Kon-tiki/Perdido enhances PS2 integrin adhesion and localizes its ligand, Thrombospondin, in the myotendinous junction.

Cell-extracellular matrix adhesion is mediated by cell receptors, mainly integrins and transmembrane proteoglycans, which can functionally interact. How these receptors are regulated and coordinated is largely unknown and key to understand cell adhesion in development. We show that the conserved transmembrane proteoglycan Kon-tiki/Perdido (Kon) interacts with αPS2βPS integrin to mediate muscle-tendon adhesion. Double mutant embryos for kon and inflated show a synergistic increase in muscle detachment. Furthermore, Kon modulates αPS2βPS signaling at the muscle attachment, since P-Fak is reduced in kon mutants. This reduction in integrin signaling can be rescued by the expression of a truncated Kon protein containing the transmembrane and extracellular domains, suggesting that these domains are sufficient to mediate this signaling. We show that these domains are sufficient to properly localize the αPS2βPS ligand, Thrombospondin, to the muscle attachment, and to partially rescue Kon dependent muscle-tendon adhesion. We propose that Kon can engage in a protein complex with αPS2βPS and enhance integrin-mediated signaling and adhesion by recruiting its ligand, which would increase integrin-binding affinity to the extracellular matrix, resulting in the consolidation of the myotendinous junction.Ramón y Cajal program and the Universidad Pablo de Olavide. Research was funded by the Ministerio de Economıa y Competitividad ́ (Spanish Ministry of Science and Innovation) (BFU2008-036550, BFU2011-26745). Proyecto de Excelencia of the Consejerıa de Econom ́ ıa, ́ Innovación, Ciencia y Empleo, Junta de Andalucıa (PO9-CVI-5058). A.G.E.-Z. and ́ the Ministerio de Ciencia e Innovación (Spanish Ministry of Science and Innovation) (BFU2008-036550, BFU2011-26745)

A colanic acid operon deletion mutation enhances induction of early antibody responses by live attenuated salmonella vaccine strains

Colanic acid (CA) is a common exopolysaccharide produced by many genera in the Enterobacteriaceae. It is critical for biofilm formation on HEp-2 cells and on chicken intestinal tissue by Salmonella. In this study, we generated different CA synthesis gene mutants and evaluated the immune responses induced by these mutants. One of these mutations, Δ(wza-wcaM)8, which deleted the whole operon for CA synthesis, was introduced into two Salmonella vaccine strains attenuated by auxotrophic traits or by the regulated delayed attenuation strategy (RDAS). The mice immunized with the auxotrophic Salmonella vaccine strain with the deletion mutation Δ(wza-wcaM)8 developed higher vaginal IgA titers against the heterologous protective antigen and higher levels of antigen-specific IgA secretion cells in lungs. In Salmonella vaccine strains with RDAS, the strain with the Δ(wza-wcaM)8 mutation resulted in higher levels of protective antigen production during in vitro growth. Mice immunized with this strain developed higher serum IgG and mucosal IgA antibody responses at 2 weeks. This strain also resulted in better gamma interferon (IFN-γ) responses than the strain without this deletion at doses of 10(8) and 10(9) CFU. Thus, the mutation Δ(wza-wcaM)8 will be included in various recombinant attenuated Salmonella vaccine (RASV) strains with RDAS derived from Salmonella enterica serovar Paratyphi A and Salmonella enterica serovar Typhi to induce protective immunity against bacterial pathogens

Analysis of the Expression, Secretion and Translocation of the Salmonella enterica Type III Secretion System Effector SteA

Many Gram-negative pathogens possess virulence-related type III secretion systems. Salmonella enterica uses two of these systems, encoded on the pathogenicity islands SPI-1 and SPI-2, respectively, to translocate more than 30 effector proteins into eukaryotic host cells. SteA is one of the few effectors that can be translocated by both systems. We investigated the conditions affecting the synthesis of this effector, its secretion to culture media and its translocation into host cells. Whereas steA was expressed under a wide range of conditions, some factors, including low and high osmolarity, and presence of butyrate, decreased expression. SteA was efficiently secreted to the culture media under both SPI-1 and SPI-2 inducing conditions. The kinetics of translocation into murine macrophages and human epithelial cells was studied using fusions with the 3xFLAG tag, and fusions with CyaA from Bordetella pertussis. Translocation into macrophages under non-invasive conditions was mainly dependent on the SPI-2-encoded type III secretion system but some participation of the SPI-1 system was also detected 6 hours post-infection. Interestingly, both type III secretion systems had a relevant role in the translocation of SteA into epithelial cells. Finally, a deletion approach allowed the identification of the N-terminal signal necessary for translocation of this effector. The amino acid residues 1–10 were sufficient to direct translocation into host cells through both type III secretion systems. Our results provide new examples of functional overlapping between the two type III secretion systems of Salmonella

Estudio seroepidemiológico y entomológico sobre la enfermedad de Chagas en un área infestada por Triatoma maculata (Erichson 1848) en el centro-occidente de Venezuela An entomological and seroepidemiological study of Chagas' disease in an area in central-western Venezuela infested with Triatoma maculata (Erichson 1848)

En el presente trabajo se realizó un estudio seroepidemiológico, entomológico y de factores de riesgo para la infestación de las viviendas en un área infestada por Triatoma maculata (Parroquia Xaguas, Municipio Urdaneta, Estado Lara, Venezuela). Se muestrearon 140 viviendas, 509 personas y 110 cánidos, a los cuales se les determinó anticuerpos séricos anti-Trypanosoma cruzi mediante ELISA y MABA, utilizando antígenos recombinantes. La infección por Tr. cruzi de los triatominos fue determinada por microscopía óptica y PCR. Los resultados mostraron una seroprevalencia en humanos de 1,57% y en cánidos de 6,36%. De los 545 triatominos capturados 97,98% fueron T. maculata, 1,65% Eratyrus mucronatus y 0,37% Panstrongylus geniculatus; con índices vectoriales de infección 0,36%, infestación 16,4%, colonización 39,1%, coinfestación 8,6% y dispersión 100%. La presencia de vectores en el domicilio y peridomicilio estuvo asociada a la presencia de gallinas, desorden en el peridomicilio, caprinos, gallineros y/o distribución del domicilio. Los resultados permiten concluir que T. maculata es el vector predominante en la región, con capacidad de infestar y colonizar el domicilio y estaría involucrado en la transmisión de la enfermedad de Chagas.<br>This article presents a study on seroepidemiological, entomologic, and risk factors for domiciliary infestation in a circumscribed area infested with Triatoma maculata in Parroquia Xaguas, Urdaneta Municipality, Lara State, Venezuela. One hundred and forty households, 509 persons, and 110 dogs were sampled. Serum anti-Trypanosoma cruzi antibodies were determined by means of ELISA and MABA techniques using recombinant antigens. Tr. cruzi infection in the triatomines was determined by direct microscopy and PCR. According to the results, 1.57% of humans and 6.36% of dogs were positive for serum anti-Tr. cruzi antibodies. Triatomine species were: 97.98% T. maculata, 1.65% Eratyrus mucronatus, and 0.37% Panstrongylus geniculatus. Vector indices were: 0.36% vector infection, 16.4% household infestation, 39.1% household colonization, 8.6% household co-infestation, and 100% vector dispersion. Domiciliary and peridomiciliary infestation was associated with the presence of chickens and disorderly goat corrals, chicken coops, and domiciliary distribution. The results strongly suggest that T. maculata is the predominant Tr. cruzi vector in the area and that due to its capacity to infest and colonize human dwellings, it could be involved in Chagas' disease transmission