scholarly journals Potential of laticifer fluids for inhibiting Aedes aegypti larval development: evidence for the involvement of proteolytic activity

2009 ◽  
Vol 104 (6) ◽  
pp. 805-812 ◽  
Author(s):  
Márcio V Ramos ◽  
Danielle A Pereira ◽  
Diego P Souza ◽  
Eliane S Araújo ◽  
Cléverson DT Freitas ◽  
...  
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ottavia Romoli ◽  
Johan Claes Schönbeck ◽  
Siegfried Hapfelmeier ◽  
Mathilde Gendrin

AbstractThe mosquito microbiota impacts the physiology of its host and is essential for normal larval development, thereby influencing transmission of vector-borne pathogens. Germ-free mosquitoes generated with current methods show larval stunting and developmental deficits. Therefore, functional studies of the mosquito microbiota have so far mostly been limited to antibiotic treatments of emerging adults. In this study, we introduce a method to produce germ-free Aedes aegypti mosquitoes. It is based on reversible colonisation with bacteria genetically modified to allow complete decolonisation at any developmental stage. We show that, unlike germ-free mosquitoes previously produced using sterile diets, reversibly colonised mosquitoes show no developmental retardation and reach the same size as control adults. This allows us to uncouple the study of the microbiota in larvae and adults. In adults, we detect no impact of bacterial colonisation on mosquito fecundity or longevity. In larvae, data from our transcriptome analysis and diet supplementation experiments following decolonisation suggest that bacteria support larval development by contributing to folate biosynthesis and by enhancing energy storage. Our study establishes a tool to study the microbiota in insects and deepens our knowledge on the metabolic contribution of bacteria to mosquito development.


Biochimie ◽  
2015 ◽  
Vol 112 ◽  
pp. 172-186 ◽  
Author(s):  
Daniele Yumi Sasaki ◽  
Ana Cristina Jacobowski ◽  
Antônio Pancrácio de Souza ◽  
Marlon Henrique Cardoso ◽  
Octávio Luiz Franco ◽  
...  

2011 ◽  
Vol 5 (11) ◽  
pp. e1369 ◽  
Author(s):  
Ranjan Ramasamy ◽  
Sinnathamby N. Surendran ◽  
Pavilupillai J. Jude ◽  
Sangaralingam Dharshini ◽  
Muthuladchumy Vinobaba

2019 ◽  
Vol 56 (6) ◽  
pp. 1739-1744 ◽  
Author(s):  
Barbara Aparecida Chaves ◽  
Ademir Bentes Vieira Junior ◽  
Karine Renata Dias Silveira ◽  
Andreia da Costa Paz ◽  
Evelyn Beatriz da Costa Vaz ◽  
...  

Abstract Zika virus (ZIKV) has emerged as a globally important arbovirus and has been reported from all states of Brazil. The virus is primarily transmitted to humans through the bite of an infective Aedes aegypti (Linnaeus, 1762) or Aedes albopictus (Skuse, 1895). However, it is important to know if ZIKV transmission also occurs from Ae. aegypti through infected eggs to her offspring. Therefore, a ZIKV and dengue virus (DENV) free colony was established from eggs collected in Manaus and maintained until the third–fourth generation in order to conduct ZIKV vertical transmission (VT) experiments which used an infectious bloodmeal as the route of virus exposure. The eggs from ZIKV-infected females were allowed to hatch. The resulting F1 progeny (larvae, pupae, and adults) were quantitative polymerase chain reaction (qPCR) assayed for ZIKV. The viability of ZIKV vertically transmitted to F1 progeny was evaluated by cultivation in C6/36 cells. The effects of ZIKV on immature development of Ae. aegypti was assessed and compared with noninfected mosquitoes. AmazonianAe. aegypti were highly susceptible to ZIKV infection (96.7%), and viable virus passed to their progeny via VT. Moreover, eggs from the ZIKV-infected mosquitoes had a significantly lower hatch rate and the slowest hatching. In addition, the larval development period was slower when compared to noninfected, control mosquitoes. This is the first study to illustrate VT initiated by oral infection of the parental population by using mosquitoes, which originated from the field and a ZIKV strain that is naturally circulating in-country. Additionally, this study suggests that ZIKV present in the Ae. aegypti can modify the mosquito life cycle. The data reported here suggest that VT of ZIKV to progeny from naturally infected females may have a critical epidemiological role in the dissemination and maintenance of the virus circulating in the vector.


2019 ◽  
Vol 116 (43) ◽  
pp. 21501-21507 ◽  
Author(s):  
Guan-Heng Zhu ◽  
Yaoyu Jiao ◽  
Shankar C. R. R. Chereddy ◽  
Mi Young Noh ◽  
Subba Reddy Palli

The yellow fever mosquito, Aedes aegypti, vectors human pathogens. Juvenile hormones (JH) control almost every aspect of an insect’s life, and JH analogs are currently used to control mosquito larvae. Since RNA interference does not work efficiently during the larval stages of this insect, JH regulation of larval development and mode of action of JH analogs are not well studied. To overcome this limitation, we used a multiple single guide RNA-based CRISPR/Cas9 genome-editing method to knockout the methoprene-tolerant (Met) gene coding for a JH receptor. The Met knockout larvae exhibited a black larval phenotype during the L3 (third instar larvae) and L4 (fourth instar larvae) stages and died before pupation. However, Met knockout did not affect embryonic development or the L1 and L2 stages. Microscopy studies revealed the precocious synthesis of a dark pupal cuticle during the L3 and L4 stages. Gene expression analysis showed that Krüppel homolog 1, a key transcription factor in JH action, was down-regulated, but genes coding for proteins involved in melanization, pupal and adult cuticle synthesis, and blood meal digestion in adults were up-regulated in L4 Met mutants. These data suggest that, during the L3 and L4 stages, Met mediates JH suppression of pupal/adult genes involved in the synthesis and melanization of the cuticle and blood meal digestion. These results help to advance our knowledge of JH regulation of larval development and the mode of action of JH analogs in Ae. aegypti.


2016 ◽  
Vol 9 (1) ◽  
Author(s):  
Igor Adolfo Dexheimer Paploski ◽  
Moreno S. Rodrigues ◽  
Vánio André Mugabe ◽  
Mariana Kikuti ◽  
Aline S. Tavares ◽  
...  

1973 ◽  
Vol 105 (3) ◽  
pp. 433-436 ◽  
Author(s):  
R. H. Gooding ◽  
A. C. Cheung ◽  
B. M. Rolseth

AbstractHoney inhibits esterolytic and proteolytic activity of trypsin from Aedes aegypti, Culex pipiens quinquefasciatus, and cattle. The inhibitor is heat stable and only a portion of the inhibition capacity is lost from the honey by dialysis. Glucose, fructose, and sucrose have no effect upon trypsin but ascorbic acid and riboflavin are inhibitory while gluconic acid is an activator. Nectar from lilies but not from honeysuckles inhibits C. pipiens quinquefasciatus trypsin.


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