Skip to main content
PLOS ONE logoLink to PLOS ONE
. 2015 Dec 21;10(12):e0144778. doi: 10.1371/journal.pone.0144778

Modeling the Transmission of Middle East Respirator Syndrome Corona Virus in the Republic of Korea

Zhi-Qiang Xia 1,2, Juan Zhang 2, Ya-Kui Xue 1,*, Gui-Quan Sun 2,*, Zhen Jin 2,*
Editor: Zhen Wang3
PMCID: PMC4686901  PMID: 26690750

Abstract

The 2015 epidemic of Middle East respiratory syndrome (MERS) in the Republic of Korea has been the largest outbreak outside Middle East. This epidemic had caused 185 laboratory-confirmed cases and 36 deaths in the Republic of Korea until September 2, 2015, which attracted public’s attention. Based on the detailed data of patients released by World Health Organization (WHO) and actual propagation of the epidemic, we construct two dynamical models to simulate the propagation processes from May 20 to June 8 and from June 9 to July 10, 2015, respectively and find that the basic reproduction number R 0 reaches up to 4.422. The numerical analysis shows that the reasons of the outbreak spread quickly are lack of self-protection sense and targeted control measures. Through partial correction analysis, the parameters β 1 and γ have strong correlations with R 0, i.e., the infectivity and proportion of the asymptomatic infected cases have much influence on the spread of disease. By sensitivity analysis, strengthening self-protection ability of susceptible and quickly isolating or monitoring close contacts are effective measures to control the disease.

Introduction

The 2015 epidemic of Middle East respiratory syndrome (MERS) in the Republic of Korea has been the largest outbreak outside Middle East since the first case was identified in Jeddah, Saudi Arabia, in June 2012 [14]. A total of 1,413 laboratory-confirmed cases infected by MERS-CoV, including 502 deaths, had been reported globally as of August 19, 2015 [5], and mortality rate was about 35% [6]. Most cases emerged in the Middle East, sporadic cases had been reported in UK, Italy, France, Spain, United States and so on [710]. Most of these cases were confirmed after a traveling in Middle East. In the Republic of Korea, the first case was an import one having a traveling experience in Middle East [8, 11]. Due to poor pre-control measures, the number of additional confirmed cases gradually increased during the period from May 20, 2015 to June 8, 2015. Then the Korean Government took effective control measures and the number of additional confirmed cases gradually decreased during the period from June 9 to July 4 [12, 13]. Therefore, the Korean Government and WHO announced the end of MERS epidemic in the Republic of Korea in the middle of July.

It is necessary to learn about the source of infection and transmission mechanism of MERS. The most probable source of Middle East respiratory syndrome coronavirus (MERS-CoV) is bats, and MERS-CoV-related viruses have been detected in bats. However, people have little chance to contact with them directly. It is generally considered that dromedary camels are the intermediate reservoirs for MERS-CoV transmission from bats to human, but the accurate role of camels in transmission of MERS-CoV has not been available [1, 10, 14, 15]. Generally, there are two main transmission routes [4, 8, 1618]: one is animal-to-human transmission, the other one is human-to-human transmission. The MERS-CoV can cause diseases ranging from the common cold to Severe Acute Respiratory Syndrome (SARS). The patients infected by MERS-CoV will have symptoms including fever, cough and shortness of breath, and the severe patients may have renal failure [1, 6, 7, 14, 19]. However, humans do not immediately show clinical symptoms after being infected and they undergo a incubation period from 2 to 14 days, during which time they are not infectious [11, 16].

Why the MERS broke out in the Republic of Korea rather than other countries such as UK, France, Italy is worth researching. It is necessary to have a look at how the epidemic emerged and developed in the Republic of Korea [8, 20, 21]. The first laboratory-confirmed patient was reported on May 20, 2015. He is a 68 year-old male who had traveled in several countries in Middle East before flying back to the Republic of Korea on May 4. Until May 11 he showed symptoms and sought for three hospitals before he was finally confirmed and isolated. During the period from being infected to being confirmed he had a close contact with many visitors, relatives, inpatients and health care workers. The new cases continued to be reported in the next few days, and they all had corrections with the first confirmed case. Through analyzing the actual transmission process, several factors appear to have contributed to the initial spread of this virus [22]:

