Literature DB >> 27342195

Alphacoronavirus in urban Molossidae and Phyllostomidae bats, Brazil.

Karen Miyuki Asano1,2, Aline Santana Hora3, Karin Côrrea Scheffer4, Willian Oliveira Fahl4, Keila Iamamoto4, Enio Mori4, Paulo Eduardo Brandão3.   

Abstract

BACKGROUND: Bats have been implicated as the main reservoir of coronavirus (CoV). Thus the role of these hosts on the evolution and spread of CoVs currently deserve the attention of emerging diseases surveillance programs. On the view of the interest on and importance of CoVs in bats the occurrence and molecular characterization of CoV were conducted in bats from Brazil.
FINDINGS: Three hundred five enteric contents of 29 bat species were tested using a panCoV nested RT-PCR. Nine specimens were positive and eight was suitable for RdRp gene sequencing. RdRp gene phylogeny showed that all CoVs strains from this study cluster in Alphacoronavirus genus, with one Molossidae and one Phlyllostomidae-CoV specific groups. Phylogenetic analyses of two S gene sequences showed a large diversity within the Alphacoronavirus genus.
CONCLUSIONS: This study indicated a CoV-to-host specificity and draws attention for CoV detection in Cynomops sp, a potential new reservoir. The phylogenetic analyses indicate that diversity of CoV in bats is higher than previously known.

Entities:  

Keywords:  Bat; Coronavirus; Molossidae; Phyllostomidae

Mesh:

Year:  2016        PMID: 27342195      PMCID: PMC4920988          DOI: 10.1186/s12985-016-0569-4

Source DB:  PubMed          Journal:  Virol J        ISSN: 1743-422X            Impact factor:   4.099


Background

Bats have been recognized as the natural reservoirs of a large variety of emerging and re-emerging viruses and have been implicated as the main reservoir of coronavirus (CoV). Thus the role of these hosts on the evolution and spread of CoVs currently deserve the attention of emerging diseases surveillance programs as illustrated by the finding of bats as reservoirs for SARS (Severe Acute Respiratory Syndrome) and MERS (Middle East Syndrome) coronavirus [1, 2]. CoV (Nidovirales:Coronaviridae:Coronavirinae) are classified into four genus: Alpha and Betacoronavirus are often found in mammals, while Gammacoronavirus were detected in wild birds, poultry, and marine mammals and Deltacoronavirus were detected in wild birds, pigs, and wild feline [3-5]. The first report of bat CoV was described in 2005 [6] in bats of Miniopterus pusillus species. Since then, several studies have identified the presence of CoV in bat population from various regions of the world, and to date have been detected both Alphacoronavirus and Betacoronavirus [6-13]. Although there is a great diversity of bats in Brazil, there are few studies related to bat CoV. Betacoronavirus has been reported in a Desmodus rotundus vampire bat and Alphacoronaviruses have been detected in Molosuss rufus, M. currentium, M. molossus, Carollia perspicillata, C. brevicauda and Tadarida brasilensis bats (14–18), but a range of bat species that might act as reservoirs for known or unknown CoVs still remains to be surveyed. On the view of the interest on and importance of bat CoV surveillance, the aim of this study was survey the occurrence of bat CoV in Brazil and to perform molecular characterization of CoVs detected.

