ; 117(4): 687-96, 1987 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17246410

RESUMO

The mitochondrial genotype of all F(1) female offspring (426 individuals) of a single Drosophila mauritiana female, heteroplasmic for two types of mtDNA (a short and a long genome), was established. All descendants were heteroplasmic. The earliest eggs laid by this female show the cytoplasmic genetic structure of ovariole stem cells at the end of development. Cohorts of females from the eggs laid day after day by this female, throughout the 31 days of its life, provide information on the evolution of the mitochondrial genotypes in the course of successive divisions of stem cells. An increase of the percentage of long DNA in offspring was observed as the female aged. Moreover, the variance of the genotypes increases as rounds of stem cell division progress. These results are supported by observations based on the adults issued from the early and late eggs, for three additional heteroplasmic females.

4.
Genetics ; 140(2): 679-95, 1995 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-7498746

RESUMO

Samples from nine populations belonging to three African (intermissa, scutellata and capensis) and four European (mellifera, ligustica, carnica and cecropia) Apis mellifera subspecies were scored for seven microsatellite loci. A large amount of genetic variation (between seven and 30 alleles per locus) was detected. Average heterozygosity and average number of alleles were significantly higher in African than in European subspecies, in agreement with larger effective population sizes in Africa. Microsatellite analyses confirmed that A. mellifera evolved in three distinct and deeply differentiated lineages previously detected by morphological and mitochondrial DNA studies. Dendrogram analysis of workers from a given population indicated that super-sisters cluster together when using a sufficient number of microsatellite data whereas half-sisters do not. An index of classification was derived to summarize the clustering of different taxonomic levels in large phylogenetic trees based on individual genotypes. Finally, individual population x loci data were used to test the adequacy of the two alternative mutation models, the infinite allele model (IAM) and the stepwise mutation models. The better fit overall of the IAM probably results from the majority of the microsatellites used including repeats of two or three different length motifs (compound microsatellites).


Assuntos
Abelhas/genética , DNA Satélite/genética , Variação Genética , Modelos Genéticos , Alelos , Animais , Sequência de Bases , Evolução Biológica , Frequência do Gene , Genética Populacional , Heterozigoto , Dados de Sequência Molecular , Mutação
5.
Genetics ; 153(4): 1989-2000, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10581301

RESUMO

A new method for assigning individuals of unknown origin to populations, based on the genetic distance between individuals and populations, was compared to two existing methods based on the likelihood of multilocus genotypes. The distribution of the assignment criterion (genetic distance or genotype likelihood) for individuals of a given population was used to define the probability that an individual belongs to the population. Using this definition, it becomes possible to exclude a population as the origin of an individual, a useful extension of the currently available assignment methods. Using simulated data based on the coalescent process, the different methods were evaluated, varying the time of divergence of populations, the mutation model, the sample size, and the number of loci. Likelihood-based methods (especially the Bayesian method) always performed better than distance methods. Other things being equal, genetic markers were always more efficient when evolving under the infinite allele model than under the stepwise mutation model, even for equal values of the differentiation parameter F(st). Using the Bayesian method, a 100% correct assignment rate can be achieved by scoring ca. 10 microsatellite loci (H approximately 0.6) on 30-50 individuals from each of 10 populations when the F(st) is near 0.1.


Assuntos
Genética Populacional , Teorema de Bayes , Mapeamento Cromossômico , Genótipo , Funções Verossimilhança , Modelos Genéticos
9.
Proc Biol Sci ; 247(1320): 163-8, 1992 Mar 23.
Artigo em Inglês | MEDLINE | ID: mdl-1350096

RESUMO

Sequences of a segment of the 16S ribosomal DNA of Wolbachia, a rickettsia-like microorganism responsible for cytoplasmic incompatibility in Drosophila simulans, have been obtained after polymerase chain reaction (PCR) amplification. Their comparison with other eubacterial sequences allows us to assign these endosymbionts to the alpha subdivision of purple bacteria. Four related sequences have been obtained for microorganisms carried by eight isofemale lines representative of the three mitochondrial types of D. simulans. Their phylogeny and level of divergence do not parallel that of the mitochondrial DNA, suggesting that several independent infections occurred. There is no direct relation between bacterial phylogeny and formerly identified incompatibility types.


Assuntos
Drosophila/microbiologia , Rickettsiaceae/genética , Animais , Sequência de Bases , Citoplasma/microbiologia , DNA Bacteriano/genética , DNA Mitocondrial/genética , Drosophila/genética , Feminino , Masculino , Dados de Sequência Molecular , Filogenia , RNA Ribossômico 16S/genética , Rickettsiaceae/isolamento & purificação , Homologia de Sequência do Ácido Nucleico , Simbiose
10.
Proc Biol Sci ; 250(1328): 91-8, 1992 Nov 23.
Artigo em Inglês | MEDLINE | ID: mdl-1361987

RESUMO

Rickettsia-like maternally inherited bacteria have been shown to be involved in a variety of alterations of arthropod sexuality, such as female-biased sex ratios, parthenogenesis, and sterility of crosses either between infected males and uninfected females or between infected individuals (cytoplasmic incompatibility). We have characterized several of these microorganisms through partial sequences of the small (16S) and large (23S) subunit ribosomal DNA. All the symbionts identified, which include several cytoplasmic incompatibility microorganisms, several endosymbionts of terrestrial isopods, and symbionts of two thelytokous Trichogramma wasp species, belong to a monophyletic group of related symbionts, some of which have previously been detected in several insects exhibiting cytoplasmic incompatibility. Three molecular lineages can be identified on the basis of 16S as well as 23S sequences. Although they are only known as endocellular symbionts, Wolbachia spread by horizontal transfer across host lineages as evidenced by their diversification which occurred long after that of their hosts, and by the non-congruence of the phylogenetic relationships of symbionts and their hosts. Indeed, symbionts of two different lineages have been found in the same host species, whereas closely related endosymbionts are found in distinct insect orders. Isopod endosymbionts form a separate lineage, and they can determine feminization as well as cytoplasmic incompatibility. The ability to determine cytoplasmic incompatibility, found in all lineages, is probably ancestral to this group.


