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Surveillance for Flaviviruses Near the Mexico–U.S. Border: Co-circulation of Dengue Virus Serotypes 1, 2, and 3 and West Nile Virus in Tamaulipas, Northern Mexico, 2014–2016
S. Viridiana Laredo-Tiscareño
S. Viridiana Laredo-Tiscareño
Laboratorio de Biomedicina Molecular, Centro de Biotecnología Genómica del Instituto Politécnico Nacional, Reynosa, Tamaulipas, México;
Laboratorio de Arbovirología, Centro de Investigaciones Regionales “Dr. Hideyo Noguchi,” Universidad Autónoma de Yucatán, Mérida, México;
Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa;
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Laboratorio de Arbovirología, Centro de Investigaciones Regionales “Dr. Hideyo Noguchi,” Universidad Autónoma de Yucatán, Mérida, México;
Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa;
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Javier A. Garza-Hernandez
Javier A. Garza-Hernandez
Laboratorio Entomología Médica, Instituto de Ciencias Biomédicas, Universidad Autónoma de Ciudad Juárez, Ciudad Juárez, Chihuahua, México;
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Ma Isabel Salazar
Ma Isabel Salazar
Laboratorio de Virología e Inmunovirología, Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México, Mexico;
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Erick J. De Luna-Santillana
Erick J. De Luna-Santillana
Laboratorio Medicina de la Conservación, Centro de Biotecnología Genómica del Instituto Politécnico Nacional, Reynosa, Tamaulipas, México;
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Chandra S. Tangudu
Chandra S. Tangudu
Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa;
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Rosa C. Cetina-Trejo
Rosa C. Cetina-Trejo
Laboratorio de Arbovirología, Centro de Investigaciones Regionales “Dr. Hideyo Noguchi,” Universidad Autónoma de Yucatán, Mérida, México;
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Gloria L. Doria-Cobos
Gloria L. Doria-Cobos
Departamento de Epidemiología de la Cuarta Jurisdicción Sanitaria, Secretaria de Salud, Reynosa, Tamaulipas, México;
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Santos Daniel Carmona-Aguirre
Santos Daniel Carmona-Aguirre
Secretaría de Salud del Estado de Tamaulipas, Dirección de Epidemiología, Ciudad Victoria, Tamaulipas, México
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Julian E. Garcia-Rejon
Julian E. Garcia-Rejon
Laboratorio de Arbovirología, Centro de Investigaciones Regionales “Dr. Hideyo Noguchi,” Universidad Autónoma de Yucatán, Mérida, México;
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Carlos Machain-Williams
Carlos Machain-Williams
Laboratorio de Arbovirología, Centro de Investigaciones Regionales “Dr. Hideyo Noguchi,” Universidad Autónoma de Yucatán, Mérida, México;
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Bradley J. Blitvich
Bradley J. Blitvich
Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa;
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Mario Alberto Rodríguez Pérez
Mario Alberto Rodríguez Pérez
Laboratorio de Biomedicina Molecular, Centro de Biotecnología Genómica del Instituto Politécnico Nacional, Reynosa, Tamaulipas, México;
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A clinical, serological, and molecular investigation was performed to determine the presence of dengue virus (DENV) and other flaviviruses among residents of the city of Reynosa, Tamaulipas, on the Mexico–U.S. border in 2014–2016. The sample population consisted of 2,355 patients with suspected dengue, in addition to 346 asymptomatic individuals recruited during a household-based epidemiological investigation designed to identify flavivirus seroconversions. Sera were collected from patients with suspected dengue in the acute phase of illness and from asymptomatic individuals at enrollment and every 5–7 months for 19 months. Sera from suspected dengue patients were tested for DENV antigen by enzyme-linked immunosorbent assay (ELISA), and select antigen-positive sera were further tested using a serotype-specific, quantitative reverse transcription–polymerase chain reaction. Sera from the household cohort were tested for flavivirus-reactive antibodies by immunoglobulin (Ig) M and IgG ELISAs using DENV antigen. A total of 418 (17.7%) patients with suspected dengue had laboratory-confirmed DENV infections, including 82 patients who were positive for DENV RNA. The most frequently detected serotype was DENV-1 (61 patients), followed by DENV-2 (16 patients) and DENV-3 (five patients). A total of 217 (62.7%) asymptomatic individuals had flavivirus-reactive antibodies at enrollment, and nine flavivirus-naïve individuals seroconverted. Sera from a subset of dengue patients and household participants, including all those who seroconverted, were further tested by plaque reduction neutralization test, resulting in the detection of antibodies to DENV-1, DENV-2, and West Nile virus. In summary, we provide evidence for the co-circulation of multiple flaviviruses in Reynosa, Tamaulipas, on the Mexico–U.S. border.
