Novel SARS-like betacoronaviruses in bats, China, 2011

previous item | next item


Material Information

Novel SARS-like betacoronaviruses in bats, China, 2011
Series Title:
Emerging infectious diseases
Yang, Li
Wu, Zhiqiang
Ren, Xianwen
Yang, Fan
He, Guimei
Zhang, Junpeng
Dong, Jie
Sun, Lilian
Zhu, Yafang
Du, Jiang
Zhang, Shuyi
Jin, Qi
Centers for Disease Control and Prevention
Publication Date:
Physical Description:
1 online resource


Subjects / Keywords:
Coronaviruses ( lcsh )
SARS (Disease) ( lcsh )
Bats -- Viruses ( lcsh )
serial ( sobekcm )
Asia -- China


To clarify the evolutionary relationships among betavoronaviruses that infect bats, we analyzed samples collected during 2010–2011 from 14 insectivorous bat species in China. We identified complete genomes of 2 novel betacoronaviruses in Rhinolophus pusillus and Chaerephon plicata bats, which showed close genetic relationships with severe acute respiratory syndrome coronaviruses.
Original Version:
Volume 19, Issue 6

Record Information

Source Institution:
University of South Florida
Holding Location:
University of South Florida
Rights Management:
All applicable rights reserved by the source institution and holding location.
Resource Identifier:
K26-05432 ( USFLDC DOI )
k26.5432 ( USFLDC Handle )

USFLDC Membership

University of South Florida
Karst Information Portal

Postcard Information



This item is only available as the following downloads:

Full Text


Novel SARS-like Betacoronaviruses in Bats, China, 2011Li Yang,1 Zhiqiang Wu,1 Xianwen Ren,1 Fan Yang,1 Guimei He, Junpeng Zhang, Jie Dong, Lilian Sun, Yafang Zhu, Jiang Du, Shuyi Zhang, and Qi JinTo clarify the evolutionary relationships among Rhinolophus pusillus and Chaerephon plicata severe acute respiratory syndrome coronaviruses.The 2003 outbreak of severe acute respiratory syndrome (SARS) was caused by a novel betacoronavirus and 900 deaths (1,2). In June 2012, a novel betacoronavirus (called human coronavirus EMC [HCoV-EMC]) also was isolated from the sputum of a patient from Saudi Arabia who died of pneumonia and renal failure (3). Similar viruses were detected in 2 additional patients who had severe pneumonia in Qatar in September 2012 and in Saudi Arabia in November 2012 (4,5). The clinical picture was remarkably similar to that of SARS and illustrates the epidemic potential of a novel coronavirus (CoV) to threaten global health. SARS-CoVs and HCoV-EMC were suspected of spreading from bats to humans because these CoVs were most closely related to bat CoVs (1,4). To clarify the evolutionary relationships among betavoronaviruses that infect bats, we analyzed samples collected during 20101 from 14 insectivorous bat species common in 8 provinces in China. The Study We obtained pharyngeal and anal swab specimens of 414 insectivorous bats. Samples of each species were pooled and then processed with a viral particle–protected 6 ). The extracted RNA species were then sequenced with the Illumina/Solexa GAII sequencer (Illumina, San Diego, CA, USA). Those reads generated by the Illumina/Solexa GAII with length of 80 bases were directly aligned to the protein sequences in the National Center for Biotechnology Information nonredundant protein database by the blastx program in the BLAST software package, version 2.2.22 (www.ncbi. with parameters “-e 1e-5 -F T -b 10 -v 10.” No assembly was performed before alignment. Sequence similarity–based taxonomic assignments were conducted as described (7 ). We found 1,075 reads of betacoronavirus in Rhinolophus pusillus bats in Shaanxi and 92 reads of betacoronavirus in Chaerephon plicata bats in Yunnan. We estimated the approximate locations of those reads on the CoV genome and their relative distances on the basis of alignment results exported with MEGAN 4– MetaGenome Analyzer ( software/megan/). The located reads were then used for reads-based nested PCR to identify genomic sequences. We established the complete genome sequences of 2 betacoronaviruses (Bat Rp-coronavirus/Shaanxi2011 and Bat Cp-coronavirus/Yunnan2011), which are 29,484 nt and 29,452 nt, respectively. The G+C content of Bat Rp-coronavirus/Shaanxi2011 and Bat Cp-coronavirus/ Yunnan2011 is 41.6% and 40.9%, respectively. We conducted complete genome comparison and phylogenetic analysis on the basis of polymerase and spike protein. Pairwise genome sequence alignment was conducted by using EMBOSS Needle software ( with default parameters. The overall nucleotide sequences between Bat Rp-coronavirus/Shaanxi2011 and Bat Cp-coronavirus/ Yunnan2011 indicated 88.7% nt identity. They shared 87.4%.5% nt identity with SARS-CoV, 88%.9% nt identity with the bat SARS-like CoV (bat SARSCoV Rm1), and 87.6%.6% nt identity with the civet SARS-like CoV (civet SARS-CoV SZ16). On the other hand, comparison between the betacoronavirus genomes and human betacoronavirus (HCoV-OC43) showed only 49.9%.4% nt overall identity, whereas the betacoronavirus genomes and HCoV-EMC showed 52.1% nt overall identity. The RNA-dependent RNA polymerase (RdRp, frame 1a,b) is a highly conserved gene of CoVs, which is frequently used for phylogenetic comparison (8 , 9 ). MEGA5.0 ( was used to construct 1