Assuntos
DNA Ribossômico/isolamento & purificação , Insetos/fisiologia , Rickettsiaceae/fisiologia , Análise para Determinação do Sexo , Vespas/fisiologia , Animais , Sequência de Bases , DNA Ribossômico/genética , Escherichia coli/genética , Feminino , Insetos/genética , Masculino , Dados de Sequência Molecular , Oligodesoxirribonucleotídeos , Ovário , Filogenia , Reação em Cadeia da Polimerase , Homologia de Sequência do Ácido Nucleico , Testículo , Vespas/genética
11.
Proc Biol Sci ; 267(1452): 1487-95, 2000 Aug 07.
Artigo em Inglês | MEDLINE | ID: mdl-11007323

RESUMO

The finding of new melanogaster sister species may help us in understanding more about how the emergence of genetic novelties, particularly in insular habitats, can result in speciation. Here we report on the discovery of Drosophila santomea, which is the first melanogaster sibling found off West-equatorial Africa, on São Tomé, one of the Gulf of Guinea islands. Although the eight other melanogaster sister species are remarkably conservative in their morphology except for their terminalia, the new find has a morphological trait distinguishing it from all of these: a pure yellow body coloration of both sexes without the normal black abdominal banding. Evidence from the terminalia, polytene and mitotic chromosomes, period gene and allozymes are provided indicating that it is nonetheless the nearest relative of Drosophila yakuba with which it coexists on the island. The new find is a clear-cut taxon as shown by the production of sterile male hybrids, eventually with developmental defects, in both directions of cross with yakuba and by the existence of an altitudinal divide accompanied by a hybrid zone at mid-elevation on the island. Molecular and karyotypic data further support this conclusion. In contrast to the significant divergence of their nuclear DNAs, an intriguing similarity in their cytochrome b sequences was observed indicating a recent coalescence common to santomea, yakuba and also teissieri cytoplasms. These were shown to harbour the same Wolbachia endosymbiotic bacteria which could possibly be responsible for mitochondrial DNA hitchhiking across the species barrier.


Assuntos
Evolução Biológica , Drosophila/classificação , Animais , Ilhas Atlânticas , Proteínas de Bactérias/genética , Quimera , Grupo dos Citocromos c/genética , Drosophila/anatomia & histologia , Drosophila/genética , Drosophila/microbiologia , Drosophila melanogaster/anatomia & histologia , Drosophila melanogaster/classificação , Drosophila melanogaster/genética , Drosophila melanogaster/microbiologia , Feminino , Genes de Insetos , Geografia , Masculino , Wolbachia/genética
12.
Parasite ; 5(2): 167-73, 1998 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9754313

RESUMO

Paromomycin is an antileishmanial chemotherapeutic agent. Leishmania donovani promastigotes resistant to 800 microM of paromomycin were selected by increasing drug pressure and cloned. These promastigotes did not acquire multidrug resistance. Paromomycin resistance was stable in the absence of the drug in the culture. It remained stable also in amastigotes isolated after a passage in mice. Furthermore the resistant parasites were still infective to macrophages in vitro and for mice in vivo. A sensitive method to detect and to quantify intracellular paromomycin by HPLC was developed and allowed to show that the main mechanism of resistance seems to be due to decreased drug uptake probably as a consequence of altered membrane composition.


Assuntos
Antibacterianos/farmacologia , Antiprotozoários/farmacologia , Leishmania donovani/efeitos dos fármacos , Paromomicina/farmacologia , Animais , Antibacterianos/análise , Antibacterianos/metabolismo , Antiprotozoários/análise , Antiprotozoários/metabolismo , Cromatografia Líquida de Alta Pressão , Resistência a Medicamentos/genética , Resistência a Múltiplos Medicamentos/genética , Leishmania donovani/genética , Leishmania donovani/metabolismo , Camundongos , Mutação , Paromomicina/análise , Paromomicina/metabolismo , Fenótipo , RNA de Protozoário/genética , RNA Ribossômico/genética
13.
Presse Med ; 30(31 Pt 1): 1525-7, 2001 Oct 27.
Artigo em Francês | MEDLINE | ID: mdl-11721490

RESUMO

DATA: The prion, which apparently enters the organism via the oral route, crosses the digestive barrier before progressively reaching the brain after multiplying in the lymphoid organs. Dendritic follicles as well as other immune cells appear to be involved in the transfer of prions from the lymphoid organs to the brain. EXPERIENCE: Experimental transfer trials with adoptive murine trembles showed that a fraction of the splenic cells enriched with CD11c+ cells have the highest infectious potential compared with the lymphocyte B enriched cell fraction and the total mononuclear population. PERSPECTIVES: While splenic B cells do not to be able to replicate the prion, their infectious potential is probably the result of contact with dendritic follicular cells, CD11c+ dendritic cells playing an important role in neuroinvasion.


Assuntos
Príons/fisiologia , Replicação Viral , Animais , Células Cultivadas , Ratos
17.
Rev Neurol (Paris) ; 156(3): 328, 2000 Mar.
Artigo em Francês | MEDLINE | ID: mdl-10740108
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