Author Notes
Financial support: The study was supported by scholarships from the Consejo Nacional de Ciencia y Tecnología of Mexico (scholarship no. 262076) and Coordinación de Cooperación Académica del Instituto Politécnico Nacional of Mexico, and in part by CONACYT grants 2014-247005 and 200664, an intramural grant from Iowa State University, and an institutional grant (Ref. No. CIP-ICB-2018-103) used to support a visiting scholar at the Universidad Autónoma de Ciudad Juárez.
Authors’ addresses: S. Viridiana Laredo-Tiscareño and Erick J. De Luna-Santillana, Centro de Biotecnología Genómica del Instituto Politécnico Nacional, Laboratorio de Biomedicina Molecular, Reynosa, Tamaulipas, México, E-mails: viridiana.laredo@gmail.com and ericklusan@yahoo.com. Javier A. Garza-Hernandez and Mario Alberto Rodríguez Pérez, Centro de Biotecnologia Genomica, Instituto Politecnico Nacional, Mexico, Tamaulipas, México, E-mails: biolgarza@gmail.com and drmarodriguez@hotmail.com. Ma Isabel Salazar, Departamento de Microbiología, Instituto Politécnico Nacional Escuela Nacional de Ciencias Biológicas, Ciudad de México, México, E-mail: maisabelsalazar@gmail.com. Chandra S. Tangudu and Bradley J. Blitvich, Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA, E-mails: ctangudu@iastate.edu and blitvich@iastate.edu. Rosa C. Cetina-Trejo, Centro de Investigaciones Regionales “Dr. Hideyo Noguchi,” Universidad Autonoma de Yucatan, Merida, Yucatán, México, E-mail: rosaccentinatrejo1234@gmail.com. Gloria L. Doria-Cobos, Epidemiología de la Cuarta Jurisdicción Sanitaria, Secretaria de Salud, Reynosa, Tamaulipas, México, E-mail: leticiaddruiz@gmail.com. Santos Daniel Carmona-Aguirre, Direccion de Epidemiologia, Secretaria de Salud del Estado de Tamaulipas, Ciudad Victoria, Tamaulipas, México, E-mail: santos.carmona@tam.gob.mx. Julian E. Garcia-Rejon, Laboratorio de Arbovirología, Universidad Autonoma de Yucatan, Merida, Yucatán, México, E-mail: julian.garcia.rejon@gmail.com. Carlos Machain-Williams, Hideo Noguchi Institute, Universidad Autónoma de Yucatán, Merida, Yucatán, México, E-mail: carlos.machain@uady.mx.
ProCite
RefWorks
Reference Manager
BibTeX
Zotero
EndNote
-
1.
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2.
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-
3.
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-
4.
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5.
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6.
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-
8.
Phuong CX et al. 2004. Clinical diagnosis and assessment of severity of confirmed dengue infections in Vietnamese children: is the world health organization classification system helpful? Am J Trop Med Hyg 70: 172–179.
-
9.
World Health Organization, 2009. Dengue: Guidelines for Diagnosis, Treatment, Prevention and Control, New Edition. Geneva, Switzerland: WHO.
-
10.
Blitvich BJ, 2008. Transmission dynamics and changing epidemiology of West Nile virus. Anim Health Res Rev 9: 71–86.
-
11.
Petersen LR, Brault AC, Nasci RS, 2013. West Nile virus: review of the literature. JAMA 310: 308–315.
-
12.
Reisen WK, 2003. Epidemiology of St. Louis encephalitis virus. Adv Virus Res 61: 139–183.
-
13.
Oyer RJ, David Beckham J, Tyler KL, 2014. West Nile and St. Louis encephalitis viruses. Handb Clin Neurol 123: 433–447.
-
14.
Petersen LR, Jamieson DJ, Powers AM, Honein MA, 2016. Zika virus. N Engl J Med 374: 1552–1563.