the phylogenetic trees on the basis of the nucleotide sequences and deduced amino acid sequences. First, we used the MUSCLE package and default parameters (www. to construct the alignment. The best substitution model was then evaluated with the Model Selection package implemented in MEGA5. Finally, we used the maximum-likelihood method with an appropriate model to process the phylogenetic analysis with 1,000 bootstrap replicates. We constructed a phylogenetic tree based on the nucleotide sequences of the RdRp gene to show the evolutionary relationship between these 2 betacoronaviruses and other CoVs (Figure 1). Reference CoV genome sequences were downloaded from GenBank and aligned with the fragments of the newly discovered CoVs. The RdRp genes of Bat Rp-coronavirus/ Shaanxi2011 and Bat Cp-coronavirus/Yunnan2011 were highly similar, sharing 93.1% nt identity. The phylogenetic analysis demonstrated that betacoronaviruses and the bat SARS-like CoVs in our study are clustered (93.1%.4% nt identity) and are close in distance to SARS-CoVs (92.9%.8% nt identity) and civet SARS-like CoVs (93.1%.8% nt identity) but that bat CoV (BtCoVHKU9) and HCoV-OC43 are placed among the relatively distant groups (65.8%.9% and 62.9%.5% nt identities with the betacoronaviruses, respectively). Therefore, collectively we called these betacoronaviruses and bat SARS-like CoVs the bat SARS-like cluster of CoVs. Bat Rp-coronavirus/Shaanxi2011 and Bat Cpcoronavirus/Yunnan2011 showed little genetic similarity (<66.2%.3% nt identity) to HCoV-EMC. The spike proteins of CoVs are responsible for receptor binding and host species adaptation, and their genes therefore constitute one of the most variable regions within CoV genomes (10, 11). The phylogenetic tree based on the amino acid sequences of spike protein (Figure 2) suggests that the selected betacoronaviruses were mainly divided into 5 clusters: SARS cluster; bat SARS-like cluster; civet SARS-like cluster; human betacoronavirus cluster; and EMC cluster. Bat Rp-coronavirus/Shaanxi2011 and Bat Cp-coronavirus/Yunnan2011 shared 89.4% aa identity in spike proteins, which consisted of 1,240 aa and 1,241 aa, respectively. The spike proteins of the CoVs in our analysis have 89.8%.7% aa identity with those of bat SARS-like CoVs, with substantial similarity in the receptor-binding domain. The close relationship also was observed with the SARS-CoVs (79.2%.4% aa identity) and civet SARS-like CoVs (78.9%.1% aa identity). In contrast, the human betacoronaviruses and EMC cluster formed separate clusters distinct from SARS-related CoVs that showed only 27.8%.4% aa and 28.8%.5% aa identities with the betacoronaviruses, respectively, in our analysis. The genome sequences reported here have been deposited into GenBank (accession nos. JX993987–JX993988). Conclusions The recent fatal human infection caused by HCoVEMC has boosted interest in the discovery of novel CoVs in humans and animals. HCoV-EMC is a novel betacoronavirus, and its closest known relatives are BtCoVs HKU4, and HKU5, which have been detected in Hong Kong only in bats (12), the same animal from which SARS is believed to have originated. Bats are increasingly recognized as natural reservoirs of CoVs and may serve as intermediate hosts for interspecies transmission of SARSCoVs (10, 13). Different bat populations from various countries harbor diverse CoVs that have a high frequency of recombination and mutation rates that enable them to DISPATCHES990 on the nucleotide sequence of the RdRp gene. The following


