Abstract
The novel coronavirus disease 2019 (COVID-19) outbreak on the Diamond Princess (DP) ship has caused over 634 cases as of February 20, 2020. We model the transmission process on DP ship as a stochastic branching process, and estimate the reproduction number at the innitial phase of 2.9 (95%CrI: 1.7–7.7). The epidemic doubling time is 3.4 days, and thus timely actions on COVID-19 control were crucial. We estimate the COVID-19 transmissibility reduced 34% after the quarantine program on the DP ship which was implemented on February 5. According to the model simulation, relocating the population at risk may sustainably decrease the epidemic size, postpone the timing of epidemic peak, and thus relieve the tensive demands in the healthcare. The lesson learnt on the ship should be considered in other similar settings.
Keywords: COVID-19, Reproduction number, Transmission, Diamond princess ship
1. Introduction
The coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first documented in Wuhan, China in the end of 2019, and spread to over 100 foreign countries in a short period of time. The World Health Organization (WHO) declared the outbreak to be a public health emergency of international concern on January 30, 2020 (2019World Health Organization). The COVID-19 outbreak on the Diamond Princess, a British-registered cruise ship that contains 3711 tourists and crew members, caused 634 confirmed cases as of February 20, 2020 (2020Ministry of Health of Japan; Mizumoto & Chowell, 2020; Mizumoto et al., 2020; Rocklov et al., 2020; Zhang et al., 2020).
Epidemiology studies had considered the situation in Diamond Princess (DP) ship as a “natural experiment” of SARS-CoV-2 exposure, and examined the epidemiological characteristics of COVID-19 (Mizumoto et al., 2020; Russell et al., 2020; Yamagishi et al., 2020). Modelling studies also attempted to uncover the transmission dynamics of COVID-19 in closed community (Azimi et al., 2021; Mizumoto & Chowell, 2020; Rockl ö v et al., 2020), as well as the effect of disease control intervention. Although recent modelling study by Emery et al. also modelled the transmission dynamics on the DP ship (Emery et al., 2020), a relatively long mean generation time of COVID-19 (at 9 days or more) was assumed, which appears larger than existing estimates from 4 to 6 days (Ali et al., 2020; Du et al., 2020; Ferretti et al., 2020; Ganyani et al., 2020; He et al., 2020; Nishiura, Linton, & Akhmetzhanov, 2020a, 2020b; Ren et al., 2021; Xu et al., 2020; Zhao, 2020; Zhao et al., 2020a, 2021a). As discussed in previous studies (Wallinga & Lipsitch, 2007; Zhao et al., 2020b), the setting of the generation time (or serial interval) is likely to affect the estimate of the disease transmissibility (Tang et al., 2021).
In this study, we model the COVID-19 outbreak on DP ship, estimate the key epidemiological parameters of this outbreak. Different types of control measures were usually implemented simultaneously, and thus their individual effects were difficult to be disentangled. We explore several hypothetical control measures, and how the effects of these measures could be reflected on epidemic curve.
2. Methods
We consider the population on the DP ship as a close cohort with N = 3711 individuals. Following (Althaus, 2015; Cori et al., 2013), we model the transmission of COVID-19 as a branching process, which considers the epidemic as a reproduction process across generations. Each individual case was modelled explicated in terms of his time of infection and number of offspring cases. In each generation, for one primary case with symptom onset (or reported for a case without symptoms) on the t-th day, the number of secondary cases generated by this primary case follows a negative binomial (NB) distribution with mean at Reff(t) and dispersion parameter at k (Adam et al., 2020; Riou & Althaus, 2020). The Reff(t) is the effective reproduction number, and Reff(t) = R0[N − C(t)]/N, where C(t) is the cumulative number of cases at the t-th day, and R0 is the basic reproduction number of COVID-19 to be estimated. The time delay between symptom onset dates of a primary case and its associated secondary cases is the serial interval (SI). Hence, given a primary case with symptom onset on the t-th day, the symptom onset time of its associated secondary case is expected to be the summation of t and SI of COVID-19. We model the SI to follow a Gamma distribution with mean at 4.5 days and standard deviation (SD) at 3.1 days (Du et al., 2020; Nishiura et al., 2020a, 2020b; You et al., 2020; Zhao et al., 2020c). All secondary cases in one generation will be considered as primary case in the next consecutive generation, and thus the simulation framework can be repeated iteratively.
