Ahead of Print -Antibodies against MERS Coronavirus in Dromedary Camels, United Arab Emirates, 2003 and 2013 - Volume 20, Number 4—April 2014 - Emerging Infectious Disease journal - CDC
Volume 20, Number 4—April 2014
Research
Antibodies against MERS Coronavirus in Dromedary Camels, United Arab Emirates, 2003 and 2013
Article Contents
Benjamin Meyer, Marcel A. Müller, Victor M. Corman, Chantal B.E.M. Reusken, Daniel Ritz, Gert-Jan Godeke, Erik Lattwein, Stephan Kallies, Artem Siemens, Janko van Beek, Jan F. Drexler, Doreen Muth, Berend-Jan Bosch, Ulrich Wernery, Marion P.G. Koopmans, Renate Wernery, and Christian Drosten
Author affiliations: University of Bonn Medical Centre, Bonn, Germany (B. Meyer, M.A. Müller, V.M. Corman, D. Ritz, S. Kallies, A. Siemens, J.F. Drexler, D. Muth, C. Drosten); National Institute for Public Health and the Environment, Bilthoven, the Netherlands. (C.B.E.M. Reusken, G.-J. Godeke, J. van Beek, M.P.G. Koopmans);Erasmus Medical Centre, Rotterdam, the Netherlands (C.B.E.M. Reusken, J.F. Drexler, M.P.G. Koopmans); EUROIMMUN AG, Lübeck, Germany (E. Lattwein); Utrecht University, Utrecht, the Netherlands (B.-J. Bosch); Central Veterinary Research Laboratory, Dubai, United Arab Emirates (U. Wernery, R. Wernery)
Abstract
Middle East respiratory syndrome coronavirus (MERS-CoV) has caused an ongoing outbreak of severe acute respiratory tract infection in humans in the Arabian Peninsula since 2012. Dromedary camels have been implicated as possible viral reservoirs. We used serologic assays to analyze 651 dromedary camel serum samples from the United Arab Emirates; 151 of 651 samples were obtained in 2003, well before onset of the current epidemic, and 500 serum samples were obtained in 2013. Recombinant spike protein–specific immunofluorescence and virus neutralization tests enabled clear discrimination between MERS-CoV and bovine CoV infections. Most (632/651, 97.1%) camels had antibodies against MERS-CoV. This result included all 151 serum samples obtained in 2003. Most (389/651, 59.8%) serum samples had MERS-CoV–neutralizing antibody titers > 1,280. Dromedary camels from the United Arab Emirates were infected at high rates with MERS-CoV or a closely related, probably conspecific, virus long before the first human MERS cases.
Middle East respiratory syndrome coronavirus (MERS-CoV) is an emerging pathogen associated with severe respiratory symptoms and renal failure in infected patients (1,2). Globally, 156 laboratory-confirmed cases of infection with MERS-CoV, including 65 deaths, were reported as of early November 2013. All human cases were linked to the Arabian Peninsula (Saudi Arabia, Jordan, Oman, Qatar, Kuwait, and the United Arab Emirates). Imported cases were detected in countries in Europe and Africa (United Kingdom, Germany, Italy, France, and Tunisia) (3).
Transmission patterns, including the putative zoonotic source of the virus, remain unclear. Hypotheses include frequent zoonotic infections with limited subsequent human-to-human transmission chains and existence of a self-sustained epidemic in humans (4). A recent study found evidence to support the existence of epidemiologically unlinked cases in a large outbreak in the al-Hasa region, Saudi Arabia (5). It was speculated that zoonotic introductions of MERS-CoV from an unknown reservoir might occur at high rates, in addition to obvious human-to-human transmission.
Coronaviruses (CoV) are positive-sense RNA viruses. Viruses in the genera Alphacoronavirus andBetacoronavirus are associated with mammals and show a particularly high level of diversification in bats. Viruses in the genera Gammacoronavirus and Deltacoronavirus are mostly avian-associated viruses (6,7). MERS-CoV belongs to Betacoronavirus phylogenetic lineage C that, in addition to MERS-CoV, contains 2 distinct bat-associated CoV species (HKU4 and HKU5) (1,8).
