Genomic Analyses of Potential Novel Recombinant Human Adenovirus C in Brazil
Roozbeh Tahmasebi,
Antonio Charlys da Costa,
Kaelan Tardy,
Rory J. Tinker,
Flavio Augusto de Padua Milagres,
Rafael Brustulin,
Maria da Aparecida Rodrigues Teles,
Rogério Togisaki das Chagas,
Cassia Vitória de Deus Alves Soares,
Aripuana Sakurada Aranha Watanabe,
Cecilia Salete Alencar,
Fabiola Villanova,
Xutao Deng,
Eric Delwart,
Adriana Luchs,
Élcio Leal,
Ester Cerdeira Sabino
Affiliations
Roozbeh Tahmasebi
Polytechnic School of University of Sao Paulo, Sao Paulo 01246-903, Brazil
Antonio Charlys da Costa
Institute of Tropical Medicine, University of Sao Paulo, Sao Paulo 01246-903, Brazil
Kaelan Tardy
Institute of Tropical Medicine, University of Sao Paulo, Sao Paulo 01246-903, Brazil
Rory J. Tinker
Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PL, UK
Flavio Augusto de Padua Milagres
LIM/46, Faculty of Medicine, University of Sao Paulo, Sao Paulo 01246-903, Brazil
Rafael Brustulin
LIM/46, Faculty of Medicine, University of Sao Paulo, Sao Paulo 01246-903, Brazil
Maria da Aparecida Rodrigues Teles
Secretary of Health of Tocantins, Tocantins 77453-000, Brazil
Rogério Togisaki das Chagas
Secretary of Health of Tocantins, Tocantins 77453-000, Brazil
Cassia Vitória de Deus Alves Soares
Secretary of Health of Tocantins, Tocantins 77453-000, Brazil
Aripuana Sakurada Aranha Watanabe
Department of Parasitology, Microbiology and Immunology, Federal University of Juiz de Fora, Juiz de Fora, MG 34092829, Brazil
Cecilia Salete Alencar
Central Laboratory Division-DLC-HCSP, Clinical Laboratory and LIM 03-Department of Pathology, Clinical Hospital, University of Sao Paulo Medical School, Sao Paulo 01246-000, Brazil
Fabiola Villanova
Institute of Biological Sciences, Federal University of Para, Para 66075-000, Brazil
Xutao Deng
Vitalant Research Institute, 270 Masonic Avenue, San Francisco, CA 94118-4417, USA
Eric Delwart
Vitalant Research Institute, 270 Masonic Avenue, San Francisco, CA 94118-4417, USA
Adriana Luchs
Enteric Disease Laboratory, Virology Center, Adolfo Lutz Institute, Sao Paulo 01246-000, Brazil
Élcio Leal
Institute of Biological Sciences, Federal University of Para, Para 66075-000, Brazil
Ester Cerdeira Sabino
Polytechnic School of University of Sao Paulo, Sao Paulo 01246-903, Brazil
Human Adenovirus species C (HAdV-C) is the most common etiologic agent of respiratory disease. In the present study, we characterized the nearly full-length genome of one potential new HAdV-C recombinant strain constituted by Penton and Fiber proteins belonging to type 89 and a chimeric Hexon protein of types 1 and 89. By using viral metagenomics techniques, we screened out, in the states of Tocantins and Pará, Northern and North regions of Brazil, from 2010 to 2016, 251 fecal samples of children between 0.5 to 2.5 years old. These children were presenting acute diarrhea not associated with common pathogens (i.e., rotavirus, norovirus). We identified two HAdV-C strains in two distinct patients. Phylogenetic analysis performed using all complete genomes available at GenBank database indicated that one strain (HAdV-C BR-245) belonged to type 1. The phylogenetic analysis also indicated that the second strain (HAdV-C BR-211) was located at the base of the clade formed by the newly HAdV-C strains type 89. Recombination analysis revealed that strain HAdV-C BR-211 is a chimera in which the variable regions of Hexon gene combined HAdV-C1 and HAdV-C89 sequences. Therefore, HAdV-C BR-211 strain possesses a genomic backbone of type HAdV-C89 and a unique insertion of HAdV-C1 in the Hexon sequence. Recombination may play an important driving force in HAdV-C diversity and evolution. Studies employing complete genomic sequencing on circulating HAdV-C strains in Brazil are needed to understand the clinical significance of the presented data.