Literature DB >> 2891346

Multiplication and distribution of type 2 dengue and Japanese encephalitis viruses in Toxorhynchites splendens after intrathoracic inoculation.

N Yamamoto1, T Kimura, A Ohyama.   

Abstract

The nonhematophagous mosquito Toxorhynchites (Tx.) splendens was found to be the most susceptible to type 2 dengue (D-2) and Japanese encephalitis (JEV) viruses among three hosts examined by virus titration and replication assays. After inoculation with D-2, the number of viral antigen positive cells in the head, thorax and abdomen increased up to day 15 and D-2 reached the maximum titer of 8.4 log10 PFU/g in the head on day 15. Hemocytes were the earliest cell type that could be detected as D-2 antigen positive on day 2. Multiplication of JEV was faster than that of D-2 in the mosquito. The number of JEV antigen positive cells in each part of the mosquito increased up to day 3, JEV reaching the maximum titer of 8.0 log10 PFU/g in the abdomen on day 3. Hemocytes and fat body cells (FBC) could be detected as JEV antigen positive cells on day 1. The time course of D-2 and JEV infection suggested that intrathoracically inoculated viruses were probably initially phagocytosed by hemocytes and/or FBC, and multiplied primarily in their cytoplasm. The infected hemocytes were then transported by the flow of body fluid and viruses were disseminated to other susceptible organs, such as ganglia, salivary glands, etc. The results obtained indicate that the course of infection of D-2 and JEV in Tx. splendens is similar to that in vector mosquitoes. Tx. splendens is therefore very useful for the study of these viruses.

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Year:  1987        PMID: 2891346     DOI: 10.1007/bf01310732

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  18 in total

1.  Japanese B encephalitis virus in the organs of infected mosquitoes.

Authors:  L C LAMOTTE
Journal:  Am J Hyg       Date:  1960-07

2.  A simple technique for the detection of dengue antigen in mosquitoes by immunofluorescence.

Authors:  T T Kuberski; L Rosen
Journal:  Am J Trop Med Hyg       Date:  1977-05       Impact factor: 2.345

3.  Studies on the mode of development of Japanese encephalitis virus in some groups of mosquitoes by the fluorescent antibody technique.

Authors:  R Doi
Journal:  Jpn J Exp Med       Date:  1970-04

4.  The use of mosquitoes to detect and propagate dengue viruses.

Authors:  L Rosen; D Gubler
Journal:  Am J Trop Med Hyg       Date:  1974-11       Impact factor: 2.345

5.  Detection of dengue virus by immunofluorescence following inoculation of mosquito larvae.

Authors:  T Pang; S K Lam; C B Chew; G K Poon; S Ramalingam
Journal:  Lancet       Date:  1983-06-04       Impact factor: 79.321

6.  Evaluation of Toxorhynchites splendens (Diptera: Culicidae) as a bioassay host for dengue viruses.

Authors:  D M Watts; B A Harrison; A Nisalak; R M Scott; D S Burke
Journal:  J Med Entomol       Date:  1982-01-28       Impact factor: 2.278

7.  Replication of dengue-2 virus in Aedes albopictus mosquitoes. An electron microscopic study.

Authors:  S Sriurairatna; N Bhamarapravati
Journal:  Am J Trop Med Hyg       Date:  1977-11       Impact factor: 2.345

8.  Comparative susceptibility of mosquito species and strains to oral and parenteral infection with dengue and Japanese encephalitis viruses.

Authors:  L Rosen; L E Roseboom; D J Gubler; J C Lien; B N Chaniotis
Journal:  Am J Trop Med Hyg       Date:  1985-05       Impact factor: 2.345

9.  The use of Toxorhynchites mosquitoes to detect and propagate dengue and other arboviruses.

Authors:  L Rosen
Journal:  Am J Trop Med Hyg       Date:  1981-01       Impact factor: 2.345

10.  The distribution and development of eastern equine encephalitis virus in its enzootic mosquito vector, Culiseta melanura.

Authors:  T W Scott; S W Hildreth; B J Beaty
Journal:  Am J Trop Med Hyg       Date:  1984-03       Impact factor: 2.345

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