  1. The appearance of MERS-CoV was unexpected and unfamiliar to most physicians;

  2. The practise of seeking hospitals may be a contribution factor;

  3. The control measures of the hospitals are not optimal;

  4. Multi-beds rooms in the hospitals are a contribution factor;

  5. The custom of many friends and relatives to visit the patient is also a contribution factor.

A lot of work has been done in studying MERS. Lee et al [8] characterized the transmission chains of MERS-CoV infection in South Korean’s outbreak. Nishura et al [21] estimated the expected size of MERS clusters and the number of generations using a stochastic epidemic model. Chowell et al [16] studied a MERS-CoV transmission model with index and secondary cases. Rivers et al [23] divided the susceptible populations into the high-risk group S 1 and the normal or low risk group S 2.

In order to describe the propagation process of MERS in the Republic of Korea during this period, we propose a deterministic SEAIHR model to study the spread of MERS among humans. Because there is no zoonotic infections of MERS-CoV in the Republic of Korea, only one transmission route (human-to-human infection) is considered in model. Since the disease is almost distributed throughout the Republic of Korea, all the Korean are viewed as research subject. Based on infection status, the population is divided into the following categories: susceptible individual, exposed individual, asymptomatic individual, symptomatic infected individual, hospitalized case and removed case [16]. According to the practical situation, there is no effective control measures included in our model before June 8, 2015.

Materials and Methods

Data

Time series of reported cases were reported by the WHO [24] and [32]. They provide detailed data of the epidemic in the Republic of Korea, including patient’s age, gender, data of symptoms, data of first hospitalization, data of laboratory confirmation and so on. We can make a related analysis of MERS based on the nice data.

Propagation Mechanism

The spread process (Table 1) of the disease is considered as follows: when a susceptible individual is infected, he or she turns to be an exposed case. Few days later, parts of the exposed cases turn to be asymptomatic cases (although no symptom, they have the ability to infect others), the remainings turn to be symptomatic cases. The symptomatic cases will go to hospital for treatment soon. After treatment, some of them will recover, and about 21% will die [25]. The asymptomatic cases will self-recover without any treatment.

Table 1. Transmission rules of compartmental Model (1).

Number Transition Transition rate
(1) (S, E) → (S − 1, E + 1) β1SAN+β2SIN+β3SHN
(2) (E, A) → (E − 1, A + 1) (1 − γ)σE
(3) (E, I) → (E − 1, I + 1) γσE
(4) (A, R) → (A − 1, R + 1) k 1 A
(5) (I, H) → (I − 1, H + 1) λI
(6) (H, R) → (H − 1, R + 1) k 2 A

Dynamical model without effective control measures

In order to facilitate research and make our model more reasonable, some assumptions are made:

  1. The whole population is initially susceptible except the first confirmed case;

  2. There is no zoonotic infections of MERS-CoV in the Republic of Korea, only considering the epidemic spread in the human beings;

  3. There is no effective control measures before June 8, 2015.

Based on the above assumptions, the spread of MERS in the human begins is shown in Fig 1. And the corresponding dynamical model is given in Eq (1):

dSdt=-β1SAN-β2SIN-β3SHN,dEdt=β1SAN+β2SIN+β3SHN-σE,dAdt=(1-γ)σE-k1A,dIdt=γσE-λI,dHdt=λI-k2H-δH,dRdt=k1A+k2H+δH, (1)

where S denotes the number of susceptible individuals; E, the number of exposed individuals; A, the number of asymptomatic infected cases; I, the total number of mild infected person and severe patients. H, the number of hospitalized cases; R, the number of removed cases. N, the total number of human population in the Republic of Korea.

Fig 1. Flow diagram of the compartmental model of MERS in the Republic of Korea.

Fig 1

β 1 is the transmission coefficient of the asymptomatic infected cases, β 2 is the transmission coefficient of the symptomatic infected cases (mild infected person and severe patients) to the susceptible, β 3 is the transmission coefficient of the hospitalized cases to the susceptible, 1σ is the mean time of incubation period, 1λ is the mean time from data of symptoms onset to data of hospitalization, 1k1 is the mean infectious period of asymptomatic infected person for survivors, 1k2 is the mean duration for hospitalized cases for survivors, 1δ is the mean duration from hospitalization to death, γ is clinical outbreak rate in all the infected cases. The unit in Model (1) is taken as days −1.

Estimation of basic reproduction number R 0 in the Republic of Korea

The transmission coefficients β 1, β 2, β 3 and γ are unknown. On the basis of the actual reported confirmed cases, we use the least-squares method to estimate these parameter values such that the sum of squared errors between the actual data and the solution of Eq (2) is minimum [2830]. The accumulated confirmed incidence (I total) in the Republic of Korea is fitted to estimate four parameters (β 1, β 2, β 3 and γ):

dItotaldt=γσE. (2)

Denoting the actual data of accumulated confirmed patients from May 20 to June 8, 2015 as Itotal¯. The estimation process is as follows (see Fig 2): first, construct a function f=t=1n[Itotal(t)-Itotal¯(t)]2 (where n is the number of actual data I total(t) which is the accumulated data of the Eq (2)); second, find a optimal set of parameter values to minimize the value of f by applying MATLAB.

Fig 2. Fitting curve of real data from May 20, 2015 to June 8, 2015 by Model (1), where the blue dots denote real data obtained from [24].

Fig 2

Through the least-squares method, the optimal set of parameter values is β 1 = 0.8756, β 2 = 0.7833, β 3 = 0.4568 and γ = 0.0348.

Substituting the parameter values (they can be found in Table 2) into the expression of the basic reproduction number R 0 (see S1 File), and estimate R 0 = 4.422 > 1 in the early epidemic. It is well-known that if R 0 is bigger than one, disease will spread in the human beings. This indicates that the disease spread quickly due to insufficient control measures and other reasons.

Table 2. Parameters value in system Eq (1).

Parameter Range Mean and 95%CI Source
1σ (3∼8) 5.2 [16]
1λ (3∼7) 5 [16]
1k1 (3∼7) 5 [16]
1k2 (5∼10) 7 [16]
1δ (0∼42) 15.16 Calculated
β 1 - 0.8756(0.853 ∼ 0.9324) Estimated
β 2 - 0.7833(0.5925 ∼ 0.8592) Estimated
β 3 - 0.4568(0.3839 ∼ 0.6751) Estimated
γ - 0.0348(0.0285 ∼ 0.353) Estimated
N 49520000 - [26]
S 0 49519960 - [26]
E 0 16 ∼ 32 - [27]
A 0 16 ∼ 36 - [27]
I 0 1 - [27]
H 0 0 - [27]
R 0 0 - [27]

The model with control measures in the Republic of Korea

The number of additional confirmed cases performs downward trend (Fig 3) from June 9, 2015. There is no additional confirmed cases from July 5, 2015, which illustrates that the control measures took by the Republic of Korea controlled the spread of the epidemic and eventually defeated the disease effectively. Here, we list the main control measures [5, 6, 22]:

  1. Early and complete identification and investigation of all contacts;

  2. Robust quarantine/isolation and monitoring of all contacts and suspected cases;

  3. Full implementation of infection prevention and control measures;

  4. Prevention of travel, especially international, of infected persons and contacts;

  5. Washing your hands regularly with soap and water and maintaining good personal hygiene;

  6. Avoiding close contact with people who are sick;

  7. Covering your mouth and nose with a tissue or your sleeve when coughing or sneezing.

Fig 3. The number of confirmed cases.

Fig 3

It is found that the main reasons of successfully controlling and eliminating disease can divide into two categories: ①: improving of self-protecting ability of susceptible. ②: isolating or monitoring all the close contacts, where asymptomatic cases and exposed cases are all belong to close contacts, and the confirmed cases and hospitalized cases are forcefully isolated. As of August 25, 2015, a total number of 16,693 cases were isolated or monitored [25]. Based on this situation we establish a dynamical Model (3) with control measures as follows:

dSdt=-l1β1SAN-l2β2SIN-l3β3SHN,dEdt=l1β1SAN+l2β2SIN+l3β3SHN-σE-d1E,dAdt=(1-γ)σE-k1A-d2A,dIdt=γσE-λI-d3I,dHdt=λI-k2H-δH-d4H,dRdt=k1A+k2H+δH+d1E+d2A+d3I+d4H, (3)

where d 1, d 2, d 3 and d 4 are isolation or monitoring rates in E, A, I and H compartment, respectively. l 1, l 2 and l 3 are self-protection coefficients with asymptomatic cases, symptomatic cases and hospitalized cases, respectively.

