Vector Surveillance for Dengue Virus Detection in the Archipelago of Fernando de Noronha, Brazil

Aedes aegypti (L.) has become an efficient vector of important arboviruses due to its anthropophilic and domiciliary behaviors. Since the 1980s, dengue affects thousands of people every year in Brazil; in Fernando de Noronha (FN), a touristic archipelago, dengue cases have occurred since 2001. Once...

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Veröffentlicht in:Journal of medical entomology 2016-05, Vol.53 (3), p.613-619
Hauptverfasser: Barbosa, P. P., Guedes, D. R. D., Melo-Santos, M. A. V., Cordeiro, M. T., Acioli, R. V., Batista, C. A. V., Gonçalves, L. S. M., Souza, M. F. M., Araújo, Y. V., Magalhães, F. J. R., Regis, L., Ayres, C. F. J.
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container_issue 3
container_start_page 613
container_title Journal of medical entomology
container_volume 53
creator Barbosa, P. P.
Guedes, D. R. D.
Melo-Santos, M. A. V.
Cordeiro, M. T.
Acioli, R. V.
Batista, C. A. V.
Gonçalves, L. S. M.
Souza, M. F. M.
Araújo, Y. V.
Magalhães, F. J. R.
Regis, L.
Ayres, C. F. J.
description Aedes aegypti (L.) has become an efficient vector of important arboviruses due to its anthropophilic and domiciliary behaviors. Since the 1980s, dengue affects thousands of people every year in Brazil; in Fernando de Noronha (FN), a touristic archipelago, dengue cases have occurred since 2001. Once Ae. aegypti populations are well established in the inhabited areas of FN, the threat of dengue or another arbovirus epidemic is continuously imminent. This study aimed to monitor the DENV serotypes in mosquito samples collected in FN, where at least one resident was clinically diagnosed as dengue patient. Entomological surveillance was conducted in 2011 and 2012. Mosquitoes were sorted by sex and location and were stored in pools. DENV detection was performed using polymerase chain reaction with reverse transcription (RT-PCR) and the Platelia Dengue NS1 Ag. RNA integrity was checked by RT-PCR using rpL8 primers, and the minimum infection rate (MIR) was calculated. In total, 339 pools were analyzed, and only one was positive (DENV-1) by Multiplex RT-PCR (MIR = 1.53). When considering only pools with RNA integrity, the MIR was 2.92. Using the Platelia kit, the MIR was 9.18 (considering all the pools) and 17.54 (only 140 pools with RNA integrity). Our results showed the importance of a constant entomological surveillance in that area, the need to improve storage and transportation protocols, and an endogenous control in the RT-PCR to avoid false-negative results. Finally, our study indicated that the NS1-Ag detection was the most sensitive method and should be used routinely for DENV surveillance in mosquitoes if the serotype identification is not required.
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P. ; Guedes, D. R. D. ; Melo-Santos, M. A. V. ; Cordeiro, M. T. ; Acioli, R. V. ; Batista, C. A. V. ; Gonçalves, L. S. M. ; Souza, M. F. M. ; Araújo, Y. V. ; Magalhães, F. J. R. ; Regis, L. ; Ayres, C. F. J.</creator><creatorcontrib>Barbosa, P. P. ; Guedes, D. R. D. ; Melo-Santos, M. A. V. ; Cordeiro, M. T. ; Acioli, R. V. ; Batista, C. A. V. ; Gonçalves, L. S. M. ; Souza, M. F. M. ; Araújo, Y. V. ; Magalhães, F. J. R. ; Regis, L. ; Ayres, C. F. J.</creatorcontrib><description>Aedes aegypti (L.) has become an efficient vector of important arboviruses due to its anthropophilic and domiciliary behaviors. Since the 1980s, dengue affects thousands of people every year in Brazil; in Fernando de Noronha (FN), a touristic archipelago, dengue cases have occurred since 2001. Once Ae. aegypti populations are well established in the inhabited areas of FN, the threat of dengue or another arbovirus epidemic is continuously imminent. This study aimed to monitor the DENV serotypes in mosquito samples collected in FN, where at least one resident was clinically diagnosed as dengue patient. Entomological surveillance was conducted in 2011 and 2012. Mosquitoes were sorted by sex and location and were stored in pools. DENV detection was performed using polymerase chain reaction with reverse transcription (RT-PCR) and the Platelia Dengue NS1 Ag. RNA integrity was checked by RT-PCR using rpL8 primers, and the minimum infection rate (MIR) was calculated. In total, 339 pools were analyzed, and only one was positive (DENV-1) by Multiplex RT-PCR (MIR = 1.53). When considering only pools with RNA integrity, the MIR was 2.92. Using the Platelia kit, the MIR was 9.18 (considering all the pools) and 17.54 (only 140 pools with RNA integrity). Our results showed the importance of a constant entomological surveillance in that area, the need to improve storage and transportation protocols, and an endogenous control in the RT-PCR to avoid false-negative results. 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Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For Permissions, please email: journals.permissions@oup.com journals.permissions@oup.com</rights><rights>The Authors 2016. Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2016</rights><rights>The Authors 2016. Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For Permissions, please email: journals.permissions@oup.com.