Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
Más filtros











Intervalo de año de publicación
1.
BMC Genomics ; 12: 223, 2011 May 10.
Artículo en Inglés | MEDLINE | ID: mdl-21569254

RESUMEN

BACKGROUND: Parasite-vector interactions are fundamental in the transmission of vector-borne diseases such as leishmaniasis. Leishmania development in the vector sand fly is confined to the digestive tract, where sand fly midgut molecules interact with the parasites. In this work we sequenced and analyzed two midgut-specific cDNA libraries from sugar fed and blood fed female Phlebotomus perniciosus and compared the transcript expression profiles. RESULTS: A total of 4111 high quality sequences were obtained from the two libraries and assembled into 370 contigs and 1085 singletons. Molecules with putative roles in blood meal digestion, peritrophic matrix formation, immunity and response to oxidative stress were identified, including proteins that were not previously reported in sand flies. These molecules were evaluated relative to other published sand fly transcripts. Comparative analysis of the two libraries revealed transcripts differentially expressed in response to blood feeding. Molecules up regulated by blood feeding include a putative peritrophin (PperPer1), two chymotrypsin-like proteins (PperChym1 and PperChym2), a putative trypsin (PperTryp3) and four putative microvillar proteins (PperMVP1, 2, 4 and 5). Additionally, several transcripts were more abundant in the sugar fed midgut, such as two putative trypsins (PperTryp1 and PperTryp2), a chymotrypsin (PperChym3) and a microvillar protein (PperMVP3). We performed a detailed temporal expression profile analysis of the putative trypsin transcripts using qPCR and confirmed the expression of blood-induced and blood-repressed trypsins. Trypsin expression was measured in Leishmania infantum-infected and uninfected sand flies, which identified the L. infantum-induced down regulation of PperTryp3 at 24 hours post-blood meal. CONCLUSION: This midgut tissue-specific transcriptome provides insight into the molecules expressed in the midgut of P. perniciosus, an important vector of visceral leishmaniasis in the Old World. Through the comparative analysis of the libraries we identified molecules differentially expressed during blood meal digestion. Additionally, this study provides a detailed comparison to transcripts of other sand flies. Moreover, our analysis of putative trypsins demonstrated that L. infantum infection can reduce the transcript abundance of trypsin PperTryp3 in the midgut of P. perniciosus.


Asunto(s)
Sangre , Carbohidratos , Perfilación de la Expresión Génica , Insectos Vectores/genética , Leishmania infantum , Phlebotomus/genética , Secuencia de Aminoácidos , Animales , Bases de Datos Genéticas , Femenino , Biblioteca de Genes , Insectos Vectores/clasificación , Insectos Vectores/citología , Insectos Vectores/enzimología , Microvellosidades/genética , Datos de Secuencia Molecular , Especificidad de Órganos , Estrés Oxidativo/genética , Phlebotomus/clasificación , Phlebotomus/citología , Phlebotomus/enzimología , Filogenia , ARN Mensajero/genética , ARN Mensajero/metabolismo , Análisis de Secuencia de ADN
2.
J Med Entomol ; 37(6): 802-6, 2000 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-11126533

RESUMEN

To establish a transient expression system for genes introduced into sand fly cell lines, we tested the expression of the luciferase reporter gene under control of different promoters. Towards this end, we lipofected cell lines obtained from New and Old World sand flies, LL-5 from Lutzomyia longipalpis Lutz & Neiva and PP-9 from Phlebotomus papatasi Scopoli, respectively. The relative levels of luciferase expression were studied under control of Drosophila melanogaster Meigen heat shock protein 70 (hsp70), human cytomegalovirus, simian virus 40 or Junonia coenia (Hübner) densovirus (P9) promoters. The Drosophila heat shock protein 70 promoter, originating from insect genes, functioned as a strong promoter in both cell lines. Promoters from the different virus genes also were capable of driving transgene expression in both cell lines.


Asunto(s)
Clonación Molecular/métodos , Luciferasas/genética , Phlebotomus/citología , Regiones Promotoras Genéticas , Psychodidae/citología , Animales , Línea Celular , Citomegalovirus/genética , Densovirus/genética , Drosophila melanogaster , Expresión Génica , Genes Reporteros , Proteínas HSP70 de Choque Térmico/genética , Humanos , Virus 40 de los Simios/genética
3.
Mem Inst Oswaldo Cruz ; 95(4): 471-2, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-10904400

RESUMEN

We describe a technique to separate male and female pupae of sand flies. This has reduced the labour to separate flies after emergence and also allows the isolation of unmated adults for behavioural and physiological studies.