Results

Sensitivity and uncertainty analysis of basic reproduction number R 0

The basic reproduction number is the threshold whether disease will outbreak and be prevalent in the crowd. When R 0 > 1, the disease will spread in the population; when R 0 < 1, the disease will gradually disappear [18, 29, 31]. So it is important to study the sensitivity and uncertainty analysis of basic reproduction number R 0 on crucial parameters. Here we adopt Latin hypercube sampling (LHS) to study the correlation between five crucial parameters (β 1, β 2, β 3, γ, λ) and R 0 to asses the effect of corresponding control measures.

Randomly choosing 1000 samples of the five crucial parameters (β 1, β 2, β 3, γ, λ), which follow a normal distribution. Based on the 1000 samples, we perform the sensitivity and uncertainty analysis through rank correlation coefficient(PRCC), there is such a relationship: the bigger the absolute value of PRCC, the stronger the correlation between the chosen parameter and R 0. From Table 3, it is easy to find that the absolute value of PRCC between β 1 and R 0 is biggest, which shows that β 1 is the most important in determining R 0. It also indicates that the key factor of the rapid spread of the epidemic in the early stage is no timely isolating close contacts with the patients. The parameter λ has a negative correction with R 0, i.e., when shorting the time from the onset to hospitalization, the value of R 0 will decrease.

Table 3. Partial rank correlation coefficient (PRCC) for the basic reproduction number R 0 and each input parameter variable.

Input parameter PRCC
β 1 0.83424
β 2 0.0510
β 3 0.018
γ 0.5377
λ -0.2042

Parameter estimation

In this section, as the same method in estimating β 1, β 2 and β 3, we apply the least squares method to estimate l 1, l 2, l 3, d 1, d 2, d 3 and d 4 (see Table 4). We assume that d 1, d 2, d 3 and d 4 are the same, and the fitting curve is shown in Fig 4.

Table 4. Parameter values and initial value in model Eq (3).

Parameter Initial variable
Parameter Value Source Initial variable Value Source
l 1 0.3239 Estimated S(0) 49516000 [A]
l 2 0.9175 Estimated E(0) 2353 [A]
l 3 0.5316 Estimated A(0) 1027 [A]
d 1 0.1922 Estimated I(0) 43 [A]
d 2 0.1922 Estimated H(0) 20 [A]
d 3 0.1922 Estimated R(0) 1047 [A]
d 4 0.1922 Estimated Itotal¯ 94 [27]

[A] denotes that the initial value (S(0), E(0), A(0), I(0), H(0), R(0)) is obtained from Model (3).

Itotal¯ is accumulated confirmed cases.

Fig 4. Fitting curve of real data from June 9, 2015 to July 10, 2015 by deterministic Model (3), where the blue dot denotes the real data of accumulated incidence.

Fig 4

Substituting parameter values into the expression of R c (see S1 File), and get R c = 0.385 which is less than one, this also illustrates that MERS epidemic in the Republic of Korea will eventually disappear, which is consistent with the actual situation that there is no additional confirmed cases form July 5, 2015.

Sensitivity analysis of the basic reproduction number R c

In this section, we apply two-dimension figures to explain how parameters affect the value of R c.

From Fig 5, it is apparent that when a transmission coefficient is fixed, how the other two transmission coefficients determine the value of R c. The region on the left of the red line represents R c < 1. The region on the right of the red line represents R c > 1. In Fig 6, it shows the change of R c with respect to d 1, d 2, d 3 and d 4, respectively. It is also easy to notice that when the isolating or monitoring rate increases, the basic reproduction number R c will reduce, where d 1 and d 2 have a bigger influence on R c than d 3 and d 4. It tells us that quickly finding and isolating exposed and asymptomatic cases can effectively control the spread of epidemic.

