scholarly journals Vector competence of Aedes aegypti from Havana, Cuba, for dengue virus type 1, chikungunya, and Zika viruses

2020 ◽  
Vol 14 (12) ◽  
pp. e0008941
Author(s):  
Gladys Gutiérrez-Bugallo ◽  
Antoine Boullis ◽  
Yanet Martinez ◽  
Lyza Hery ◽  
Magdalena Rodríguez ◽  
...  

Background Like many countries from the Americas, Cuba is threatened by Aedes aegypti-associated arboviruses such as dengue (DENV), Zika (ZIKV), and chikungunya (CHIKV) viruses. Curiously, when CHIKV was actively circulating in the region in 2013–2014, no autochthonous transmission of this virus was detected in Havana, Cuba, despite the importation of chikungunya cases into this city. To investigate if the transmission ability of local mosquito populations could explain this epidemiological scenario, we evaluated for the first time the vector competence of two Ae. aegypti populations (Pasteur and Párraga) collected from Havana for dengue virus type 1 (DENV-1), CHIKV, and ZIKV. Methodology/Principal findings Mosquito populations were fed separately using blood containing ZIKV, DENV-1, or CHIKV. Infection, dissemination, and transmission rates, were estimated at 3 (exclusively for CHIKV), 7, and 14 days post exposure (dpe) for each Ae. aegypti population-virus combination. Both mosquito populations were susceptible to DENV-1 and ZIKV, with viral infection and dissemination rates ranging from 24–97% and 6–67% respectively. In addition, CHIKV disseminated in both populations and was subsequently transmitted. Transmission rates were low (<30%) regardless of the mosquito population/virus combination and no ZIKV was detected in saliva of females from the Pasteur population at any dpe. Conclusions/Significance Our study demonstrated the ability of Ae. aegypti from Cuba to transmit DENV, ZIKV, and CHIKV. These results, along with the widespread distribution and high abundance of this species in the urban settings throughout the island, highlight the importance of Ae. aegypti control and arbovirus surveillance to prevent future outbreaks.

2006 ◽  
Vol 100 (4) ◽  
pp. 327-336 ◽  
Author(s):  
A. Imrie ◽  
Z. Zhao ◽  
S. N. Bennett ◽  
P. Kitsutani ◽  
M. Laille ◽  
...  

iScience ◽  
2018 ◽  
Vol 6 ◽  
pp. 38-51 ◽  
Author(s):  
Carmen Koo ◽  
Wei Ping Tien ◽  
Helen Xu ◽  
Janet Ong ◽  
Jayanthi Rajarethinam ◽  
...  

2015 ◽  
Vol 4 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Sheng-Fan Wang ◽  
Ko Chang ◽  
Ruo-Wei Lu ◽  
Wen-Hung Wang ◽  
Yen-Hsu Chen ◽  
...  
Keyword(s):  

2010 ◽  
Vol 16 (11) ◽  
pp. 1783-1785 ◽  
Author(s):  
Boon-Teong Teoh ◽  
Sing-Sin Sam ◽  
Juraina Abd-Jamil ◽  
Sazaly AbuBakar
Keyword(s):  

2006 ◽  
Vol 12 (2) ◽  
pp. 343-346 ◽  
Author(s):  
Yoko Nukui ◽  
Shigeru Tajima ◽  
Akira Kotaki ◽  
Mikako Ito ◽  
Tomohiko Takasaki ◽  
...  
Keyword(s):  

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Mami Matsuda ◽  
Atsushi Yamanaka ◽  
Keigo Yato ◽  
Kentaro Yoshii ◽  
Koichi Watashi ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Yuanzhi Liu ◽  
Anchun Cheng ◽  
Mingshu Wang ◽  
Sai Mao ◽  
Xumin Ou ◽  
...  

Duck hepatitis A virus type 1 (DHAV-1) is one of the most deadly pathogens that endanger the duck industry. Most viruses usually turn off host translation after infection to facilitate viral replication and translation. For the first time report to our knowledge, DHAV-1 can induce eIF2α phosphorylation and inhibit cellular translation in duck embryo fibroblasts (DEFs). Moreover, the activity of DHAV-1 in the cells caused obvious eIF2α phosphorylation, which has nothing to do with the viral protein. Subsequently, we screened two kinases (PERK and GCN2) that affect eIF2α phosphorylation through inhibitors and shRNA. Notably, the role of GCN2 in other picornaviruses has not been reported. In addition, when the phosphorylation of eIF2α induced by DHAV-1 is inhibited, the translation efficiency of DEFs restores to a normal level, indicating that DHAV-1 induced cellular translation shutoff is dependent on eIF2α phosphorylation.


2021 ◽  
Vol 67 (02/2021) ◽  
Author(s):  
Juan Teng ◽  
Qingliang Wang ◽  
Xiaojie Li ◽  
Li Chen ◽  
Dayong Gu ◽  
...  

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