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Eurosurveillance, Volume 17, Issue 49, 06 December 2012
Rapid communications
Assays for laboratory confirmation of novel human coronavirus (hCoV-EMC) infections
  1. Institute of Virology, University of Bonn Medical Centre, Bonn, Germany
  2. These authors contributed equally to this work
  3. Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany
  4. Institute of Virology, University of Duisburg-Essen, Essen, Germany
  5. Robert Koch Institute, Berlin, Germany
  6. Euroimmun AG, Lübeck, Germany
  7. TibMolbiol, Berlin, Germany
  8. Virosciences Laboratory, Erasmus MC, Rotterdam, the Netherlands

Citation style for this article: Corman VM, Müller MA, Costabel U, Timm J, Binger T, Meyer B, Kreher P, Lattwein E, Eschbach-Bludau M, Nitsche A, Bleicker T, Landt O, Schweiger B, Drexler JF, Osterhaus AD, Haagmans BL, Dittmer U, Bonin F, Wolff T, Drosten C. Assays for laboratory confirmation of novel human coronavirus (hCoV-EMC) infections. Euro Surveill. 2012;17(49):pii=20334. Available online:
Date of submission: 05 December 2012

We present a rigorously validated and highly sensitive confirmatory real-time RT-PCR assay (1A assay) that can be used in combination with the previously reported upE assay. Two additional RT-PCR assays for sequencing are described, targeting the RdRp gene (RdRpSeq assay) and N gene (NSeq assay), where an insertion/deletion polymorphism might exist among different hCoV-EMC strains. Finally, a simplified and biologically safe protocol for detection of antibody response by immunofluorescence microscopy was developed using convalescent patient serum.


A novel human coronavirus, hCoV-EMC, has recently emerged in the Middle East region [1-3]. The virus has caused severe acute respiratory infection (SARI) in at least nine patients to date. Latest reports from the World Health Organization (WHO) suggest that infections have occurred since April 2012, as hCoV-EMC was found retrospectively in two patients from a group of 11 epidemiologically linked cases of SARI in Jordan, eight of whom were healthcare workers [4].

We have recently presented methods for the rapid detection of hCoV-EMC by real-time reverse transcription polymerase chain reaction (RT-PCR) [2]. One of these protocols, the upE gene assay, has been used as a first-line diagnostic assay for all human cases to date. More than 100 laboratories worldwide have since been equipped with positive-control material necessary to conduct the upE assay. We also presented a confirmatory RT-PCR assay targeting the open reading frame (ORF) 1b gene, with slightly lower sensitivity than the upE assay.

In view of the growing knowledge of the epidemiology of hCoV-EMC infections, WHO is continuously updating its guidelines for laboratory testing. During an expert consultation on 28 November 2012, it was concluded that first-line screening should involve the upE assay [2]. Confirmatory testing can involve any appropriately validated RT-PCR assay for alternative targets within the viral genome, followed by sequencing of at least a portion of one viral gene that can then be compared with hCoV-EMC sequences deposited in GenBank.

Recent investigations into a cluster of cases in Saudi Arabia have revealed the possibility that the virus may not be detected by RT-PCR in all patients with symptoms and proven epidemiological linkage [5]. From our previous experience during the severe acute respiratory syndrome (SARS) epidemic in 2003, such issues were predicted to occur when testing by RT-PCR alone [2]. In SARS patients, in particular those seen more than 10 days after symptom onset, serological testing by immunofluorescence assay (IFA) has been successfully used to complement RT-PCR findings [6,7].

On 22 November 2012, German health authorities were notified of a patient who had been treated for SARI in a hospital in Essen, Germany [5]. On the basis of clinical samples from this case, we present here a set of validated assays for the confirmation of cases of hCoV-EMC infection, including a confirmatory real-time RT-PCR assay in the ORF1a gene, two sequencing amplicons in the RNA-dependent RNA polymerase (RdRp) and nucleocapsid (N) protein genes, as well as a straightforward methodology for biologically safe immunofluorescence testing.


