Literature DB >> 27940937

Risk factors for transmission of Middle East respiratory syndrome coronavirus infection during the 2015 outbreak in South Korea.

Seung Woo Kim1, Jung Wan Park1, Hee-Dong Jung2, Jeong-Sun Yang2, Yong-Shik Park1, Changhwan Lee1, Kyung Min Kim1, Keon-Joo Lee1, Donghyok Kwon1, Young Joo Hur3, Bo Youl Choi4, Moran Ki5.   

Abstract

Background: Transmission heterogeneity was observed during the 2015 South Korean outbreak of Middle East respiratory syndrome coronavirus (MERS-CoV) infection. Only 22 of 186 cases transmitted the infection, and 5 super-spreading events caused 150 transmissions. We investigated the risk factors for MERS-CoV transmission.
Methods: Epidemiological reports were used to classify patients as non-spreaders, spreaders (1-4 transmission), or those associated with super-spreading event (≥4 transmissions). Logistic regression analyses were used to evaluate the factors that influenced MERS-CoV transmission.
Results: Compared to non-spreaders, spreaders exhibited a longer interval from symptom onset to isolation (7 days vs. 3 days) and more frequent pre-isolation pneumonia diagnoses (68.2% vs. 17.1%). Spreaders also exhibited higher values for pre-isolation contacts (149 vs. 17.5), pre-isolation hospitalization (68.2% vs. 16.5%), and emergency room visits (50% vs. 7.3%). Spreaders exhibited lower cycle thresholds for the upE and ORF1a genes (22.7 vs. 27.2 and 23.7 vs. 27.9, respectively). Transmission was independently associated with the cycle threshold (odds ratio [OR]: 0.84, 95% confidence interval [CI]: 0.75-0.96) and pre-isolation hospitalization or emergency room visits (OR: 6.82, 95% CI: 2.06-22.84). The spreaders with ≥4 transmissions exhibited higher values for pre-isolation contacts (777 vs. 78), pre-isolation emergency room visits (100% vs. 35.3%), and doctor-shopping (100% vs. 47.1%), compared to other spreaders. Conclusions: These findings indicate that transmission is determined by host infectivity and the number of contacts, whereas super-spreading events were determined by the number of contacts and hospital visits. These relationships highlight the importance of rapidly enforcing infection control measures to prevent outbreaks.
© The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail journals.permissions@oup.com.

Entities:  

Keywords:  Middle East respiratory syndrome coronavirus; South Korea; epidemiology; super-spreading event; transmission

Year:  2016        PMID: 27940937      PMCID: PMC7108049          DOI: 10.1093/cid/ciw768

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


Transmission heterogeneity was a significant characteristic of the 2015 South Korean outbreak of Middle East respiratory syndrome coronavirus (MERS-CoV) infection [1]. Transmission heterogeneity describes a state in which most transmissions are related to a few patients and most patients do not transmit the disease. Numerous other infectious diseases exhibit transmission heterogeneity [2], and this concept is important for understanding epidemics. The course of an epidemic is influenced by the basic reproduction number (R0 = the average number of cases that 1 case produces in a susceptible population) and transmission heterogeneity [3]. As R0 represents an average quantity, it is often insufficient to explain individual variation, and as transmission heterogeneity reflects individual variation, it can help predict the likelihood of super-spreading events. Even in instances with a low R0, a disease with high transmission heterogeneity (eg, severe acute respiratory syndrome [SARS]) can cause super-spreading events [2], such as the super-spreading that occurred during the 2003 SARS outbreak [2, 4]. Transmission heterogeneity was observed during early MERS-CoV outbreaks [1] and became prominent during the 2015 South Korean outbreak. Among the 186 confirmed Korean cases of MERS-CoV infection, >80% of the transmissions were epidemiologically associated with 5 patients [5], and almost 90% of the cases caused no transmission. Furthermore, a recent study revealed that MERS has greater transmission heterogeneity compared to SARS [6]. Therefore, to successfully control MERS-CoV infection, it is essential to identify high-risk patients and perform targeted infection control [2]. However, these patients are difficult to identify, as an individual’s infectiousness is affected by complex interactions between the pathogen, host, and environment. Several researchers have attempted to identify risk factors for super-spreading events during the SARS outbreak [3, 4, 7], although there is little information regarding the high-risk group(s) from the MERS-CoV outbreak. The recent South Korean MERS-CoV outbreak was triggered by a single imported case, and epidemiological tracing was performed for all laboratory-confirmed cases and their close contacts [5, 8–13]. Thus, it is possible to precisely reconstruct the transmission chain and identify patients who transmitted MERS-CoV infection. Therefore, we analyzed the epidemiological characteristics that were associated with MERS-CoV transmission and super-spreading events.

