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Review

Middle East Respiratory Syndrome Coronavirus (MERS-CoV): A Review

Department of Agriculture, Faculty of Agricultural and Food Sciences (FAFS), American University of Beirut (AUB), Riad El Solh 1107-2020, Beirut P.O. Box 11-0236, Lebanon
*
Author to whom correspondence should be addressed.
GERMS 2019, 9(1), 35-42; https://doi.org/10.18683/germs.2019.1155
Submission received: 6 November 2018 / Revised: 8 January 2019 / Accepted: 26 January 2019 / Published: 1 March 2019

Abstract

As a novel coronavirus first reported by Saudi Arabia in 2012, the Middle East respiratory syndrome coronavirus (MERS-CoV) is responsible for an acute human respiratory syndrome. The virus, of 2C beta-CoV lineage, expresses the dipeptidyl peptidase 4 (DPP4) receptor and is densely endemic in dromedary camels of East Africa and the Arabian Peninsula. MERS-CoV is zoonotic but human-to-human transmission is also possible. Surveillance and phylogenetic researches indicate MERS-CoV to be closely associated with bats’ coronaviruses, suggesting bats as reservoirs, although unconfirmed. With no vaccine currently available for MERS-CoV nor approved prophylactics, its global spread to over 25 countries with high fatalities highlights its role as ongoing public health threat. An articulated action plan ought to be taken, preferably from a One Health perspective, for appropriately advanced countermeasures against MERS-CoV.

Introduction

June 19th, 2017, a case of Middle East respiratory syndrome coronavirus (MERS-CoV) is reported by the National International Health Regulation (IHR) focal point of Lebanon [1]. As a novel coronavirus, MERS-CoV was first identified in a patient from the Kingdom of Saudi Arabia in June 2012 and was originally named human coronavirus-EMC, as in Erasmus Medical Center [2]. The case involved a man in Saudi Arabia who was admitted to the hospital with pneumonia and acute kidney injury [3]. The virus was later isolated from the patient’s sputum. A different report appeared in September 2012, detecting a similar virus with 99.5% identity in a previous patient who initially developed symptoms in Qatar and had traveled to Saudi Arabia before the disease progression exacerbated [4]. Seroepidemiologic and virologic research revealed MERS-CoV infection in dromedary camels (Camelus dromedarius) with isolated viruses from dromedaries competent in infecting the human respiratory tract [5,6]. All cases of MERS-CoV have been established in the Middle East and North Africa region, Europe, East Asia and the United States [7]. With numerous consecutive cases and clusters of infections having been reported since September 2012, the World Health Organization (WHO) was notified to date with 2,040 laboratory-confirmed cases of MERS-CoV infection, 712 fatalities and a total of 27 differing countries reporting cases [1].
This paper discusses the virology, pathogenesis, and epidemiology of MERS-CoV, highlighting possible sources and modes of transmission and clinical manifestation along with treatment and prevention while providing a One Health approach to tackle the complex issue of MERS-CoV.

Literature review

Virology and pathogenesis

MERS-CoV belongs to the family Coronaviridae and has a large RNA viral genome of approximately 26-33 kb and G+C contents varying from 32 to 43% [8,9].
MERS-CoV descends from the 2C beta-coronavirus lineage existing in humans and camels [10]. Although genomically related, it is separate from other human beta-coronaviruses such as severe acute respiratory syndrome (SARS) coronavirus, but it is similarly associated with few bat coronaviruses [2,3,11]. The functional receptor of MERS-CoV is dipeptidyl peptidase 4 (DPP4) and its expression induces the infection. The DPP4 protein expresses large quantity conversion of amino acid sequences in various species [11,12]. MERS-CoV has the capability of infecting multiple human cell lines [13]. This mainly comprises the lower respiratory tract in which respiratory epithelial cells are highly susceptible, encouraging viral replication productivity in human macrophages and dendritic cells, inducing production of pro-inflammatory cytokines, targeting T lymphocytes and leading to their apoptosis [14]. Kidneys are also significantly affected by MERS-Co viruses, in addition to intestinal, liver cells, and histiocytes [14].
Furthermore, in vitro studies illustrate that MERS-CoV can infect non-human primate, porcine, bat, civet, rabbit, as well as horse cell lines [13,15]. The pathogenesis of MERS-CoV infection to date is not well understood and further research is necessary. MERS-CoV causes disease of the lower respiratory tract and can be found in tracheal aspirates, sputum, or bronchoalveolar lavage fluid of symptomatic patients. According to highly conserved coronavirus RNA polymerase chain reaction (PCR) analysis (or Pan-Corona-PCR), viral shedding from nasal secretions, sneezing, coughing and sputum can be continuous up to six weeks, which builds concerns that asymptomatic individuals could also transmit the infection to others [6,16]. It is important to note that DPP4 is expressed in the upper respiratory tract of camels, while in humans it is solely expressed in the lower respiratory tract, a fact which may explain the limited detection of human-to-human transmission to date [17]. MERS coronaviruses are capable of causing human and veterinary outbreaks. This is due to the fact that CoV have the potential to recombine, mutate and jump between animals, thus infecting a wide variety of species [18]. Moreover, recent phylogenetic analysis has demonstrated that MERS-CoV reported from camels and humans are clustered together, while bat and hedgehog MERS-CoVs established a basal paraphyletic group to the camel and human MERS-CoV clade [19]. It is estimated that the genome-wide substitution rate of nucleotides in camels and humans MERS-CoVs is 4.81 × 10−4 per site per year [19].
Five bat cells (M. ricketti lung, P. abramus kidney, R. sinicus kidney and lung, and R. leschenaultii kidney cells) have been reported to be susceptible to MERS-CoV EMC/2012 [20]. In addition, various MERS-CoV strains have exhibited different infectivity on bat cell lines. For instance, M. ricketti lungs sustained infection by strains D1189.1/15 and D1271.1/15, while R. sinicus lung and R. leschenaultii kidney exhibited infection by strain D1189.1/15. None of the bat cell lines have shown sustainable infection by strain D998/15 [20].
MERS-CoV causes mild or no respiratory and clinical symptoms in camels and as a consequence it is not easily recognized or difficult to clinically diagnose. MERS-CoV is mainly acquired in dromedaries of less than one year of age [21]. A case in 2013 has been reported in a camel with MERS-CoV, symptomatic with fever and rhinorrhea [22]. Bats on the other hand are believed to be carriers of MERS-CoV without demonstrating apparent clinical signs of the disease [23].
The genome of MERS-CoV contains 30,119 nucleotides and a minimum of 10 predicted open reading frames, 9 of which are suggested to be displayed from a set of nested 7 sub-genomic mRNA. ORF1a and ORF1b are the replicase opening frames which cover the 5′ end region of the genome, while the 3′ end encodes structural proteins,including spike (S), membrane (M), nucleocapsid (N), envelope (E), as well as various accessory proteins such as 3, 4a, 4b, 5 and 8b [24]. MERS-CoV prompts cytopathic effects and replicates at high titers allowing for a rapid genome characterization [24]. Replicase gene phylogenetic analysis has demonstrated that the full sequenced genome of coronavirus HCoV-EMC/2012 is closely related to Tylonycteris bat coronavirus HKU4 (BtCoV-HKU4) and to Pipistrellus bat coronavirus HKU5 (BtCoV-HKU5) [16,25].
The spike (S) protein of β-CoV is a key in cross-species transmission as it mediates virus-receptor recognition and induces viral pathogenesis. The receptor binding domain (RBD) on S protein’s N-terminal is vital for the penetration of β-CoV into host cells. Further, the severity of infection and cross-species efficiency is influenced by the mutations in CoV RBD [26].
Nine sites in the S protein of MERS-CoV have been found to have significant positive selection. This entails that the S protein has encountered strong evolutionary pressure during its transmission from its natural host to humans. In addition, six of these positively selected sites occupy the RBD [19].

Epidemiology

As large, enveloped, positive-stranded RNA viruses, coronaviruses are known to cause respiratory and enteric disease in various animals (including cattle, chicken, bat, mice, alpacas, swine, dogs, horse) and in humans [8,27]. Four separate human coronavirus (hCoV) genera circulate the globe, of which some are promoters of the common cold, with an additional hCoV being SARS-CoV that caused an outbreak in 2003 [1]. In 2012, as discussed above, two cases of severe hCoV infection were notified, and were caused by a novel virus type. Both patients had travelled to or resided in Saudi Arabia. Shortly thereafter, numerous cases were reported, with at least 62% of human symptomatic cases having not been detected, indicating the true number of cases inclined to be greater than reported [28]. A retrospective analysis traced the initial outbreak in April 2012 to a hospital in the city of Al-Zarqa, Jordan [29]. Although outbreaks of MERS-CoV have been majorly reported in the Middle East, namely in Kuwait, Yemen, Oman, Iran, Lebanon, United Arab Emirates (Table 1), and specifically in Saudi Arabia (with 85.8% of the reported cases), imported cases have also been observed in Europe, Asia and North America. These include countries such as the United Kingdom, France, Germany, Italy, Greece, Netherlands, Egypt, Tunis, Malaysia, South Korea and the USA [30,31].
In the Middle East, the number of cases has significantly increased during March and April 2014, later declining in mid-May of 2014 [3,10]. However, there has been a notable outbreak of 186 confirmed cases across 16 hospitals present in South Korea in the period of May and June 2015 from an index case [32]. Two positive cases of MERS-CoV have been reported in Lebanon so far. The national IHR Focal Point of Lebanon reported the country’s first MERS-CoV infection on May 8th, 2014 as laboratory-confirmed case [33]. A Lebanese 60-year-old male healthcare worker presenting high fever was admitted to the hospital, with symptoms of dyspnea and productive cough, and tested positive for MERS-CoV [1]. The patient reported neither contact with laboratory confirmed cases nor with animals and no travel history during the 14 days prior to symptom onset. However, the patient had previously travelled around a couple of Gulf regions. The second Lebanese case involved a 39-year-old male from Saudi Arabia. He developed mild symptoms and as a healthcare worker along the enhanced MERS-CoV surveillance in Saudi Arabia, a nasal swab was collected on June 11th, 2017 testing negative for the infection; the same day the patient travelled to Lebanon with no reporting symptoms [1]. On June 15th, the patient developed gastrointestinal symptoms, diagnosis confirmed pneumonia, and the following day he tested positive for MERS-CoV. MERS-CoV appears to possess a predilection for males as approximately 64% cases are male with a median age of 48 years (range 9 months to 94 years) with nearly 35% case-fatality rate [1,31].
A seasonal pattern of cases has been observed, with a peak each year between April and June, although the reason has yet to be elucidated [10]. A potential explanation for this could be the camel birthing season, when younger camels are more prone to infection as opposed to mature ones. Moreover, it may be argued that the current upsurge in the number of infected patients is due to enhanced case detection and active surveillance programs [10].

Sources and transmission

In an effort to examine the possibilities of domestic animals as reservoir, serological studies were performed in Saudi Arabia from 2010 to 2013, and in 2014, where sera from sheep, goats, cattle, and chickens from various geographical areas within the country were collected. All samples tested seronegative for MERS-CoV. Similar studies on equids in the United Arab Emirates and Spain, goats, sheep and cattle in Jordan and Europe also indicated negative results [34,35,36,37]. Dromedary camels have been demonstrated to be the primary animal host for MERS-CoV [5,6,14,38]. Yet, all tested healthy alpacas in a recent Qatar study have been demonstrated to be positive for MERS-CoV [38]. Human-to-human transmission occurs but seems limited to families and close contacts, or is due to nosocomial infection [2,39]. Camel-to-human transmission of MERS-CoV has been evident in Saudi Arabia where full-genome sequencing of MERS-CoV isolated from a patient with fatal infection and from one of his dromedary camels proved to be positive for MERS-CoV RNA and the isolates were identical [6]. Both stool and nasal secretions of dromedaries have homologous genome sequencing to MERS-CoV [2]. As the virus targets the respiratory tract, nasal and mucosal secretions in humans and dromedaries eliminated through sneezing and coughing are primary spreading mechanisms in zoonotic and inter-human transmissions [7].
MERS-CoV is closely associated with coronaviruses found in bats, suggesting that bats may be a reservoir of MERS-CoV.3 This prompted several researchers to screen bats in Lebanon, yet no evidence for antibodies to MERS-CoV were found [40]. The majority of the CoV-positive camels existed in Saudi Arabian wholesale markets; this is where indigenous camels were mixed with imported camels from Sudan and Somalia while local camels demonstrated significantly higher rates of infection with MERS-CoVs as well as other CoVs than those imported [39]. However, since its presence in the 1980s, high seropositivity against MERS-CoV among camels in the Arabian Peninsula and Africa indicates that the virus has circulated in camels prior to being introduced to the human population [35,37,39].
MERS-CoV infectivity is dependent upon the median incubation period, which is approximately 5 days for limited human-to-human transmission, ranging from 2 to 14 days. The approximate time from the onset of MERS-CoV illness to hospitalization is 4 days, with an approximate duration of 5 days for critically ill patients to intensive care unit (ICU) admission and approximately 12 days from onset of viral symptoms to death [7]. Immunosuppression caused by malnutrition, deficiencies, stress, parasites, concurrent infections, etc., could aggravate the course of MERS-CoV infection [41].
Phylogenetic analysis of MERS-CoV’s full-genome indicated that MERS-CoV’s evolution within camels has resulted in diverse lineages of which all have caused human infections, perpetuating a low barrier for interspecies transmission [39]. Training and milking of camels have been associated with MERS-CoV infection [42]. Consumption of raw camel milk or improperly cooked meat has illustrated high risk of MERS-CoV infection [1]. The emergence of intensive camel livestock system and large trade between countries, particularly from Somalia to Gulf regions, leading to roughly 77,000 live camels being exported each year, can significantly contribute to multiple disease transmissions [43].