RT-PCR assays for the screening and confirmation of infections with hCoV-EMC
Figure 1 provides a summary of the target regions on the viral genome for screening, confirmation and sequence determination. Documentation on sources of materials used is provided in the Acknowledgements section.

Figure 1. RT-PCR target regions for screening, confirmation and sequencing of novel human coronavirus (hCoV-EMC)

RNA preparation
The procedures for RNA preparation have been described previously [2].

Confirmatory real-time RT-PCR assay in ORF 1a (1A assay)
A 25 µl reaction was set up containing 5 µl of RNA, 12.5 µl of 2 X reaction buffer from the Superscript III one step RT-PCR system with Platinum Taq Polymerase (Invitrogen; containing 0.4 mM of each dNTP and 3.2 mM MgSO4), 1 µl of reverse transcriptase/Taq mixture from the kit, 0.4 µl of a 50 mM MgCl2 solution (Invitrogen – not provided with the kit), 1 μg of non-acetylated bovine serum albumin (Sigma), 400 nM of primers EMC-Orf1a-Fwd (CCACTACTCCCATTTCGTCAG) and EMC-Orf1a-Rev (CAGTATGTGTAGTGCGCATATAAGCA), as well as 200 nM of probe EMCOrf1a-Prb (6-carboxyfluorescein (FAM)-TTGCAAATTGGCTTGCCCCCACT -6-carboxy-N,N,N,N´-tetramethylrhodamine (TAMRA)). Thermal cycling was performed at 55 °C for 20 min for the RT, followed by 95 °C for 3 min and then 45 cycles of 95 °C for 15 s, 58 °C for 30 s.

RT-PCR for generating amplicons for sequencing the RdRp gene target (RdRpSeq assay)
For the first round, a 25 µl reaction was set up containing 5 µl of RNA, 12.5 µl of 2 X reaction buffer from the Superscript III one step RT-PCR system with Platinum Taq Polymerase (Invitrogen; containing 0.4 mM of each dNTP and 3.2 mM MgSO4), 1 µl of reverse transcriptase/Taq mixture from the kit, 0.4 µl of a 50 mM MgSO4 solution (Invitrogen – not provided with the kit), 1 μg of non-acetylated bovine serum albumin (Sigma), 400 nM of each primer RdRpSeq-Fwd (TGC TAT WAG TGC TAA GAA TAG RGC; R=A/G, W=A/T) and RdRpSeq-Rev (GCA TWG CNC WGT CAC ACT TAG G; W=A/T, N=A/C/T/G). Thermal cycling was performed at 50 °C for 20 min, followed by 95 °C for 3 min and then 45 cycles of 95 °C for 15 s, 56 °C for 15 s and 72 °C for 30 s, with a terminal elongation step of 72 °C for 2 min.

In cases where no amplification products were obtained with the RT-PCR assay, a 50 µl second-round reaction was set up containing 1 µl of reaction mixture from the first round, 5 µl of 10 X reaction buffer provided with the Platinum Taq Polymerase Kit (Invitrogen), 2 µl of a 50 mM MgCl2 solution (provided with the kit), 200 µM of each dNTP, 400 nM concentrations of each second round primer RdRpSeq-Fwd (the same as in the first round) and RdRpSeq-Rnest (CAC TTA GGR TAR TCC CAW CCC A) and 0.2 μl of Platinum Taq from the kit. Thermal cycling was performed at 95 °C for 3 min and 45 cycles of 95 °C for 15 s, 56 °C for 15 s and 72 °C for 30 s, followed by a 2 min extension step at 72 °C.

RT-PCR for sequencing in the N gene (NSeq assay)
The assay employed the same conditions as the RdRpSeq assay, except that the primer sequences were  NSeq-Fwd (CCT TCG GTA CAG TGG AGC CA) and NSeq-Rev (GAT GGG GTT GCC AAA CAC AAA C) for the first round and NSeq-Fnest (TGA CCC AAA GAA TCC CAA CTA C) and NSeq-Rev (the same as in the first round) for the second round. The second round was only done if no product was visible by agarose gel electrophoresis after the first round.

