Implementation of the artificial feeders in hematophagous arthropod research cooperates to the vertebrate animal use replacement, reduction and refinement (3Rs) principle

Vector-borne diseases are transmitted to humans by hematophagous arthropods and these blood-sucking organisms are target to researches worldwide. The laboratory colonization of these species is an important factor in the development of innovative strategies to control these vectors. However, this maintenance requires blood to make these invertebrates able to complete their life cycle. Although live vertebrate animals are frequently used for this feeding procedure, artificial feeders are available as potential alternatives to replace the use of live animals in some situations, especially in vector colony maintenance. The aim of this commentary is to discuss the use of artificial feeding methods concerning the 3Rs principle application. The scientific community focused on vector-borne diseases studies needs to strongly consider these artificial feeding options as a bioethical alternative to maintain blood-feeding arthropods in laboratory

Expression analyses of Plasmodium sp. Circumsporozoite protein regions in Plasmodium gallinaceum infected Aedes aegypti.

Mosquitos transgênicos incapazes de transmitir malária podem ser um controle alternativo, mas atualmente não estão disponíveis. O estudo da interação mosquitopatógeno é importante para melhorar o desenho de genes. A proteína circumsporozoita (CSP) tem dois domínios conservados que podem estar envolvidos na penetração dos esporozoítos na glândula salivar. Nosso objetivo foi expressar peptídeos contendo essas regiões na hemolinfa do mosquito usando o sistema de expressão transiente vírus Sindbis e a tecnologia de transgênese. Se a CSP está envolvida neste processo, os peptídeos competirão com spz impedindo a penetração. Cinco vírus sindbis e quatro linhagens transgênicas foram construídos e desafiados por P. gallinaceum. Nossos resultados mostram que os peptídeos não impediram a penetração de spz na glândula salivar, principalmente porque os peptídeos recombinantes não foram produzidos ou detectados. Aprimorar o desenho de genes, usando a otimização de códons e outras tecnologias, será essencial para a expressão de proteínas exógenas em mosquitos transgênicos.Transgenic mosquitoes that impair malaria transmission can be an alternative control but currently an effective line is not available. A better understanding of mosquito interaction with pathogens is very important to improve refractory transgene design. Circumsporozoite protein (CSP) has two conserved domains that could be involved in spz penetration into mosquito salivary glands. Our aim was to express peptides encompassing these conserved regions in the mosquito hemolymph using Sindbis virus transient expression system and transgenesis technology. If CSP is involved in this process these peptides will compete with sporozoites impairing its penetration. Five Sindbis virus and four transgenic lines were constructed and challenged with P. gallinaceum. Our results showed these peptides could not impair sporozoites penetration in salivary glands, mainly because the recombinant proteins could not be produced or detected. Improving transgene design using codon usage and other technologies will be essential for expressing foreign proteins in transgenic mosquitoes

Sex determination and Aedes population control

Abstract The global economic cost of Aedes-borne diseases, such as dengue, is estimated to be in the billions of dollars annually. In this scenario, a sustained vector control strategy is the only alternative to control dengue, as well as other diseases transmitted by Aedes, including Zika and chikungunya. The use of transgenic mosquitoes is a promising weapon in the improvement of approaches currently applied in Aedes aegypti control. Field trials using genetically modified mosquitoes for population control have been conducted and offer an excellent opportunity to evaluate what can be improved. In a mass-rearing mosquito facility, the absence of a transgenic line that produces male-only progeny is undoubtedly a limiting factor; thus, being able to manipulate sex determination in this species is a fundamental step for the success of this strategy. Likewise, the possibility of manipulation of the sex determination pathway opens-up a new opportunity for disease control

Aedes aegypti D7 long salivary proteins modulate blood feeding and parasite infection

Mosquito saliva facilitates blood meal acquisition through pharmacologically active compounds that prevent host hemostasis and immune responses. Here, we generated two knockout (KO) mosquito lines by CRISPR/Cas9 to functionally characterize D7L1 and D7L2, two abundantly expressed salivary proteins from the yellow fever mosquito vector Aedes aegypti. The D7s bind and scavenge biogenic amines and eicosanoids involved in hemostasis at the bite site. The absence of D7 proteins in the salivary glands of KO mosquitoes was confirmed by mass spectrometry, enzyme-linked immunosorbent assay, and fluorescence microscopy of the salivary glands with specific antibodies. D7-KO mosquitoes had longer probing times than parental wildtypes. The differences in probing time were abolished when mutant mice resistant to inflammatory insults were used. These results confirmed the role of D7 proteins as leukotriene scavengers in vivo. We also investigated the role of D7 salivary proteins in Plasmodium gallinaceum infection and transmission. Both KO lines had significantly fewer oocysts per midgut. We hypothesize that the absence of D7 proteins in the midgut of KO mosquitoes might be responsible for creating a harsh environment for the parasite. The information generated by this work highlights the biological functionality of salivary gene products in blood feeding and pathogen infection. IMPORTANCE: During blood feeding, mosquitoes inject saliva into the host skin, preventing hemostasis and inflammatory responses. D7 proteins are among the most abundant components of the saliva of blood-feeding arthropods. Aedes aegypti, the vector of yellow fever and dengue, expresses two D7 long-form salivary proteins: D7L1 and D7L2. These proteins bind and counteract hemostatic agonists such as biogenic amines and leukotrienes. D7L1 and D7L2 knockout mosquitoes showed prolonged probing times and carried significantly less Plasmodium gallinaceum oocysts per midgut than wild-type mosquitoes. We hypothesize that reingested D7s play a vital role in the midgut microenvironment with important consequences for pathogen infection and transmission.This research was supported by the Division of Intramural Research Program of the NIH/NIAID (AI001246, to E.C.) and by a subcontract from grant 1R01AI099483 (to Z.N.A.)S

nanos-Driven expression of piggyBac transposase induces mobilization of a synthetic autonomous transposon in the malaria vector mosquito, Anopheles stephensi.