METHODS

Definitions

Cases of MERS-CoV infection were confirmed using real-time reverse-transcription polymerase chain reaction (RT-PCR) assays, regardless of their clinical manifestations. The epidemiological reports were analyzed by epidemic intelligence service officers who participated in the MERS-CoV outbreak investigation. When a case was exposed to multiple confirmed cases, the transmission was attributed to the case with the highest likelihood of transmission, and any conflicts were resolved through the consensus of the epidemic intelligence service officers. Spreaders were defined as confirmed cases of MERS-CoV infection that were epidemiologically suspected of transmitting MERS-CoV to 1 or more persons. Super-spreading events were arbitrarily defined as transmission of MERS-CoV infection to 5 or more cases. The patient who triggered the outbreak was defined as patient zero. Cases that were infected by patient zero were defined as first-generation cases; cases that were infected by first-generation cases were defined as second-generation cases; and cases that were infected by second-generation cases were defined as third-generation cases [14]. Isolation was defined as separating symptomatic patients from others to prevent spreading, and quarantine was defined as separating or restricting the movement of healthy individuals who may have been exposed to the infection within the maximum incubation period. The transmission date was defined as the date of contact between the spreader and suspected secondary case during the spreader’s infectious period. In cases with an exposure duration of longer than 1 day, the transmission date was defined as the day with the highest likelihood of transmission or as the median day during the exposure period in cases with consistent contact throughout the exposure. The date of sampling was the day on which the first positive respiratory specimen was collected. Close contacts were defined using the Guidelines on Middle East Respiratory Syndrome [15], which include persons who stayed in a room or ward with a confirmed case, who directly contacted respiratory secretions from confirmed cases, or who stayed within 2 m from the confirmed cases without wearing appropriate personal protective equipment. Pre-isolation pneumonia diagnoses were based on radiographic evidence. Doctor shopping was defined as visiting multiple healthcare facilities without an official interhospital transfer after developing MERS-CoV symptoms [16].

Data Collection

Epidemiological reports from the outbreak were evaluated to collect data regarding basic demographic characteristics, medical history, MERS-CoV exposure, symptoms and their onset date(s), sampling date(s), contact history, and post-exposure infection control. The reports were drafted during the outbreak based on direct interviews with the confirmed cases and follow-up epidemiological investigations that were performed to identify the exposure route and close contacts. Hospital information systems were reviewed to identify patients who stayed in the hospital during the exposure period and healthcare providers who contacted the patient(s). Persons who contacted confirmed cases outside healthcare facilities were also traced. Data from closed circuit television, credit card transactions, and health insurance services were also reviewed [5]. The numbers of close contacts were calculated based on the number of quarantines during the outbreak. All data were collected as part of the public health response and in accordance with the Infectious Disease Control and Prevention Act [17].

Laboratory Confirmation

Clinical specimens were collected in sterile containers and immediately transferred to qualified facilities. Sputum samples were mixed with 0–1× phosphate-buffered saline and vortexed vigorously to reduce their viscosity. Viral RNA was extracted from the clinical specimens using a Qiagen viral RNA mini kit (Qiagen, Hilden, Germany). All laboratory diagnoses of MERS-CoV were confirmed using the World Health Organization guidelines [18] and results from real-time RT-PCR assays that target upstream of the MERS-CoV envelope protein gene (upE) and the open reading frame 1a gene (ORF1a) [19]. Cycle threshold (Ct) values for the upE and ORF1a genes were obtained during testing. We analyzed the Ct value from the first positive MERS-CoV specimen (or the specimen obtained immediately after a positive screening test).

Statistical Analyses

Categorical variables were compared using the χ2 test and Fisher exact test, and the Mann–Whitney test was used for continuous variables. The variables’ associations with MERS-CoV transmission were evaluated using multiple logistic regression analyses, and covariates were selected based on a P value of < .1 in the univariate analyses. A P value of < .05 was considered statistically significant. All analyses were performed using R software (version 3.2.2; R Foundation, Vienna, Austria).

RESULTS

Transmission Chain

We identified 186 cases of confirmed MERS-CoV infection. Patient zero infected 28 first-generation cases. Among the 28 cases, 8 were responsible for transmission to 121 second-generation cases. Among the 121 cases, 12 infected 30 third-generation cases. One patient with an unclear source of infection (case 119) transmitted the infection to another patient. Four patients exhibited unclear sources of transmission (cases 43, 178, 184, and 185). Each confirmed case transmitted the infection to 0–83 secondary cases (Figure 1). There were 164 nonspreaders and 22 spreaders (1 or more transmission). Of the spreaders, 5 cases transmitted the infection to 5 or more cases (super-spreading event).
Figure 1.

Transmission chain for the 186 laboratory-confirmed cases of Middle East respiratory syndrome coronavirus infection in South Korea during 2015. Figures in squares indicate the spreaders that transmitted the infection to 5 or more cases. One case with an unclear infection generation (case 119) transmitted the infection to an additional case. The source of infection was unclear in 4 additional cases (cases 43, 178, 184, and 185).

