Urban wild meat consumption and trade in Central Amazonia

The switch from hunting wild meat for home consumption to supplying more lucrative city marketsin Amazonia can adversely affect some game species. Despite this, information on the amounts of wild meateaten in Amazonian cities is still limited. We estimated wild meat consumption rates in 5 cities in the State ofAmazonas in Brazil through 1046 door-to-door household interviews conducted from 2004 to 2012. With thesedata, we modeled the relationship between wild meat use and a selection of socioeconomic indices. We thenscaled up our model to determine the amounts of wild meat likely to be consumed annually in the 62 urbancenters in central Amazonia. A total of 80.3% of all interviewees reported consuming wild meat during an averageof 29.3 (CI 11.6) days per year. Most wild meat was reported as bought in local markets (80.1%) or hunted by afamily member (14.9%). Twenty-one taxa were cited as consumed, mostly mammals (71.6%), followed by reptiles(23.2%) and then birds (5.2%). The declared frequency of wild meat consumption was positively correlated withthe proportion of rural population as well as with the per capita gross domestic product of the municipality(administrative divisions) where the cities were seated. We estimated that as much as 10,691 t of wild meat mightbe consumed annually in the 62 urban centers within central Amazonia, the equivalent of 6.49 kg per person peryear. In monetary terms, this amounts to US$21.72 per person per year or US$35.1 million overall, the latter figureis comparable to fish and timber production in the region. Given this magnitude of wild meat trade in centralAmazonia, it is fundamental to integrate this activity into the formal economy and actively develop policies thatallow the trade of more resilient taxa and restrict trade in species sensitive to hunting

Complex SUMO-1 Regulation of Cardiac Transcription Factor Nkx2-5

Reversible post-translational protein modifications such as SUMOylation add complexity to cardiac transcriptional regulation. The homeodomain transcription factor Nkx2-5/Csx is essential for heart specification and morphogenesis. It has been previously suggested that SUMOylation of lysine 51 (K51) of Nkx2-5 is essential for its DNA binding and transcriptional activation. Here, we confirm that SUMOylation strongly enhances Nkx2-5 transcriptional activity and that residue K51 of Nkx2-5 is a SUMOylation target. However, in a range of cultured cell lines we find that a point mutation of K51 to arginine (K51R) does not affect Nkx2-5 activity or DNA binding, suggesting the existence of additional Nkx2-5 SUMOylated residues. Using biochemical assays, we demonstrate that Nkx2-5 is SUMOylated on at least one additional site, and this is the predominant site in cardiac cells. The second site is either non-canonical or a “shifting” site, as mutation of predicted consensus sites and indeed every individual lysine in the context of the K51R mutation failed to impair Nkx2-5 transcriptional synergism with SUMO, or its nuclear localization and DNA binding. We also observe SUMOylation of Nkx2-5 cofactors, which may be critical to Nkx2-5 regulation. Our data reveal highly complex regulatory mechanisms driven by SUMOylation to modulate Nkx2-5 activity

Comparative genomics of the major parasitic worms

Parasitic nematodes (roundworms) and platyhelminths (flatworms) cause debilitating chronic infections of humans and animals, decimate crop production and are a major impediment to socioeconomic development. Here we report a broad comparative study of 81 genomes of parasitic and non-parasitic worms. We have identified gene family births and hundreds of expanded gene families at key nodes in the phylogeny that are relevant to parasitism. Examples include gene families that modulate host immune responses, enable parasite migration though host tissues or allow the parasite to feed. We reveal extensive lineage-specific differences in core metabolism and protein families historically targeted for drug development. From an in silico screen, we have identified and prioritized new potential drug targets and compounds for testing. This comparative genomics resource provides a much-needed boost for the research community to understand and combat parasitic worms

PARTICIPATION OF TICKS IN THE INFECTIOUS CYCLE OF CANINE VISCERAL LEISHMANIASIS, IN TERESINA, PIAUÍ, BRAZIL

In this study, we detected Leishmania spp. infection in R. sanguineus collected from dogs that were naturally infected with L. (L.) infantum. We examined 35 dogs of both sexes and unknown ages. The infected dogs were serologically positive by the immunofluorescence antibody test (IFAT), enzyme-linked immunosorbent assay (ELISA), and Quick Test-DPP (Dual Path Platform), as well as parasitological examination of a positive skin biopsy or sternal bone marrow aspiration. Ten negative dogs were included as controls. The ticks that infested these dogs were collected in pools of 10 adult females per animal. The PCR was performed with specific primers for Leishmania spp., which amplified a 720-bp fragment. Of the 35 analyzed samples, a product was observed in eight samples (8/35; 22.9%). We conclude that the presence of parasite DNA suggests that ticks participate in the zoonotic cycle of canine visceral leishmaniasis, in the city of Teresina, Piauí