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Animals as potential reservoirs for dengue transmission: A systematic review

期刊

ONE HEALTH
卷 12, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.onehlt.2021.100216

关键词

Dengue infection; Animal reservoir; Enzootic transmission; Systematic review

资金

  1. Ministry of Defence, Singapore [N-608-000-065-001]
  2. Fulbright United States-ASEAN Visiting Scholar Award [PS00266705]

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Dengue virus positivity has been detected in various animals, primarily in bats, non-human primates, and pigs. Serological testing suggests possible enzootic transmission, while regular dengue virus spillback cannot be ruled out. Acute infections among animals are limited, indicating the need for further investigation into the potential role of animals in dengue transmission.
Dengue is a rapidly spreading mosquito-borne flavivirus infection that is prevalent in tropical and sub-tropical regions. Humans are known to be the main reservoir host maintaining the epidemic cycles of dengue but it is unclear if dengue virus is also maintained in a similar enzootic cycle. The systematic review was conducted in accordance to Cochrane's PRISMA recommendations. A search was done on PubMed, EMBASE, Scopus and Cochrane Library. Key data on animal dengue positivity was extracted and classified according to animal type and diagnostic modes. Of the 3818 articles identified, 56 articles were used in this review. A total of 16,333 animals were tested, 1817 of which were positive for dengue virus by RT-PCR or serology. Dengue positivity was detected in bats (10.1%), non-human primates (27.3%), birds (11%), bovid (4.1%), dogs (1.6%), horses (5.1%), pigs (34.1%), rodents (3.5%), marsupials (13%) and other small animals (7.3%). While majority of dengue positivity via serology suggests potential enzootic transmission, but regular dengue virus spillback cannot be excluded. With the exception of bats, acute infection among animals is limited. Further investigation on animals is critically required to better understand their role as potential reservoir in dengue transmission.

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