Transmission chain for the 186 laboratory-confirmed cases of Middle East respiratory syndrome coronavirus infection in South Korea during 2015. Figures in squares indicate the spreaders that transmitted the infection to 5 or more cases. One case with an unclear infection generation (case 119) transmitted the infection to an additional case. The source of infection was unclear in 4 additional cases (cases 43, 178, 184, and 185).

The Spreaders’ Epidemiological Characteristics

After excluding the 5 cases with unclear infection sources, we identified 180 transmissions generated by 22 spreaders. A total of 150 transmission events (83.3%) were epidemiologically linked to the 5 super-spreading events. Twenty-five transmission events (13.9%) occurred within 3 days after symptom onset, 136 transmissions (75.6%) occurred 4–7 days after symptom onset, and 19 transmissions (10.6%) occurred >7 days after symptom onset. A total of 170 transmission events (94.4%) occurred on the day of or after a radiographically confirmed diagnosis of pneumonia. A total of 173 transmissions (96.1%) occurred before appropriate in-hospital isolation. Seven transmissions (3.9%) occurred between confirmed cases and healthcare personnel after in-hospital isolation: 4 (cases164, 169, 181, and 183) were doctors or nurses who managed confirmed cases, 1 (case148) participated in cardiopulmonary resuscitation of a confirmed case, 1 (case 162) involved portable radiography for a confirmed case, and 1 (case 179) rode in an ambulance with a confirmed case during a hospital transfer.

Comparing the Spreaders and Nonspreaders

Table 1 shows the spreaders’ and nonspreaders’ epidemiological characteristics. These individuals exhibited similar values for age, sex, and presence of cough at symptom onset. However, spreaders exhibited significantly more frequent underlying respiratory disease (27.3% vs 11%; P = .044). The spreaders also had significantly lower Ct values (upE: median [interquartile range], 22.7 [19.5–29.1] vs 27.2 [23.5–30.4]; P = .004 and ORF1a: 23.7 [20.3–29.8] vs 27.9 [24.9–30.8]; P = .009). The intervals from symptom onset to diagnosis or obtaining a respiratory specimen were also significantly longer among spreaders (to diagnosis: 9 [5.5–10] days vs 5 [3-8] days; P = .008 and to sampling: 8 [5–9.3] days vs 4 [2-6] days; P < .001). Furthermore, the interval from symptom onset to isolation was longer among spreaders (7 [4.5–9] days vs 3 [1-6] days; P = .002). Spreaders exhibited a significantly higher proportion of pre-isolation pneumonia diagnoses (68.2% vs 17.1%; P < .001) and a longer interval from the pneumonia diagnosis to isolation (4 [3-7] days vs 1 [0-3] days; P = .008). The overall number of contacts was significantly larger among spreaders compared to nonspreaders (149 [22.3–640.5] vs 17.5 [2–92.5]; P = .004). Compared to nonspreaders, spreaders exhibited a significantly higher proportion for pre-isolation hospitalization (68.2% vs 16.5%; P < .001), visiting outpatient clinics (59.1% vs 33.5%; P = .019), and visiting emergency rooms (ERs; 50% vs 7.3%; P < .001).
Table 1.

Comparing the Demographic and Epidemiological Characteristics of Middle East Respiratory Syndrome Coronavirus Infection Spreaders and Nonspreaders During the 2015 South Korean Outbreak

Variables, n (%) or median [interquartile range]Spreaders (n = 22)Nonspreaders (n = 164) P Value
Host factors
Age, y55.5 [35.0–67.0]55 [42.5–66.0].938
Sex, male16 (72.7)95 (57.9).184
Case classification.013a
 Healthcare personnel0 (0)25 (15.2)
 Patients9 (40.9)74 (45.1)
 Family members5 (22.7)46 (28.0)
 Paid caregivers2 (9.1)7 (4.3)
 Othersb6 (27.3)12 (7.3)
Stage of transmissionc<.001a
 Patient zero1 (4.8)0 (0)
 1st generation8 (38.1)20 (12.5)
 2nd generation12 (57.1)111 (69.4)
 3rd generation0 (0)29 (18.1)
Underlying respiratory diseased6 (27.3)18 (11.0).044a
Cough at symptom onset5 (22.7)30 (18.3).571a
Cycle threshold value (reverse transcription polymerase chain reaction)
upE22.7 [19.5–29.1]27.2 [23.5–30.4].004
ORF1a23.7 [20.3–29.8]27.9 [24.9–30.8].009
Duration
Symptom onset to sampling, days8 [5.0–9.3]4 [2.0–6.0]<.001
Symptom onset to diagnosis, dayse9 [5.5–10.0]5 [3.0–8.0].008
Symptom onset before isolatione21 (95.5)124 (78.0).083a
 Onset to isolation, days7 [4.5–9.0]3 [1.0–6.0].002
Diagnosis of pneumonia before isolationf15 (68.2)28 (17.1)<.001
 Pneumonia to isolation, days4 [3.0–7.0]1 [0–3.0].008
Contacts
Contact with other persons before isolation21 (95.5)138 (84.1).209a
 Number of contacts149 [22.3–640.5]17.5 [2.0–92.5].004
Hospital visit before isolation
Hospitalization15 (68.2)27 (16.5)<.001a
 Duration of hospitalization, days5 [4.0–8.0]4 [2.0–7.0].354
Outpatient clinic visit13 (59.1)55 (33.5).019
 Frequency of visits2 [1.0–2.0]2 [1.0–3.0].472
ER visit11 (50.0)12 (7.3)<.001a
 Frequency of visits2 [1.0–2.0]1.5 [1.0–2.0].499
Number of hospitals visited2 [1.0–2.3]0 [0–1.0]<.001
 For hospitalization or ER visit1 [0–2.0]0 [0–0]<.001
 For outpatient clinic visit1 [1.0–2.0]1 [1.0–2.0].364