Clinical manifestation and diagnosis

In terms of fatality rates, around one third of patients with MERS have died; however, as mild cases of MERS-CoV might have been missed by the current surveillance techniques, specifically in the developing countries, this ratio might be an overestimation of the actual mortality rate [1,2].
In infected people, MERS-CoV causes a range of illnesses from asymptomatic to acute respiratory illness with mild to severe respiratory courses and death [1,2]. Symptomatic MERS-CoV is typically introduced following an incubation period of 2 to 14 days [7]. Confirmed cases include any patient sample with q-PCR positive or shown seropositivity for MERS-CoV irrespective of the presence of clinical signs and symptoms [7]. It is suggested to use q-PCR for targeting the region upstream of the envelope gene (upE) as a screening assay in addition to ORF1a target gene as a confirmatory assay [44]. Chest X-ray shows lung fibrosis, ground glass opacity, and pleural thickening, yet the abnormalities may not always be present in MERS CoV-infected individuals. Presentation with fever, chills, cough, shortness of breath (most likely with severe hypoxemic respiratory failure), and myalgia have been reported with MERS-CoV. Mild cases are found among children and young adults. These include low-grade fever, runny nose, sore throat, headache, and abdominal pain [7]. In critically ill patients, gastrointestinal symptoms have been observed such as nausea, vomiting, or diarrhea, while acute kidney damage has been reported in approximately half of these patients [45]. Severe MERS-CoV infection is outlined by progression to acute respiratory distress, with a 2 days median period between hospitalization and ICU admission [7,45].
Laboratory confirmed cases reported first signs that included fever, cough and upper respiratory tract illness, followed within a week by progressive lower respiratory tract signs and lymphopenia. MERS-CoV can progress to acute respiratory distress syndrome and multiorgan system failure. Patients commonly present to a hospital with pneumonia in addition to concurrent bacterial infections [7,46].
Three cases of MERS-CoV reported onset with widespread bilateral hyperintense lesions via T2 weighted image on magnetic resonance imaging (T2WI MRI) within the white matter and subcortical regions of the frontal, temporal and parietal lobes including the basal ganglia, corpus callosum, pons, cerebellum, and upper cervical cord, suggestive of encephalitis [47]. A high risk of severe course of MERS-CoV infection is seen in patients with comorbid conditions, such as diabetes, renal, cardiac and chronic pulmonary disease, cancer, as well as in immunocompromised persons. Prognostic signs of fatal courses include acute nephritis and shock [1,2,47].

