RESUMO
The Equatorial Pacific Region (EPR) in Ecuador is characterized by high rates of vegetation diversity, and rapid loss of vegetation cover due to anthropogenic pressures. In this study, general ecological aspects of the Tabanidae family, including richness, endemism, and seasonality, were evaluated. Analyses reveal that approximately 42% of the species recorded for Ecuador are present in the EPR, and out of the 84 species cataloged in the EPR, 6 are endemic, representing an endemism of 7.14%. Furthermore, it was established that tabanid populations in a coastal dry forest significantly increased their population density during the dry season, while decreasing during the wet season.
RESUMO
The type III secretion systems (T3SS) encoded in pathogenicity islands SPI-1 and SPI-2 are key virulence factors of Salmonella. These systems translocate proteins known as effectors into eukaryotic cells during infection. To characterize the functionality of T3SS effectors, gene fusions to the CyaA' reporter of Bordetella pertussis are often used. CyaA' is a calmodulin-dependent adenylate cyclase that is only active within eukaryotic cells. Thus, the translocation of an effector fused to CyaA' can be evaluated by measuring cAMP levels in infected cells. Here, we report the construction of plasmids pCyaA'-Kan and pCyaA'-Cam, which contain the ORF encoding CyaA' adjacent to a cassette that confers resistance to kanamycin or chloramphenicol, respectively, flanked by Flp recombinase target (FRT) sites. A PCR product from pCyaA'-Kan or pCyaA'-Cam containing these genetic elements can be introduced into the bacterial chromosome to generate gene fusions by homologous recombination using the Red recombination system from bacteriophage λ. Subsequently, the resistance cassette can be removed by recombination between the FRT sites using the Flp recombinase. As a proof of concept, the plasmids pCyaA'-Kan and pCyaA'-Cam were used to generate unmarked chromosomal fusions of 10 T3SS effectors to CyaA' in S. Typhimurium. Each fusion protein was detected by Western blot using an anti-CyaA' monoclonal antibody when the corresponding mutant strain was grown under conditions that induce the expression of the native gene. In addition, T3SS-1-dependent secretion of fusion protein SipA-CyaA' during in vitro growth was verified by Western blot analysis of culture supernatants. Finally, efficient translocation of SipA-CyaA' into HeLa cells was evidenced by increased intracellular cAMP levels at different times of infection. Therefore, the plasmids pCyaA'-Kan and pCyaA'-Cam can be used to generate unmarked chromosomal cyaA' translational fusion to study regulated expression, secretion and translocation of Salmonella T3SS effectors into eukaryotic cells.
RESUMO
The coli surface antigen 26 (CS26) of enterotoxigenic Escherichia coli (ETEC) had been described as a putative adhesive pilus based on the partial sequence of the crsH gene, detected in isolates from children with diarrhea in Egypt. However, its production and activity as adherence determinant has not been experimentally addressed. The crsH was identified as a homolog of genes encoding structural subunits of ETEC colonization factors (CFs) CS12, CS18, and CS20. These CFs, along with the recently discovered CS30, belong to the γ2 family of pili assembled by the chaperone-usher pathway (CU pili). Further, the complete CS26 locus, crsHBCDEFG, was described in an O141 ETEC strain (ETEC 100664) obtained from a diarrhea case in The Gambia, during the Global Enterics Multicenter Study. Here, we report that CS26 is a pilus of â¼10 nm in diameter, with the capacity to increase the cell adherence of the non-pathogenic strain E. coli DH10B. As for other related pili, production of CS26 seems to be regulated by phase variation. Deletion of crsHBCDEFG in ETEC 100664 significantly decreased its adherence capacity, which was recovered by in trans complementation. Furthermore, CrsH was cross-recognized by polyclonal antibodies directed against the major structural subunit of CS20, CsnA, as determined by Western blotting and immunogold labeling. ETEC CS26+ strains were found to harbor the heat-labile enterotoxin only, within three different sequence types of phylogroups A and B1, the latter suggesting acquisition through independent events of horizontal transfer. Overall, our results demonstrate that CS26 is an adhesive pilus of human ETEC. In addition, cross-reactivity with anti-CsnA antibodies indicate presence of common epitopes in γ2-CFs.
RESUMO
El estudio físico del suelo ha recibido atención por su importancia para mantener la producción de caña de azúcar en forma sustentable. Se evaluó densidad aparente (DAP) en un vertisol en los agrosistemas de caña de azúcar, pastos y selva mediana perennifolia. Para el muestreo de los ciclos de caña se seleccionaron los entresurcos donde no hubo tránsito de equipo, donde pasaron camiones y donde pasó la alzadora durante la cosecha. Se tomaron al azar 9 repeticiones de cada sitio por ciclo de cultivo. Para los agrosistemas de pasto y selva los muestreos se efectuaron al azar con seis repeticiones. La DAp entre 0-10cm de profundidad se determinó con el método del cilindro.
Assuntos
Fauna , Assistência Religiosa , México , PlantasRESUMO
Hay indicios en la literatura médica nacional, sugestivos de la existencia de casos de leishmaniasis muco-cutánea (Espundia). Nosotros, estudiamos las formas cutáneas localizada y diseminada, hemos tambien reconocido 3 casos de la variante muco-cutánea, con las suficientes bases de metodología diagnóstica, que de manera inequívocada sustentan a esta entidad, como una forma patológica primaria en nuestro país. Se discute la literatura mexicana, lo mismo que nuestras observaciones .