</rights><rights>Copyright Oxford University Press, UK May 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b378t-91d06b206dedb8aeb7e0bbfd8059ab9db66f03cdd4dc611dae9cb4282b8a5bfa3</citedby><cites>FETCH-LOGICAL-b378t-91d06b206dedb8aeb7e0bbfd8059ab9db66f03cdd4dc611dae9cb4282b8a5bfa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27067800$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbosa, P. P.</creatorcontrib><creatorcontrib>Guedes, D. R. D.</creatorcontrib><creatorcontrib>Melo-Santos, M. A. V.</creatorcontrib><creatorcontrib>Cordeiro, M. T.</creatorcontrib><creatorcontrib>Acioli, R. V.</creatorcontrib><creatorcontrib>Batista, C. A. V.</creatorcontrib><creatorcontrib>Gonçalves, L. S. M.</creatorcontrib><creatorcontrib>Souza, M. F. M.</creatorcontrib><creatorcontrib>Araújo, Y. V.</creatorcontrib><creatorcontrib>Magalhães, F. J. R.</creatorcontrib><creatorcontrib>Regis, L.</creatorcontrib><creatorcontrib>Ayres, C. F. J.</creatorcontrib><title>Vector Surveillance for Dengue Virus Detection in the Archipelago of Fernando de Noronha, Brazil</title><title>Journal of medical entomology</title><addtitle>J Med Entomol</addtitle><description>Aedes aegypti (L.) has become an efficient vector of important arboviruses due to its anthropophilic and domiciliary behaviors. Since the 1980s, dengue affects thousands of people every year in Brazil; in Fernando de Noronha (FN), a touristic archipelago, dengue cases have occurred since 2001. Once Ae. aegypti populations are well established in the inhabited areas of FN, the threat of dengue or another arbovirus epidemic is continuously imminent. This study aimed to monitor the DENV serotypes in mosquito samples collected in FN, where at least one resident was clinically diagnosed as dengue patient. Entomological surveillance was conducted in 2011 and 2012. Mosquitoes were sorted by sex and location and were stored in pools. DENV detection was performed using polymerase chain reaction with reverse transcription (RT-PCR) and the Platelia Dengue NS1 Ag. RNA integrity was checked by RT-PCR using rpL8 primers, and the minimum infection rate (MIR) was calculated. In total, 339 pools were analyzed, and only one was positive (DENV-1) by Multiplex RT-PCR (MIR = 1.53). When considering only pools with RNA integrity, the MIR was 2.92. Using the Platelia kit, the MIR was 9.18 (considering all the pools) and 17.54 (only 140 pools with RNA integrity). Our results showed the importance of a constant entomological surveillance in that area, the need to improve storage and transportation protocols, and an endogenous control in the RT-PCR to avoid false-negative results. Finally, our study indicated that the NS1-Ag detection was the most sensitive method and should be used routinely for DENV surveillance in mosquitoes if the serotype identification is not required.</description><subject>Aedes - physiology</subject><subject>Aedes - virology</subject><subject>Animals</subject><subject>Aquatic insects</subject><subject>arbovirus</subject><subject>Archipelagoes</subject><subject>Brazil - epidemiology</subject><subject>Dengue - epidemiology</subject><subject>Dengue - transmission</subject><subject>Dengue - virology</subject><subject>Dengue fever</subject><subject>Dengue Virus - classification</subject><subject>Dengue Virus - genetics</subject><subject>Dengue Virus - isolation &amp; purification</subject><subject>Dengue Virus - physiology</subject><subject>diagnostic</subject><subject>Female</subject><subject>Fernando de Noronha</subject><subject>Humans</subject><subject>Insect Vectors - physiology</subject><subject>Insect Vectors - virology</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Mosquitoes</subject><subject>NS1</subject><subject>RT-PCR</subject><subject>Sentinel Surveillance</subject><subject>Serogroup</subject><subject>Vector-borne diseases</subject><subject>VECTOR-BORNE DISEASES, SURVEILLANCE, PREVENTION</subject><subject>Viruses</subject><issn>0022-2585</issn><issn>1938-2928</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp90M1O3DAUBWALFcFA2fQBKktVJYRI59pJHHtJ-a00oou2bIMd3zAeZeKpnRTRp8ejGViwYGVd69ORziHkE4NvDFQ-XSxxOiweIS92yISpXGZccfmBTAA4z3gpy31yEOMCACQr1B7Z5xWISgJMyP0dNoMP9NcY_qHrOt03SNv0cYH9w4j0zoUxpmNIzPmeup4Oc6RnoZm7FXb6wVPf0isMve6tpxbprQ--n-tT-j3o_677SHZb3UU82r6H5M_V5e_zm2z28_rH-dksM3klh0wxC8JwEBatkRpNhWBMayWUShtljRAt5I21hW0EY1ajakzBJU-4NK3OD8nxJncV_N8R41AvXWxw3Qj9GGsmuRCiUmWZ6Jc3dOHHVKBbq1KlVFBFUicb1QQfY8C2XgW31OGpZlCvd6_T7vVm94Q_byNHs0T7Sl-GTuDrBvhx9X7QtoZx3vf4Hn0GLqSaJg</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Barbosa, P. 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subjects Aedes - physiology
Aedes - virology
Animals
Aquatic insects
arbovirus
Archipelagoes
Brazil - epidemiology
Dengue - epidemiology
Dengue - transmission
Dengue - virology
Dengue fever
Dengue Virus - classification
Dengue Virus - genetics
Dengue Virus - isolation & purification
Dengue Virus - physiology
diagnostic
Female
Fernando de Noronha
Humans
Insect Vectors - physiology
Insect Vectors - virology
Male
Medical diagnosis
Mosquitoes
NS1
RT-PCR
Sentinel Surveillance
Serogroup
Vector-borne diseases
VECTOR-BORNE DISEASES, SURVEILLANCE, PREVENTION
Viruses
title Vector Surveillance for Dengue Virus Detection in the Archipelago of Fernando de Noronha, Brazil
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