Methods

This work was conducted with samples from 73 municipalities of São Paulo State, Southern Brazil, using 305 samples of enteric content of 29 bat species of three families (Molossidae, Phyllostomidae and Vespertilionidae). These animals were submitted to Instituto Pasteur (São Paulo, Brazil) from March/2013 to July/2014, as a part of rabies surveillance program, and were stored at −20 °C. Each animal was necropsied, the entire intestine was removed from abdominal cavity and all intestinal content was extracted and stored at −20 °C. Feces suspensions (v/v, 10 %) were prepared with DEPC-treated water. Suspensions were clarified at 12,000 × g for 30 min at 4 °C and the supernatants were used in the assays. Extraction of total RNA was carried out with TRIzol Reagent™ (Life Technologies, Carlsbad, CA, USA) according to the manufacture’s instruction followed by reverse transcription with Random Primers and M-MLV™ Reverse Transcriptase (Life Technologies, Carlsbad, CA, USA) as per manufacturer’s instructions. All samples were submitted to a pancoronavirus nested RT-PCR targeting the RNA-dependent RNA-polimerase (RdRp) [14], using Taq Platinum™ DNA Polymerase (Life Technologies, Carlsbad, CA, USA) as per manufacturer’s instructions. Positive samples were submitted to a RT-PCR targeting to S gene for phylogenetic inference [9]. Amplicons were purified using the ExoSap-IT® reagent (USB, Cleveland, OH, USA) or Illustra™ GFX™ Gel Extraction Kit (GE Healthcare, Buckinghamshire, UK) and bi-directional Sanger sequencing with the respective primers was carried out with BigDye v.3.1™ and ABI 3500 Genetic Analyzer™ (Life Technologies, Carlsbad, CA, USA). Chromatograms generated were subjected to Phred online application (http://asparagin.cenargen.embrapa.br/phph/) for assessment of their quality and the final consensus sequences were obtained with CAP Contig application in Bioedit 7.2.5 program [15]. Sequences obtained were aligned with homologous sequences retrieved from GenBank using CLUSTAL/W software in Bioedit 7.2.5 program [15]. Alignments were used for phylogenetic trees construction with distance optimization criterion with neighbor-joining algorithm and Composite Maximum Likelihood evolutionary model with 1000 “bootstrap” repetitions, using the MEGA 6 program [16].

Results and discussion

Nine out of the 305 samples (2,95 %) were found positive and DNA sequences were obtained for the RdRp for eight of them: sequences 4292/2013/Desmodus rotundus; 4539/2013/Cynomops planirostris, 4620/2013/Glossophaga soricina, 4702/2013/Cynomops abrasus, 4705/2013/Cynomops abrasus, 5026/2013/Cynomops abrasus, 2173/2014/Cynomops planirostris, 2218/2014/Cynomops planirostris (Genbank accession numbers KU552072 to KU552079). Five species tested were positive: Cynomops abrasus (3/11 = 27.3 %), Cynomops planirostris (3/5 = 60 %), Desmodus rotundus (1/41 = 2.4 %), Glossophaga soricina (1/33 = 3 %) and Platyrrhinus lineatus (1/12 = 8.3 %). Only the sample of P. lineatus was not confirmed by DNA sequencing. The occurrence of CoV per specie demonstrates a high frequency in Cynomops genus: 60 % for C. abrasus and 27.3 % for C. planirostris, indicating these species must have an important role in CoV maintenance in bat population in this region. In South America, CoV detection on bats have shown a low occurrence of CoV per species [12, 17, 18], however, none of these studies included the Cynomops genus. Though CoVs have been described in Brazilian Molossidae bats [19, 20], Cynomops sp were previously unknown hosts for CoVs. The Alphacoronaviruses found in Cynomops sp (Molossidae) were closely related with Alphacoronaviruses already detected in South Brazil (RdRp nt identities 81.4–82.9 %). D. rotundus is one of the three hematophagous bat species and can be found only in the Americas, from northern Mexico to northern Argentina [21]. Although the presence of Betacoronavirus has already been described [22], this is the first report of an Alphacoronavirus in common vampire bat, showing that this species can carry both Alpha and Betacoronavirus. G. soricina is a nectarivorous neotropical bat that might be found inside houses and has already been described as a host for Alphacoronaviruses [23]. Although separated by a large geographic area of more than 4000 km, G. soricina CoV found in São Paulo showed high nucleotide and amino acids identities when compared with G. soricina CoV of Trinidad and Tobago (90.3 and 98.4 %, respectively). G. soricina species does not migrate over long distances [24], therefore it is unlikely that transmission has occurred among these specimens, suggesting a virus-host adaptation. RdRp phylogeny (Fig. 1) showed that all CoVs strains from this study clustered in the Alphacoronavirus genus, with one Molossidae and one Phyllostomidae-CoV specific groups. The Molossidae CoV of this study clustered with Molossidae bat CoV from South Brazil with high bootstrap value (85 %). Although phylogenetic analysis indicates a geographic relation, the Alphacoronaviruses of this study was separated by a geographic area of 1000 km approximately from Molossidae batCoV previously detected in Brazil [19]. Besides, there are few studies regarding batCoV in Brazil, which difficult a phylogeographic relatedness hypothesis confirmation. Phyllostomidae CoV of this study clustered with sequences of Carollia perspicillata and G. soricina, two Phyllostomid bats from Trinidad and Tobago, with high bootstrap value (70 %) (Fig. 1). Taking together these results supports the theory that host specificity is more important than geographic pattern as previously noticed [13, 17, 25, 26].
Fig. 1