Fig 5. The combined influence of transmission coefficients on R c.

Fig 5

Fig 6. The relationships between isolation or monitor rate (d 1, d 2, d 3 and d 4) and R c.

Fig 6

The relationship between self-protective coefficient, transmission coefficient and the final size of accumulated confirmed cases

From Fig 7, it is obvious that the bigger value the self-protective coefficient, the smaller the final size of accumulated confirmed cases. Moreover, the bigger the transmission coefficient, the bigger size the final size of accumulated infected cases. The parameters l 1 and β 1 have a bigger influence on the final size of accumulated confirmed cases, and this is consistent with the sensitivity analysis results of R 0. As a result, it is critical to isolate asymptomatic cases. Through calculating, we get the theoretical expression of final accumulated confirmed cases size which is shown in S1 File.

Fig 7. The relationships between total number of confirmed cases and transmission coefficient and self-protection coefficient (here the smaller value of self-protection coefficient, the lower probability of being infected).

Fig 7

Discussion

Combining with the actual propagation situation and patients’ data from May 20 to July 4, 2015 in the Republic of Korea, we establish two dynamical Models (1) and (3) study the process of MERS in the Republic of Korea. When the novel disease emerged, there were no effective control measures for many reasons, in this case the basic reproduction number R 0 = 4.42, i.e., the epidemic spread quickly. Since South Korean Government isolated or monitored all the close contacts with the patients infected by MERS-CoV, the additional confirmed cases gradually reduced and epidemic was controlled quickly. At this moment, R c = 0.385. After July 5, there is no additional confirmed cases reported anymore.

Applying our Models (1) and (3), it comes to a consistent conclusion through the sensitivity of the basic reproduction and the final size of accumulated confirmed cases: isolating all the close contacts and strengthening the self-protection ability of susceptible are the most effective control measures.

During this period, the spread situation of MERS in China also confirmed the above results. In May 29, 2015, the first confirmed case in China was reported in Huizhou, Guongdong province [33]. The patient is a Korean in his mid-40s, who traveled to Guangdong province, China via Hong Kong on May 26. Subsequently, the China Government isolated all close contacts as soon as possible and publicized the progress of the event to the society, killed the source of disease in the bud. Therefore, MERS cannot spread across population under proper control measures.

Based on the successful experience in control MERS, we give some specific suggestions in face with emerging diseases: ①: Limit or stop taking fairs, rallies and theaters performances; ②: Provide necessary personal protective equipment to staff participated in emergency response; ③: Timely publish the information of emergence disease to the community, including the number confirmed cases, suspected cases, hospitalized cases and so on; ④: Carry out targeted health care education, raise public awareness and slef-protection and eliminate public mental disorder.

The MERS mainly occurs in the Middle East countries, where the epidemic is most severe in Saudi Arabia. There was a large-scale outbreak from early April to late June in Saudi Arabia in 2014, while the outbreak in the Republic of Korea mainly emerged from mid-May to early July in 2015. Why the outbreaks of MERS are centralized from April to July and whether the outbreak of MERS has relation with season [34] are needed to be checked by more investigations. In addition, it is also a good method in studying infectious disease on complex networks [3537] and we will try to study disease-behavior dynamics on complex networks in the future study.

Supporting Information

S1 File. Mathematical analysis.

(PDF)

Data Availability

All relevant data are within the paper and its Supporting Information files.

Funding Statement

The research is funded by the National Natural Science Foundation of China (under grants 11501338, 11171314, 11331009, and 11301490), 131 Talents of Shanxi University, Top Young Academic Leaders of Higher Learning Institutions of Shanxi Province, and International Exchange Program of Postdoctor in Fudan University.