Asunto(s)
Phlebotomus/fisiología , Caracteres Sexuales , Animales , Femenino , Masculino , Phlebotomus/citología , Pupa/fisiología
4.
Mem. Inst. Oswaldo Cruz ; 95(4): 471-2, July-Aug. 2000.
Artículo en Inglés | LILACS | ID: lil-264225

RESUMEN

We describe a technique to separate male and female pupae of sand flies. This has reduced the labour to separate flies after emergence and also allows the isolation of unmated adults for behavioural and physiological studies.


Asunto(s)
Animales , Masculino , Femenino , Phlebotomus/fisiología , Caracteres Sexuales , Phlebotomus/citología , Pupa
5.
Mem Inst Oswaldo Cruz ; 93(6): 773-85, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9921302

RESUMEN

Numerical analyses (correspondence analysis, ascending hierarchical classification, cladistic approach) were applied to the morphological characters of the adults of the genus Phlebotomus Rondani & Berté 1840. They confirm the reliability of the classic classifications, and also redefine the taxonomic and phylogenetic position of certain taxa. Thus, Spelaeophlebotomus Theodor 1948. Idiophlebotomus Quate & Fairchild 1961 and Australophlebotomus Theodor 1948 deserve generic rank. Among the vectors of leishmaniasis, the subgenus Phlebotomus Rondani & Berté 1840 is probably ancient. The results attribute an intermediate taxonomic and phylogenetic position to the taxa Euphlebotomus Theodor 1948 and Anaphlebotomus Theodor 1948, and reveal the probable artificial nature of the latter. The comparatively large numbers of species of subgenera Paraphlebotomus Theodor 1948, Synphlebotomus Theodor 1948 and, above all, Larroussius Nitzulescu 1931 and Adlerius Nitzulescu 1931, suggest that they are relatively recent. The development of adult morphological characters, the validity of their use in taxonomy and proposals for further studies are discussed.


Asunto(s)
Phlebotomus/clasificación , Animales , Clasificación/métodos , Phlebotomus/citología , Filogenia , Especificidad de la Especie
6.
Mem Inst Oswaldo Cruz ; 93(6): 787-93, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9921303

RESUMEN

Numerical analyses (correspondence analysis, ascending hierarchical classification, and cladistics) were done with morphological characters of adult phlebotomine sand flies. The resulting classification largely confirms that of classical taxonomy for supra-specific groups from the Old World, though the positions of some groups are adjusted. The taxa Spelaeophlebotomus Theodor 1948, Idiophlebotomus Quate & Fairchild 1961, Australophlebotomus Theodor 1948 and Chinius Leng 1987 are notably distinct from other Old World groups, particularly from the genus Phlebotomus Rondani & Berté 1840. Spelaeomyia Theodor 1948 and, in particular, Parvidens Theodor & Mesghali 1964 are clearly separate from Sergentomyia França & Parrot 1920.


Asunto(s)
Phlebotomus/clasificación , Animales , Clasificación/métodos , Phlebotomus/citología , Filogenia , Especificidad de la Especie
7.
J Med Entomol ; 31(6): 890-7, 1994 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-7815403

RESUMEN

A histologic technique was used to detect multiple hamster blood meals taken by Phlebotomus duboscqi Neveu-Lemaire during a 5-d period. Forty-eight flies were fed two or three blood meals separated by 48, 72, or 120 h and sampled immediately; multiple meals were detected in 27 flies (56%). Double meals separated by 72 h within a single gonotrophic cycle were documented in 11/19 (58%) flies; double meals separated by 120 h were detected in only 4/17 (24%) flies. Triple blood meals taken at 0, 72, and 120 h were detected in 5/12 (42%) flies; all of these flies contained the second and third meals. Early blood meals were detected clearly within later blood meals as a delimited body of dark digested blood, heme (sometimes also with pink undigested blood), the presence of an associated pale pink-staining peritrophic plug, the presence and appearance of the peritrophic membrane surrounding the meals, and a physical space between meals; the first two characteristics were the most important. Development of the ovarian follicles including apparent dilatations was also observable using this histologic technique. The results of this study indicate that the rate of multiple feeding can be determined using histology. The technique would be useful in evaluating the blood feeding frequency of field-caught sand flies in endemic areas of leishmaniasis, bartonellosis, and phleboviruses.


Asunto(s)
Alimentación Animal , Sangre , Conducta Alimentaria , Phlebotomus/fisiología , Animales , Cricetinae , Femenino , Hemo/análisis , Folículo Ovárico/citología , Ovario/citología , Phlebotomus/citología , Factores de Tiempo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA