The Middle East respiratory syndrome coronavirus (MERS-CoV) is a priority zoonotic pathogen of humans highlighted in the WHO research and development blueprint list requiring urgent action1 because it has epidemic potential, a high fatality rate with no specific treatment or vaccine, and a wide geographical distribution of the host reservoir of dromedary camels in the Middle East, Africa, and Asia.2
Globally, as of May 31, 2019, 2442 laboratory-confirmed MERS cases, with 842 deaths (case-fatality ratio of 34·5%), had been reported to WHO since September, 2012.3 2031 of these cases occurred in Saudi Arabia and the largest outbreak outside the Middle East occurred in South Korea in May, 2015, with 186 cases reported between May 15 and July 6, 2015, showing its epidemic potential.4 An upsurge in the number of MERS cases has been seen in Saudi Arabia and Oman, with 189 cases reported between July, 2017, and June, 2018, compared with 126 cases between January and March, 2019.3 Worryingly, although MERS-CoV continues to circulate in the Middle East, progress in advancing priority research and development on the epidemiology, rapid diagnostics, treatments, and vaccines, including regional One Health activities5 have been slow. Importantly, despite many WHO MERS expert group and other stakeholder meetings that have defined priority research needs, major knowledge gaps remain in the epidemiology, transmission, pathogenesis, and phylogenetic evolution of MERS-CoV.6, 7
Major opportunities for appropriate longitudinal and cross-sectional studies to fill these gaps from the recurrent community and nosocomial outbreaks of MERS in Saudi Arabia are being missed. By contrast, several studies done after the 2015 MERS outbreak in South Korea yielded important epidemiological, clinical, virological, and management outcome data.8 MERS-CoV sequence variants were detected during the South Korean outbreak, with some mutations incorporated into the circulating virus. Remarkably, the most extensively studied mutations, which occurred in the surface glycoprotein were not predicted.8 The surface glycoprotein is crucial for virus entry and during the severe acute respiratory syndrome epidemic it evolved to bind more tightly to its cellular receptor. By contrast, changes detected in MERS-CoV-surface glycoprotein appeared to decrease binding and were expected to decrease virulence and transmissibility;8 however, these changes could be beneficial to the MERS-CoV by facilitating evasion of the antibody response.
MERS-CoV transmission occurs in community or household settings or in health-care facilities.2, 3 Nosocomial outbreaks were a major feature but have decreased due to increased awareness and implementation of infection control measures.10 Although zoonotic transmission from camels is thought to be the primary mode of transmission, a substantial proportion of patients describe no camel contact.2, 6, 10, 11 MERS-CoV infection of camels throughout Africa is common, although no convincing serological or virological evidence exists of human MERS-CoV infection in Africa.11, 12 The key questions are why did human MERS-CoV infection only begin in the Middle East in 2012 and not in Africa? And how do patients without contact with camels acquire the disease? Sequence analysis of MERS-CoV isolated from patients in the Middle East revealed mutations in the virus, most of which were transient with reversion to wild type sequence,9 which is inconsistent with continuing adaptation to humans. Many of the virus variants were observed circulating in camels at the same time,13 suggesting continuing camel-to-human transmission, which might have obscured adaptive changes in the human virus. Small differences in sequences were observed when east African and Saudi Arabian MERS-CoV isolates were compared, with more substantial differences observed when compared with west African MERS-CoV, including deletions detected in west African MERS-CoV.12 These differences might contribute to diminished transmission; however, another possibility is that differences might occur in human–camel contact in Africa versus the Middle East. Camel workers and owners have close contact with camels and thus have increased prevalence of MERS-CoV immunopositivity (3–67%) than the general population (0·15%).14, 15 Camel workers have mild or subclinical disease, and they might transmit MERS-CoV either directly or indirectly to more susceptible individuals (eg, those with comorbidities) who would present as sporadic cases.
These studies point to several directions for priority research and interventions to decrease the persistent threat of MERS-CoV transmission. First, continuous sequence analysis of MERS-CoV in endemic countries is needed to establish viral evolution, as was the case in the South Korean outbreak. Second, increased understanding of camel–human interactions and patterns of camel grazing in Africa and the Middle East could provide insight into transmission differences. Third, an effective vaccine for humans is the best way to prevent spread of MERS but logistical issues because of the small number of sporadic MERS cases in different geographical locations need to be overcome. Alternatively, vaccination of juvenile camels might block transmission. Fourth, development of antiviral and other therapies for MERS-CoV would improve patient outcomes and, by decreasing virus burden, could decrease transmission. Finally, continued efforts to educate camel workers about infection control measures, such as handwashing and wearing protective gear when handling camels, especially juvenile ones with upper respiratory tract infections, will be crucial in minimising transmission.
The persistence of MERS-CoV transmission in the Middle East 7 years after it was first discovered, and the many unanswered questions regarding MERS6, 7 that have been raised recurrently at WHO MERS expert group annual meetings, now require a major change from the current status quo. If we are to prevent MERS-CoV evolving into the next global pandemic, serious financial and political commitments, especially from MERS-endemic countries, are needed to establish and take forward an effective multidisciplinary One Health consortia to establish more effective multidisciplinary research collaborations.
Acknowledgments
All authors have an academic interest in Middle East respiratory syndrome coronavirus. AZ is a member of the PANDORA-ID-NET Consortium funded by Grant RIA2016E-1609 from the European and Developing Countries Clinical Trials Partnership (EDCTP2) programme and he is in receipt of a National Institutes of Health Research senior investigator award. SP is supported by grants from the US National Institutes of Health (AI060699).
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