References

  • 1. Xia S, Liu Q, Wang Q, Sun ZW, Su S, Du LY, et al. Middle East respiratory syndrome coronavirus (MERS-CoV) entry inhibitors targeting spike protein. Virus research. 2014;194: 200–210. 10.1016/j.virusres.2014.10.007 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Drosten C, Seilmaier M, Corman VM, Hartmann W, Scheible G, Sack S, et al. Clinical features and virological analysis of a case of Middle East respiratory syndrome coronavirus infection. The Lancet infectious diseases. 2013;13(9): 745–751. 10.1016/S1473-3099(13)70154-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Jansen A, Chiew M, Konings F, Lee CK, Li A. Sex matters-a preliminary analysis of Middle East respiratory syndrome in the Republic of Korea,2015. Western Pacific Surveillance and Response. 2015;6(3). 10.5365/wpsar.2015.6.3.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Sharif-Yakan A, Kanj S S. Emergence of MERS-CoV in the Middle East: origins, transmission, treatment, and perspectives. PLoS pathogens. 2014;10(12): e1004457 10.1371/journal.ppat.1004457 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. http://www.who.int/emergencies/mers-cov/en/.
  • 6. World Health Organization. Investigation of cases of human infection with Middle East respiratory syndrome coronavirus (MERS-CoV): interim guidance. World Health Organization; 2015. [Google Scholar]
  • 7. Drosten C. Is MERS another SARS?. The Lancet Infectious Diseases. 2013;13(9): 727–728. 10.1016/S1473-3099(13)70159-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Lee SS, Wong NS. Probable transmission chains of Middle East respiratory syndrome coronavirus and the multiple generations of secondary infection in South Korea. International Journal of Infectious Diseases. 2015;38: 65–67. 10.1016/j.ijid.2015.07.014 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Assiri A, Al-Tawfiq J A, Al-Rabeeah A A, Al-Rabiah F A, Al-Hajjar S, Al-Barrak A, et al. Epidemiological, demographic, and clinical characteristics of 47 cases of Middle East respiratory syndrome coronavirus disease from Saudi Arabia: a descriptive study. The Lancet infectious diseases. 2013;13(9): 752–761. 10.1016/S1473-3099(13)70204-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Ferguson N M, Van Kerkhove M D. Identification of MERS-CoV in dromedary camels. The Lancet infectious diseases. 2014;14(2): 93–94. 10.1016/S1473-3099(13)70691-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Lim P L. Middle East respiratory syndrome (MERS) in Asia: lessons gleaned from the South Korean outbreak. Transactions of The Royal Society of Tropical Medicine and Hygiene. 2015;109(9): 541–542. 10.1093/trstmh/trv064 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. http://www.mers.go.kr/mers/html/jsp/MenuC/listC4.jsp.
  • 13. http://www.who.int/csr/disease/coronavirusinfections/archive−cases/en/.
  • 14. Memish Z A, Al-Tawfiq J A, Alhakeem R F, Assiri A, Alharby K D, Almahallawi M S, et al. Middle East respiratory syndrome coronavirus (MERS-CoV): A cluster analysis with implications for global management of suspected cases. Travel medicine and infectious disease. 2015;13(4): 311–314. 10.1016/j.tmaid.2015.06.012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Zhang RH. MERS-CoV: current research progress and prospect. Journal of Applied Virology. 2015;4(2): 30–36. [Google Scholar]
  • 16. Chowell G, Blumberg S, Simonsen L, Miller M A, Viboud C. Synthesizing data and models for the spread of MERS-CoV, 2013: Key role of index cases and hospital transmission. Epidemics. 2014;9: 40–51. 10.1016/j.epidem.2014.09.011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Khan A, Farooqui A, Guan Y, Kelvin D J. Lessons to learn from MERS-CoV outbreak in South Korea. The Journal of Infection in Developing Countries. 2015;9(06): 543–546. 10.3855/jidc.7278 [DOI] [PubMed] [Google Scholar]
