Volume 25, Number 10—October 2019
Transmissibility of MERS-CoV Infection in Closed Setting, Riyadh, Saudi Arabia, 2015
To investigate a cluster of Middle East respiratory syndrome (MERS) cases in a women-only dormitory in Riyadh, Saudi Arabia, in October 2015, we collected epidemiologic information, nasopharyngeal/oropharyngeal swab samples, and blood samples from 828 residents during November 2015 and December 2015–January 2016. We found confirmed infection for 19 (8 by reverse transcription PCR and 11 by serologic testing). Infection attack rates varied (2.7%–32.3%) by dormitory building. No deaths occurred. Independent risk factors for infection were direct contact with a confirmed case-patient and sharing a room with a confirmed case-patient; a protective factor was having an air conditioner in the bedroom. For 9 women from whom a second serum sample was collected, antibodies remained detectable at titers >1:20 by pseudoparticle neutralization tests (n = 8) and 90% plaque-reduction neutralization tests (n = 2). In closed high-contact settings, MERS coronavirus was highly infectious and pathogenicity was relatively low.
Middle East respiratory syndrome (MERS) coronavirus (CoV) is a zoonotic virus (1). Approximately 2,266 laboratory-confirmed cases of MERS have been reported to the World Health Organization (WHO) (2) since the identification of the first human cases in 2012 (3,4).
Although the primary source of human infections is MERS-CoV–infected dromedaries, the modes of transmission from dromedaries to humans remain unclear (5). Human-to-human transmission has occurred primarily in healthcare settings (6), sometimes resulting in large explosive outbreaks (7,8). However, to date, no sustained human-to-human infection has been detected. Few outbreaks of MERS-CoV outside of healthcare settings have been documented, and limited transmission within families has been reported, but secondary attack rates in households or in settings outside of healthcare facilities (e.g., farms) seem to be low (9).
The nonspecificity of clinical definitions for MERS-CoV and the tendency of surveillance to focus on severe cases suggest that the prevalence of mild or asymptomatic infection cannot be estimated from case-based clinical surveillance alone (10). Mild or asymptomatic cases have been identified from contact tracing of laboratory-confirmed case-patients in several countries, including Saudi Arabia, the United Arab Emirates, Qatar, and South Korea (11–16).
In early October 2015, a cluster of MERS-CoV infections was identified among expatriate women working for a women-only university in Riyadh, Saudi Arabia. At the time the outbreak investigation was initiated, Kingdom of Saudi Arabia (KSA) Ministry of Health officials had identified 8 MERS case-patients by reverse transcription PCR (RT-PCR) (17); all patients were epidemiologically linked through their place of residence, a dormitory that housed expatriate women. Two additional laboratory-confirmed cases were identified among healthcare workers who had been exposed to the first case-patient, who had sought treatment at a medical clinic near the residence (17).
As part of this outbreak investigation, we conducted a molecular and seroepidemiologic study of the residents of an expatriate dormitory where the initial case-patients lived. Our goal was to describe and characterize the outbreak, determine potential source(s) of the outbreak, estimate the extent of MERS-CoV infection among residents, and evaluate risk factors for infection among residents.
Selection and Recruitment of Study Participants
We used the MERS-CoV standardized serologic investigation protocol developed by WHO and the Consortium for the Standardization of Influenza Seroepidemiology (18) and adapted it to the context of this outbreak. All 828 residents of the women-only expatriate dormitory in Riyadh were informed of the purpose of the outbreak investigation by KSA Ministry of Health official field teams and asked in person to participate. The KSA Ministry of Health, WHO, and Institut Pasteur field teams provided information sessions about the study and about MERS-CoV. The response team established a nursing station within the residential compound and assigned 2 nurses to reside within the compound to follow up with exposed persons and keep a log of any medical complaints from the residents throughout the outbreak period. Because this outbreak investigation was part of a public health response, it was not considered by the KSA Ministry of Health, Institut Pasteur, or The University of Hong Kong to be research that was subject to review by an institutional review board. As such, written informed consent was not required.
Included in the investigation were all residents of the dormitory who orally provided consent for completion of a questionnaire; collection of a nasopharyngeal or oropharyngeal swab sample, or both; and collection of a blood sample for serologic testing. Exclusion criteria included being <16 years of age at the time of recruitment, having any contraindication to venipuncture, or both.
The interviewers were trained to use the data collection forms developed for this investigation; because most residents were from the Philippines, the questionnaire was translated into Tagalog (Appendix). Each question was read aloud to women in groups of 15–25 in the dormitory while they filled in the questionnaire by hand. A subset of more sensitive questions was administered one-on-one by a member of the investigation team over the course of the 3-day field investigation. Before study implementation, frontline staff, including all outbreak investigation personnel, were trained with regard to infection control procedures, including proper hand hygiene and the correct use of respiratory face masks, to minimize their own risk for infection when in close contact with patients during home visits and elsewhere and to minimize the potential risk for MERS-CoV transmission between participants or between households.
Specimen Collection and Testing for MERS-CoV
Any participant who reported respiratory symptoms during the initial investigation (October 19–28, 2015) or during a 14-day follow-up period (after last contact with a confirmed/suspected MERS-CoV patient) was immediately isolated, and nasopharyngeal/oropharyngeal swab samples were collected and tested for MERS-CoV by RT-PCR. RT-PCR testing of human biological specimens was conducted at the Riyadh Regional Laboratory by use of standardized RT-PCR methods for MERS-CoV testing (19). Any participants with a positive MERS-CoV result by RT-PCR according to WHO criteria (10) were reported to WHO under the requirements of the International Health Regulations (2005) (https://www.who.int/ihr/9789241596664/en).
On November 1–2, 2015, a total of 5 mL of blood was collected from consenting residents of the compound. The blood was collected in a serum collection tube according to standard procedures and labeled with a coded identification number linked to the data collection forms. Transport of specimens within national borders complied with the applicable national regulations of Saudi Arabia. International transport of MERS-CoV specimens followed applicable international regulations (20).
Serologic assays used to detect and confirm seropositivity in the serum samples were MERS-CoV S1 IgG ELISA (EUROIMMUN EI 2604–9601G kit, https://www.euroimmun.com), MERS-CoV spike pseudoparticle neutralization test (ppNT), and 90% plaque-reduction neutralization test (PRNT90). Serologic testing for MERS-CoV antibodies was conducted at the University of Hong Kong, as previously described (21). All serum samples were screened by MERS-CoV S1 ELISA, and positive or equivocal samples were further tested by ppNT and PRNT90. Serologic results were interpreted as positive if PRNT90 or ppNT titer for either the first or second serum specimen was >1:20.
We entered all data for analysis in the entry form in Epi Info 3.5.4 (https://www.cdc.gov/epiinfo) and exported it to statistical software Stata 14 (https://www.stata.com). We estimated risk factors for infection among case-patients and non–case-patients (risk ratios [RRs] and 95% CIs) and within a nested case–control study (odds ratios [ORs] and 95% CIs) by restricting analyses to residents living in villas in which laboratory-confirmed cases had been identified.
The first patient in this cluster who had laboratory-confirmed MERS was a 27-year-old woman who worked as a janitor in a women-only university in Riyadh. She reported experiencing dry cough and fatigue on October 1, 2015; she sought care at a private healthcare clinic on October 4 and was provided treatment and sent home the same day. On October 7, after signs and symptoms worsened to include fever, shortness of breath, productive cough, and signs of pneumonia, she again sought care in the same healthcare clinic, and a diagnosis of MERS was suspected. On October 8, a nasopharyngeal sample was collected and the patient was transferred to a public hospital in Riyadh, designated for isolation and treatment of MERS patients. MERS-CoV infection was confirmed on October 9. A second case in this cluster has recently been described (22).
The first patient resided in an enclosed, women-only, expatriate dormitory composed of 24 villas (Figure 1). Each villa is a 3-story building with 7 bedrooms (2 on the ground floor, 3 on the first floor, and 2 on the second floor) and is inhabited by 24–50 women. On inspection of the living quarters, the field team found that most of the windows in the bedrooms were closed and sealed and that ventilation within the bedrooms was poor. Initial open-ended interviews with some residents informed the study team that residents shared the same kitchen and dining room within the villa but did not typically eat together or share food at mealtimes. There were no designated social spaces; however, residents reported gathering around laptops to watch movies together.
A total of 828 women who lived in the residence complex were included in the seroepidemiologic study; none of the eligible women refused to participate. All participants were female, and median age was 35.1 (26.6–41.3) years. None were Saudi Arabia nationals; they were from the Philippines (84.6%), Sri Lanka (6.4%), Indonesia (2.9%), Nepal (1.6%), and India (1.1%) (Table 1). A total of 49 participants (1 case-patient and 48 non–case-patients) reported having >1 chronic condition (e.g., asthma, diabetes, heart disease, hypertension, breast cancer) (Table 1). The MERS case-patient reported having asthma; among non–case-patients, the most common chronic conditions reported were asthma (31%), diabetes (25%), and hypertension (18%).
In terms of occupation, almost half (49.1%) of participants reported working at the women-only university in Riyadh, including 17 (89.5%) of the MERS case-patients (Table 1). Participants reported working in 1 of 4 hospitals as either their primary or secondary occupation (Table 1).
Contact tracing of the initial patient and molecular and serologic laboratory test results identified an additional 18 MERS-CoV infections (Figure 2; Table 2). Of the 19 total case-patients, 12 (63.2%) were from villa 2A; 2 (10.5%) were from a facing villa (1B); and 1 case (5.3%) was reported from each of 5 villas either close to the mostly affected villa (2A) or 2 other villas (10A and 7A) populated with residents from the Philippines (Figure 1).
Among the 8 MERS-CoV cases positive by PCR, 8 were also serologically positive for MERS-CoV (Table 2). According to PRNT90 or ppNT serology results for either the first or second serum sample, an additional 11 persons were serologically positive for MERS-CoV infections. Therefore, a total of 19 of the 828 dormitory residents had evidence of MERS-CoV infection by molecular or serologic testing or both; the infection attack rate [IAR] for the cohort was 2.3%.
Of the 9 patients from whom a second sample was collected in March 2016, a total of 8 had ppNT titers of >1:20, and only 2 of these had PRNT90 titers of >1:20. For 2 of these 8 patients, ppNT indicated a >4-fold fall in antibody titer; for the others, ppNT antibody levels remained within 2-fold that of the initial serum sample.
Bivariate analyses indicated significant assocations between MERS and the following risk factors: having direct contact with a known MERS patient (RR 10.9, 95% CI 6.7–17.6); sharing a bedroom (RR 25.5, 95% CI 10.3–63.1), kitchen (RR 15.5, 95% CI 5.4–44.2), bathroom (RR 25.5, 95% CI 10.3–63.1), meal (RR 19.4, 95% CI 7.5–50.3), or transportation vehicle (RR 11.8, 95% CI 4.9–28.5); and having indirect contact with a known patient (RR 15.5, 95% CI 5.4–44.2) (Table 3). The presence of a chronic condition did not vary by MERS infection status. According to multivariate analyses, direct contact with a known MERS patient (OR 27.6, 95% CI 8.4–91.0) and sharing a bedroom with a MERS patient (OR 5.7, 95% CI 1.5–22.5) remained statistically significant. Having a functioning air conditioner in the bedroom was protective (OR 0.15, 95% CI 0.03–0.82). None of the women reported traveling outside of Saudi Arabia in the 14 days before symptom onset (data not shown).
This study details the comprehensive investigation of a cluster of MERS cases reported outside a healthcare-associated or camel industry–associated occupational setting. In this women-only, expatriate worker dormitory in Riyadh, Saudi Arabia, the overall IAR of 2.3% is similar to that found in a household contact study conducted in 2014 (IAR of 4.3%) (9). However, in this outbreak, the residential setting was more crowded than typical single-family households. Although we found the IAR in some villas to be low, we identified IARs as high as 35.3% (12/34) in 1 villa (2A), probably because of the exceptionally crowded living and sleeping conditions. Within this villa, 12 women were infected with MERS-CoV but only 10 reported any symptoms. Rates of IAR were not affected by the presence or absence of underlying conditions or the median age of residents by villa.
This study identified the independent risk factors for infection to be direct contact and sharing a bedroom with a MERS patient. Findings from other serologic studies have been similar (23). We hypothesize that the increased human-to-human transmission within villas resulted from the clustering of the women’s activities. For example, the same women who lived together typically ate and socialized together, worked together, and traveled to and from work together. These activities added to the likelihood of intense direct physical contact among the women and probably led to limited but effective human-to-human transmission within their residence.
Globally, the extent of human-to-human transmission outside of healthcare facilities is uncertain, and whether MERS-CoV has the potential for sustained community transmission is unclear. Transmission among family members seems to be limited but can be amplified in healthcare settings (24,25) among persons with underlying medical conditions and to healthcare workers. Contributors to propagation of MERS-CoV infection in healthcare facilities include aerosol-generating procedures such as intubation, suction, and collection of nasopharyngeal swabs (26). Compared with the total number of MERS-CoV infections reported to WHO to date, patients in our study cohort were significantly younger (median age 32 vs. 52 years, respectively), healthier (6.3% vs. 41.0% reporting >1 chronic condition), and more likely to be female (0 vs. 68.1% male) (27).
Healthcare staff can prevent human-to-human transmission of MERS-CoV through stringent adherence and implementation of detailed and clear protocols for standard, droplet, and aerosol infection prevention and control (IPC) measures among the various persons within a healthcare setting (i.e., healthcare workers, patients, and visitors) (28). Such IPC measures were not followed by the inhabitants of the dormitory in this study.
Although we were able to rule out a connection to dromedary camels, we were not able to specifically determine the source of this outbreak. Of the 19 laboratory-confirmed case-patients, 17 reported working at the same women-only university in Riyadh and the other 2 worked primarily as cleaners at the same healthcare facility in Riyadh (hospital B). Of these 19 case-patients, 3 also reported having a secondary place of employment, including working as cleaners at 2 other hospitals in Riyadh (hospitals A and D). We hypothesize that 1 of the 19 infected women identified in this investigation may have been exposed to and infected with MERS-CoV while working as a cleaner in a healthcare facility where persons with undiagnosed MERS had been cared for. In August 2015, hospital B, reportedly the primary occupation location for 2 women who were MERS-CoV positive according to PCR, was the location of a small cluster of laboratory-confirmed MERS cases (n = 5). Unfortunately, viral genetic sequencing was conducted on only 1 of those patients (22); without further epidemiologic and sequencing data from other patients in this cluster, or from the laboratory-confirmed patients in the small cluster in hospital B in August 2015, we cannot surmise further.
The time lag between identification of MERS patients in hospital B in August 2015 and the timing of this outbreak in October 2015 suggests that persons with subclinical cases may have been in or working in this hospital during August–October 2015; however, because testing for MERS-CoV in Saudi Arabia was substantial (29), missing symptomatic cases was unlikely. A subject of some debate and recent focus has been the potential role of mildly symptomatic or asymptomatic infections and possible environmental contamination in the spread of MERS-CoV in healthcare facilities (22,30–33). The rapid initiation of this investigation and use of an existing protocol (34) (developed for such use after the rapid isolation of close contacts regardless of the development of symptoms and the implementation of a no-fly policy among residents of the compound until the full 14-day follow-up was completed) probably limited further human-to-human transmission inside and potentially outside of Saudi Arabia.
Our study highlights the potential role of healthcare workers not responsible for direct patient care (e.g., hospital cleaners) in the spread of MERS-CoV. Often, hospital cleaning staff may be from other countries, may speak several languages, and may be missed by efforts to increase IPC specific to MERS-CoV. Specific MERS-CoV IPC training should be directed to cleaning staff in healthcare facilities, in addition to healthcare providers, in appropriate languages, particularly to protect them from infection and from facilitating virus spread within the healthcare facility.
For the 8 women with RT-PCR–confirmed infection, antibody titers ranged from 1:10 to 1:80 by PRNT and from 1:20 to 1:160 by ppNT. For 9 of the 19 women with confirmed evidence of infection by RT-PCR, serologic testing, or both, for whom follow-up serum samples were available 3 months after the putative exposure, 7 women had PRNT titers of <1:20 and 1 woman had ppNT titers of <1:20. Thus, the ppNT antibody test was somewhat more sensitive for detecting evidence of past infection. A ppNT titer of 1:20 is therefore an optimal indicator of past infection in seroepidemiologic assays. The ppNT, although more sensitive, correlated well with PRNT among persons with RT-PCR–confirmed MERS-CoV infection (35) and was uniformly negative in serum from persons in areas where MERS-CoV is not endemic (e.g., Hong Kong ). For this study, we categorized those without RT-PCR evidence of MERS-CoV infection but PRNT or ppNT antibody titers >1:20 as being MERS-CoV infected.
Of the 8 women who had RT-PCR–confirmed infection, 2 were asymptomatic, as were 6 of the 11 women whose diagnosis was made solely by serologic testing. Serologic studies of cohorts of patients positive for MERS-CoV by RT-PCR have shown that milder disease and asymptomatic infections may not be associated with detectable serologic responses (37). Thus, our serologic testing probably underestimates the true number of MERS-CoV infections that may have occurred. However, our data provide evidence that even asymptomatic infections can sometimes lead to detectable serologic responses and that such investigations are useful. Furthermore, the serologic results at 5 months after putative exposure show evidence of antibody titers waning to below diagnostic limits in some patients but also show that antibodies may remain detectable in others. This information is useful when interpreting seroepidemiologic studies in high-risk populations.
Our study had several limitations. Because of multicollinearity of the exposure variables (38), the accuracy of individual predictors may be compromised. The lack of collection of acute blood samples during the outbreak limited our ability to detect seroconversion. In addition, we were not able to conduct sequencing for patients of this outbreak and therefore were not able to use this information to potentially confirm that all 19 infected women acquired their infection from a common source or to identify the source of the outbreak.
The rapid initiation of contact tracing, isolation, and subsequent investigation probably contributed to the quick halt of human-to-human transmission in this outbreak. On the basis of the possible source of infection, to reduce secondary human-to-human transmission outside the occupational setting, our study indicates that IPC measures introduced in healthcare facilities should focus on not only healthcare personnel but also those working within the wider facility, including cleaners.
Dr. Van Kerkhove is an infectious disease epidemiologist who specializes in outbreaks of emerging and re-emerging high-threat pathogens. She is the MERS-CoV technical lead at the WHO Health Emergencies Programme in Geneva, Switzerland. Her research interests include zoonotic, respiratory, and emerging/re-emerging viruses, and her work focuses on investigating factors associated with transmission between animals and humans, studying the epidemiology of zoonotic pathogens, and ensuring that research on infectious diseases directly informs public health policy for action.
We thank the KSA Ministry of Health field staff for their support in collecting biological samples and administering questionnaires during the study.
Serologic testing for this study was supported by a research grant from the US National Institutes of Health (contract no. HHSN272201400006C).
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TablesCite This Article
Original Publication Date: August 19, 2019
1Current affiliation: World Health Organization, Geneva, Switzerland.
2Current affiliation: King Saud University, Riyadh, Saudi Arabia.
Table of Contents – Volume 25, Number 10—October 2019
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Maria D. Van Kerkhove, World Health Organization, High Threat Pathogens, Global Infectious Hazards Management Health Emergencies Program, Avenue Appia, Geneva 1211, Switzerland