Transposons are a class of selfish DNA elements that can mobilize within a genome. If mobilization is accompanied by an increase in copy number (replicative transposition), the transposon may sweep through a population until it is fixed in all of its interbreeding members. This introgression has been proposed as the basis for drive systems to move genes with desirable phenotypes into target species. One such application would be to use them to move a gene conferring resistance to malaria parasites throughout a population of vector mosquitos. We assessed the feasibility of using the piggyBac transposon as a gene-drive mechanism to distribute anti-malarial transgenes in populations of the malaria vector, Anopheles stephensi. We designed synthetic gene constructs that express the piggyBac transposase in the female germline using the control DNA of the An. stephensi nanos orthologous gene linked to marker genes to monitor inheritance. Two remobilization events were observed with a frequency of one every 23 generations, a rate far below what would be useful to drive anti-pathogen transgenes into wild mosquito populations. We discuss the possibility of optimizing this system and the impetus to do so

Correction: Laboratory strains of Aedes aegypti are competent to Brazilian Zika virus.

[This corrects the article DOI: 10.1371/journal.pone.0171951.]

Mosquito pornoscopy: Observation and interruption of <i>Aedes aegypti</i> copulation to determine female polyandric event and mixed progeny

<div><p>Ades aegypti is the most important arbovirus vector in the world, and new strategies are under evaluation. Biological studies mentioning the occurrence of a second mate in <i>Aedes aegypti</i> can interfere with vector control program planning, which involves male mosquito release technique. This study presents different experiments to show the occurrence of mixed progeny. Mixed male crosses (using a combination of different type of males in confinement with virgin females) showed no polyandric female. Individual crosses with male substitution in every gonotrophic cycle also did not show any polyandric female. Individual crosses with a 20 minutes interval, with subsequent male change, showed that only a few females presented mixed offspring. The copulation breach in three different moments, group A with full coitus length, group B the coitus was interrupted in 5–7 seconds after the start; and group C, which the copulation was interrupted 3 seconds after started. In summary, group A showed a majority of unique progeny from the first male; group B showed the higher frequency of mixed offspring and group C with the majority of the crosses belonging to the second male. To conclude, the occurrence of a viable second mate and mixed offspring is only possible when the copulation is interrupted; otherwise, the first mate is responsible for mixed progeny.</p></div

Laboratory strains of <i>Aedes aegypti</i> are competent to Brazilian Zika virus

<div><p>The Zika virus outbreaks are unprecedented human threat in relation to congenital malformations and neurological/autoimmune complications. Since this virus has high potential to spread in regions presenting the vectors, improvement in mosquito control is a top priority. Thus, <i>Aedes aegypti</i> laboratory strains will be fundamental to support studies in different research fields implicated on Zika-mosquito interactions which are the basis for the development of innovative control methods. In this sense, our aim was to determine the main infection aspects of a Brazilian Zika strain in reference <i>Aedes aegypti</i> laboratory mosquitoes. We orally exposed Rockefeller, Higgs and Rexville mosquitoes to the Brazilian ZIKV (ZIKV^BR) and qRT-PCR was applied to determine the infection, dissemination and detection rates of ZIKV in the collected saliva as well as viral levels in mosquito tissues. The three strains sustain the virus development but Higgs showed significantly lower viral loads in bodies at 14 days post-infection (dpi) and the lowest prevalences in bodies and heads. The Rockefeller strain was the most susceptible at 7 dpi but similar dissemination rates were observed at 14 dpi. Although variations exist, the ZIKV^BR RNA shows detectable levels in saliva of the three strains at 14 dpi but is only detected in Rockefeller at 7 dpi. Moreover, saliva samples from the three strains were confirmed to be infectious when intrathoracically injected into mosquitoes. The ZIKV^BR kinetics was monitored in Rockefeller mosquitoes and virus could be identified in the heads at 4 dpi but was more consistently detected late in infection. Our study presents the first evaluation on how Brazilian Zika virus behaves in reference <i>Aedes aegypti</i> strains and shed light on how the infection evolves over time. Vector competence and hallmarks of the ZIKV^BR development were revealed in laboratory mosquitoes, providing additional information to accelerate studies focused on ZIKV-mosquito interactions.</p></div

Average number of eggs, mean hatch rate and number of crosses with mixed/unique type of progeny in 20 minutes interval for first male cross.

<p>Average number of eggs, mean hatch rate and number of crosses with mixed/unique type of progeny in 20 minutes interval for first male cross.</p