Abstract

BackgroundA Chikungunya (CHIK) outbreak hit La Réunion Island in 2005–2006. The implicated vector was Aedes albopictus. Here, we present the first study on the susceptibility of Ae. albopictus populations to sympatric CHIKV isolates from La Réunion Island and compare it to other virus/vector combinations.Methodology and FindingsWe orally infected 8 Ae. albopictus collections from La Réunion and 3 from Mayotte collected in March 2006 with two Chikungunya virus (CHIKV) from La Réunion: (i) strain 05.115 collected in June 2005 with an Alanine at the position 226 of the glycoprotein E1 and (ii) strain 06.21 collected in November 2005 with a substitution A226V. Two other CHIKV isolates and four additional mosquito strains/species were also tested. The viral titer of the infectious blood-meal was 107 plaque forming units (pfu)/mL. Dissemination rates were assessed by immunofluorescent staining on head squashes of surviving females 14 days after infection. Rates were at least two times higher with CHIKV 06.21 compared to CHIKV 05.115. In addition, 10 individuals were analyzed every day by quantitative RT-PCR. Viral RNA was quantified on (i) whole females and (ii) midguts and salivary glands of infected females. When comparing profiles, CHIKV 06.21 produced nearly 2 log more viral RNA copies than CHIKV 05.115. Furthermore, females infected with CHIKV 05.115 could be divided in two categories: weakly susceptible or strongly susceptible, comparable to those infected by CHIKV 06.21. Histological analysis detected the presence of CHIKV in salivary glands two days after infection. In addition, Ae. albopictus from La Réunion was as efficient vector as Ae. aegypti and Ae. albopictus from Vietnam when infected with the CHIKV 06.21.ConclusionsOur findings support the hypothesis that the CHIK outbreak in La Réunion Island was due to a highly competent vector Ae. albopictus which allowed an efficient replication and dissemination of CHIKV 06.21.

Highlights

  • First isolated in Tanzania in 1952 [1], Chikungunya virus (CHIKV) is a zoonotic arthropod-borne virus (Alphavirus genus, Togaviridae family) endemic to Africa, India and South-East Asia

  • We showed that (i) examined populations of Ae. albopictus from La Reunion and Mayotte exhibited differential susceptibilities to La Reunion CHIKV isolates, (ii) CHIKV 05.115 replication was restricted when compared to CHIKV 06.21, (iii) both CHIKV 05.115 and CHIKV 06.21 invaded salivary glands in a similar pattern, the crossing of midgut was the critical step in the susceptibility of Ae. albopictus to CHIKV isolates, (iv) females infected with CHIKV 05.115 could be divided in two categories: weakly susceptible or strongly susceptible, comparable to those infected by CHIKV 06.21 and (v) Ae. albopictus from La Reunion Island and Asian CHIKV vectors showed similar ability to support CHIKV 06.21 replication

  • Whereas CHIKV often circulated in Africa and Asia, it has never been reported in the Indian Ocean and in La Reunion Island where Ae. albopictus has been incriminated

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Summary

Introduction

First isolated in Tanzania in 1952 [1], Chikungunya virus (CHIKV) is a zoonotic arthropod-borne virus (Alphavirus genus, Togaviridae family) endemic to Africa, India and South-East Asia. Considered to be a secondary vector, Ae. albopictus (Skuse), the Asian ‘‘tiger mosquito’’, is involved in the CHIK outbreak in the Indian Ocean in 2005–2006 This species native from South-East Asia [7] has spread as far West as Madagascar and most islands in the Indian Ocean and East through the Indomalayan and Oriental regions. We present the first study on the susceptibility of Ae. albopictus populations to sympatric CHIKV isolates from La Reunion Island and compare it to other virus/vector combinations. Ae. albopictus from La Reunion was as efficient vector as Ae. aegypti and Ae. albopictus from Vietnam when infected with the CHIKV 06.21. Our findings support the hypothesis that the CHIK outbreak in La Reunion Island was due to a highly competent vector Ae. albopictus which allowed an efficient replication and dissemination of CHIKV 06.21

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