phylogenetic tree constructed with neighbor-joining method and maximum likelihood composite substitution model for partial 393 bp fragment of coronavirus RdRp gene. Numbers on each node represents the bootstrap values. The scale represents the number of substitutions sites. Samples of this study are identified with a black triangle

phylogenetic tree constructed with neighbor-joining method and maximum likelihood composite substitution model for partial 393 bp fragment of coronavirus RdRp gene. Numbers on each node represents the bootstrap values. The scale represents the number of substitutions sites. Samples of this study are identified with a black triangle Two 547 nt sequences of S gene (GenBank accession numbers KU552080 and KU552081) were obtained for C. planirostris and C. abrasus CoV. The nucleotide identity between these two sequences was high (99.8 %), suggesting the transmission of CoV among different bats species. However, the nucleotide identity with sequences retrieved from GenBank was low, varying from 39,1 and 65,8 %, showing a large genetic diversity with Alphacoronavirus from others countries. The phylogenetic tree performed for partial S gene (Fig. 2) shows that the samples of this study formed a separate group from others Alphacoronavirus sequences retrieved from GenBank, with bootstrap value of 100 %. Although the fragment analyzed was small, the tree indicates that samples of this study are unique, forming a completely separate group.
Fig. 2

phylogenetic tree constructed with the neighbor-joining method and maximum likelihood composite substitution model for partial 547 bp fragment of coronavirus S gene. Numbers on each node represents the bootstrap values. The scale represents the number of substitutions sites. Samples of this study are identified with a black triangle

phylogenetic tree constructed with the neighbor-joining method and maximum likelihood composite substitution model for partial 547 bp fragment of coronavirus S gene. Numbers on each node represents the bootstrap values. The scale represents the number of substitutions sites. Samples of this study are identified with a black triangle Environmental changes caused by man have promoted a major impact on ecology, affecting the movement of several wild animals species from their natural habitat to urban or rural areas [27], increasing the chances of contact between humans and domestic animals with wild animals. Furthermore approximately 75 % of emerging infectious diseases have zoonotic origin and wildlife as source of infection [28, 29]. Therefore, it is essential to survey and identify possible sources of infection, especially in relation to bats that are considered important reservoirs of viral agents [30, 31].

Conclusion

The significance of CoVs detected during this survey on Public Health remains to be investigated, but the finding of CoV in new viral reservoirs justifies the need for CoV surveillance. This study indicates a CoV-to-host specificity and draws attention for CoV detection in Cynomops sp, suggesting the importance of this species for CoV maintenance in the region studied. The phylogenetic analyses indicate a great diversity of CoV in bats, particularly for S gene.

Abbreviations

CoV: coronavirus; MERS: Middle East respiratory syndrome; RT-PCR: reverse transcription polymerase chain reaction; SARS: severe acute respiratory syndrome
  26 in total

Review 1.  Population biology of emerging and re-emerging pathogens.

Authors:  Mark E J Woolhouse
Journal:  Trends Microbiol       Date:  2002       Impact factor: 17.079

2.  Genomic characterization of severe acute respiratory syndrome-related coronavirus in European bats and classification of coronaviruses based on partial RNA-dependent RNA polymerase gene sequences.

