15 research outputs found
Recent Technological Advances and Strategies for Arbovirus Vector Control
In recent decades, we have seen the emergence and re-emergence of many arthropod-transmitted viruses (arboviruses) that pose important public health challenges worldwide [...
Two New Y-Linked Genes in Drosophila melanogaster
The Y chromosome and other heterochromatic regions present special challenges for genome sequencing and for the annotation of genes. Here we describe two new genes (ARY and WDY) on the Drosophila melanogaster Y, bringing its number of known single-copy genes to 12. WDY may correspond to the fertility factor kl-1
Biology of Triatoma klugi Carcavallo, Jurberg, Lent & GalvĂŁo 2001 (Heteroptera: Reduviidae) under laboratory conditions: Effects of distinct blood sources and susceptibility to Trypanosoma cruzi and Trypanosoma rangeli
The life cycle of Triatoma klugi  Carcavallo, Jurberg, Lent
& GalvĂŁo 2001 was compared under laboratory conditions using
two groups of the F1 generation obtained from field-collected bugs.
Among the 100 nymphs weekly fed on mice (Group A) or chicken (Group B),
77% of Group A and 67% of Group B reached the adult stage, and the mean
time from the first nymphal stage to adult was 190.08 ± 28.31 days
and 221.23 ± 40.50, respectively. The average span in days for
each stage per group and the number of blood meals required for each
stage were also evaluated. The overall mortality rate was 23% and 33%
for Groups A and B, respectively. The mean number of eggs laid per
month in a three-month period was of 56.20, 51.70 and 73.20 for Group
A, and 64.50, 53.50 and 38.71 for Group B. Despite the blood source,
comparative analysis revealed no statistically significant differences
in the life cycle of T. klugi under laboratory conditions. Infection
rates over 60% were observed for both Trypanosoma cruzi Â
strains tested. Even revealing high infection rates of the hemolymph by
T. rangeli strains, T. klugi revealed no salivary gland infections and
was not able to transmit the parasite
An Anopheles aquasalis GATA factor Serpent is required for immunity against Plasmodium and bacteria.
Innate immunity is an ancient and conserved defense system that provides an early effective response against invaders. Many immune genes of Anopheles mosquitoes have been implicated in defense against a variety of pathogens, including plasmodia. Nevertheless, only recent work identified some immune genes of Anopheles aquasalis mosquitoes upon P. vivax infection. Among these was a GATA transcription factor gene, which is described here. This is an ortholog of GATA factor Serpent genes described in Drosophila melanogaster and Anopheles gambiae. Gene expression analyses showed an increase of GATA-Serpent mRNA in P. vivax-infected A. aquasalis and functional RNAi experiments identified this transcription factor as an important immune gene of A. aquasalis against both bacteria and P. vivax. Besides, we were able to identify an effect of GATA-Serpent knockdown on A. aquasalis hemocyte proliferation and differentiation. These findings expand our understanding of the poorly studied A. aquasalis-P. vivax interactions and uncover GATA-Serpent as a key player of the mosquito innate immune response
Characterization of the complete mitogenome of Anopheles aquasalis, and phylogenetic divergences among Anopheles from diverse geographic zones.
Whole mitogenome sequences (mtDNA) have been exploited for insect ecology studies, using them as molecular markers to reconstruct phylogenies, or to infer phylogeographic relationships and gene flow. Recent Anopheles phylogenomic studies have provided information regarding the time of deep lineage divergences within the genus. Here we report the complete 15,393 bp mtDNA sequences of Anopheles aquasalis, a Neotropical human malaria vector. When comparing its structure and base composition with other relevant and available anopheline mitogenomes, high similarity and conserved genomic features were observed. Furthermore, 22 mtDNA sequences comprising anopheline and Dipteran sibling species were analyzed to reconstruct phylogenies and estimate dates of divergence between taxa. Phylogenetic analysis using complete mtDNA sequences suggests that A. aquasalis diverged from the Anopheles albitarsis complex ~28 million years ago (MYA), and ~38 MYA from Anopheles darlingi. Bayesian analysis suggests that the most recent ancestor of Nyssorhynchus and Anopheles + Cellia was extant ~83 MYA, corroborating current estimates of ~79-100 MYA. Additional sampling and publication of African, Asian, and North American anopheline mitogenomes would improve the resolution of the Anopheles phylogeny and clarify early continental dispersal routes