Human IgG responses to the Aedes albopictus 34k2 salivary protein: analyses in Réunion Island and Bolivia confirm its suitability as marker of host exposure to the tiger mosquito
The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomologi...
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Published in | Parasites & vectors Vol. 15; no. 1; p. 260 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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BioMed Central Ltd
20.07.2022
BioMed Central BMC |
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Abstract | The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission.
IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France).
Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. |
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AbstractList | The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission. IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France). Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. Abstract Background The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission. Methods IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France). Results and conclusion Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. Graphical Abstract BACKGROUND: The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission. METHODS: IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France). RESULTS AND CONCLUSION: Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission. IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France). Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. Background: The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission.Methods IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France).Results and conclusion Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus . Bolivian subjects, exposed to bites of Ae. aegypti , carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti . On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti . Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. Graphical Abstract The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission.BACKGROUNDThe rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission.IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France).METHODSIgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France).Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist.RESULTS AND CONCLUSIONAnti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. Background The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to improve monitoring and control of mosquito vector populations. Assessment of human-vector contact, currently estimated by classical entomological methods, is crucial to guide planning and implementation of control measures and evaluate transmission risk. Antibody responses to mosquito genus-specific salivary proteins are emerging as a convenient complementary tool for assessing host exposure to vectors. We previously showed that IgG responses to the Ae. albopictus 34k2 salivary protein (al34k2) allow detection of seasonal and geographic variation of human exposure to the tiger mosquito in two temperate areas of Northeast Italy. The main aim of this study was to confirm and extend these promising findings to tropical areas with ongoing arboviral transmission. Methods IgG responses to al34k2 and to the Ae. aegypti orthologous protein ae34k2 were measured by ELISA in cohorts of subjects only exposed to Ae. albopictus (Réunion Island), only exposed to Ae. aegypti (Bolivia) or unexposed to both these vectors (North of France). Results and conclusion Anti-al34k2 IgG levels were significantly higher in sera of individuals from Réunion Island than in unexposed controls, indicating that al34k2 may be a convenient and reliable proxy for whole saliva or salivary gland extracts as an indicator of human exposure to Ae. albopictus. Bolivian subjects, exposed to bites of Ae. aegypti, carried in their sera IgG recognizing the Ae. albopictus al34k2 protein, suggesting that this salivary antigen can also detect, even though with low sensitivity, human exposure to Ae. aegypti. On the contrary, due to the high background observed in unexposed controls, the recombinant ae34k2 appeared not suitable for the evaluation of human exposure to Aedes mosquitoes. Overall, this study confirmed the suitability of anti-al34k2 IgG responses as a specific biomarker of human exposure to Ae. albopictus and, to a certain extent, to Ae. aegypti. Immunoassays based on al34k2 are expected to be especially effective in areas where Ae. albopictus is the main arboviral vector but may also be useful in areas where Ae. albopictus and Ae. aegypti coexist. Graphical Keywords: Aedes albopictus, Aedes aegypti, 34k2 salivary protein, Host exposure, Serological marker, Vector control, Human-vector contact |
ArticleNumber | 260 |
Audience | Academic |
Author | Buezo Montero, Sara Gabrieli, Paolo Zamble, Bi Zamble Hubert Lombardo, Fabrizio Remoue, Franck Poinsignon, Anne Arcà, Bruno |
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CitedBy_id | crossref_primary_10_3390_pathogens12030371 crossref_primary_10_3389_fitd_2023_1145340 crossref_primary_10_1038_s41598_023_43751_1 |
Cites_doi | 10.2807/1560-7917.ES.2019.24.47.1900346 10.3390/insects12030191 10.1186/s13071-017-2139-z 10.1371/journal.pntd.0001487 10.3390/tropicalmed3030080 10.1371/journal.pntd.0007806 10.1016/j.cois.2018.07.012 10.1016/j.ibmb.2010.08.002 10.1111/tmi.12280 10.1371/journal.pone.0002472 10.1371/journal.pone.0040170 10.2807/1560-7917.ES.2020.25.36.2001606 10.12688/gatesopenres.13061.1 10.1371/journal.pntd.0005109 10.1016/j.trstmh.2005.06.032 10.1016/S0140-6736(19)32790-4 10.1056/NEJMoa2030243 10.1089/vbz.2009.0005 10.1371/journal.pntd.0007482 10.1186/1475-2875-11-439 10.1186/1475-2875-8-121 10.1371/journal.pntd.0007615 10.1371/journal.pone.0017980 10.3389/fcimb.2020.00377 10.1038/s41564-018-0214-7 10.1038/s41564-019-0376-y 10.3390/insects11110770 10.4269/ajtmh.2007.77.727 10.1186/s12936-020-3128-9 10.1016/S0140-6736(12)61151-9 10.1093/infdis/jiz289 10.1016/j.ibmb.2006.10.007 10.1186/1471-2164-8-6 10.1186/1475-2875-11-318 10.1186/s12936-019-2975-8 10.3389/fpubh.2018.00111 10.1111/j.1365-2915.2012.01062.x 10.1186/1475-2875-7-195 10.1186/s13071-014-0549-8 10.4269/ajtmh.2012.11-0477 10.1371/journal.pntd.0001905 10.1186/s12864-017-3579-8 10.1371/journal.pntd.0009440 10.3390/ijms21030691 |
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References | B Arcà (5383_CR43) 2007; 37 5383_CR9 MUG Kraemer (5383_CR5) 2019; 4 E Elanga Ndille (5383_CR38) 2012; 6 P Ya-Umphan (5383_CR32) 2017; 215 E Elanga Ndille (5383_CR39) 2016; 10 ZM Ali (5383_CR33) 2012; 11 AM Kilpatrick (5383_CR6) 2012; 380 WR Shaw (5383_CR15) 2019; 4 F Remoue (5383_CR22) 2006; 100 JM Ribeiro (5383_CR44) 2007; 8 S Buezo Montero (5383_CR46) 2020; 10 BB Andrade (5383_CR19) 2009; 8 B Arcà (5383_CR34) 2017; 18 AB Sagna (5383_CR42) 2019; 220 S Buezo Montero (5383_CR45) 2019; 13 B Arcà (5383_CR23) 2018; 29 A Poinsignon (5383_CR28) 2008; 3 P Renault (5383_CR3) 2007; 77 CF Oliva (5383_CR14) 2021; 12 S Doucoure (5383_CR20) 2012; 6 JM Ribeiro (5383_CR24) 2010; 40 L Bagny Beilhe (5383_CR47) 2013; 27 S Doucoure (5383_CR21) 2012; 87 BL Londono-Renteria (5383_CR36) 2018; 6 EJM Pollard (5383_CR29) 2019; 18 W Stone (5383_CR31) 2012; 7 B Londono-Renteria (5383_CR35) 2020; 21 C Paupy (5383_CR2) 2010; 10 AB Sagna (5383_CR37) 2018; 3 A Utarini (5383_CR17) 2021; 384 ZM Idris (5383_CR26) 2017; 10 PA Ryan (5383_CR16) 2019; 3 M Vincent (5383_CR4) 2019 G Espana (5383_CR12) 2019; 13 I Dusfour (5383_CR13) 2019; 13 LC Gouagna (5383_CR50) 2020; 11 PH Corran (5383_CR48) 2008; 7 B Fustec (5383_CR40) 2021; 15 OJ Brady (5383_CR7) 2019; 394 C Rizzo (5383_CR49) 2014; 7 C Rizzo (5383_CR30) 2011; 6 5383_CR11 5383_CR10 K Badu (5383_CR25) 2012; 11 J Montiel (5383_CR27) 2020; 19 5383_CR18 5383_CR1 EE Ndille (5383_CR41) 2014; 19 CM Gossner (5383_CR8) 2018; 23 |
References_xml | – year: 2019 ident: 5383_CR4 publication-title: Euro Surveill doi: 10.2807/1560-7917.ES.2019.24.47.1900346 – volume: 12 start-page: 191 year: 2021 ident: 5383_CR14 publication-title: Insects doi: 10.3390/insects12030191 – volume: 10 start-page: 204 year: 2017 ident: 5383_CR26 publication-title: Parasit Vectors doi: 10.1186/s13071-017-2139-z – volume: 6 start-page: e1487 year: 2012 ident: 5383_CR20 publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0001487 – volume: 215 start-page: 396 year: 2017 ident: 5383_CR32 publication-title: J Infect Dis – volume: 23 start-page: 1800268 year: 2018 ident: 5383_CR8 publication-title: Euro Surveill – volume: 3 start-page: 80 year: 2018 ident: 5383_CR37 publication-title: Trop Med Infect Dis doi: 10.3390/tropicalmed3030080 – volume: 13 start-page: e0007806 year: 2019 ident: 5383_CR45 publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0007806 – volume: 29 start-page: 102 year: 2018 ident: 5383_CR23 publication-title: Curr Opin Insect Sci doi: 10.1016/j.cois.2018.07.012 – volume: 40 start-page: 767 year: 2010 ident: 5383_CR24 publication-title: Insect Biochem Mol Biol doi: 10.1016/j.ibmb.2010.08.002 – volume: 19 start-page: 576 year: 2014 ident: 5383_CR41 publication-title: Lao PDR Trop Med Int Health doi: 10.1111/tmi.12280 – ident: 5383_CR18 – volume: 3 start-page: e2472 year: 2008 ident: 5383_CR28 publication-title: PLoS ONE doi: 10.1371/journal.pone.0002472 – volume: 7 start-page: e40170 year: 2012 ident: 5383_CR31 publication-title: PLoS ONE doi: 10.1371/journal.pone.0040170 – ident: 5383_CR9 doi: 10.2807/1560-7917.ES.2020.25.36.2001606 – volume: 3 start-page: 1547 year: 2019 ident: 5383_CR16 publication-title: Australia Gates Open Res doi: 10.12688/gatesopenres.13061.1 – volume: 10 start-page: e0005109 year: 2016 ident: 5383_CR39 publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0005109 – volume: 100 start-page: 363 year: 2006 ident: 5383_CR22 publication-title: Trans R Soc Trop Med Hyg doi: 10.1016/j.trstmh.2005.06.032 – volume: 394 start-page: 1991 year: 2019 ident: 5383_CR7 publication-title: Lancet doi: 10.1016/S0140-6736(19)32790-4 – volume: 384 start-page: 2177 year: 2021 ident: 5383_CR17 publication-title: N Engl J Med doi: 10.1056/NEJMoa2030243 – ident: 5383_CR11 – volume: 10 start-page: 259 year: 2010 ident: 5383_CR2 publication-title: Vector Borne Zoonotic Dis doi: 10.1089/vbz.2009.0005 – volume: 13 start-page: e0007482 year: 2019 ident: 5383_CR12 publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0007482 – volume: 11 start-page: 439 year: 2012 ident: 5383_CR33 publication-title: Malar J doi: 10.1186/1475-2875-11-439 – volume: 8 start-page: 121 year: 2009 ident: 5383_CR19 publication-title: Malar J doi: 10.1186/1475-2875-8-121 – volume: 13 start-page: e0007615 year: 2019 ident: 5383_CR13 publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0007615 – ident: 5383_CR1 – volume: 6 start-page: e17980 year: 2011 ident: 5383_CR30 publication-title: PLoS ONE doi: 10.1371/journal.pone.0017980 – volume: 10 start-page: 377 year: 2020 ident: 5383_CR46 publication-title: Front Cell Infect Microbiol doi: 10.3389/fcimb.2020.00377 – volume: 4 start-page: 20 year: 2019 ident: 5383_CR15 publication-title: Nat Microbiol doi: 10.1038/s41564-018-0214-7 – volume: 4 start-page: 854 year: 2019 ident: 5383_CR5 publication-title: Nat Microbiol doi: 10.1038/s41564-019-0376-y – volume: 11 start-page: 770 year: 2020 ident: 5383_CR50 publication-title: Insects doi: 10.3390/insects11110770 – volume: 77 start-page: 727 year: 2007 ident: 5383_CR3 publication-title: Am J Trop Med Hyg doi: 10.4269/ajtmh.2007.77.727 – ident: 5383_CR10 – volume: 19 start-page: 42 year: 2020 ident: 5383_CR27 publication-title: Malar J doi: 10.1186/s12936-020-3128-9 – volume: 380 start-page: 1946 year: 2012 ident: 5383_CR6 publication-title: Lancet doi: 10.1016/S0140-6736(12)61151-9 – volume: 220 start-page: 1199 year: 2019 ident: 5383_CR42 publication-title: J Infect Dis doi: 10.1093/infdis/jiz289 – volume: 37 start-page: 107 year: 2007 ident: 5383_CR43 publication-title: Insect Biochem Mol Biol doi: 10.1016/j.ibmb.2006.10.007 – volume: 8 start-page: 6 year: 2007 ident: 5383_CR44 publication-title: BMC Genomics doi: 10.1186/1471-2164-8-6 – volume: 11 start-page: 318 year: 2012 ident: 5383_CR25 publication-title: Malar J doi: 10.1186/1475-2875-11-318 – volume: 18 start-page: 334 year: 2019 ident: 5383_CR29 publication-title: Malar J doi: 10.1186/s12936-019-2975-8 – volume: 6 start-page: 111 year: 2018 ident: 5383_CR36 publication-title: Front Public Health doi: 10.3389/fpubh.2018.00111 – volume: 27 start-page: 387 year: 2013 ident: 5383_CR47 publication-title: Med Vet Entomol doi: 10.1111/j.1365-2915.2012.01062.x – volume: 7 start-page: 195 year: 2008 ident: 5383_CR48 publication-title: Malar J doi: 10.1186/1475-2875-7-195 – volume: 7 start-page: 549 year: 2014 ident: 5383_CR49 publication-title: Parasit Vectors doi: 10.1186/s13071-014-0549-8 – volume: 87 start-page: 504 year: 2012 ident: 5383_CR21 publication-title: Am J Trop Med Hyg doi: 10.4269/ajtmh.2012.11-0477 – volume: 6 year: 2012 ident: 5383_CR38 publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0001905 – volume: 18 start-page: 153 year: 2017 ident: 5383_CR34 publication-title: BMC Genomics doi: 10.1186/s12864-017-3579-8 – volume: 15 start-page: e0009440 year: 2021 ident: 5383_CR40 publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0009440 – volume: 21 start-page: 691 year: 2020 ident: 5383_CR35 publication-title: Int J Mol Sci doi: 10.3390/ijms21030691 |
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Snippet | The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the urgent need to... Background The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the... BACKGROUND: The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the... Background: The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out the... Abstract Background The rapid worldwide spreading of Aedes aegypti and Aedes albopictus is expanding the risk of arboviral diseases transmission, pointing out... |
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Title | Human IgG responses to the Aedes albopictus 34k2 salivary protein: analyses in Réunion Island and Bolivia confirm its suitability as marker of host exposure to the tiger mosquito |
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