AI Article Synopsis

  • * A review of 29 global studies showed that reverse transcription PCR (RT-PCR) is the most common method for detecting dengue virus in mosquito larvae, with detection rates varying from 0% to 50%.
  • * To improve dengue control programs, there is a need for more sensitive and cost-effective active surveillance methods for early detection of the virus in larvae.

Article Abstract

The burden of dengue has emerged as a serious public health issue due to its impact on morbidity, mortality, and economic burden. Existing surveillance systems are inadequate to provide the necessary data for the prompt and efficient control of dengue. Passive surveillance of dengue cases may lead to underreporting and delayed mitigation responses. Improved dengue control program requires sensitive and proactive methods for early detection of dengue. We collected and reviewed existing research articles worldwide on detecting dengue virus in species larvae. Searches were conducted in PUBMED and Google Scholar, including all the studies published in English and Bahasa Indonesia. Twenty-nine studies were included in this review in terms of assay used, positivity rate, and dengue serotype detected. The presence of dengue virus in immature mosquitoes was mostly detected using reverse transcription PCR (RT-PCR) in pooled larvae. In one study, dengue virus was detected in larvae from laboratory-infected mosquitoes using enzyme-linked immunosorbent assay (ELISA). The positivity rate of dengue virus detection ranged from 0 to 50% in field-caught larvae. Although various methods can detect the dengue virus, further research encourages the use of low-cost and less laborious methods for active surveillance of dengue in larvae.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10975107PMC
http://dx.doi.org/10.3390/tropicalmed9030060DOI Listing

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