  • 18. Cauchemez S, Van Kerkhove MD, Riley S, Donnelly CA, Fraser C, Ferguso NM, et al. Transmission scenarios for Middle East Respiratory Syndrome Coronavirus (MERS-CoV) and how to tell them apart. Euro surveillance: bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 2013;18(24). [PMC free article] [PubMed] [Google Scholar]
  • 19. World Health Organization. Clinical management of severe acute respiratory infection when Middle East respiratory syndrome coronavirus (MERS-CoV) infection is suspected: interim guidance. World Health Organization; 2015. [Google Scholar]
  • 20. Cowling B J, Park M, Fang V J, Wu P, Leung G M, Wu J T. Preliminary epidemiologic assessment of MERS-CoV outbreak in South Korea, May–June 2015. Euro surveillance: bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 2015;20(25). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Nishiura H, Miyamatsu Y, Chowell G, Saitoh M. Assessing the risk of observing multiple generations of Middle East respiratory syndrome (MERS) cases given an imported case. Euro Surveill. 2015;20: 27 10.2807/1560-7917.ES2015.20.27.21181 [DOI] [PubMed] [Google Scholar]
  • 22. http://www.mers.go.kr/mers/html/jsp/MenuC/listC4.jsp?menuIds=fid=5767qtype=qvalue=cid=63477pageNum=.
  • 23. Rivers C. Modeling Emerging Infectious Diseases for Public Health Decision Support. Virginia Tech. 2015. [Google Scholar]
  • 24. http://www.who.int/csr/don/14−july−2015−mers−korea/en/.
  • 25. Mizumoto K, Saitoh M, Chowell G, Miyamatsu Y, Nishiura H. Estimating the risk of Middle East respiratory syndrome (MERS) death during the course of the outbreak in the Republic of Korea, 2015. International Journal of Infectious Diseases. 2015;39: 7–9. 10.1016/j.ijid.2015.08.005 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. http://www.360doc.com/content/14/1005/10/1937977414507414.shtml.
  • 27. http://www.who.int/emergencies/mers−cov/MERS−CoV−cases−rok.pdf?ua=1.
  • 28. Zhang J, Sun GQ, Sun XD, Hou Q, Li MT, Huang BX, et al. Prediction and control of brucellosis transmission of dairy cattle in Zhejiang Province, China. Plos one. 2014;9(11): e108592 10.1371/journal.pone.0108592 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Xia ZQ, Wang SF, Li SL, Huang LY, Zhang WY, Sun GQ, et al. Modeling the transmission dynamics of Ebola virus disease in Liberia. Scientific reports. 2015;5 10.1038/srep13857 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Li MT and Sun GQ and Zhang J and Jin Z and Sun XD and Wang YM, et al. Transmission dynamics and control for a brucellosis model in Hinggan League of Inner Mongolia, China. Math Biosci Eng. 2014;11: 1115–1137. 10.3934/mbe.2014.11.1115 [DOI] [PubMed] [Google Scholar]
  • 31. Lovecraft H P. The epidemiology of MERS-CoV. Lancet. 2013;382: 694–99.23831141 [Google Scholar]
  • 32. http://www.mers.go.kr/mers/html/jsp/MenuC/listC4.jsp.
  • 33. Su S, Wong G, Liu YX, Gao G F, Li SJ, Bi YH, et al. MERS in South Korea and China: a potential outbreak threat? The Lancet. 2015;385(9985): 2349–2350. 10.1016/S0140-6736(15)60859-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Altizer S, Dobson A, Hosseini P, Hudson P, Pascual M, Rohani P, et al. Seasonality and the dynamics of infectious diseases. Ecology letters. 2006;9(4): 467–484. 10.1111/j.1461-0248.2005.00879.x [DOI] [PubMed] [Google Scholar]
  • 35. Wang Z, Andrews M A, Wu ZX, Wang L, Bauch C T. Coupled disease-behavior dynamics on complex networks: A review. Physics of life reviews. 2015;15: 1–29. 10.1016/j.plrev.2015.07.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Wang Z, Kokubo S, Jusup M, Tanimoto J. Universal scaling for the dilemma strength in evolutionary games. Physics of life reviews. 2015;14: 1–30. [DOI] [PubMed] [Google Scholar]
  • 37. Wang Z, Wang L, Szolnoki A, Perc M. Evolutionary games on multilayer networks: a colloquium. The European Physical Journal B. 2015;88(5): 1–15. 10.1140/epjb/e2015-60270-7 [DOI] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

S1 File. Mathematical analysis.

(PDF)

Data Availability Statement

All relevant data are within the paper and its Supporting Information files.


Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES