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Ahead of Print -Replicative Capacity of MERS Coronavirus in Livestock Cell Lines - Volume 20, Number 2—February 2014 - Emerging Infectious Disease journal - CDC

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Ahead of Print -Replicative Capacity of MERS Coronavirus in Livestock Cell Lines - Volume 20, Number 2—February 2014 - Emerging Infectious Disease journal - CDC

link to Volume 20, Number 1—January 2014

Volume 20, Number 2—February 2014


Replicative Capacity of MERS Coronavirus in Livestock Cell Lines

Isabella Eckerle, Victor M. Corman, Marcel A. Müller, Matthias Lenk, Rainer G. Ulrich, and Christian DrostenComments to Author 
Author affiliations: University of Bonn Medical Centre, Bonn, Germany (I. Eckerle, V.M. Corman, M.A. Müller, C. Drosten);Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany (M. Lenk, R.G. Ulrich)


Replicative capacity of Middle East respiratory syndrome coronavirus (MERS-CoV) was assessed in cell lines derived from livestock and peridomestic small mammals on the Arabian Peninsula. Only cell lines originating from goats and camels showed efficient replication of MERS-CoV. These results provide direction in the search for the intermediate host of MERS-CoV.
Coronaviruses (CoV) in the genera Alphacoronavirus and Betacoronavirus (order Nidovirales, family Coronaviridae, subfamily Coronavirinae) infect a broad range of mammals, including humans (1). The human CoVs (HCoVs) HCoV-HKU1, HCoV-229E, HCoV-NL63, and HCoV-OC43 typically cause mild to moderate respiratory tract infection; however, the disease course can be more severe in a minority of patients. In 2002–2003, an epidemic of severe lower respiratory tract infection with a case-fatality rate of ≈10% was caused by severe acute respiratory syndrome (SARS)–CoV (2). In 2012, another CoV associated with severe respiratory disease emerged on the Arabian Peninsula and was termed Middle East respiratory syndrome (MERS)–CoV (3).
Both SARS-CoV and MERS-CoV are zoonotic viruses, and their presumed origin is in bats. SARS-related CoVs were identified in Rhinolophus spp. bats in China and Europe (4,5), and MERS-related CoVs were found in Pipistrellus bats in Europe and in Neoromicia bats in South Africa (6,7). As with SARS-CoV, it is expected that MERS-CoV might be transmitted to humans by an intermediate animal host, and neutralizing antibodies against MERS-CoV have been found in Arabian camels originating from Oman, Spain, and Egypt (8,9).
We investigated replication of MERS-CoV in cell lines of the most abundant mammalian livestock species and representative peridomestic small mammals on the Arabian Peninsula. To estimate MERS-CoV permissiveness of cell cultures derived from these animals, we compared MERS-CoV replication and infectious virus production with that in bat- and primate-derived cells known to be permissive for MERS-CoV. The MERS-CoV receptor dipeptidyl peptidase 4 (DPP-4) is expressed in epithelial cells of the lung and kidney, and patients with MERS-CoV consistently show severe involvement of both organs; thus, we focused on lung and kidney cells in potential animal hosts (10,11).

The Study

Figure 1
Thumbnail of Immunofluorescence staining of the Middle East respiratory syndrome coronavirus receptor dipeptidyl peptidase 4 (DPP-4; rabbit anti-CD26/DPP-4 polyclonal antibody; Bioss Inc., Woburn, USA) in cell lines used to guide the search for the intermediate host of the virus. Counterstaining of nuclei was done by using 4′,6-diamidino-2-phenylindole. Cell lines: A) ZN-R, B) ZLu-R, C) LGK-1-R, D) TT-R.B, E) PO, F) KN-R, G) KLu-R, H) MyglaAEC.B, I) Crocsu-Lu, J) PipNi, K) A549, and L) Vero E6.
Figure 1. [[caption]]
Figure 2
Thumbnail of Analysis of the replication of Rift Valley fever virus (RVFV) clone 13 (A), bovine coronavirus (BCoV) (B), and Middle East respiratory syndrome coronavirus (MERS-CoV) (C) and of the production of infectious MERS-CoV particles (D) in cell lines derived from livestock and peridomestic small mammals on the Arabian Peninsula. Cell lines of human, bat, and primate origin were used as controls. Replication levels for each virus used are given as log of the genome equivalents (GEs) (A–C) o
Figure 2. [[caption]]
Using enhanced respiratory personal protection equipment in a Biosafety Level 3 facility, we cultivated, in parallel, cell lines from goats, sheep, cattle, camelids (dromedary and alpaca), rodents, insectivores, bats, and human and nonhuman primates (Table). Cells were checked to ensure the absence of mycoplasma contamination and genotyped for their species of origin by sequencing of the mitochondrial cytochrome c subunit oxidase I gene (12). All cells expressed DPP-4, as determined by immunofluorescence staining (Figure 1) and Western blot analysis (data not shown). Because several of the ungulate cell lines had not previously been used for viral infection experiments, we determined permissiveness of all cell lines for Rift Valley fever virus (RVFV) clone 13, a virus mutant known to be attenuated yet broadly infectious for ungulate cell lines (13). Triplicate infections with multiplicities of infection (MOIs) of 0.5 infectious units/cell resulted in highly consistent levels between cells (maximal variation 3.2-fold) (Figure 2, panel A). In addition, to demonstrate the ability of the cells to support CoV replication, we infected all cell lines in triplicate (MOIs of 0.5) with bovine CoV strain Nebraska. The strain replicated to high levels in all cell lines; replication varied by <52.9-fold, which constitutes small relative variations in light of the overall levels of replication (Figure 2, panel B). We conducted MERS-CoV infections under the same conditions and with MOIs of 0.5.
In addition to livestock cell lines, we used rodent, insectivore, bat, and primate cell lines in the experiments (Table). Bat and primate cells known to be permissive for MERS-CoV served as controls. MERS-CoV–inoculated cells were incubated for 1 h and then washed twice before supernatant was harvested (0 h after incubation) (Figure 2, panel C). We quantified virus replication by using the upE assay (14), a MERS-CoV real-time reverse transcription PCR that screens upstream of the E gene. Replication was seen in lung and kidney cell lines derived from goats (Capra hircus) and in umbilical cord and kidney cells from camelids (Camelus dromedariusand Llama pacos) (Figure 2, panel C). Efficient replication (>9.3 log10 virus RNA genome equivalents/mL of cell culture supernatant) was seen in the goat kidney cells; this replication level was similar to that in Vero E6 cells (interferon-deficient primate kidney cells). Goat lung cells, alpaca kidney cells, and dromedary umbilical cord cells also showed strong replication, but virus did not replicate in sheep, cattle, rodent, or insectivore cells. In addition, expression of the receptor, DPP-4, was confirmed in all cells, including the nonpermissive sheep, cattle, rodent, and insectivore cells.
After following virus growth in all permissive cells for another 20 h, we harvested supernatants and, to confirm the production of infectious virus particles, we titrated the supernatants by using a plaque assay in Vero cells. MERS-CoV replication was seen in all permissive cells except TT-R.B (Figure 2, panel D), and all permissive cells showed cytopathic effects. The highest production of virus particles was in goat lung and kidney cells (1.0 × 107 and 2.7 × 106 PFU/mL, respectively). This level of replication was comparable to that in human lung cells (A549) and Vero E6 (Figure 2, panel D).


Transmission of MERS-CoV between humans is still limited, and the identification of an intermediate animal host could enable the development of public health measures to prevent future spread of the virus among humans. Although MERS-CoV neutralizing antibodies have been detected in camels from Oman, Spain, and Egypt, the virus has not previously been detected in camels (8,9). An informed focusing of investigations on a select group of species, such as camels, could benefit epidemiologic investigations. To identify potential intermediate host species of MERS-CoV, we used in vitro testing to determine virus permissiveness in select cell culture models. In general, cell lines cannot depict the full pathogenicity of in vivo infection because infection is influenced by epithelium-specific differentiation of target cells and the presence of immune cells. However, for viruses such as CoVs, whose tropism is believed to be determined mainly by the availability of an appropriate entry receptor (10), epithelial cell cultures could indeed constitute valid surrogates of virus permissiveness in vivo. With these limitations in mind, our results are in concordance with the findings of MERS-CoV neutralizing antibodies in camels and with information regarding patient contact with animals in reports of 2 human cases of MERS-CoV infection (11,15). One of the patients owned a farm on which camels and goats were kept. Before onset of his own illness, the patient reported illness in several goats on his farm. The patient did not have direct contact with animals, but he reported having eaten goat meat and having had contact with one of the animal caretakers, who suffered from respiratory disease (15). The second patient reported direct contact with a diseased camel shortly before onset of his symptoms (11).
In our study, production of infectious virus particles was seen in goat lung and kidney cells and in camelid kidney cells. Excretion patterns indicative of kidney infection should be investigated once further clues to the identity of the MERS-CoV animal reservoir become available. Our preliminary findings suggest that ungulates, such as goats and camels, are a possible intermediate host of MERS-CoV; thus, exposure to urine and feces from these animals might constitute a source of human infection. Moreover, food products derived from these animals (e.g., meat and milk) should be tested for their potential to transmit MERS-CoV. The results of our study suggest that investigations into the MERS-CoV animal reservoir and intermediate host should focus on caprid (e.g., goats) and camelid hosts, and we identified several new cell lines for use in virus isolation studies.
Dr Eckerle is a virologist at the Institute of Virology in Bonn, Germany. Her primary research interest is characterization of novel and emerging zoonotic viruses.


We thank Benjamin Meyer, Stephan Kallies, and Jan-Erik Mittler for excellent technical assistance; Sandra Junglen, Marco Marklewitz, and Valerie Biewener for providing insectivore samples; Ulrike M. Rosenfeld for providing rodent samples for the generation of cell lines; Friedemann Weber for providing Rift Valley fever virus clone 13; and Martin Beer and Malte Dauber for providing bovine coronavirus.
This study was supported by the European Commission under project ANTIGONE (contract no. 278976) and the German Centre for Infection research.


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Suggested citation for this article: Eckerle I, Corman VM, Müller MA, Lenk M, Ulrich RG, Drosten C. Replicative capacity of MERS coronavirus in livestock cell lines. Emerg Infect Dis. 2014 Feb [date cited]. Web Site Icon
DOI: 10.3201/eid2002.131182

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