P values were obtained using the chi-square test or Fisher’s exact test for categorical variables, and the Mann-Whitney test for continuous variables.

Abbreviation: ER, emergency room.

Fisher exact test.

Includes hospital security agents in the emergency department, emergency medical technicians, visitors, police officers, and hospital office workers.

Excludes 5 cases with unclear stages of transmission.

Includes chronic obstructive pulmonary disease, asthma, pulmonary tuberculosis, and pneumonia before the exposure to Middle East respiratory syndrome coronavirus.

Excludes 5 cases with unclear symptom onset dates.

Cases with radiographic evidence of pneumonia before their isolation.

Comparing the Demographic and Epidemiological Characteristics of Middle East Respiratory Syndrome Coronavirus Infection Spreaders and Nonspreaders During the 2015 South Korean Outbreak P values were obtained using the chi-square test or Fisher’s exact test for categorical variables, and the Mann-Whitney test for continuous variables. Abbreviation: ER, emergency room. Fisher exact test. Includes hospital security agents in the emergency department, emergency medical technicians, visitors, police officers, and hospital office workers. Excludes 5 cases with unclear stages of transmission. Includes chronic obstructive pulmonary disease, asthma, pulmonary tuberculosis, and pneumonia before the exposure to Middle East respiratory syndrome coronavirus. Excludes 5 cases with unclear symptom onset dates. Cases with radiographic evidence of pneumonia before their isolation. We used logistic regression analyses to evaluate the risk factors for transmission (Table 2). In the univariate analyses, transmission was associated with underlying respiratory disease, Ct value, interval from symptom onset to diagnosis, number of contacts, and pre-isolation hospitalization or ER visits. In the multivariate analyses, transmission was independently associated with a low Ct value for upE (odds ratio [OR], 0.84; 95% confidence interval [CI], 0.75–0.96) and pre-isolation hospitalization or ER visits (OR, 6.82; 95% CI, 2.06–22.84).
Table 2.

Epidemiological Factors Associated With Middle East Respiratory Syndrome Coronavirus Transmission During the 2015 South Korean Outbreak

Variable (reference)Univariate Logistic RegressionMultivariate Logistic Regression
OR95% CI P ValueOR95% CI P Value
Underlying respiratory disease (no)3.041.06–8.76.0393.020.80–11.40.103
Cycle threshold value (upE)0.850.76–0.94.0020.840.75–0.96.007
Symptom onset to diagnosis (days)1.131.01–1.27.0311.020.87–1.18.846
Number of contacts (<10).0041.490.75–2.97.260
 10–991.030.27–4.03.963
 ≥1004.861.61–14.65.005
Hospitalization or emergency room visit before isolation (no)10.593.84–29.15<.0016.822.06–22.84.002

There was no multicollinearity between the independent variables (all variables: R score of <0.5).

Abbreviations: CI, confidence interval; OR, odds ratio.

Epidemiological Factors Associated With Middle East Respiratory Syndrome Coronavirus Transmission During the 2015 South Korean Outbreak There was no multicollinearity between the independent variables (all variables: R score of <0.5). Abbreviations: CI, confidence interval; OR, odds ratio.

Comparing the Spreaders With 5 or More Transmissions and Spreaders With 4 or Fewer Transmissions

We compared the epidemiological characteristics of the 5 spreaders with 5 or more transmissions and the 17 spreaders with 4 or fewer transmissions (Table 3). Both groups exhibited similar host factors and contact durations. However, spreaders with 5 or more transmissions exhibited higher values for pre-isolation contacts (777 [459.5–862] vs 78 [8.5–281.5]; P = .017), pre-isolation ER visits (100% vs 35.3%; P = .035), and the number of healthcare facilities that each patient visited for hospitalization or ER treatment (2 [2.0–2.5] vs 1 [0–1.5]; P = .009). In addition, super-spreading events were marginally associated with doctor shopping (100% vs 47.1%; P = .054).
Table 3.

Comparison of the Epidemiological Characteristics of Spreaders With 5 or More Cases and Spreaders With 4 or Fewer Cases

Variables, n (%) or Median [interquartile range]Spreaders With 5 or More Cases (n = 5)Spreaders With 4 or Fewer cases (n = 17) P Value
Host factors
Underlying respiratory diseasea2 (40)4 (23.5).585b
Cough at symptom onset3 (60)2 (11.8).055b
Cycle threshold value (reverse transcription polymerase chain reaction)
upE22.2 [17.4–29.9]22.8 [20.7–26.9].820
ORF1a23.2 [18.2–32.2]23.9 [21.3–28.1].880
Duration
Symptom onset to sampling, days9 [4.5–10.5]6 [5.0–8.5].284
Symptom onset to diagnosis, days9 [5.5–11]8 [5.0–9.5].320
Symptom onset before isolation5 (100)16 (94.1)1b
 Onset to isolation, days8 [4.0–9.5]6.5 [4.3–8.8].453
Diagnosis of pneumonia before isolationc5 (100)10 (58.8).135b
 Pneumonia to isolation, days5 [2.0–8.0]3.5 [2.3–6.3].419
Contacts
Contact with other persons before isolation5 (100)16 (94.1)1b
 Number of contacts777 [459.5–862]78 [8.5–281.5].017
Hospital visit before isolation
Hospitalization5 (100)10 (58.8).135b
 Duration of hospitalization, days5 [2.5–9]4.5 [3.5–8.3].852
Outpatient clinic visit3 (60)10 (58.8)1b
ER visit5 (100)6 (35.3).035b
 Frequency of visits2 [2–2.5]1.5 [1.0–2.0].054
Number of hospitals visited2 [2.0–3.5]1 [1.0–2.0].055
 For hospitalization or ER visit2 [2.0–2.5]1 [0–1.5].009
 For outpatient clinic visit1 [0–1.5]1 [0–1.0].966
Doctor shopping5 (100)8 (47.1).054b

P values were obtained using the χ2 test or Fisher exact test for categorical variables, and the Mann–Whitney test for continuous variables.

Abbreviation: ER, emergency room.

Includes chronic obstructive pulmonary disease, asthma, pulmonary tuberculosis, and pneumonia before the exposure to Middle East respiratory syndrome coronavirus.

Fisher exact test.

Cases with radiographic evidence of pneumonia before their isolation.

Comparison of the Epidemiological Characteristics of Spreaders With 5 or More Cases and Spreaders With 4 or Fewer Cases P values were obtained using the χ2 test or Fisher exact test for categorical variables, and the Mann–Whitney test for continuous variables. Abbreviation: ER, emergency room. Includes chronic obstructive pulmonary disease, asthma, pulmonary tuberculosis, and pneumonia before the exposure to Middle East respiratory syndrome coronavirus. Fisher exact test. Cases with radiographic evidence of pneumonia before their isolation.

DISCUSSION

We evaluated the epidemiological characteristics of patients who transmitted MERS-CoV during the recent South Korean outbreak. Among the 186 confirmed MERS-CoV cases, only 22 cases transmitted the infection to other individuals. These spreaders had higher host infectivity and wider and prolonged contacts compared to nonspreaders. The risk factors for super-spreading events included a larger number of contacts and a pre-isolation ER visit. Doctor shopping was marginally associated with a super-spreading event. However, both spreaders with 5 or more transmissions and spreaders with 4 or fewer transmissions exhibited similar levels of host infectivity. It appears that both host infectivity and the number of contacts influenced MERS-CoV transmission, whereas super-spreading events were mostly associated with a greater likelihood of encountering other people under diverse environmental conditions. During the 2015 outbreak, approximately 75% of the transmissions occurred during days 4–7 after symptom onset, and this may be a period when the risk of transmission is particularly high. Furthermore, this high-risk period was temporally associated with other epidemiological factors. First, the period overlapped with the confirmed cases’ visits to healthcare facilities, as hospitalization and ER visits peaked during days 4–7 after symptom onset. It is well known that MERS-CoV outbreaks generally occur in the healthcare setting [1, 5, 13, 20], and the high-risk period may be associated with healthcare-seeking behaviors. Second, the high-risk period was several days (1–4 days) after the radiographic diagnoses of pneumonia, which generally occurred on days 3–4 after symptom onset. Although the significance of pre-isolation pneumonia has not been discussed previously, a radiographic diagnosis of pneumonia may influence transmission in 2 ways. First, it may directly increase the chance of transmission by actively generating lower respiratory tract secretions and a productive cough. Second, it may be an indirect index of disease severity and hospital visiting status. In our study, cases with pre-isolation pneumonia had lower Ct values and more frequent pre-isolation hospital visits. The epidemiological significance of the high-risk period could also be observed when we compared the spreaders and nonspreaders. The spreaders were typically isolated after the high-risk period (median, 7 days after symptom onset and 4 days after a diagnosis of pneumonia), whereas nonspreaders were typically isolated before this period (median, 3 days after symptom onset and 1 day after a diagnosis of pneumonia). Similar results were observed in a study of the SARS outbreak, which revealed that late admission to healthcare facilities (especially >4 days after symptom onset) was associated with super-spreading events [21]. Thus, infection prevention measures should target isolation before this critical period (ie, within 4–7 days after symptom onset and within 1 day after the detection of pneumonia). Interestingly, the average duration from symptom onset to isolation dropped to <4 days during the first week of June 2015, and reports of new cases have rapidly decreased since that time. Among the host factors that were associated with transmission, only the Ct value was statistically significant in the multivariate analyses. The Ct value is a semiquantitative continuous variable that is inversely proportional to the viral load. Ct values are associated with the severity of MERS-CoV infection [22], although its relationship with transmission has rarely been studied. In the present study, spreaders had significantly lower Ct values compared to nonspreaders, which suggests that Ct values might reliably predict transmission. Moreover, the cases with very low Ct values (Ct <23) tended to transmit the infection in uncommon circumstances. In both the present study and previous studies, MERS-CoV transmission usually occurred in the hospital setting [1, 11, 13, 23]. In contrast, cases with very low Ct values transmitted the infection in more diverse settings in the present outbreak (eg, their household, in an ambulance, in an outpatient clinic, or to healthcare personnel after in-hospital isolation). These findings suggest that cases with very low Ct values can potentially transmit the infection in unexpected conditions. However, our data regarding the Ct values have several limitations. First, various amounts of phosphate-buffered saline were added to dilute the respiratory specimens, and this may have affected the Ct values. Second, the Ct value is influenced by the specimen type and the interval between symptom onset and sample collection [22, 24], but various different types of specimens were collected at different time points in the present study. However, we only evaluated 5 nonsputum specimens, and there was no linear correlation between the Ct values and the interval from onset to sampling. Our comparison of the spreaders with 5 or more transmissions and spreaders with 4 or fewer transmissions revealed that the spreaders with 5 or more transmissions had an approximately 10-fold higher number of contacts. Furthermore, there were no significant differences in host infectivity. These findings may suggest that the underlying likelihood of transmission has the greatest influence on super-spreading events rather than an intrinsic difference in host infectivity. A similar finding was observed in a previous study of the SARS super-spreading event [4], with those super-spreaders having 11–74 contacts compared to 1–4 contacts for the spreaders with 1–2 transmissions. Our study also revealed that a pre-isolation ER visit and doctor shopping were associated with super-spreading events. In addition, super-spreading events were associated with the number of healthcare facilities that each patient visited for hospitalization or ER treatment but not with the number of hospitals visited for outpatient treatment. In South Korea, patients who seek hospitalization without prior arrangements tend to visit the ER, and a history of 2 or more ER visits strongly suggests that the patient had been doctor shopping during hospitalization. Specific environmental conditions have been suggested to increase the likelihood of a super-spreading event [3], and doctor shopping may increase the likelihood of encountering these conditions. For example, when a confirmed case changes hospital during hospitalization without an official interhospital transfer, multiple environments are exposed to the infected case (an ambulance, an ER, and a ward). Thus, doctor shopping can greatly increase the likelihood of encountering conditions that are suitable for a super-spreading event. In the present outbreak, 4 of the 5 super spreaders (cases 1, 14, 16, and 76) transmitted the infection at 2 or more hospitals, as they had visited multiple healthcare facilities. Therefore, it is very important to have an early suspicion of MERS-CoV infection and minimize doctor shopping during the early stage of an outbreak. Our study has several limitations. First, some of the confirmed cases had multiple potential sources of infection, and we attributed the transmission to the case with the highest epidemiological probability. The source of infection was clear in >95% of the transmissions, and we excluded 3 cases that had contact with multiple cases and an unclear source of transmission. However, as the analyses of the epidemiological data are ongoing, the list of spreaders may change if new epidemiological evidence is uncovered. Second, we did not have access to genomic sequencing data, which might have provided information regarding the relatedness of transmitted strains. Third, transmission may be affected by other epidemiological factors, including aerosol-generating procedures, differences in environmental conditions, and variations in crowdedness [3, 13, 25]. However, these factors were not included in the present analysis. Fourth, serological testing was not performed for every close contact, and additional asymptomatic cases may have been present. However, the seropositive rate was 0.7% in a recent serological study of close contacts [26]. Thus, the absence of serological testing likely did not significantly influence our results. We evaluated the epidemiological risk factors for MERS-CoV transmission during the recent South Korean outbreak. Super-spreading events were not related to intrinsic host characteristics and were attributable to the likelihood of transmission. Therefore, strict ER triage and minimizing doctor shopping during an outbreak’s early stage may help prevent super-spreading events.
  22 in total

1.  Hospital outbreak of Middle East respiratory syndrome coronavirus.

Authors:  Abdullah Assiri; Allison McGeer; Trish M Perl; Connie S Price; Abdullah A Al Rabeeah; Derek A T Cummings; Zaki N Alabdullatif; Maher Assad; Abdulmohsen Almulhim; Hatem Makhdoom; Hossam Madani; Rafat Alhakeem; Jaffar A Al-Tawfiq; Matthew Cotten; Simon J Watson; Paul Kellam; Alimuddin I Zumla; Ziad A Memish
Journal:  N Engl J Med       Date:  2013-06-19       Impact factor: 91.245

2.  Middle East Respiratory Syndrome Coronavirus Outbreak in the Republic of Korea, 2015.

Authors: 
Journal:  Osong Public Health Res Perspect       Date:  2015-09-05

3.  Epidemiologic features of the first MERS outbreak in Korea: focus on Pyeongtaek St. Mary's Hospital.

Authors:  Kyung Min Kim; Moran Ki; Sung-Il Cho; Minki Sung; Jin Kwan Hong; Hae-Kwan Cheong; Jong-Hun Kim; Sang-Eun Lee; Changhwan Lee; Keon-Joo Lee; Yong-Shik Park; Seung Woo Kim; Bo Youl Choi
Journal:  Epidemiol Health       Date:  2015-09-17

4.  An observational, laboratory-based study of outbreaks of middle East respiratory syndrome coronavirus in Jeddah and Riyadh, kingdom of Saudi Arabia, 2014.

Authors:  Christian Drosten; Doreen Muth; Victor M Corman; Raheela Hussain; Malaki Al Masri; Waleed HajOmar; Olfert Landt; Abdullah Assiri; Isabella Eckerle; Ali Al Shangiti; Jaffar A Al-Tawfiq; Ali Albarrak; Alimuddin Zumla; Andrew Rambaut; Ziad A Memish
Journal:  Clin Infect Dis       Date:  2014-10-16       Impact factor: 9.079

5.  Association of Higher MERS-CoV Virus Load with Severe Disease and Death, Saudi Arabia, 2014.

Authors:  Daniel R Feikin; Basem Alraddadi; Mohammed Qutub; Omaima Shabouni; Aaron Curns; Ikwo K Oboho; Sara M Tomczyk; Bernard Wolff; John T Watson; Tariq A Madani
Journal:  Emerg Infect Dis       Date:  2015-11       Impact factor: 6.883

6.  Super-spreaders in infectious diseases.

Authors:  Richard A Stein
Journal:  Int J Infect Dis       Date:  2011-07-06       Impact factor: 3.623

7.  MERS-CoV outbreak following a single patient exposure in an emergency room in South Korea: an epidemiological outbreak study.

Authors:  Sun Young Cho; Ji-Man Kang; Young Eun Ha; Ga Eun Park; Ji Yeon Lee; Jae-Hoon Ko; Ji Yong Lee; Jong Min Kim; Cheol-In Kang; Ik Joon Jo; Jae Geum Ryu; Jong Rim Choi; Seonwoo Kim; Hee Jae Huh; Chang-Seok Ki; Eun-Suk Kang; Kyong Ran Peck; Hun-Jong Dhong; Jae-Hoon Song; Doo Ryeon Chung; Yae-Jean Kim
Journal:  Lancet       Date:  2016-07-09       Impact factor: 79.321

8.  Surveillance of the Middle East respiratory syndrome (MERS) coronavirus (CoV) infection in healthcare workers after contact with confirmed MERS patients: incidence and risk factors of MERS-CoV seropositivity.

Authors:  C-J Kim; W S Choi; Y Jung; S Kiem; H Y Seol; H J Woo; Y H Choi; J S Son; K-H Kim; Y-S Kim; E S Kim; S H Park; J H Yoon; S-M Choi; H Lee; W S Oh; S-Y Choi; N-J Kim; J-P Choi; S Y Park; J Kim; S J Jeong; K S Lee; H C Jang; J Y Rhee; B-N Kim; J H Bang; J H Lee; S Park; H Y Kim; J K Choi; Y-M Wi; H J Choi
Journal:  Clin Microbiol Infect       Date:  2016-07-27       Impact factor: 8.067

Review 9.  Aerosol generating procedures and risk of transmission of acute respiratory infections to healthcare workers: a systematic review.

Authors:  Khai Tran; Karen Cimon; Melissa Severn; Carmem L Pessoa-Silva; John Conly
Journal:  PLoS One       Date:  2012-04-26       Impact factor: 3.240

10.  MERS epidemiological investigation to detect potential mode of transmission in the 178th MERS confirmed case in Pyeongtaek, Korea.

Authors:  Kyujin Chang; Moran Ki; Eun Gyu Lee; Soon Young Lee; Byoungin Yoo; Jong Hyuk Choi
Journal:  Epidemiol Health       Date:  2015-08-15
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  32 in total

1.  Medical School Hotline: Pacific Center for Emerging Infectious Diseases Research.

Authors:  Richard Yanagihara; Vivek R Nerurkar; George Hui; Gwen A Jacobs
Journal:  Hawaii J Med Public Health       Date:  2017-01

2.  Practical Guidance for Clinical Microbiology Laboratories: Viruses Causing Acute Respiratory Tract Infections.

Authors:  Carmen L Charlton; Esther Babady; Christine C Ginocchio; Todd F Hatchette; Robert C Jerris; Yan Li; Mike Loeffelholz; Yvette S McCarter; Melissa B Miller; Susan Novak-Weekley; Audrey N Schuetz; Yi-Wei Tang; Ray Widen; Steven J Drews
Journal:  Clin Microbiol Rev       Date:  2018-12-12       Impact factor: 26.132

Review 3.  Middle East respiratory syndrome: what we learned from the 2015 outbreak in the Republic of Korea.

Authors:  Myoung-Don Oh; Wan Beom Park; Sang-Won Park; Pyoeng Gyun Choe; Ji Hwan Bang; Kyoung-Ho Song; Eu Suk Kim; Hong Bin Kim; Nam Joong Kim
Journal:  Korean J Intern Med       Date:  2018-02-27       Impact factor: 2.884

4.  Asymptomatic Middle East Respiratory Syndrome coronavirus infection using a serologic survey in Korea.

Authors:  Yeong-Jun Song; Jeong-Sun Yang; Hee Jung Yoon; Hae-Sung Nam; Soon Young Lee; Hae-Kwan Cheong; Woo-Jung Park; Sung Han Park; Bo Youl Choi; Sung Soon Kim; Moran Ki
Journal:  Epidemiol Health       Date:  2018-04-15

5.  Nosocomial outbreak of the Middle East Respiratory Syndrome coronavirus: A phylogenetic, epidemiological, clinical and infection control analysis.

Authors:  Mazin Barry; My Vt Phan; Layan Akkielah; Fahad Al-Majed; Abdulkarim Alhetheel; Ali Somily; Sarah Suliman Alsubaie; Scott Jn McNabb; Matthew Cotten; Alimuddin Zumla; Ziad A Memish
Journal:  Travel Med Infect Dis       Date:  2020-06-27       Impact factor: 6.211

6.  Comparative Analysis of Eleven Healthcare-Associated Outbreaks of Middle East Respiratory Syndrome Coronavirus (Mers-Cov) from 2015 to 2017.

Authors:  Sibylle Bernard-Stoecklin; Birgit Nikolay; Abdullah Assiri; Abdul Aziz Bin Saeed; Peter Karim Ben Embarek; Hassan El Bushra; Moran Ki; Mamunur Rahman Malik; Arnaud Fontanet; Simon Cauchemez; Maria D Van Kerkhove
Journal:  Sci Rep       Date:  2019-05-14       Impact factor: 4.379

Review 7.  Host Determinants of MERS-CoV Transmission and Pathogenesis.

Authors:  W Widagdo; Syriam Sooksawasdi Na Ayudhya; Gadissa B Hundie; Bart L Haagmans
Journal:  Viruses       Date:  2019-03-19       Impact factor: 5.048

8.  Pathogenicity and Viral Shedding of MERS-CoV in Immunocompromised Rhesus Macaques.

Authors:  Joseph Prescott; Darryl Falzarano; Emmie de Wit; Kath Hardcastle; Friederike Feldmann; Elaine Haddock; Dana Scott; Heinz Feldmann; Vincent Jacobus Munster
Journal:  Front Immunol       Date:  2018-02-12       Impact factor: 7.561

9.  MERS transmission and risk factors: a systematic review.

Authors:  Ji-Eun Park; Soyoung Jung; Aeran Kim; Ji-Eun Park
Journal:  BMC Public Health       Date:  2018-05-02       Impact factor: 3.295

10.  Epidemiologic Characteristics, Transmission Chain, and Risk Factors of Severe Infection of COVID-19 in Tianjin, a Representative Municipality City of China.

Authors:  Jin Wang; Zhihui Li; Xiaomin Cheng; Huan Hu; Conghui Liao; Pengyuan Li; Jiahai Lu; Zeliang Chen
Journal:  Front Public Health       Date:  2020-05-20
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