As the quarantine program starting on February 5, 2020, we account for the effect of this event by reducing R0 to λ∙R0, where λ (0 ≤ λ ≤ 1) is the change ratio of transmissibility due to quarantine program. We estimate both R0 and λ simultaneously.
We collect the number of confirmed cases time series, including both symptomatic and asymptomatic infections, on the DP ship released in the situation reports of COVID-19 infections in Japan (2020Ministry of Health of Japan). To set up the model, we simulate the courses of the COVID-19 outbreaks stochastically starting from one infectious index case on January 20, 2020. We fix k at 0.43 as estimated in (Adam et al., 2020; Wang et al., 2021; Zhao et al., 2021b), which is considered as the main results. For sensitivity analysis, we also consider k = 1, with which the NB distribution is reduced to geometric distribution, and k = 1000000, with which the NB distribution is reduced to Poisson distribution.
We fitted model generated number of cases to the observed number of cases with Poisson-distributed likelihood framework. We adopted a Bayesian fitting procedure with Metropolis-Hastings Markov chain Monte Carlo (MCMC) algorithm with noninformative uniform distribution ranging from 1 to 9 as prior distribution for R0. The MCMC is conducted with 10 chains and 100000 iterations for each chain, including 40000 as for the burn-in period, to obtain the estimates. The median estimate and 95% credible intervals (95%CrI) of R0 are calculated.
To explore an alternative scenario with a larger SI, we repeat the fitting and estimation procedures above with mean SI at 7.5 days and SD at 3.4 days, which was estimated in (Li et al., 2020). We evaluate the modelling performance with mean SI at 4.5 or 7.5 days by the Akaike information criterion (AIC). Under the latter scenario with mean SI at 7.5 days, we find that the R0 is larger than 5, which is not in line with WHO estimates and unlikely under a ‘quarantine’ setting in DP ship. In particular, the latter scenario yields a higher AIC by 10 units than the former scenario with mean SI at 4.5 days, and thus we argue the former scenario is most likely the reality.
Furthermore, we explore several hypothetical COVID-19 control measures, and how these measures may be reflected by epidemic curve. We consider five ‘what-if’ scenarios, and they were.
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scenario (0): the best-fit R0 but λ fixed at 1, i.e., baseline scenario;
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scenario (1): the best-fit model, i.e., main results;
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scenario (2): based on (1), 1000 susceptibles were removed on February 11, 2020;
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scenario (3): based on (1), the R0 was set at 2; and
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scenario (4): based on (1), combining scenarios (2) and (3).
Scenario (0) was the worst scenario in terms of disease control measures, where we assume the quarantine program was never places and thus reproduction number was not decreased. Scenario (1) was our main results, where a quarantine program was placed on February 5, 2020 and reproduction number decreased from R0 to λ∙R0. Under scenario (1), both model parameters λ and R0 were set to be the best estimates by fitting to real-world dataset, which were summarized in Table 1. Scenarios (2)–(4) were based on scenario (1), and different control measures that different from the actual situation were considered. We simulated the model under five different scenarios, and estimate the key epidemiological metric that quantify the timing and size of the outbreak. We estimate the cumulative number of cases on February 20, the outbreak final size, the epidemic doubling time, and the peaking time to capture the patterns of outbreak.
Table 1.
Summary of the reproduction number (R0) and its change ratio (λ) estimates of the outbreak with dispersion parameter k fixed at 0.43, 1, and 1000000. The scenarios where k was fixed at 0.43 was considered as the main results.
| dispersion | reproduction number | change ratio |
|---|---|---|
| 0.43 | 2.86 (1.66, 7.68) | 0.66 (0.11, 0.96) |
| 1 | 2.53 (1.86, 6.60) | 0.78 (0.12, 0.95) |
| 1000000 | 2.99 (2.05, 3.67) | 0.85 (0.37, 0.92) |
The analysis in this study was carried out using R statistical software (version 3.6.3).
3. Results
With the dispersion parameter k fixed at 0.43, we estimate the R0 to be 2.9 (95%CrI: 1.7–7.7), which is consistent with previous estimates (Riou & Althaus, 2020; You et al., 2020; Zhao et al., 2020d). We find that the quarantine program (since February 5, 2020) in DP ship was likely to reduce [(1 − λ) × 100% = ] 34% of R0 (95%CrI: 4–89), see Fig. 1. The fitting results are shown in Fig. 2(a), which match the observed data well. For the sensitivity analysis, the estimating results of R0 and λ with different dispersion term (k) were largely consistent, see Table 1 and Fig. 1, which implies the virus is hard to go extinction that other two coronavirus. Note that low k implies high chance of superspreading events and high chance of extinction.
Fig. 1.
The prior (green) and posterior (blue) distributions of reproduction number R0 (upper panels) and change ratio of reproduction number λ (lower panels) with dispersion parameter k = 0.43 (panel (a)), 1 (panel (b)), and 1000000 (panel (c)). In each panel, the vertical gold bar shows the median of posterior estimate. The top panels were the prior (green) and posterior (blue) distributions of reproduction number (R0) before the quarantine program, which was on February 5, 2020. The bottom panels were the prior (green) and posterior (blue) distributions of the change ratio of reproduction number (λ) since February 5, 2020, when reproduction number decreased from R0 to λ∙R0.
Fig. 2.
The observed (dots) and fitted (curves) number of COVID-19 cases on the Diamond Princess ship. Panel (a) shows the daily number of cases, and panel (b) shows the estimated epidemic curves under different scenarios. In panel (a), the black dots are the observed number of cases time series, the blue curve is the simulation median, and the grey curves are 100 simulation samples. In panel (b), the bold curves are the simulation median, and the dashed curves are the 95% centiles. The black curves are for scenario (0), blue curves are for scenario (1), green curves are for scenario (2), gold curves are for scenario (3), and red curves are for scenario (4). The key settings and simulation outcomes of all scenarios were summarized in Table 2. In panels (a) and (b), the blue curves show the baseline scenario, and they are the same.
Without the quarantine program on February 5, we estimate that the COVID-19 outbreak is likely to cause 1340 COVID-19 cases (95%CI: 190–2493) as of February 21, and the epidemic curve is likely to peak around February 16, 2020 with a doubling time at 3.4 days (95%CI: 1.8–8.1), see Fig. 2(b) and Table 1. Under scenario (1), we find the quarantine program mitigated the epidemic size at 1118 (95%CI: 39–2389) as of February 21, and postponed the timing of epidemic peak on February 22. Under scenario (2), timely reduction in the susceptible population could lower the final size and sustainably reduce the daily incidences. Under scenario (3), the lower the R0, decreasing from 2.9 to 2.0, the lower the epidemic size and the later the peaking time will be. If the susceptible pools and R0 are reduced simultaneously, the COVID-19 outbreak on the ship will be likely mitigated and postponed largely, see Fig. 2(b).
4. Discussion
The R0 of COVID-19 on the Diamond Princess ship is likely to be lower than that of the severe acute respiratory syndrome (SARS) ranging from 2.2 to 3.6 (Lipsitch et al., 2003), but lower than estimates in previous studies assuming relatively long SI (Emery et al., 2020; Rockl ö v et al., 2020). The situation on the Diamond Princess cruise implies that the virus could spread rapidly, most likely with a short SI than previously estimated (Li et al., 2020). Note that a recent study on the 1099 patients found that the median of incubation period is only 3 days, thus a short effective SI is also possible (Guan et al., 2020). With a shorter SI, a relatively lower R0 could also result in a rapid growth of the epidemic size (Tuite & Fisman, 2020), and with a shorter epidemic doubling time as we show in Table 1. Therefore, timely contact tracing and effectively quarantine were crucial to shutoff transmission chains.
The simulation results under scenarios (1)–(4) indicate that the public health control measures could effectively mitigate the COVID-19 outbreak on the ship in terms of the epidemic size, see Table 2. The estimated 34% reduction in R0 was associated with the quarantine program on February 5, and similar reduction in transmissibility was also reported in (Emery et al., 2020; Rockl ö v et al., 2020). Decreasing the disease transmissibility in terms of R0 could postpone the peak, which may gain valuable time to prepare and allocate the resources in response to incoming patients. Relocating the population at risk (if possible) could sustainably decrease the daily incidences, and thus relieve the tensive demands in the healthcare, and improve in the treatment outcome.
Table 2.
Summary of the key epidemiological estimates of the outbreak under different scenarios. The epidemic curve of each scenario was visualized in Fig. 2.
| scenario | description | cum. # on Feb 21 | doubling time (day) | peak time | Visualization |
|---|---|---|---|---|---|
| (0) | baseline, λ = 1 | 1340 (190, 2493) | 3.4 (1.8, 8.1) | Feb 16 (Feb 7, Mar 2) | black curve in Fig. 2 |
| (1) | main result, R0 = 2.86, λ = 0.66 | 1118 (39, 2389) | 3.4 (1.7, 12.6) | Feb 22 (Feb 7, Mar 18) | blue curve in Fig. 2 |
| (2) | based on (1), remove 1000 susceptibles | 1195 (26, 2701) | 3.9 (2.0, 9.3) | Feb 18 (Feb 9, Mar 18) | green curve in Fig. 2 |
| (3) | based on (1), R0 reduced by 0.5 | 562 (26, 2154) | 4.1 (1.5, 9.1) | Mar 3 (Feb 14, Apr 11) | gold curve in Fig. 2 |
| (4) | based on (1), implement (2) and (3) | 512 (31, 1706) | 3.5 (1.7, 9.3) | Mar 1 (Feb 12, Mar 30) | red curve in Fig. 2 |
From Japan official reports (https://www.mhlw.go.jp/stf/newpage_09542.html), we obtain the following facts:
“2/15/2020 陽性が確認されたのは、延べ930名の検査中285名(うち無症状病原体保有者延べ73名)となりました。2/20/2020陽性が確認されたのは、延べ3063名の検査中634名(うち無症状病原体保有者延べ328名)となりました。”
The English translation from Google translation:
“February 15, 2020: Positive cases were confirmed in 285 of the 930 people tested (including 73 asymptomatic pathogen carriers). February 20, 2020: A total of 634 people (including 328 asymptomatic pathogen carriers) tested positive for a total of 3063 people.”
From the above official announcement of Japan, we calculate the ratio of asymptomatic cases out of all confirmed cases increased from (73/285 = ) 25.6% to (328/634 = ) 51.7% between February 15 and 20, 2020. It was unlikely that such a large increase in asymptomatic cases were infected before the quarantine starting on February 5, 2020, but unascertained in February 15. As such, the quarantine was less effective to prevent the emergence of asymptomatic cases, while it successfully reduced the occurrence of symptomatic cases, which is also suggested by studies only including symptomatic cases (Mizumoto & Chowell, 2020). Recent modelling study also inferred that there were 74% of infections proceeded asymptomatically, and the prevalence of asymptomatic infections appears higher after February 5 than before (Emery et al., 2020). They also estimate that asymptomatic individuals were the source for 69% of all infections. In other words, 74% of all infections are asymptomatic and may generate 69% offsprings, and thus asymptomatic or symptomatic infections made roughly equal contributions to the COVID-19 transmission.
In this study, we avoid separating the asymptomatic and symptomatic cases, and we model all laboratory confirmed infections regardless their symptoms. We capture the overall transmissibility of COVID-19 on DP ship, and evaluate the effect of the quarantine program in terms of the reduction in R0. One of the contributions is to explore several ‘what-if’ scenarios, under which the epidemic outcomes were assessed and projected, see Table 2. We suggest maintaining the enhancement in both populational level public health control as well as the individual level self-protection actions in combating the COVID-19 outbreak. With detailed information on public intervention, the analytical framework in this study can be extended to a complex context and used for evaluating the effects of certain control measures.
5. Ethics approval and consent to participate
The data were collected via public domain (2020Ministry of Health of Japan), and thus neither ethical approval nor individual consent was not applicable.
Availability of materials
All data used in this work were publicly available via (2020Ministry of Health of Japan).
Consent for publication
Not applicable.
Funding
DH was supported by General Research Fund (Grant Number 15205119) of the Research Grants Council (RGC) of Hong Kong, China and an Alibaba-Hong Kong Polytechnic University Collaborative Research project. WW was supported by National Natural Science Foundation of China (Grant Number 61672013) and Huaian Key Laboratory for Infectious Diseases Control and Prevention (Grant Number HAP201704), Huaian, Jiangsu, China.
Disclaimer
The funding agencies had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; or decision to submit the manuscript for publication.
Authors’ contributions
SZ and DH conceived the study, carried out the analysis, and drafted the first manuscript. All authors discussed the results, critically read and revised the manuscript, and gave final approval for publication.
Declaration of competing interest
This study was partially supported by a grant from the Research Grants Council of the Hong Kong Special Administrative Region, China (HKU C7123-20G).
Acknowledgements
None.
Handling Editor: Dr. J Wu
Footnotes
Peer review under responsibility of KeAi Communications Co., Ltd.
Supplementary data to this article can be found online at https://doi.org/10.1016/j.idm.2022.05.005.
Contributor Information
Shi Zhao, Email: zhaoshi.cmsa@gmail.com.
Peihua Cao, Email: cphcc@smu.edu.cn.
Daozhou Gao, Email: dzgao@shnu.edu.cn.
Zian Zhuang, Email: larry.zhuangzian@gmail.com.
Weiming Wang, Email: weimingwang2003@163.com.
Jinjun Ran, Email: jimran@connect.hku.hk.
Kai Wang, Email: wangkaimath@sina.com.
Lin Yang, Email: l.yang@polyu.edu.hk.
Yijun Lou, Email: yijun.lou@polyu.edu.hk.
Daihai He, Email: daihai.he@polyu.edu.hk.
Maggie H. Wang, Email: maggiew@cuhk.edu.hk.
Appendix A. Supplementary data
The following is the Supplementary data to this article:
References
- Adam D.C., Wu P., Wong J.Y., Lau E.H.Y., Tsang T.K., Cauchemez S., et al. Clustering and superspreading potential of SARS-CoV-2 infections in Hong Kong. Nature Medicine. 2020;26(11):1714–1719. doi: 10.1038/s41591-020-1092-0. [DOI] [PubMed] [Google Scholar]
- Ali S.T., Wang L., Lau E.H.Y., Xu X.K., Du Z., Wu Y., et al. Serial interval of SARS-CoV-2 was shortened over time by nonpharmaceutical interventions. Science. 2020;369(6507):1106–1109. doi: 10.1126/science.abc9004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Althaus C.L. Ebola superspreading. Lancet Infect Dis. 2015;15(5):507–508. doi: 10.1016/S1473-3099(15)70135-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Azimi P., Keshavarz Z., Laurent J.G.C., Stephens B., Allen J.G. Mechanistic transmission modeling of COVID-19 on the Diamond Princess cruise ship demonstrates the importance of aerosol transmission. Proceedings of the National Academy of Sciences. 2021;118(8) doi: 10.1073/pnas.2015482118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cori A., Ferguson N.M., Fraser C., Cauchemez S. A new framework and software to estimate time-varying reproduction numbers during epidemics. American Journal of Epidemiology. 2013;178(9):1505–1512. doi: 10.1093/aje/kwt133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Du Z., Xu X., Wu Y., Wang L., Cowling B.J., Meyers L.A. Serial interval of COVID-19 among publicly reported confirmed cases. Emerging Infectious Diseases. 2020;26(6):1341–1343. doi: 10.3201/eid2606.200357. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Emery J.C., Russell T.W., Liu Y., Hellewell J., Pearson C.A., Group C.C.-W., et al. The contribution of asymptomatic SARS-CoV-2 infections to transmission on the Diamond Princess cruise ship. Elife. 2020;9 doi: 10.7554/eLife.58699. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferretti L., Wymant C., Kendall M., Zhao L., Nurtay A., Abeler-Dorner L., et al. Quantifying SARS-CoV-2 transmission suggests epidemic control with digital contact tracing. Science. 2020;368(6491) doi: 10.1126/science.abb6936. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ganyani T., Kremer C., Chen D., Torneri A., Faes C., Wallinga J., et al. Estimating the generation interval for coronavirus disease (COVID-19) based on symptom onset data. Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. March 2020;25(17) doi: 10.2807/1560-7917.ES.2020.25.17.2000257. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guan W-j, Ni Z-y, Hu Y., Liang W-h, Ou C-q, He J-x, et al. Clinical characteristics of 2019 novel coronavirus infection in China. medRxiv. 2020;2020 02.06.20020974. [Google Scholar]
- He X., Lau E.H.Y., Wu P., Deng X., Wang J., Hao X., et al. Temporal dynamics in viral shedding and transmissibility of COVID-19. Nature Medicine. 2020:1–4. doi: 10.1038/s41591-020-0869-5. [DOI] [PubMed] [Google Scholar]
- Li Q., Guan X., Wu P., Wang X., Zhou L., Tong Y., et al. Early transmission dynamics in wuhan, China, of novel coronavirus-infected pneumonia. New England Journal of Medicine. 2020;382(13):1199–1207. doi: 10.1056/NEJMoa2001316. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lipsitch M., Cohen T., Cooper B., Robins J.M., Ma S., James L., et al. Transmission dynamics and control of severe acute respiratory syndrome. Science. 2003;300(5627):1966–1970. doi: 10.1126/science.1086616. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ministry of Health of Japan Identification of novel coronavirus infection on cruise ship in quarantine at Vokohama port. Ministry of Health, Labour and welfare of Japan. 2020 https://www.mhlw.go.jp/stf/newpage_09425.html [Available from: [Google Scholar]
- Mizumoto K., Chowell G. Transmission potential of the novel coronavirus (COVID-19) onboard the diamond Princess Cruises Ship. Infectious Disease Modelling. 2020;5:264–270. doi: 10.1016/j.idm.2020.02.003. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mizumoto K., Kagaya K., Zarebski A., Chowell G. Estimating the asymptomatic proportion of coronavirus disease 2019 (COVID-19) cases on board the Diamond Princess cruise ship, Yokohama, Japan. Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 2020;25(10) doi: 10.2807/1560-7917.ES.2020.25.10.2000180. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nishiura H., Linton N.M., Akhmetzhanov A.R. Serial interval of novel coronavirus (COVID-19) infections. International Journal of Infectious Diseases. 2020;93:284–286. doi: 10.1016/j.ijid.2020.02.060. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nishiura H., Linton N.M., Akhmetzhanov A.R. Serial interval of novel coronavirus (2019-nCoV) infections. medRxiv. 2020:2020. doi: 10.1016/j.ijid.2020.02.060. 02.03.20019497. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ren X., Li Y., Yang X., Li Z., Cui J., Zhu A., et al. Evidence for pre-symptomatic transmission of coronavirus disease 2019 (COVID-19) in China. Influenza Other Respir Viruses. 2021;15(1):19–26. doi: 10.1111/irv.12787. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Riou J., Althaus C.L. Pattern of early human-to-human transmission of Wuhan 2019 novel coronavirus (2019-nCoV) Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin. 2020;25(4) doi: 10.2807/1560-7917.ES.2020.25.4.2000058. December 2019 to January 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rocklov J., Sjodin H., Wilder-Smith A. COVID-19 outbreak on the diamond princess cruise ship: Estimating the epidemic potential and effectiveness of public health countermeasures. Journal of Travel Medicine. 2020;27(3) doi: 10.1093/jtm/taaa030. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rocklöv J., Sjödin H., Wilder-Smith A. COVID-19 outbreak on the diamond princess cruise ship: Estimating the epidemic potential and effectiveness of public health countermeasures. Journal of Travel Medicine. 2020;27(3) doi: 10.1093/jtm/taaa030. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Russell T.W., Hellewell J., Jarvis C.I., Van Zandvoort K., Abbott S., Ratnayake R., et al. Estimating the infection and case fatality ratio for coronavirus disease (COVID-19) using age-adjusted data from the outbreak on the Diamond Princess cruise ship. Eurosurveillance. February 2020;25(12) doi: 10.2807/1560-7917.ES.2020.25.12.2000256. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tang X., Musa S.S., Zhao S., Mei S., He D. Using proper mean generation intervals in modeling of COVID-19. Frontiers in Public Health. 2021;9 doi: 10.3389/fpubh.2021.691262. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tuite A.R., Fisman D.N. Reporting, epidemic growth, and reproduction numbers for the 2019 novel coronavirus (2019-nCoV) epidemic. Annals of Internal Medicine. 2020;172(8):567–568. doi: 10.7326/M20-0358. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallinga J., Lipsitch M. How generation intervals shape the relationship between growth rates and reproductive numbers. Proc Biol Sci. 2007;274(1609):599–604. doi: 10.1098/rspb.2006.3754. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang J., Chen X., Guo Z., Zhao S., Huang Z., Zhuang Z., et al. Superspreading and heterogeneity in transmission of SARS, MERS, and COVID-19: A systematic review. Computational and Structural Biotechnology Journal. 2021;19:5039–5046. doi: 10.1016/j.csbj.2021.08.045. [DOI] [PMC free article] [PubMed] [Google Scholar]
- World Health Organization Statement on the second meeting of the International Health Regulations Emergency Committee regarding the outbreak of novel coronavirus (2019-nCoV) https://www.who.int/news-room/detail/30-01-2020-statement-on-the-second-meeting-of-the-international-health-regulations-(2005)-emergency-committee-regarding-the-outbreak-of-novel-coronavirus-(2019-ncov World Health Organization (WHO). 2020 [Available from:
- Xu X.K., Liu X.F., Wu Y., Ali S.T., Du Z., Bosetti P., et al. Reconstruction of transmission pairs for novel coronavirus disease 2019 (COVID-19) in mainland China: Estimation of superspreading events, serial interval, and hazard of infection. