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Dive into the research topics where Roberto Navarro-Lopez is active.

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Featured researches published by Roberto Navarro-Lopez.


Emerging Infectious Diseases | 2003

West Nile virus in Mexico: evidence of widespread circulation since July 2002.

Jose G. Estrada-Franco; Roberto Navarro-Lopez; David W. C. Beasley; Lark L. Coffey; Anne-Sophie Carrara; Amelia Travassos da Rosa; Tamara Clements; Eryu Wang; George V. Ludwig; Arturo Campomanes Cortes; Pedro Paz Ramirez; Robert B. Tesh; Alan D. T. Barrett; Scott C. Weaver

West Nile virus (WNV) antibodies were detected in horses from five Mexican states, and WNV was isolated from a Common Raven in the state of Tabasco. Phylogenetic studies indicate that this isolate, the first from Mexico, is related to strains from the central United States but has a relatively high degree of sequence divergence.


Emerging Infectious Diseases | 2004

Genome sequence and attenuating mutations in West Nile virus isolate from Mexico.

David W. C. Beasley; C. Todd Davis; Jose G. Estrada-Franco; Roberto Navarro-Lopez; Arturo Campomanes-Cortes; Robert B. Tesh; Scott C. Weaver; Alan D. T. Barrett

The complete genome sequence of a Mexican West Nile virus isolate, TM171-03, included 46 nucleotide (0.42%) and 4 amino acid (0.11%) differences from the NY99 prototype. Mouse virulence differences between plaque-purified variants of TM171-03 with mutations at the E protein glycosylation motif suggest the emergence of an attenuating mutation.


Emerging Infectious Diseases | 2006

Introductions of West Nile Virus Strains to Mexico

Eleanor R. Deardorff; Jose G. Estrada-Franco; Aaron C. Brault; Roberto Navarro-Lopez; Arturo Campomanes-Cortes; Pedro Paz-Ramirez; Mario Solis-Hernandez; Wanichaya N. Ramey; C. Todd Davis; David W. C. Beasley; Robert B. Tesh; Alan D. T. Barrett; Scott C. Weaver

Complete genome sequencing of 22 West Nile virus isolates suggested 2 independent introductions into Mexico. A previously identified mouse-attenuated glycosylation variant was introduced into southern Mexico through the southeastern United States, while a common US genotype appears to have been introduced incrementally into northern Mexico through the southwestern United States.


Emerging Infectious Diseases | 2004

Venezuelan Equine Encephalitis Virus, Southern Mexico

Jose G. Estrada-Franco; Roberto Navarro-Lopez; Jerome E. Freier; Dionicio Cordova; Tamara Clements; Abelardo C. Moncayo; Wenli Kang; Carlos Hugo Gómez-Hernández; Gabriela Rodríguez-Domínguez; George V. Ludwig; Scott C. Weaver

Evidence of enzootic and endemic Venezuelan equine encephalitis virus circulation in southern Mexico since the 1996 epizootic was obtained from serosurveys and virus isolations.


PLOS Neglected Tropical Diseases | 2012

Venezuelan equine encephalitis virus activity in the Gulf Coast region of Mexico, 2003-2010.

A. Paige Adams; Roberto Navarro-Lopez; Francisco J. Ramirez-Aguilar; Irene Lopez-Gonzalez; Grace Leal; Jose M. Flores-Mayorga; Amelia Travassos da Rosa; Kali D. Saxton-Shaw; Amber J. Singh; Erin M. Borland; Ann M. Powers; Robert B. Tesh; Scott C. Weaver; Jose G. Estrada-Franco

Venezuelan equine encephalitis virus (VEEV) has been the causative agent for sporadic epidemics and equine epizootics throughout the Americas since the 1930s. In 1969, an outbreak of Venezuelan equine encephalitis (VEE) spread rapidly from Guatemala and through the Gulf Coast region of Mexico, reaching Texas in 1971. Since this outbreak, there have been very few studies to determine the northward extent of endemic VEEV in this region. This study reports the findings of serologic surveillance in the Gulf Coast region of Mexico from 2003–2010. Phylogenetic analysis was also performed on viral isolates from this region to determine whether there have been substantial genetic changes in VEEV since the 1960s. Based on the findings of this study, the Gulf Coast lineage of subtype IE VEEV continues to actively circulate in this region of Mexico and appears to be responsible for infection of humans and animals throughout this region, including the northern State of Tamaulipas, which borders Texas.


Emerging Infectious Diseases | 2009

Experimental Infection of Potential Reservoir Hosts with Venezuelan Equine Encephalitis Virus, Mexico

Eleanor R. Deardorff; Naomi L. Forrester; Amelia Travassos da Rosa; Jose G. Estrada-Franco; Roberto Navarro-Lopez; Robert B. Tesh; Scott C. Weaver

Multiple wild rodent species can serve as amplifying reservoir hosts for virus subtype IE.


American Journal of Tropical Medicine and Hygiene | 2011

Candidate Vectors and Rodent Hosts of Venezuelan Equine Encephalitis Virus, Chiapas, 2006–2007

Eleanor R. Deardorff; Jose G. Estrada-Franco; Jerome E. Freier; Roberto Navarro-Lopez; Amelia Travassos da Rosa; Robert B. Tesh; Scott C. Weaver

Enzootic Venezuelan equine encephalitis virus (VEEV) has been known to occur in Mexico since the 1960s. The first natural equine epizootic was recognized in Chiapas in 1993 and since then, numerous studies have characterized the etiologic strains, including reverse genetic studies that incriminated a specific mutation that enhanced infection of epizootic mosquito vectors. The aim of this study was to determine the mosquito and rodent species involved in enzootic maintenance of subtype IE VEEV in coastal Chiapas. A longitudinal study was conducted over a year to discern which species and habitats could be associated with VEEV circulation. Antibody was rarely detected in mammals and virus was not isolated from mosquitoes. Additionally, Culex (Melanoconion) taeniopus populations were found to be spatially related to high levels of human and bovine seroprevalence. These mosquito populations were concentrated in areas that appear to represent foci of stable, enzootic VEEV circulation.


American Journal of Tropical Medicine and Hygiene | 2010

Experimental Infections of Oryzomys couesi with Sympatric Arboviruses from Mexico

Eleanor R. Deardorff; Naomi L. Forrester; Amelia Travassos da Rosa; Jose G. Estrada-Franco; Roberto Navarro-Lopez; Robert B. Tesh; Scott C. Weaver

Coues rice rat (Oryzomys couesi), a species abundant throughout Central America, was evaluated experimentally for the ability to serve as an amplifying host for three arboviruses: Patois (Bunyaviridae, Orthobunyavirus), Nepuyo (Orthobunyavirus), and Venezuelan equine encephalitis virus subtype ID (Togaviridae, Alphavirus). These three viruses have similar ecologies and are known to co-circulate in nature. Animals from all three cohorts survived infection and developed viremia with no apparent signs of illness and long-lasting antibodies. Thus, O. couesi may play a role in the general maintenance of these viruses in nature.


Proceedings of the National Academy of Sciences of the United States of America | 2004

Venezuelan equine encephalitis emergence: Enhanced vector infection from a single amino acid substitution in the envelope glycoprotein

Aaron C. Brault; Ann M. Powers; Diana Ortiz; Jose G. Estrada-Franco; Roberto Navarro-Lopez; Scott C. Weaver


Future Virology | 2011

Endemic Venezuelan equine encephalitis in the Americas: hidden under the dengue umbrella

Patricia V. Aguilar; Jose G. Estrada-Franco; Roberto Navarro-Lopez; Cristina Ferro; Andrew D. Haddow; Scott C. Weaver

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Jose G. Estrada-Franco

University of Texas Medical Branch

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Scott C. Weaver

University of Texas Medical Branch

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Robert B. Tesh

University of Texas Medical Branch

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Amelia Travassos da Rosa

University of Texas Medical Branch

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Alan D. T. Barrett

University of Texas Medical Branch

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David W. C. Beasley

University of Texas Medical Branch

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C. Todd Davis

Centers for Disease Control and Prevention

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Aaron C. Brault

Centers for Disease Control and Prevention

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Ann M. Powers

Centers for Disease Control and Prevention

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