Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
The endosymbiotic bacterium blocks replication of several arboviruses in transinfected mosquitoes. However, the mechanism of virus blocking remains poorly understood. Here, we characterized an gene from , which is rapidly induced in response to dengue virus (DENV) infection. Knocking down using antisense RNA in -transinfected mosquito cell lines and mosquitoes led to increased DENV replication. Furthermore, overexpression of RNase HI, in the absence of , led to reduced replication of a positive sense RNA virus, but had no effect on a negative sense RNA virus, a familiar scenario in -infected cells. Altogether, our results provide compelling evidence for the missing link between early -mediated virus blocking and degradation of viral RNA. These findings and the successful pioneered knockdown of genes using antisense RNA in cell line and mosquitoes enable new ways to manipulate and study the complex endosymbiont-host interactions.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830209 | PMC |
http://dx.doi.org/10.1016/j.isci.2022.105836 | DOI Listing |
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