Treatment and prevention

No vaccination or treatment is currently available for MERS-CoV [1]. A great challenge exists in developing MERS-CoV infection models for several reasons. For one, small and larger animal models that aid in initial screening do not express the DPP4 receptor [48].
In addition, pharmaceutical companies have meager incentive for producing MERS-CoV vaccine as clinical trials are very costly and the timeline to approved vaccine use is 10 years or longer [49]. If, however, sustained human-to-human MERS-CoV transmission were to occur, the benefit of developing a safe and effective vaccine would outweigh any cost [49].
Supportive therapy necessitates respiration and circulatory support, preservation of renal and hepatic function, and prevention of secondary infections [2,50]. Administration of both ribavirin and interferon-a2b may decrease viral load, as they decrease the multiplication of MERS-CoV in Vero as well as LLC-MK2 cells [2,50]. It is hypothesized that DPP4 inhibitors may restrain viral replication; this yet requires further study [2]. Further, the development of vaccination targeting receptor binding subdomain (RBSD) of MERS-CoV is under investigation. Recently, a candidate DNA vaccine developed from MERS-Cov spike protein subunit 1 (S1) is under study [48]. As dromedaries are speculated as the source of transmission of MERS-CoV to humans particularly in the Arabian Peninsula, travelers are advised to follow basic safety precautions, including proper hand washing prior and post touching an animal, and to refrain from consuming raw meat and milk and direct contact with camels [7].

Discussion

One Health approach

Controlling MERS-CoV requires interdisciplinary efforts with the One Health concept focusing on human, animal and environmental health, intimately in order to understand the exact dynamics of MERS-CoV. Multidisciplinary teams with collaboration between public health officers and veterinarians ought to be primarily organized. This must include ranges of expertise such as academic researchers, physicians, ecologists, microbiologists/virologists, and phylogeneticists cooperating and investigating valuable information on MERS-CoV. Secondly, laboratory equipment and proven diagnostic assays should be available for use by public health laboratories early in an outbreak; or perhaps new techniques may be developed since the isolation and initial characterization of this virus requires a biosafety level 3 lab. Outbreak preparedness response infrastructures must be considered with specialized training for responders for early effective prevention. This also calls for early anticipation of extensive production of vaccines, should these become available. Using the notion of natural nidality can aid in understanding reservoir dynamics of MERS-CoV, and in turn help in implementing policies for future prevention of the disease and its transmission. Since dromedaries are primary hosts of MERS-CoV, their vaccination would decrease the risk of zoonotic transmission. It is questionable if camels and bats are the only reservoirs of MERS-CoV, this is why surveillance particularly towards wildlife is essential, and considerable gaps in the knowledge of MERS-CoV demands better case definitions. As vaccine productions are generally costly and as MERS-CoV is not yet widespread, from a theoretical point of view, should vaccination become available, it ought to primarily begin with camel handlers, healthcare workers and veterinarians. Moreover, attention should be paid to any mass gathering (such as pilgrimage-Hajj). Also, gene or viral signatures determination should be performed by analyzing symptomatic and asymptomatic MERS-CoV infections. Geographic Information Systems can serve for evaluating spatialized risk and identifying high risk areas. Lastly, education and raising awareness must be promptly carried out on topics of hygiene and food safety.

Conclusions

This manuscript has discussed various elements of MERS-CoV infection and control, and the role of the One Health approach in containing and preventing the spread of this disease. The One Health approach should not be affected by the increasing globalization pullback voices. On the contrary, it should turn into a movement, having supporting organizations worldwide, for a better control of emerging diseases, including MERS-CoV.

Author Contributions

NR wrote the first draft. All authors have read and approved the final version of the manuscript.

Funding

None to disclose.

Conflicts of Interest

All authors—none to disclose.

References

  1. World Health Organization. Middle East Respiratory Syndrome Coronavirus (MERS-CoV)-Lebanon. 2017. Available online: https://www.who.int/csr/don/04-july-2017-mers-lebanon/en/ (accessed on 05 July 2017).
  2. Bauerfeind, R.; von Graevenitz, A.; Kimmig, P.; et al. Zoonoses: Infectious Diseases Transmissible from Animals to Humans, 4th Ed. ed; ASM Press: Washington, DC, USA, 2016. [Google Scholar]
  3. McIntosh, K.; Hirsch, M.; Thorner, A. Middle East respiratory syndrome coronavirus: Virology, pathogenesis, and epidemiology. In UpToDate; Post, T.W., Ed.; . UpToDate Inc: Waltham, MA, USA, 2017. [Google Scholar]
  4. Wise, J. Patient with new strain of coronavirus is treated in intensive care at London hospital. BMJ 2012, 345, e6455. [Google Scholar] [CrossRef]
  5. Al-Tawfiq, A. Middle East Respiratory Syndrome-coronavirus infection: An overview. J Infect Public Health 2013, 6, 319–322. [Google Scholar]
  6. Azhar, E.I.; El-Kafrawy, S.A.; Farraj, S.A.; Hassan, A.M.; Al-Saeed, M.S.; Hashem, A.M. Evidence for camel-to-human transmission of MERS coronavirus. N Engl J Med. 2014, 370, 2499–2505. [Google Scholar]
  7. World Health Organization. Middle East Respiratory Syndrome Coronavirus (MERS-CoV). 2018. Available online: https://www.who.int/news-room/fact-sheets/detail/middle-east-respiratory-syndrome-coronavirus-(mers-cov) (accessed on 18 December 2018).
  8. Fehr, A.R.; Perlman, S. Coronaviruses: an overview of their replication and pathogenesis. Methods Mol Biol 2015, 1282, 1–23. [Google Scholar]
  9. Woo, P.C.; Huang, Y.; Lau, S.K.; Yuen, K.Y. Coronavirus genomics and bioinformatics analysis. Viruses 2010, 2, 1804–1820. [Google Scholar] [CrossRef]
  10. Sharif-Yakan, A.; Kanj, S.S. Emergence of MERS-CoV in the Middle East: origins, transmission, treatment, and perspectives. PLoS Pathog 2014, 10, e1004457. [Google Scholar]
  11. Chan, J.F.; Lau, S.K.; To, K.K.; Cheng, V.C.; Woo, P.C.; Yuen, K.Y. Middle East respiratory syndrome coronavirus: another zoonotic betacoronavirus causing SARS-like disease. Clin Microbiol Rev 2015, 28, 465–522. [Google Scholar] [PubMed]
  12. Raj, V.S.; Mou, H.; Smits, S.L.; et al. Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC. Nature 2013, 495, 251–254. [Google Scholar] [CrossRef]
  13. Kindler, E.; Jónsdóttir, H.R.; Muth, D.; et al. Efficient replication of the novel human betacoronavirus EMC on primary human epithelium highlights its zoonotic potential. MBio 2013, 4, e00611–2. [Google Scholar]
  14. Chan, R.W.; Hemida, M.G.; et al. Tropism and replication of Middle East respiratory syndrome coronavirus from dromedary camels in the human respiratory tract: an in-vitro and ex-vivo study. Lancet Respir Med 2014, 2, 813–822. [Google Scholar]
  15. Müller, M.A.; Raj, V.S.; Muth, D.; et al. Human coronavirus EMC does not require the SARS-coronavirus receptor and maintains broad replicative capability in mammalian cell lines. MBio 2012, 3, e00515–12. [Google Scholar]
  16. Chan, J.F.; Choi, G.K.; Tsang, A.K.; et al. Development and evaluation of novel real-time reverse transcription-PCR assays with locked nucleic acid probes targeting leader sequences of human-pathogenic coronaviruses. J Clin Microbiol 2015, 53, 2722–2726. [Google Scholar] [PubMed]
  17. Widagdo, W.; Raj, V.S.; Schipper, D.; et al. Differential expression of the Middle East respiratory syndrome coronavirus receptor in the upper respiratory tracts of humans and dromedary camels. J Virol 2016, 90, 4838–4842. [Google Scholar] [PubMed]
  18. Mackay, I.M.; Arden, K.E. MERS coronavirus: diagnostics, epidemiology and transmission. Virol J 2015, 12, 222. [Google Scholar] [CrossRef]
  19. Zhang, Z.; Shen, L.; Gu, X. Evolutionary dynamics of MERS-CoV: potential recombination, positive selection and transmission. Sci Rep 2016, 6, 25049. [Google Scholar] [CrossRef]