Authors:  Jan Felix Drexler; Florian Gloza-Rausch; Jörg Glende; Victor Max Corman; Doreen Muth; Matthias Goettsche; Antje Seebens; Matthias Niedrig; Susanne Pfefferle; Stoian Yordanov; Lyubomir Zhelyazkov; Uwe Hermanns; Peter Vallo; Alexander Lukashev; Marcel Alexander Müller; Hongkui Deng; Georg Herrler; Christian Drosten
Journal:  J Virol       Date:  2010-08-04       Impact factor: 5.103

3.  Identification of a novel coronavirus in bats.

Authors:  L L M Poon; D K W Chu; K H Chan; O K Wong; T M Ellis; Y H C Leung; S K P Lau; P C Y Woo; K Y Suen; K Y Yuen; Y Guan; J S M Peiris
Journal:  J Virol       Date:  2005-02       Impact factor: 5.103

4.  Bats are natural reservoirs of SARS-like coronaviruses.

Authors:  Wendong Li; Zhengli Shi; Meng Yu; Wuze Ren; Craig Smith; Jonathan H Epstein; Hanzhong Wang; Gary Crameri; Zhihong Hu; Huajun Zhang; Jianhong Zhang; Jennifer McEachern; Hume Field; Peter Daszak; Bryan T Eaton; Shuyi Zhang; Lin-Fa Wang
Journal:  Science       Date:  2005-09-29       Impact factor: 47.728

5.  A coronavirus detected in the vampire bat Desmodus rotundus.

Authors:  Paulo Eduardo Brandão; Karin Scheffer; Laura Yaneth Villarreal; Samira Achkar; Rafael de Novaes Oliveira; Willian de Oliveira Fahl; Juliana Galera Castilho; Ivanete Kotait; Leonardo José Richtzenhain
Journal:  Braz J Infect Dis       Date:  2008-12       Impact factor: 1.949

6.  Alphacoronaviruses in New World bats: prevalence, persistence, phylogeny, and potential for interaction with humans.

Authors:  Christina Osborne; Paul M Cryan; Thomas J O'Shea; Lauren M Oko; Christina Ndaluka; Charles H Calisher; Andrew D Berglund; Mead L Klavetter; Richard A Bowen; Kathryn V Holmes; Samuel R Dominguez
Journal:  PLoS One       Date:  2011-05-12       Impact factor: 3.240

7.  Bat coronavirus in Brazil related to appalachian ridge and porcine epidemic diarrhea viruses.

Authors:  Paulo Vitor Marques Simas; Ana Caroline de Souza Barnabé; Ricardo Durães-Carvalho; Daniel Ferreira de Lima Neto; Leonardo Cardia Caserta; Luiza Artacho; Fábio André Facco Jacomassa; Matheus Cavalheiro Martini; Márcia Mercês Aparecida Bianchi Dos Santos; Paulo Anselmo Nunes Felippe; Helena Lage Ferreira; Clarice Weis Arns
Journal:  Emerg Infect Dis       Date:  2015-04       Impact factor: 6.883

8.  Novel bat coronaviruses, Brazil and Mexico.

Authors:  Luiz Gustavo Bentim Góes; Sicilene Gonzalez Ruvalcaba; Angélica Almeida Campos; Luzia Helena Queiroz; Cristiano de Carvalho; José Antonio Jerez; Edison Luiz Durigon; Luis Ignacio Iñiguez Dávalos; Samuel R Dominguez
Journal:  Emerg Infect Dis       Date:  2013-10       Impact factor: 6.883

9.  Bat origins of MERS-CoV supported by bat coronavirus HKU4 usage of human receptor CD26.

Authors:  Qihui Wang; Jianxun Qi; Yuan Yuan; Yifang Xuan; Pengcheng Han; Yuhua Wan; Wei Ji; Yan Li; Ying Wu; Jianwei Wang; Aikichi Iwamoto; Patrick C Y Woo; Kwok-Yung Yuen; Jinghua Yan; Guangwen Lu; George F Gao
Journal:  Cell Host Microbe       Date:  2014-09-10       Impact factor: 21.023

Review 10.  Mass extinctions, biodiversity and mitochondrial function: are bats 'special' as reservoirs for emerging viruses?

Authors:  Lin-Fa Wang; Peter J Walker; Leo L M Poon
Journal:  Curr Opin Virol       Date:  2011-11-09       Impact factor: 7.090

View more
  9 in total

1.  Erratum to: Alphacoronavirus in urban Molossidae and Phyllostomidae bats, Brazil.

Authors:  Karen Miyuki Asano; Aline Santana Hora; Karin Côrrea Scheffer; Willian Oliveira Fahl; Keila Iamamoto; Enio Mori; Paulo Eduardo Brandão
Journal:  Virol J       Date:  2016-07-07       Impact factor: 4.099

2.  Detection of coronavirus in vampire bats (Desmodus rotundus) in southern Brazil.

Authors:  Raquel Silva Alves; Juliana do Canto Olegário; Matheus Nunes Weber; Mariana Soares da Silva; Raissa Canova; Jéssica Tatiane Sauthier; Letícia Ferreira Baumbach; André Alberto Witt; Ana Paula Muterle Varela; Fabiana Quoos Mayer; Renata da Fontoura Budaszewski; Cláudio Wageck Canal
Journal:  Transbound Emerg Dis       Date:  2021-05-28       Impact factor: 4.521

3.  Coronavirus and paramyxovirus in bats from Northwest Italy.

Authors:  Francesca Rizzo; Kathryn M Edenborough; Roberto Toffoli; Paola Culasso; Simona Zoppi; Alessandro Dondo; Serena Robetto; Sergio Rosati; Angelika Lander; Andreas Kurth; Riccardo Orusa; Luigi Bertolotti; Maria Lucia Mandola
Journal:  BMC Vet Res       Date:  2017-12-22       Impact factor: 2.741

4.  Viral Diversity of Microbats within the South West Botanical Province of Western Australia.

Authors:  Diana Prada; Victoria Boyd; Michelle L Baker; Mark O'Dea; Bethany Jackson
Journal:  Viruses       Date:  2019-12-13       Impact factor: 5.048

5.  Detection of adenovirus, papillomavirus and parvovirus in Brazilian bats of the species Artibeus lituratus and Sturnira lilium.

Authors:  Fernando Finoketti; Raíssa Nunes Dos Santos; Aline Alves Scarpellini Campos; André Luís da Silva Zani; Camila Mosca Barboza; Marcélia Emanuele Sad Fernandes; Tatiane de Cassia Pardo de Souza; Driele Delanira Dos Santos; Giovana Werneck Bortolanza; Henrique Ortêncio Filho; Paulo Michel Roehe; Ana Cláudia Franco; Helena Beatriz de Carvalho Ruthner Batista
Journal:  Arch Virol       Date:  2019-02-10       Impact factor: 2.574

6.  Alphacoronavirus Detection in Lungs, Liver, and Intestines of Bats from Brazil.

Authors:  Cíntia Bittar; Rafael Rahal Guaragna Machado; Manuela Tosi Comelis; Larissa Mayumi Bueno; Mateus Rodrigues Beguelini; Eliana Morielle-Versute; Maurício Lacerda Nogueira; Paula Rahal
Journal:  Microb Ecol       Date:  2019-05-29       Impact factor: 4.552

Review 7.  Systematic review and meta-analysis of the prevalence of coronavirus: One health approach for a global strategy.

Authors:  Ricardo Faustino; Miguel Faria; Mónica Teixeira; Filipe Palavra; Paulo Sargento; Maria do Céu Costa
Journal:  One Health       Date:  2022-04-04

8.  Coronaviruses in Brazilian bats: A matter of concern?

Authors:  Samuel Cibulski; Francisco Esmaile Sales de Lima; Paulo Michel Roehe
Journal:  PLoS Negl Trop Dis       Date:  2020-10-26

Review 9.  Coronaviruses in Bats: A Review for the Americas.

Authors:  Itandehui Hernández-Aguilar; Consuelo Lorenzo; Antonio Santos-Moreno; Eduardo J Naranjo; Darío Navarrete-Gutiérrez
Journal:  Viruses       Date:  2021-06-25       Impact factor: 5.048

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.