Insectivorous bats of the family Vespertilionidae were recently shown to carry viruses that are probably conspecific with MERS-CoV (9). However, the limited rate of contact between humans and insectivorous bats makes a continuous and frequent acquisition of MERS-CoV from bats an unlikely scenario. In a manner similar to observations regarding severe acute respiratory syndrome CoV (SARS-CoV), an intermediate reservoir host might exist from which human infections are acquired. Dromedary camels from different regions in Africa and the Arabian Peninsula have been shown to have antibodies against MERS-CoV (10,11). Animals from the Arabian Peninsula had high neutralizing serum activities overall and reciprocal antibody titers ≤320–1,280, which support recent infection with MERS-CoV or a highly related virus. Thus, dromedary camels might serve as intermediate hosts. However, detailed serologic studies in countries with actual incidence of MERS-CoV infections in humans have not been conducted.
Serologic analysis of CoVs is challenging because of cross-reactivity between CoVs infecting the same host and the broad distribution of CoVs in diverse mammalian species (6,7,12–14). Antibodies directed against some of the major antigens of different CoVs are known to cross-react in standard serologic assays (15,16). Potential cross-reactivity is a diagnostic challenge because camelids are known to be infected with bovine CoV (BCoV), a distinct betacoronavirus of phylogenetic lineage A unrelated to the MERS-CoV (17,18). As an additional challenge, camel immunoglobulins lack a light chain peptide, which affects specific physical properties, such as altered size and stability, compared with immunoglobulins of other mammals (19,20). The influence of this feature on serologic assays has not been thoroughly investigated. Thus, serologic assays should be applied with caution, and different assay formats should be tested concurrently.
We reported a 2-staged approach for MERS-CoV serologic analysis in humans (15,16). Expanding upon these studies, we used in the present study a recombinant MERS-CoV spike protein immunofluroescence assay (rIFA) augmented by a validated protein microarray (10,21), followed by MERS-CoV–specific neutralization assay, to screen 651 dromedary camel serum samples from the United Arabian Emirates. Cross-reactivity against clade A betacoronaviruses was assessed by using a immunofluorescence assay (IFA) and a BCoV-specific neutralization assay. Serum samples obtained in 2003 and 2013 were compared to obtain information for the time in which MERS-related CoV has been circulating in camels.
Acknowledgments
We thank Tobias Bleicker for providing excellent technical assistance.
The work was supported by a European research project on emerging diseases detection and response (EMPERIE; www.emperie.eu/emp/) (contract no. 223498) and ANTIGONE (contract no. 278976). C.D. has received infrastructural support from the German Centre for Infection Research, the German Ministry for Research and Education, and the German Research Council (grants 01KIO701 and DR 772/3-1).
References
- 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;367:1814–20. DOIPubMed
- Drosten C, Seilmaier M, Corman VM, Hartmann W, Scheible G, Sack S, Clinical features and virological analysis of a case of Middle East respiratory syndrome coronavirus infection. Lancet Infect Dis. 2013;13:745–51. DOIPubMed
- World Health Organization. Middle East respiratory syndrome coronavirus (MERS-CoV)—update, 2013 [cited 2013 Dec 10].http://www.who.int/csr/don/2013_06_26/en/index.html
- Cauchemez S, Van Kerkhove MD, Riley S, Donnelly CA, Fraser C, Ferguson NM.Transmission scenarios for Middle East respiratory syndrome coronavirus (MERS-CoV) and how to tell them apart. Euro Surveill. 2013;18:20503.PubMed
