Viral metagenomics unveils MW (Malawi) polyomavirus infection in Brazilian pediatric patients with acute respiratory disease

Author:

da Silva Anielly S.1ORCID,de Campos Gabriel Montenegro1,Giovanetti Marta234,Zucherato Victória Simonatto1,Lima Alex Ranieri Jerônimo5,Santos Elaine Vieira1,Haddad Rodrigo6ORCID,Ciccozzi Massimo7ORCID,Carlos Júnior Alcantara Luiz24,Elias Maria Carolina5,Sampaio Sandra Coccuzzo5,Covas Dimas Tadeu15,Kashima Simone1ORCID,Slavov Svetoslav Nanev15

Affiliation:

1. Blood Center of Ribeirão Preto, Faculty of Medicine of Ribeirão Preto University of São Paulo Ribeirão Preto São Paulo Brazil

2. Laboratory of Flaviviruses Oswaldo Cruz Institute Rio de Janeiro Rio de Janeiro Brazil

3. Department of Science and Technology for Humans and Environment University of Campus‐Bio Medico di Roma Rome Italy

4. Interunit Postgraduate Program in Bioinformatics Federal University of Minas Gerais Belo Horizonte Minas Gerais Brazil

5. Center for Scientific Development (CDC) Butantan Institute São Paulo São Paulo Brazil

6. Faculty of Ceilândia University of Brasília Brasília Federal District Brazil

7. Epidemiology and Statistics Unit University of Campus Bio‐Medico di Roma Rome Italy

Abstract

AbstractViral metagenomics has been extensively applied for the identification of emerging or poorly characterized viruses. In this study, we applied metagenomics for the identification of viral infections among pediatric patients with acute respiratory disease, but who tested negative for SARS‐CoV‐2. Twelve pools composed of eight nasopharyngeal specimens were submitted to viral metagenomics. Surprisingly, in two of the pools, we identified reads belonging to the poorly characterized Malawi polyomavirus (MWPyV). Then, the samples composing the positive pools were individually tested using quantitative polymerase chain reaction for identification of the MWPyV index cases. MWPyV‐positive samples were also submitted to respiratory virus panel testing due to the metagenomic identification of different clinically important viruses. Of note, MWPyV‐positive samples tested also positive for respiratory syncytial virus types A and B. In this study, we retrieved two complete MWPyV genome sequences from the index samples that were submitted to phylogenetic inference to investigate their viral origin. Our study represents the first molecular and genomic characterization of MWPyV obtained from pediatric patients in South America. The detection of MWPyV in acutely infected infants suggests that this virus might participate (coparticipate) in cases of respiratory symptoms. Nevertheless, future studies based on testing of a larger number of clinical samples and MWPyV complete genomes appear to be necessary to elucidate if this emerging polyomavirus might be clinically important.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

International Centre for Genetic Engineering and Biotechnology

Publisher

Wiley

Subject

Infectious Diseases,Virology

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