adapt to new hosts and ecologic niches (14, 15). Therefore, continuous studies of CoVs from different bat species and different countries would help better prevent the new global pandemics resulting from novel viral infection. We detected and characterized 2 novel betacoronaviruses–Bat Rp-coronavirus/Shaanxi2011 in R. pusillus bats and Bat Cp-coronavirus/Yunnan2011 in C. plicata bats–in China. The high similarity shown relationship among the CoVs (SARS-like CoVs and SARS-CoVs) that we analyzed. In contrast, Bat Rpcoronavirus/Shaanxi2011 and Bat Cp-coronavirus/ Yunnan2011 showed little genetic similarity with human betacoronaviruses and HCoV-EMC. Although several CoVs are found in horseshoe bats (Rhinolophus spp.), to our knowledge, the SARS-like CoVs in R. pusillus and C. plicata description presented here will further the understanding of CoVs distribution in different bat species found in human habitats and provide clues for rapid response to potential public health threats.This work was supported by the National Science and Technology Major Project, “China Mega-Project for Infectious Disease” (grant no. 2011ZX10004-001) from China. Dr Li Yang is a research assistant at the Institute of Pathogen Biology in Beijing. Her research interest is virus discovery. References 1. Peiris JS, Yuen KY, Osterhaus AD, Stohr K. The severe acute respiratory syndrome. N Engl J Med. 2003;349:2431. http:// 2. Drosten C, Gunther S, Preiser W, van der Werf S, Brodt HR, Becker acute respiratory syndrome. N Engl J Med. 2003;348:1967. 3. Zaki AM, van Boheemen S, Bestebroer TM, Osterhaus AD, Fouchier RA. Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia. N Engl J Med. 2012;367:1814. http://dx.doi. org/10.1056/NEJMoa1211721 4. Corman V, Eckerle I, Bleicker T, Zaki A, Landt O, EschbachBludau M, et al. Detection of a novel human coronavirus by realtime reverse-transcription polymerase chain reaction. Euro Surveill. 2012;17: pii: 20285. 5. ProMEDmail. Novel coronavirus—Saudi Arabia: new case. ProMED-mail 2012 Nov 04 [cited 2012 Nov 4]. http://www., article no. 20121104.1391285. 6. Wu Z, Ren X, Yang L, Hu Y, Yang J, He G, et al. Virome analysis Chinese provinces. J Virol. 2012;86:10999. http://dx.doi. org/10.1128/JVI.01394-12 7. Yang J, Yang F, Ren L, Xiong Z, Wu Z, Dong J, et al. Unbiased parallel detection of viral pathogens in clinical samples by use of a metagenomic approach. J Clin Microbiol. 2011;49:3463. http:// 8. Woo PC, Lau SK, Chu CM, Chan KH, Tsoi HW, Huang Y, et al. Characterization and complete genome sequence of a novel coronavirus, coronavirus HKU1, from patients with pneumonia. J Virol. 2005;79:884. 9. Lau SK, Li KS, Tsang AK, Shek CT, Wang M, Choi GK, et al. Recent transmission of a novel alphacoronavirus, bat coronavirus HKU10, from Leschenault’s rousettes to Pomona leaf-nosed bats: bats of different suborders. J Virol. 2012;86:11906. http://dx.doi. org/10.1128/JVI.01305-12 10. Li W, Shi Z, Yu M, Ren W, Smith C, Epstein JH, et al. Bats are natural reservoirs of SARS-like coronaviruses. Science. 2005;310:676. 11. Lau SK, Woo PC, Li KS, Huang Y, Wang M, Lam CS, et al. Complete genome sequence of bat coronavirus HKU2 from Chinese horseshoe bats revealed a much smaller spike gene with a different evolutionary lineage from the rest of the genome. Virology. 2007;367:428. 12. Woo PC, Lau SK, Li KS, Poon RW, Wong BH, Tsoi HW, et al. Molecular diversity of coronaviruses in bats. Virology. 2006;351:180. 13. Balboni A, Battilani M, Prosperi S. The SARS-like coronaviruses: the role of bats and evolutionary relationships with SARS coronavirus. New Microbiol. 2012;35:1. 14. Lau SK, Lee P, Tsang AK, Yip CC, Tse H, Lee RA, et al. Molecular epidemiology of human coronavirus OC43 reveals evolution of different genotypes over time and recent emergence of a novel genotype due to natural recombination. J Virol. 2011;85:11325. 15. Woo PC, Lau SK, Huang Y, Yuen KY. Coronavirus diversity, phylogeny and interspecies jumping. Exp Biol Med (Maywood). 2009;234:1117. Address for correspondence: Qi Jin, Ministry of Health Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 6, Rongjing East St, BDA, Beijing 100176, China; email: deduced amino acid sequence of spike protein. SARS, severe acute respiratory syndrome; CoV, coronavirus; HCoV, human CoV; BtCoV,


Download Options [CUSTOM IMAGE]

No images are available for this item.
Cite this item close


Cras ut cursus ante, a fringilla nunc. Mauris lorem nunc, cursus sit amet enim ac, vehicula vestibulum mi. Mauris viverra nisl vel enim faucibus porta. Praesent sit amet ornare diam, non finibus nulla.


Cras efficitur magna et sapien varius, luctus ullamcorper dolor convallis. Orci varius natoque penatibus et magnis dis parturient montes, nascetur ridiculus mus. Fusce sit amet justo ut erat laoreet congue sed a ante.


Phasellus ornare in augue eu imperdiet. Donec malesuada sapien ante, at vehicula orci tempor molestie. Proin vitae urna elit. Pellentesque vitae nisi et diam euismod malesuada aliquet non erat.


Nunc fringilla dolor ut dictum placerat. Proin ac neque rutrum, consectetur ligula id, laoreet ligula. Nulla lorem massa, consectetur vitae consequat in, lobortis at dolor. Nunc sed leo odio.