- Cotten M, Watson SJ, Kellam P, Al-Rabeeah AA, Makhdoom HQ, Assiri A, Transmission and evolution of the Middle East respiratory syndrome coronavirus in Saudi Arabia: a descriptive genomic study. Lancet. 2013;382:1993–2002. DOIPubMed
- Woo PC, Lau SK, Lam CS, Lau CC, Tsang AK, Lau JH, Discovery of seven novel mammalian and avian coronaviruses in the genus deltacoronavirus supports bat coronaviruses as the gene source of alphacoronavirus and betacoronavirus and avian coronaviruses as the gene source of gammacoronavirus and deltacoronavirus. J Virol.2012;86:3995–4008. DOIPubMed
- Drexler JF, Gloza-Rausch F, Glende J, Corman VM, Muth D, Goettsche M, Genomic characterization of SARS-related coronavirus in European bats and classification of coronaviruses based on partial RNA-dependent RNA polymerase gene sequences. J Virol.2010;84:11336–49. DOIPubMed
- van Boheemen S, de Graaf M, Lauber C, Bestebroer TM, Raj VS, Zaki AM, Genomic characterization of a newly discovered coronavirus associated with acute respiratory distress syndrome in humans. MBio. 2012;3:e00473–12. DOIPubMed
- Ithete NL, Stoffberg S, Corman VM, Cottontail VM, Richards LR, Schoeman MC, Close relative of human middle East respiratory syndrome coronavirus in bat, South Africa.Emerg Infect Dis. 2013;19:1697–9. DOIPubMed
- Reusken CB, Haagmans BL, Muller MA, Gutierrez C, Godeke GJ, Meyer B, Middle East respiratory syndrome coronavirus neutralising serum antibodies in dromedary camels: a comparative serological study. Lancet Infect Dis. 2013;13:859–66. DOIPubMed
- Perera RA, Wang P, Gomaa M, El-Shesheny R, Kandeil A, Bagato O, Seroepidemiology for MERS coronavirus using microneutralisation and pseudoparticle virus neutralisation assays reveal a high prevalence of antibody in dromedary camels in Egypt, June 2013.Euro Surveill. 2013;18:20574.PubMed
- Woo PC, Lau SK, Li KS, Poon RW, Wong BH, Tsoi HW, Molecular diversity of coronaviruses in bats. Virology. 2006;351:180–7. DOIPubMed
- Pfefferle S, Oppong S, Drexler JF, Gloza-Rausch F, Ipsen A, Seebens A, Distant relatives of severe acute respiratory syndrome coronavirus and close relatives of human coronavirus 229E in bats, Ghana. Emerg Infect Dis. 2009;15:1377–84. DOIPubMed
- Gloza-Rausch F, Ipsen A, Seebens A, Gottsche M, Panning M, Felix Drexler J, Detection and prevalence patterns of group I coronaviruses in bats, northern Germany. Emerg Infect Dis. 2008;14:626–31. DOIPubMed
- Buchholz U, Muller MA, Nitsche A, Sanewski A, Wevering N, Bauer-Balci T, Contact investigation of a case of human novel coronavirus infection treated in a German hospital, October–November 2012. Euro Surveill. 2013;18:20406.PubMed
- Aburizaiza AS, Mattes FM, Azhar EI, Hassan AM, Memish ZA, Muth D, Investigation of anti–Middle East respiratory syndrome antibodies in blood donors and slaughtethouse workers in Jeddah and Makkah, Saudi Arabia, fall 2013. [Epub ahead of print]. J Infect Dis. 2013.
- Jin L, Cebra CK, Baker RJ, Mattson DE, Cohen SA, Alvarado DE, Analysis of the genome sequence of an alpaca coronavirus. Virology. 2007;365:198–203. DOIPubMed
- Wünschmann A, Frank R, Pomeroy K, Kapil S. Enteric coronavirus infection in a juvenile dromedary (Camelus dromedarius). J Vet Diagn Invest. 2002;14:441–4. DOIPubMed
- van der Linden RH, Frenken LG, de Geus B, Harmsen MM, Ruuls RC, Stok W, Comparison of physical chemical properties of llama VHH antibody fragments and mouse monoclonal antibodies. Biochim Biophys Acta. 1999;1431:37–46. DOIPubMed
- Hamers-Casterman C, Atarhouch T, Muyldermans S, Robinson G, Hamers C, Songa EB,Naturally occurring antibodies devoid of light chains. Nature. 1993;363:446–8. DOIPubMed
- Reusken C, Mou H, Godeke GJ, van der Hoek L, Meyer B, Muller MA, Specific serology for emerging human coronaviruses by protein microarray. Euro Surveill. 2013;18:20441 .PubMed
- FAOSTAT. 2013 [cited 2013 Dec16].http://faostat3.fao.org/faostat-gateway/go/to/download/Q/QA/E
- CVRL. 26th annual report 2012. 2013 [cited 2013 Dec 16].http://www.cvrl.ae/%5Can%5Canrp%5C2012%5CANRP2012.pdf
- Corman VM, Eckerle I, Bleicker T, Zaki A, Landt O, Eschbach-Bludau M, Detection of a novel human coronavirus by real-time reverse-transcription polymerase chain reaction.Euro Surveill. 2012;17:20285.PubMed
- Annan A, Baldwin HJ, Corman VM, Klose SM, Owusu M, Nkrumah EE, Human betacoronavirus 2c EMC/2012-related viruses in bats, Ghana and Europe. Emerg Infect Dis. 2013;19:456–9. DOIPubMed
- Corman VM, Muller M, Costabel U, Timm J, Binger T, Meyer B, Assays for laboratory confirmation of novel human coronavirus (hCoV-EMC) infections. Euro Surveill.2012;17:20334.PubMed
- de Souza Luna LK, Heiser V, Regamey N, Panning M, Drexler JF, Mulangu S, Generic detection of coronaviruses and differentiation at the prototype strain level by reverse transcription–PCR and nonfluorescent low-density microarray. J Clin Microbiol.2007;45:1049–52. DOIPubMed
- Gerna G, Cereda PM, Revello MG, Cattaneo E, Battaglia M, Gerna MT. Antigenic and biological relationships between human coronavirus OC43 and neonatal calf diarrhoea coronavirus. J Gen Virol. 1981;54:91–102. DOIPubMed
- Müller MA, Raj VS, Muth D, Meyer B, Kallies S, Smits SL, Human coronavirus EMC does not require the SARS-coronavirus receptor and maintains broad replicative capability in mammalian cell lines. MBio. 2012;3:e00515–12. DOIPubMed
- Raj VS, Mou H, Smits SL, Dekkers DH, Muller MA, Dijkman R, Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC. Nature. 2013;495:251–4. DOIPubMed
- Chan CM, Tse H, Wong SS, Woo PC, Lau SK, Chen L, Examination of seroprevalence of coronavirus HKU1 infection with S protein-based ELISA and neutralization assay against viral spike pseudotyped virus. J Clin Virol. 2009;45:54–60. DOIPubMed
- Horzinek MC, Lutz H, Pedersen NC. Antigenic relationships among homologous structural polypeptides of porcine, feline, and canine coronaviruses. Infect Immun.1982;37:1148–55.PubMed
- Hofmann H, Pyrc K, van der Hoek L, Geier M, Berkhout B, Pohlmann S. Human coronavirus NL63 employs the severe acute respiratory syndrome coronavirus receptor for cellular entry. Proc Natl Acad Sci U S A. 2005;102:7988–93. DOIPubMed
- Anthony SJ, Ojeda-Flores R, Rico-Chavez O, Navarrete-Macias I, Zambrana-Torrelio CM,Rostal MK, Coronaviruses in bats from Mexico. J Gen Virol. 2013;94:1028–38. DOIPubMed
- Wacharapluesadee S, Sintunawa C, Kaewpom T, Khongnomnan K, Olival KJ, Epstein JH,Group C betacoronavirus in bat guano fertilizer, Thailand. Emerg Infect Dis.2013;19:1349–51. DOIPubMed
- Drexler JF, Gloza-Rausch F, Glende J, Corman VM, Muth D, Goettsche M, 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. J Virol. 2010;84:11336–49. DOIPubMed
- Ge XY, Li JL, Yang XL, Chmura AA, Zhu G, Epstein JH, Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor. Nature. 2013;503:535–8. DOIPubMed
Figure
Tables
- Table 1. Validation of serologic assays for coronaviruses with differentially reactive dromedary camel serum samples, United Arab Emirates, 2003 and 2013
- Table 2. MERS-CoV serologic results for camel serum and fecal samples, United Arab Emirates, 2003 and 2013
- Table 3. BCoV neutralization test results for MERS-CoV–positive dromedary camel serum samples, United Arab Emirates, 2003 and 2013
Suggested citation for this article: Meyer B, Müller MA, Corman VM, Reusken CBEM, Ritz D, Godeke G-D, et al. Antibodies against MERS coronavirus in dromedary camels, United Arab Emirates, 2003 and 2013. Emerg Infect Dis [Internet]. 2014 Apr [date cited].http://dx.doi.org/10.3201/eid2004.131746
DOI: 10.3201/eid2004.131746
No hay comentarios:
Publicar un comentario