Virus quantification by real-time RT-PCR using in-vitro transcribed RNA
In-vitro transcribed RNA was prepared as described previously [2]. Serial 10-fold dilutions of this RNA were amplified in parallel with samples in a Roche LightCycler 480II after entering the known RNA concentrations of standards in the quantification module of the operation software. Virus concentrations in terms of genome copies per ml of original sample were extrapolated using a conversion factor of 85.7, as explained previously [2].  

Virus growth, infection and titration
Virus stocks of the clinical isolate hCoV-EMC/2012 (kindly provided by Ron Fouchier [1]) were grown on African green monkey kidney (Vero B4) cells. Cells were infected at a multiplicity of infection (MOI) of 0.01 and supernatants were harvested two days post infection. Titres were determined by plaque assay on Vero B4 cells as described previously [8].

hCoV-EMC antibody detection assays
Two IFAs have been developed.

(i) Conventional IFA
Vero cells were seeded onto glass coverslips in 24-well plates, grown to subconfluence, and infected at an MOI of 0.5. After 24 hours, cell monolayers were fixed with acetone [9].

(ii) Rapid, biologically safe IFA
Vero B4 cells in flasks were infected at an MOI of 0.01 and harvested two days post infection. Infected cells were mixed with non-infected Vero B4 cells (ratio 1:1) and spotted on glass slides by dispensing and immediately aspirating the cell suspension. The concentration of the cell suspension was 10e7 cells per ml in medium. The time between dispensing and back-aspiration was 2 seconds. About 6 wells could be loaded with the content of one 50 µl pipette tip. It was important for the success of cell spotting that the IFA slides used for the procedure should have undergone aggressive cleaning and autoclaving before use. After drying, the slides were fixed and virus inactivated with 4% paraformaldehyde for 30 minutes. Slides were immersed into ice-cold acetone/methanol (ratio 1:1) to permeabilise the cells. In the assay, patient sera (25 µl per dilution) were subjected to serial dilution in sample buffer (Euroimmun AG, Lübeck, Germany) starting at 1:40 and applied at 25 l per well. As a positive control, a macaque-anti-hCoV-EMC (day 14 post infection), provided by author B. H. was used in a 1:20 dilution. Slides were incubated at 37 °C for 1 hour (rapid slides) or at room temperature for 30 minutes (conventional coverslips) and washed three times with phosphate-buffered saline (PBS)-Tween (0.1%) for 5 minutes. The secondary antibody was a goat-anti human Cy2-labelled immunoglobulin G conjugate. After incubation at 37 °C (spotted slides) or room temperature (conventional coverslips) for 30 minutes, they were washed three times with PBS-Tween for 5 minutes, rinsed with water and mounted with DAPI ProLong mounting medium (Life Technologies).

Recombinant assays for confirmatory IFA and western blot analysis
The hCoV-EMC/2012 spike (S) and N genes were amplified from cDNA. For PCR amplification of FLAG-tagged N and S and subsequent cloning into a pCG1 vector (kindly provided by Georg Herrler, TIHO, Hannover), the following primers were used: 2c-nhCoV-SflagN-BamHI-F (TACGGATCCGCCACCATGGATTACAAGGATGACGATGACAAGGGAGGCATACACTCAGTGTTTCTACTGATGT), 2c-nhCoV-S-SalI-R (AGCGTCGACTTAGTGAACATGAACCTTATGCGG), 2c-nhCoV-NflagN-BamHI-F (TACGGATCCGCCACCATGGATTACAAGGATGACGATGACAAGGGAGGCGCATCCCCTGCTGCACCTCGT) and 2c-nhCoV-N-XbaI-R (AGCTCTAGACTAATCAGTGTTAACATCAATCATTG).

For IFA, Vero B4 cells were transfected in suspension using 0.5 µg of plasmid DNA and the FuGENE HD protocol (Roche, Basel, Switzerland). Transfected cells were seeded into a 24-well plate containing glass coverslips. After 24 hours, cells were fixed with 4% paraformaldehyde, washed twice with PBS-Tween and permeabilised with PBS containing 0.1% Triton X-100. For western blot analysis of recombinant spike and nucleocapsid proteins, transfections were performed similarly but in six-well plates with HEK-293T cells using 2 µg of plasmid DNA. After 24 hours post-transfection, cells were washed three times with ice-cold PBS and harvested for western blot analysis. Cell lysis was performed with RIPA lysis buffer containing Protease Inhibitor Cocktail III (Calbiochem, San Diego, United States), 5mM DTT and nuclease (25 U/ml). Lysates from untransfected HEK-293T cells were used as controls. Patient serum was serially diluted 1:100 to 1:8,000 in PBS-Tween with 1% milk powder. Blot strips were incubated for 1.5 hours at room temperature. The secondary antibody, a horseradish peroxidase-conjugated goat-anti human immunoglobulin, was applied (1:20,000 in PBS-Tween with 1% milk powder). Detection was performed by using SuperSignal West Pico Chemiluminescence Substrate (Pierce Biotechnology).


1A assay
The 1A RT-PCR assay is directed to the Orf1a gene: this was optimised for sensitivity by testing several different candidate primers. The assay was compared with the upE assay by testing dilution series of the cell culture supernatant containing hCoV-EMC. There was complete concordance of the endpoints of the two assays. A total of 40 reactions using water instead of RNA were performed, in order to exclude any artificial signals due to irregular primer-/probe hybridisations. In-vitro transcribed RNA was generated for the peri-amplicon region of the 1A assay and used for parallel end-point dilution testing and probit regression analysis. The target concentration at which >95% of 1A assays can be expected to yield positive results was 4.1 RNA copies per reaction tube, i.e. a sensitivity equivalent to that of the upE assay ([2] and Figure 2). To exclude the possibility of false-positive results, human coronaviruses 229E, NL63, OC43, as well as SARS-CoV were tested in form of cell-culture supernatants in both assays (Table). A total of 42  clinical samples known to contain other respiratory viruses were tested as well, eight of which contained human coronaviruses including the unculturable hCoV-HKU1: all samples yielded negative results (Table).
Figure 2. Technical limit of detection for the 1A assay, novel human coronavirus (hCoV-EMC)

Table. Summary of experiments to determine sensitivity and cross-reactivity, novel human coronavirus (hCoV-EMC)

For a final comparison of sensitivity, the upE, ORF1b, and 1A assays were applied in parallel reactions to test a bronchoalveolar lavage sample from the patient treated in Essen, Germany. This sample had a very low RNA concentration of 360 copies per ml as determined with the upE assay using in-vitro transcribed RNA as the quantification standard [2]. The upE and 1A assays consistently detected RNA in this sample in repeated tests. The concentration determined by the 1A assay was between 66.5 and 100 copies per ml, reflecting slightly lower target abundance in the non-structural gene RNA, as observed previously for SARS-CoV [10]. Critically, the ORF1b assay presented in [2] did not detect virus in this sample.

RdRpSeq and NSeq assays
Two different RT-PCRs to produce amplicons for sequencing were designed. One amplicon was from the RdRp gene, a common target for CoV detection and a genome region where sequences for most coronaviruses are available (RdRpSeq assay, Figure 1). The assay was designed to provide broad detection of Betacoronavirus clade C sequences including hCoV-EMC as well as related viruses from animal sources such as bats (unpublished observations). The other amplicon was from a highly specific fragment within the hCoV-EMC N gene (NSeq assay, Figure 1). This region was chosen because it comprised a two amino acid (6 nt) deletion in the corresponding sequence published from a patient treated in London, United  Kingdom [11].  As shown in Figure 3, both amplicons were sensitive enough to detect cell culture-derived virus at very low concentrations. Both assays also yielded amplification products from the bronchoalveolar lavage sample from the Essen patient, in spite of its very low RNA concentration. Sequencing results are shown in Figure 4.

Figure 3. Comparison of RdRpSeq and NSeq assays, novel human coronavirus (hCoV-EMC)

Figure 4. Sequence alignments comparing the results of RdRpSeq and NSeq sequencing assays, novel human coronavirus (hCoV-EMC) and sequence obtained from a patient from Essen, Germany

hCoV-EMC antibody detection
Finally, slides for immunofluorescence microscopy were produced following two different common protocols. While the first method, growing cells on coverslips, provides better cell morphology, the second is commonly used to circumvent the necessity to optimise infection dose and duration, and to obtain slides with no infectious virus, to meet the biosafety requirements for shipment. For the first (conventional) protocol, Vero cells were seeded on microscope coverslips and infected with virus in situ. Infection conditions had been previously optimised to ensure infection of about 30% of cells in a series of experiments. For the second option, Vero cells were infected in conventional cell culture and mixed with an equivalent quantity of uninfected cells, after which they were spotted on glass microscope slides and further inactivated with paraformaldehyde. Both types of slides were stained with serum of a cynomolgus macaque infected with hCoV-EMC or with serum from the Essen patient. Figure 5, panel A, shows a typical coronavirus cytoplasmic fine-to-medium granular fluorescence with pronounced perinuclear accumulation, sparing the nucleus on the coverslip culture. The same result was also achieved with the convalescent serum from an experimentally infected cynomolgus macaque, suggesting that this can be used as a valid positive control in absence of available patient material. Figure 5, panel B, shows results from two convalescent sera of the patient, taken about four weeks apart, on simplified biologically safe slides. As expected, the fluorescence pattern was less well differentiated compared with slides infected and tested in situ. However, a very clear cytoplasmic perinuclear pattern is discernible, suggesting those slides will be appropriate for diagnostic application in spite of their simpler production and safer handling.

Sera from a limited number of German blood donors were tested by this IFA assay, with no relevant false-positive findings in a non-exposed population. However, much more validation is needed, because antibodies against betacoronaviruses are generally known to cross-react within the genus.  Sera from patients with a high antibody titre against any other human coronavirus such as OC43 or HKU1 may well lead to false-positive results if tested by IFA alone.  We propose to use this IFA only for patients with a very clear epidemiological linkage, ideally presenting positive results with a first-line assay such as upE. Paired sera should be investigated wherever possible.

Figure 5.  Examples of serological assays, novel human coronavirus (hCoV-EMC)


As shown in Figure 5, panel C, IFA reactivity was also demonstrated in cells overexpressing recombinant S or N proteins. Anti-S and anti-N antibodies were also confirmed by western blot.


Here we present nucleic acid-based and serological assays for the confirmation of hCoV-EMC infections. The current strategy and recommendations by WHO require reference laboratories to be involved in cases where first-line screening has provided positive results. However, with the potential occurrence of more cases of hCoV-EMC infection, the demand for confirmatory testing might grow in a way that it could overwhelm the capacity of reference laboratories. The major challenge in setting up confirmatory methodology will be the validation of tests. Technical studies can be tedious and clinical validation is hard to achieve if no patient samples are at hand. The documentation here of proven methodology is presented with those laboratories in mind that will have to provide diagnostic testing and additional reference services in the future, but cannot rely on their own validation studies.

The 1A real-time RT-PCR assay provides the same sensitivity as the upE first-line assay, and should provide consistent results in case of truly positive patients. It should be mentioned that the ORF1b assay along with the upE assay can also serve as a highly robust confirmatory test [2]. However, patients may be seen at times when they excrete small amounts of virus, e.g. very early or very late after symptom onset [6]. Moreover, samples may be diluted due to clinical processes such as lavage, as exemplified by the case investigated here. In such instances, confirmatory assays must have the same sensitivity as the first-line test. Such high sensitivity is achieved by the 1A assay, providing an appropriate complement to the upE assay proposed previously [2].

While real-time RT-PCR products can be sequenced, the shortness of their fragments makes DNA preparation inefficient and limits the length of useful sequence information. We present here two different sequencing amplicons (RdRpSeq and NSeq assays) that will yield reasonably large fragments even from samples containing very low virus concentration. We are not proposing to preferentially use either of those two assays, as both have different properties that suggest using them in combination. The RdRpSeq assay provides sequencing results that can be compared with a large database of cognate sequences, as it is commonly used for typing coronaviruses. The amplicon overlaps to a large extent with that proposed earlier by Vijgen et al. for pan-coronavirus detection, ensuring good comparability between laboratory results from different groups [12]. The primers of the RdRpSeq assay are highly conserved and will cross-react with other betacoronaviruses including hCoV-OC43 or -HKU1. Critically, this amplicon should not be used for screening if not connected with subsequent sequence analysis, as false-positive results are possible in patients infected with other human coronaviruses. In contrast, the NSeq assay provides highly sensitive and specific detection for hCoV-EMC, enabling a sequence-based confirmation even for cases that present with very low virus concentration. Here it is interesting to note that a sequence presented from a patient treated in London has a deletion in the amplified fragment. We should not draw early conclusions on virus diversity from these limited data, but it will be interesting to sequence and compare the NSeq fragment from more viruses in the future, in order to determine whether lineages with and without the deletion might have formed already. The NSeq assay might be used as a tool for provisional strain classification in the future.

For the augmentation of confirmatory testing by serology, IFA, ideally in paired sera taken several days apart, proved highly robust during the SARS epidemic [6,7]. In contrast to EIA, IFA provides additional criteria for result interpretation via the localisation of signals within cells. False-positive reactivity can thus be circumvented. The data presented here are intended as reference for those laboratories willing to confirm cases of hCoV-EMC infection by IFA. We have shown in this single patient that antibodies were detectable by IFA at a time when the patient still presented severe disease and the virus was not yet eliminated from respiratory secretions as detectable by RT-PCR (case report to be presented elsewhere). As in many SARS patients, the antibody titre was in the medium range, below 1:1,000, even in convalescence [6]. In SARS patients, IFA seroconversions usually began to show from day 10 of symptoms onward, while virus RNA could not be detected by RT-PCR in respiratory secretions starting from day 15 onward [6,7].

It is important to mention that IFA slides contain virus-infected cells which in theory could retain infectious virus. However, it has been shown in a meticulous investigation of SARS-CoV that acetone fixation of IFA slides results in the reduction of infectivity to undetectable levels. The extent of reduction of infectivity was at least 6.55 log 10 infectious virus doses [9] (greater reductions could not be measured by the assay applied). In the rapid and biologically safe IFA procedure we presented here, further reduction of any conceivable residues of infectivity was achieved by combining acetone fixation with paraformaldehyde treatment. This treatment was shown to confer efficient reduction on SARS-CoV [9] and is also effective against other enveloped RNA viruses [13]. No residual infectivity should exist in the rapid and biologically safe IFA slides described here. 

We have also shown that there is good correlation between IFA results and western blot against the two major structural proteins, S and N. Western blotting might therefore be an option as a confirmatory diagnostic for serology. However, in absence of data from a considerably larger number of patients, care must be taken in interpreting the results from western blot alone, as SARS patients were found to vary in their immune responses against single proteins in western blot [14,15]. Not only western blot but also neutralisation tests should be evaluated for their capacity to afford a highly specific confirmation of serological results [7]. This is of particular importance because it is unknown to what extent hCoV-EMC antibodies cross-react with those against common human coronaviruses such as OC43 and HKU1. In the present study, we have not investigated cross-reactivity in a larger group of patients, as this requires meticulous counter-testing and selection of samples with high titres against other human coronaviruses, as well as confirmation by additional methods such as differential virus neutralisation tests. The serological data presented here should be regarded as suggestions for confirmatory testing of epidemiologically linked individuals, or of cases under investigation due to positive results in first-line tests.

The development and provision of these assays was done by a European research project on emerging diseases detection and response, EMPERIE (, contract number 223498, coordinated by author A.D.O. Author C.D. has received infrastructural support from the German Centre for Infection Research (DZIF) that included full funding of the position of author V.M.C.

Oligonucleotides can be ordered from stock at Tib-Molbiol, Berlin ( Limited numbers of IFA slides as well as in-vitro transcribed control RNA for the upE and 1A assays can be acquired from author C. D. through the European Virus Archive platform (, funded by the European Commission under contract number 228292. Further information and assay updates can be obtained from


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