-
15.
Weaver SC, Costa F, Garcia-Blanco MA, Ko AI, Ribeiro GS, Saade G, Shi PY, Vasilakis N, 2016. Zika virus: history, emergence, biology, and prospects for control. Antiviral Res 130: 69–80.
-
16.
Ibanez-Bernal S, Briseno B, Mutebi JP, Argot E, Rodriguez G, Martinez-Campos C, Paz R, de la Fuente-San Roman P, Tapia-Conyer R, Flisser A, 1997. First record in America of Aedes albopictus naturally infected with dengue virus during the 1995 outbreak at Reynosa, Mexico. Med Vet Entomol 11: 305–309.
-
17.
Rawlings J et al. 1996. Dengue fever at the US-Mexico border, 1995–1996 (reprinted from MMWR, vol 45, pg 841, 1996). JAMA 276: 1464–1465.
-
18.
Ramos MM et al. 2008. Epidemic dengue and dengue hemorrhagic fever at the Texas-Mexico border: results of a household-based seroepidemiologic survey, December 2005. Am J Trop Med Hyg 78: 364–369.
-
19.
Brunkard JM, Robles Lopez JL, Ramirez J, Cifuentes E, Rothenberg SJ, Hunsperger EA, Moore CG, Brussolo RM, Villarreal NA, Haddad BM, 2007. Dengue fever seroprevalence and risk factors, Texas-Mexico border, 2004. Emerg Infect Dis 13: 1477–1483.
-
20.
Thomas DL et al. 2016. Reemergence of dengue in southern Texas, 2013. Emerg Infect Dis 22: 1002–1007.
-
21.
Secretaría de Salud México, Boletín Epidemiológico SNdVESÚdI, 2015. Available at: https://www.gob.mx/cms/uploads/attachment/file/10564/sem27.pdf. Accessed January 1, 2018.
-
22.
Secretaria de Salud, 2015. Lineamientos para la Vigilancia Epidemiológica de Dengue por Laboratorio (Guidelines for Epidemiological Surveillance of Dengue in the Laboratory). Available at: https://www.gob.mx/cms/uploads/attachment/file/23789/Lineamientos_para_la_vigilancia_epidemiologica_de_dengue.pdf. Accessed April 9, 2018.
-
23.
Chien LJ, Liao TL, Shu PY, Huang JH, Gubler DJ, Chang GJ, 2006. Development of real-time reverse transcriptase PCR assays to detect and serotype dengue viruses. J Clin Microbiol 44: 1295–1304.
-
24.
Beaty B, Calisher C, Shope R, 1995. Arboviruses. Lennette E, Lennette D, Lennette E, eds. Diagnostic Procedures for Viral, Rickettsial, and Chlamydial Infections. Washington, DC: American Public Health Association, 189–212.
-
25.
Chappell WA, Sasso DR, Toole RF, Monath TP, 1971. Labile serum factor and its effect on arbovirus neutralization. Appl Microbiol 21: 79–83.
-
26.
Laredo-Tiscareño SV et al. 2018. Arbovirus surveillance near the Mexico-U.S. border: isolation and sequence analysis of chikungunya virus from patients with dengue-like symptoms in Reynosa, Tamaulipas. Am J Trop Med Hyg 99: 191–194.
-
27.
Leduc-Galindo D et al. 2015. Characterization of the dengue outbreak in Nuevo Leon state, Mexico, 2010. Infection 43: 201–206.
-
28.
Dantes HG, Farfan-Ale JA, Sarti E, 2014. Epidemiological trends of dengue disease in Mexico (2000–2011): a systematic literature search and analysis. PLoS Negl Trop Dis 8: e3158.
-
29.
Shrivastava S, Tiraki D, Diwan A, Lalwani SK, Modak M, Mishra AC, Arankalle VA, 2018. Co-circulation of all the four dengue virus serotypes and detection of a novel clade of DENV-4 (genotype I) virus in Pune, India during 2016 season. PLoS One 13: e0192672.
-
30.
Andrade EH et al. 2016. Spatial-temporal co-circulation of dengue virus 1, 2, 3, and 4 associated with coinfection cases in a hyperendemic area of Brazil: a 4-week survey. Am J Trop Med Hyg 94: 1080–1084.
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