Peridomestic Infection as a Determining Factor of Dengue Transmission

Ruth Aralí Martínez-Vega, Rogelio Danis-Lozano, Fredi Alexander Díaz-Quijano, Jorge Velasco-Hernández, René Santos-Luna, Susana Román-Pérez, Pablo Kuri-Morales, José Ramos-Castañeda, Ruth Aralí Martínez-Vega, Rogelio Danis-Lozano, Fredi Alexander Díaz-Quijano, Jorge Velasco-Hernández, René Santos-Luna, Susana Román-Pérez, Pablo Kuri-Morales, José Ramos-Castañeda

Abstract

Background: The study of endemic dengue transmission is essential for proposing alternatives to impact its burden. The traditional paradigm establishes that transmission starts around cases, but there are few studies that determine the risk.

Methods: To assess the association between the peridomestic dengue infection and the exposure to a dengue index case (IC), a cohort was carried out in two Mexican endemic communities. People cohabitating with IC or living within a 50-meter radius (exposed cohort) and subjects of areas with no ICs in a 200-meter radius (unexposed cohort) were included.

Results: Exposure was associated with DENV infection in cohabitants (PRa 3.55; 95%CI 2.37-5.31) or neighbors (PRa 1.82; 95%CI 1.29-2.58). Age, location, toilets with no direct water discharge, families with children younger than 5 and the House Index, were associated with infection. Families with older than 13 were associated with a decreased frequency. After a month since the IC fever onset, the infection incidence was not influenced by exposure to an IC or vector density; it was influenced by the local seasonal behavior of dengue and the age. Additionally, we found asymptomatic infections accounted for 60% and a greater age was a protective factor for the presence of symptoms (RR 0.98; 95%CI 0.97-0.99).

Conclusion: The evidence suggests that dengue endemic transmission in these locations is initially peridomestic, around an infected subject who may be asymptomatic due to demographic structure and endemicity, and it is influenced by other characteristics of the individual, the neighborhood and the location. Once the transmission chain has been established, dengue spreads in the community probably by the adults who, despite being the group with lower infection frequency, mostly suffer asymptomatic infections and have higher mobility. This scenario complicates the opportunity and the effectiveness of control programs and highlights the need to apply multiple measures for dengue control.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1. Accumulated Distribution of Groups in…
Fig 1. Accumulated Distribution of Groups in Axochiapan (A) and Tepalcingo (B).
IC houses in red, IC neighbor houses in blue (exposed group) and unexposed group houses in green. Areas have 50, 100 and 200 meters in diameter with the center at the IC house or in the centroid of unexposed the neighbor houses. Source: Esri, DigitalGlobe, GeoEye, i-cubed, USDA, USGS, AEX, Getmapping, Aerogrid, IGN, IGP, swisstopo, and the GIS User Community.
Fig 2. Cohort Enrollment and Follow-up.
Fig 2. Cohort Enrollment and Follow-up.
*Two 3-year-old children were included because they had pre-enrollment symptomatic infections diagnosed by the SSM.
Fig 3. Pre-enrollment DENV Infections per Age.
Fig 3. Pre-enrollment DENV Infections per Age.
A. Pre-enrollment infection cases (n = 213/1,172), B. Frequency of pre-enrollment infections.
Fig 4. Post-enrollment DENV Infections per Age.
Fig 4. Post-enrollment DENV Infections per Age.
A. Post-enrollment infection cases (n = 40/922), B. Frequency of post-enrollment infections.
Fig 5. Proposed Dengue Transmission in Studied…
Fig 5. Proposed Dengue Transmission in Studied Communities.
Force of infection (λ). Symptomatic (Sx). Asymptomatic (Asx). Index Case (IC). Infection (Inf). Years old (y/o). Destination, includes workplace and other locations where subjects spend enough time to be bitten by vectors located in that area; except for schools.

