Frequência e etiologia da mastite caprina na região do Cariri paraibano

Com o objetivo de estimar a freqüência da mastite caprina e de identificar os principais agentes etiológicos envolvidos na infecção da glândula mamária de cabras leiteiras na Região do Cariri Paraibano, foram examinadas 654 metades mamárias de 327 cabras, provenientes de 15 propriedades. A glândula mamária das cabras em lactação foi examinada e o leite submetido aos testes da caneca telada e do CMT. Nenhuma metade mamária apresentou alteração no exame clínico. Das 654 amostras de leite analisadas, uma (0,15%) apresentou alteração no teste da caneca telada, indicando mastite clínica, e 201 (30,70%) apresentaram algum grau de gelificação (1+, 2+ ou 3+) no teste do CMT, sendo procedida à coleta para lactocultura. Das 201 amostras cultivadas, 45 (22,39%) apresentaram crescimento bacteriano. 6,88% (45/654) das glândulas mamárias examinadas apresentavam mastite subclínica. Na lactocultura, isolouse Staphylococcus spp (84,44%), Streptococcus spp (4,44%), Bacillus spp. (4,44%), Micrococcus spp. (4,44%) e Bastonete Gram negativo (2,22%). Conclui-se que a mastite caprina na região do Cariri Paraibano apresenta o mesmo padrão de outras regiões do Brasil e do mundo, tendo o Staphylococcus spp. como principal agente causal; e que o CMT pode ser utilizado como teste de triagem da saúde da glândula mamária caprina, mas a lactocultura é o método mais indicado para o diagnóstico da mastite subclínica em cabras leiteiras

Significance of glycolytic metabolism-related protein expression in colorectal cancer, lymph node and hepatic metastasis

Background: Colorectal cancer (CRC) is one of the most common malignancies and a leading cause of cancer death worldwide. Most cancer cells display high rates of glycolysis with production of lactic acid, which is then exported to the microenvironment by monocarboxylate transporters (MCTs). The main aim of this study was to evaluate the significance of MCT expression in a comprehensive series of primary CRC cases, lymph node and hepatic metastasis. Methods: Expressions of MCT1, MCT4, CD147 and GLUT1 were studied in human samples of CRC, lymph node and hepatic metastasis, by immunohistochemistry. Results: All proteins were overexpressed in primary CRC, lymph node and hepatic metastasis, when compared with non-neoplastic tissue, with exception of MCT1 in lymph node and hepatic metastasis. MCT1 and MCT4 expressions were associated with CD147 and GLUT1 in primary CRC. These markers were associated with clinical pathological features, reflecting the putative role of these metabolism-related proteins in the CRC setting. Conclusion: These findings provide additional evidence for the pivotal role of MCTs in CRC maintenance and progression, and support the use of MCTs as biomarkers and potential therapeutic targets in primary and metastatic CRC.This work was supported by the Fundação para a Ciência e a Tecnologia (FCT) grant ref. PTDC/SAU-FCF/104347/2008, under the scope of ‘Programa Operacional Temático Factores de Competitividade’ (COMPETE) of ‘Quadro Comunitário de Apoio III’ and co-financed by the Fundo Europeu De Desenvolvimento Regional (FEDER). Ricardo Amorim was recipient of the fellowship SFRH/BD/98002/2013, from Fundação para a Ciência e a Tecnologia (FCT Portugal).info:eu-repo/semantics/publishedVersio

Ss-Sl2, a Novel Cell Wall Protein with PAN Modules, Is Essential for Sclerotial Development and Cellular Integrity of Sclerotinia sclerotiorum

The sclerotium is an important dormant body for many plant fungal pathogens. Here, we reported that a protein, named Ss-Sl2, is involved in sclerotial development of Sclerotinia sclerotiorum. Ss-Sl2 does not show significant homology with any protein of known function. Ss-Sl2 contains two putative PAN modules which were found in other proteins with diverse adhesion functions. Ss-Sl2 is a secreted protein, during the initial stage of sclerotial development, copious amounts of Ss-Sl2 are secreted and accumulated on the cell walls. The ability to maintain the cellular integrity of RNAi-mediated Ss-Sl2 silenced strains was reduced, but the hyphal growth and virulence of Ss-Sl2 silenced strains were not significantly different from the wild strain. Ss-Sl2 silenced strains could form interwoven hyphal masses at the initial stage of sclerotial development, but the interwoven hyphae could not consolidate and melanize. Hyphae in these interwoven bodies were thin-walled, and arranged loosely. Co-immunoprecipitation and yeast two-hybrid experiments showed that glyceraldehyde-3-phosphate dehydrogenase (GAPDH), Woronin body major protein (Hex1) and elongation factor 1-alpha interact with Ss-Sl2. GAPDH-knockdown strains showed a similar phenotype in sclerotial development as Ss-Sl2 silenced strains. Hex1-knockdown strains showed similar impairment in maintenance of hyphal integrity as Ss-Sl2 silenced strains. The results suggested that Ss-Sl2 functions in both sclerotial development and cellular integrity of S. sclerotiorum