Abundance of Procamallanus (Spirocamallanus) inopinatus (Nematoda: Camallanidae) in Characiformes fish and associated factors in Midwest Brazil.

The success of Procamallanus (Spirocamallanus) inopinatus infection in fish involves a complexity of variables. This study aims to evaluate the relationship between abundance of P. (S.) inopinatus with biometric and somatic parameters, sex, relative condition factor (Kn) and hosts diet, as well as to evaluate length relationship of the parasites and the hosts. The fishes were collected by the mesh method and data, length, weight, sex, gonad and liver weight, Gonadosomatic index (GSI) and hepatosomatic index (HSI), Kn and stomach content were recorded. Twenty-seven specimens of P. (S.) inopinatus were collected in the intestine from Serrasalmus rhombeus and 52 from Leporinus friderici. In general, the prevalence, mean intensity and mean abundance of infection was higher in L. friderici. The total abundance was explained by the variables GSI, HSI total length, gonad and liver weight. Fish relative condition factor (kn) and sex were not influenced by the infection, being that the parasite infection did not impair the body condition of the hosts. There is no relationship between host length and parasite length in any of the evaluated fish species. On average, S. rhombeus parasites are 0.69 cm larger than L. friderici parasites.

Eomes expression reports the progressive differentiation of IFN-γ-producing Th1-like γδ T cells.

The transcription factor Eomesodermin (Eomes) plays a crucial role in regulating cytotoxic function, development, and survival of immune cells. γδ T cells can express Eomes, but its contribution to their differentiation is unknown. Using Eomes-IRES-GFP mice, we show that Eomes+ γδ T cells are unequally distributed among organs, with the highest proportion in spleen. While the majority of Eomes+ γδ T cells expressed Vγ1+ and Vγ4+ TCRs, Eomes was absent in Vγ5+ , Vγ6+ , and Vγ7+ subsets. Moreover, Eomes was co-expressed in γδ T cells with Th1 lineage-related factors such as CD27, T-bet, and Ly6C, but not with Th17 lineage-related genes. Eomes+ and Eomes- γδ T-cell populations showed distinct gene expression profiles, with an increase of cytotoxic-related genes in Eomes+ γδ T cells. Furthermore, Eomes could be induced in peripheral γδ T cells by IL-12 and IL-4, and Eomes+ γδ T cells presented a higher proliferation rate and IFN-γ production when stimulated in vitro with IL-12 and IL-18. However, γδ T cells with very high Eomes levels displayed an exhausted phenotype with high levels of PD-1, and were less capable of IFN-γ production. Together, this study highlights Eomes as a marker for the differentiation of Th1-like effector γδ T cells.

Exposure to Aedes aegypti Bites Induces a Mixed-Type Allergic Response following Salivary Antigens Challenge in Mice.

Classical studies have shown that Aedes aegypti salivary secretion is responsible for the sensitization to mosquito bites and many of the components present in saliva are immunogenic and capable of inducing an intense immune response. Therefore, we have characterized a murine model of adjuvant-free systemic allergy induced by natural exposure to mosquito bites. BALB/c mice were sensitized by exposure to A. aegypti mosquito bites and intranasally challenged with phosphate-buffered saline only or the mosquito's salivary gland extract (SGE). Blood, bronchoalveolar lavage (BAL) and lung were collected and evaluated for cellularity, histopathological analyses, cytokines and antibody determination. Respiratory pattern was analyzed by Penh measurements and tracheal segments were obtained to study in vitro reactivity to methacholine. BAL recovered from sensitized mice following challenge with SGE showed an increased number of eosinophils and Th2 cytokines such as IL-4, IL-5 and IL-13. Peribronchoalveolar eosinophil infiltration, mucus and collagen were also observed in lung parenchyma of sensitized mice, suggesting the development of a typical Th2 response. However, the antibody profile in serum of these mice evidenced a mixed-type response with presence of both, IgG1/IgE (Th2-related) and IgG2a (Th1-related) isotypes. In addition, changes in breathing pattern and tracheal reactivity to methacholine were not found. Taken together, our results show that A. aegypti bites trigger an atypical allergic reaction, with some classical cellular and soluble Th2 components in the lung, but also systemic Th1 and Th2 antibody isotypes and no change in either the respiratory pattern or the trachea responsiveness to agonist.