  20. Lau, S.K.P.; Fan, R.Y.Y.; Luk, H.K.H.; et al. Replication of MERS and SARS coronaviruses in bat cells offers insights to their ancestral origins. Emerg Microbes Infect 2018, 7, 209. [Google Scholar]
  21. Food and Agriculture Organization of the United Nations. Dromedary Camels and MERS-CoV: Filling Knowledge Gaps. 2017. Available online: http://www.fao.org/3/a-i7350e.pdf (accessed on 20 November 2018).
  22. Center for Infectious Disease Research and Policy. Camel with MERS-CoV Had Signs of Illness. 2013. Available online: http://www.cidrap.umn.edu/news-perspective/2013/11/camel-mers-cov-had-signs-illness (accessed on 25 November 2018).
  23. Chan, J.F.; Chan, K.H.; Choi, G.K.; et al. Differential cell line susceptibility to the emerging novel human betacoronavirus 2c EMC/2012: implications for disease pathogenesis and clinical manifestation. J Infect Dis 2013, 207, 1743–1752. [Google Scholar]
  24. van Boheemen, S.; de Graaf, M.; Lauber, C.; et al. Genomic characterization of a newly discovered coronavirus associated with acute respiratory distress syndrome in humans. MBio 2012, 3, e00473–12. [Google Scholar]
  25. Hu, B.; Ge, X.; Wang, L.F.; Shi, Z. Bat origin of human coronaviruses. Virol J 2015, 12, 221. [Google Scholar]
  26. Wang, N.; Shi, X.; Jiang, L.; et al. Structure of MERS-CoV spike receptor-binding domain complexed with human receptor DPP4. Cell Res 2013, 23, 986–993. [Google Scholar]
  27. Woo, P.C.; Lau, S.K.; Lam, C.S.; et al. 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. [Google Scholar]
  28. Cauchemez, S.; Fraser, C.; Van Kerkhove, M.D.; et al. Middle East respiratory syndrome coronavirus: quantification of the extent of the epidemic, surveillance biases, and transmissibility. Lancet Infect Dis 2014, 14, 50–56. [Google Scholar] [CrossRef]
  29. Hijawi, B.; Abdallat, M.; Sayaydeh, A.; et al. Novel coronavirus infections in Jordan, April 2012: epidemiological findings from a retrospective investigation. East Mediterr Health J 2013, 19 (Suppl. 1), S12–S18. [Google Scholar] [CrossRef]
  30. MERS Corona Map. 23017. Available online: http://coronamap.com (accessed on day month year).
  31. Banerjee, A.; Rawat, R.; Subudhi, S. Outbreak control policies for Middle East Respiratory Syndrome (MERS): the present and the future. J Trop Dis Public Health. 2015, 3, 166. [Google Scholar]
  32. Korea Centers for Disease Control and Prevention. Middle East respiratory syndrome coronavirus outbreak in the Republic of Korea. Osong Public Health Res Perspect 2015, 6, 269–278. [Google Scholar] [CrossRef] [PubMed]
  33. World Health Organization. Middle East Respiratory Syndrome Coronavirus (MERS-CoV)—Update. 2014. Available online: https://www.who.int/csr/don/2014_05_15_mers/en/ (accessed on 29 June 2017).
  34. Hemida, M.G.; Perera, R.A.; Wang, P.; et al. Middle East Respiratory Syndrome (MERS) coronavirus seroprevalence in domestic livestock in Saudi Arabia, 2010 to 2013. Euro Surveill 2013, 18, 20659. [Google Scholar] [CrossRef] [PubMed]
  35. Centers for Disease Control and Prevention. Middle East Respiratory Syndrome (MERS). Transmission. 2016. Available online: https://www.cdc.gov/coronavirus/mers/about/transmission.html (accessed on 29 June 2017).
  36. Meyer, B.; García-Bocanegra, I.; Wernery, U.; et al. Serologic assessment of possibility for MERS-CoV infection in equids. Emerg Infect Dis 2015, 21, 181–182. [Google Scholar] [CrossRef]
  37. Reusken, C.B.; Ababneh, M.; Raj, V.S.; et al. Middle East Respiratory Syndrome coronavirus (MERS-CoV) serology in major livestock species in an affected region in Jordan, June to September 2013. Euro Surveill 2013, 18, 20662. [Google Scholar] [CrossRef]
  38. Reusken, C.B.; Schilp, C.; Raj, V.S.; et al. MERS-CoV infection of alpaca in a region where MERS-CoV is endemic. Emerg Infect Dis 2016, 22, 1129–1131. [Google Scholar] [CrossRef]
  39. Sabir, J.S.; Lam, T.T.; Ahmed, M.M.; et al. Co-circulation of three camel coronavirus species and recombination of MERS-CoVs in Saudi Arabia. Science 2016, 351, 81–84. [Google Scholar] [CrossRef]
  40. Shehata, M.M.; Chu, D.K.; Gomaa, M.R.; et al. Surveillance for coronaviruses in bats, Lebanon and Egypt, 2013-2015. Emerg Infect Dis 2016, 22, 148–150. [Google Scholar] [CrossRef]
  41. Funk, A.L.; Goutard, F.L.; Miguel, E.; et al. MERS-CoV at the animal–human interface: inputs on exposure pathways from an expert-opinion elicitation. Front Vet Sci 2016, 3, 88. [Google Scholar] [CrossRef]
  42. Sikkema, R.S.; Farag, E.A.B.A.; Himatt, S.; et al. Risk factors for primary Middle East respiratory syndrome coronavirus infection in camel workers in Qatar during 2013-2014: A case-control study. J Infect Dis 2017, 215, 1702–1705. [Google Scholar] [CrossRef]
  43. Zumla, A.; Rustomjee, R.; Ntoumi, F.; et al. Middle East respiratory syndrome—need for increased vigilance and watchful surveillance for MERS-CoV in Sub-Saharan Africa. Int J Infect Dis 2015, 37, 77–79. [Google Scholar] [CrossRef] [PubMed]
  44. Lu, X.; Whitaker, B.; Sakthivel, S.K.; et al. Real-time reverse transcription-PCR assay panel for Middle East respiratory syndrome coronavirus. J Clin Microbiol 2014, 52, 67–75. [Google Scholar] [CrossRef] [PubMed]
  45. Arabi, Y.M.; Arifi, A.A.; Balkhy, H.H.; et al. Clinical course and outcomes of critically ill patients with Middle East respiratory syndrome coronavirus infection. Ann Intern Med 2014, 160, 389–397. [Google Scholar] [CrossRef]
  46. Al-Hameed, F.; Wahla, A.S.; Siddiqui, S.; et al. Characteristics and outcomes of Middle East respiratory syndrome coronavirus patients admitted to an intensive care unit in Jeddah, Saudi Arabia. J Intensive Care Med 2016, 31, 344–348. [Google Scholar] [CrossRef]
  47. Arabi, Y.M.; Harthi, A.; Hussein, J.; et al. Severe neurologic syndrome associated with Middle East respiratory syndrome corona virus (MERS-CoV). Infection 2015, 43, 495–501. [Google Scholar] [CrossRef]
  48. Excler, J.L.; Delvecchio, C.J.; Wiley, R.E.; et al. Toward developing a preventive MERS-CoV vaccine—Report from a workshop organized by the Saudi Arabia Ministry of Health and the International Vaccine Institute, Riyadh, Saudi Arabia, November 14-15, 2015. Emerg Infect Dis 2016, 22. [Google Scholar] [CrossRef]
  49. Papaneri, A.B.; Johnson, R.F.; Wada, J.; Bollinger, L.; Jahrling, P.B.; Kuhn, J.H. Middle East respiratory syndrome: obstacles and prospects for vaccine development. Expert Rev Vaccines 2015, 14, 949–962. [Google Scholar] [CrossRef]
  50. Chan, J.F.; Lau, S.K.; Woo, P.C. The emerging novel Middle East respiratory syndrome coronavirus: the “knowns” and “unknowns”. J Formos Med Assoc 2013, 112, 372–381. [Google Scholar] [CrossRef] [PubMed]
Table 1. Reported human cases of MERS-CoV in the Arabian Peninsula.
Table 1. Reported human cases of MERS-CoV in the Arabian Peninsula.
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Ramadan, N.; Shaib, H. Middle East Respiratory Syndrome Coronavirus (MERS-CoV): A Review. GERMS 2019, 9, 35-42. https://doi.org/10.18683/germs.2019.1155

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Ramadan N, Shaib H. Middle East Respiratory Syndrome Coronavirus (MERS-CoV): A Review. GERMS. 2019; 9(1):35-42. https://doi.org/10.18683/germs.2019.1155

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Ramadan, Nour, and Houssam Shaib. 2019. "Middle East Respiratory Syndrome Coronavirus (MERS-CoV): A Review" GERMS 9, no. 1: 35-42. https://doi.org/10.18683/germs.2019.1155

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Ramadan, N., & Shaib, H. (2019). Middle East Respiratory Syndrome Coronavirus (MERS-CoV): A Review. GERMS, 9(1), 35-42. https://doi.org/10.18683/germs.2019.1155

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