References

    1. Gubler DJ. The economic burden of dengue. Am J Trop Med Hyg. 2012; 86:743–44. 10.4269/ajtmh.2012.12-0157
    1. Thammapalo S, Chongsuvivatwong V, Geater A, Dueravee M. Environmental factors and incidence of dengue fever and dengue haemorrhagic fever in an urban area, Southern Thailand. Epidemiol Infect. 2008; 136:135–43.
    1. Honório NA, Nogueira RM, Codeço CT, Carvalho MS, Cruz OG, Magalhães Mde A, et al. Spatial evaluation and modeling of Dengue seroprevalence and vector density in Rio de Janeiro, Brazil. PLoS Negl Trop Dis. 2009; 3:e545 10.1371/journal.pntd.0000545
    1. Sanchez L, Vanlerberghe V, Alfonso L, Marquetti Mdel C, Guzman MG, Bisset J, et al. Aedes aegypti larval indices and risk for dengue epidemics. Emerg Infect Dis. 2006; 12:800–6.
    1. Mammen MP, Pimgate C, Koenraadt CJ, Rothman AL, Aldstadt J, Nisalak A, et al. Spatial and temporal clustering of dengue virus transmission in Thai villages. PLoS Med. 2008; 5:e205 10.1371/journal.pmed.0050205
    1. Reyes M, Mercado JC, Standish K, Matute JC, Ortega O, Moraga B, et al. Index cluster study of dengue virus infection in Nicaragua. Am J Trop Med Hyg. 2010; 83:683–89. 10.4269/ajtmh.2010.10-0023
    1. Yoon IK, Getis A, Aldstadt J, Rothman AL, Tannitisupawong D, Koenraadt CJ, et al. Fine scale spatiotemporal clustering of dengue virus transmission in children and Aedes aegypti in rural Thai villages. PLoS Negl Trop Dis. 2012; 6:e1730 10.1371/journal.pntd.0001730
    1. Yew YW, Ye T, Ang LW, Ng LC, Yap G, James L, et al. Seroepidemiology of dengue virus infection among adults in Singapore. Ann Acad Med Singapore. 2009; 38:667–75. (pdf)
    1. Rodríguez Rodríguez D, Garza Rodríguez M, Chavarria AM, Ramos-Jiménez, Rivera MA, Taméz RC, et al. Dengue virus antibodies in blood donors from an endemic area. Transfus Med. 2009; 19:125–31. 10.1111/j.1365-3148.2009.00922.x
    1. Dussart P, Baril L, Petit L, Beniguel L, Quang LC, Ly S, et al. Clinical and virological study of dengue cases and the members of their households: the multinational DENFRAME Project. PLoS Negl Trop Dis. 2012; 6:e1482 10.1371/journal.pntd.0001482
    1. Xu G, Dong H, Shi N, Liu S, Zhou A, Cheng Z, et al. An outbreak of dengue virus serotype 1 infection in Cixi, Ningbo, People's Republic of China, 2004, associated with a traveler from Thailand and high density of Aedes albopictus. Am J Trop Med Hyg. 2007; 76:1182–88.
    1. Méndez F, Barreto M, Arias JF, Rengifo G, Muñoz J, Burbano ME, et al. Human and mosquito infections by dengue viruses during and after epidemics in a dengue-endemic region of Colombia. Am J Trop Med Hyg. 2006; 74:678–83.
    1. Vanwambeke SO, van Benthem BH, Khantikul N, Burghoorn-Maas C, Panart K, Oskam L, et al. Multi-level analyses of spatial and temporal determinants for dengue infection. Int J Health Geogr. 2006; 5:5
    1. Porter KR, Beckett CG, Kosasih H, Tan RI, Alisjahbana B, Rudiman PI, et al. Epidemiology of dengue and dengue hemorrhagic fever in a cohort of adults living in Bandung, West Java, Indonesia. Am J Trop Med Hyg. 2005; 72:60–6.
    1. Rodrigues EM, Dal-Fabbro AL, Salomao R, Ferreira IB, Rocco IM, Fonseca BA. Epidemiologia da infecção pela dengue em Ribeirão Preto, SP, Brasil. Rev Saude Publica. 2002; 36:160–65.
    1. Endy TP, Chunsuttiwat S, Nisalak A, Libraty DH, Green S, Rothman, et al. Epidemiology of inapparent and symptomatic acute dengue virus infection: a prospective study of primary school children in Kamphaeng Phet, Thailand. Am J Epidemiol. 2002; 156:40–51.
    1. Vasconcelos PF, Lima JW, da Rosa AP, Timbó MJ, da Rosa ES, Lima HR, et al. Epidemia de dengue em Fortaleza, Ceará: Inquérito soro-epidemiológico aleatório. Rev Saude Publica. 1998; 32:447–54.
    1. Da Cunha RV, Dias M, Nogueira RM, Chagas N, Miagostovich MP, Schatzmayr HG. Secondary dengue infection in schoolchildren in a dengue endemic area in the state of Rio de Janeiro, Brazil. Rev Inst Med Trop Sao Paulo. 1995; 37:517–21.
    1. Vasconcelos PF, Travassos da Rosa ES, Travassos da Rosa JF, de Freitas RB, Dégallier N, Rodrigues SG, et al. Epidemia de febre clássica de dengue causada pelo sorotipo 2 em Araguaina, Tocantins, Brasil. Rev Inst Med Trop Sao Paulo. 1993; 35:141–48.
    1. Chevillon C, Failloux A-B. Questions on viral population biology to complete dengue puzzle. TRENDS in Microbiol. 2003; 11:415–21.
    1. Beckett CG, Kosasih H, Faisal I, Nurhayati, Tan R, Widjaja S, et al. Early detection of dengue infections using cluster sampling around index cases. Am J Trop Med Hyg. 2005; 72:777–82.
    1. Siqueira JB, Martelli CM, Maciel IJ, Oliveira RM, Ribeiro MG, Amorim FP, et al. Household survey of dengue infection in central Brazil: spatial point pattern analysis and risk factors assessment. Am J Trop Med Hyg. 2004; 71:646–51.
    1. Braga C, Luna CF, Martelli CM, Souza WV, Cordeiro MT, Alexander N, et al. Seroprevalence and risk factors for dengue infection in socioeconomically distinct areas of Recife, Brazil. Acta Trop. 2010; 113:234–40. 10.1016/j.actatropica.2009.10.021
    1. Stoddard ST, Morrison AC, Vazquez-Prokopec GM, Paz Soldan V, Kochel TJ, Kitron U, et al. The role of human movement in the transmission of vector-borne pathogens. PLoS Negl Trop Dis. 2009; 3:e481 10.1371/journal.pntd.0000481
    1. Adams B, Kapan DD. Man bites mosquito: understanding the contribution of human movement to vector-borne disease dynamics. PLoS One 2009; 4:e6763 10.1371/journal.pone.0006763
    1. Martínez-Vega RA, Danis-Lozano R, Velasco-Hernández J, Díaz-Quijano FA, González-Fernández M, Santos R, Román S, et al. A prospective cohort study to evaluate peridomestic infection as a determinant of dengue transmission: protocol. BMC Public Health. 2012; 12:262 10.1186/1471-2458-12-262
    1. Amaya-Larios IY, Martínez-Vega RA, Mayer SV, Galeana-Hernández M, Comas-García A, Sepúlveda-Salinas KJ, et al. Seroprevalence of neutralizing antibodies against dengue virus in two localities in the state of Morelos, Mexico. Am J Trop Med Hyg. 2014; 91:1057–65. 10.4269/ajtmh.14-0145
    1. Sa-Ngasang A, Anantapreecha S, A-Nuegoonpipat A, Chanama S, Wibulwattanakij S, Pattanakul K, et al. Specific IgM and IgG responses in primary and secondary dengue virus infections determined by enzyme-linked immunosorbent assay. Epidemiol Infect. 2006; 134:820–5.
    1. Sistema Nacional de Vigilancia Epidemiológica [Internet]. México: Dirección General de Epidemiología;
    1. Lee J, Chia KS. Estimation of prevalence rate ratios for cross sectional data: an example in occupational epidemiology. Br J Ind Med. 1993; 50:861–64.
    1. Nijem K, Kristensen P, Al-Khatib A, Bjertness E. Application of different statistical methods to estimate relative risk for self-reported health complaints among shoe factory workers exposed to organic solvents and plastic compounds. Nor Epidemiol. 2005; 15:111–16.
    1. Diaz-Quijano FA. A simple method for estimating relative risk using logistic regression. BMC Med Res Methodol. 2012; 12:14 10.1186/1471-2288-12-14
    1. Anders KL, Nga le H, Thuy NT, et al. Households as foci for dengue transmission in highly urban Vietnam. PLoS Negl Trop Dis. 2015; 9:e0003528 10.1371/journal.pntd.0003528
    1. Smith DL, Perkins TA, Reiner RC Jr, Barker CM, Niu T, Chaves LF, et al. Recasting the theory of mosquito-borne pathogen transmission dynamics and control. Trans R Soc Trop Med Hyg. 2014; 108:185–97. 10.1093/trstmh/tru026
    1. Montoya M, Gresh L, Mercado JC, Williams KL, Vargas MJ, Gutierrez G, et al. Symptomatic versus inapparent outcome in repeat dengue virus infections is influenced by the time interval between infections and study year. PLoS Negl Trop Dis. 2013; 7:e2357 10.1371/journal.pntd.0002357
    1. Olkowski S, Forshey BM, Morrison AC, Rocha C, Vilcarromero S, Halsey ES, et al. Reduced risk of disease during postsecondary dengue virus infections. J Infect Dis. 2013; 208:1026–33. 10.1093/infdis/jit273
    1. Grange L, Simon-Loriere E, Sakuntabhai A, Gresh L, Paul R, Harris E. Epidemiological risk factors associated with high global frequency of inapparent dengue virus infections. Front Immunol. 2014; 5:280 10.3389/fimmu.2014.00280
    1. Nguyet MN, Duong TH, Trung VT, Nguyen TH, Tran CN, Long VT, et al. Host and viral features of human dengue cases shape the population of infected and infectious Aedes aegypti mosquitoes. Proc Natl Acad Sci U S A. 2013; 110:9072–77. 10.1073/pnas.1303395110
    1. Barmak DH, Dorso CO, Otero M, Solari HG. Modelling interventions during a dengue outbreak. Epidemiol Infect. 2014; 142:545–61. 10.1017/S0950268813001301

Source: PubMed

3
Se inscrever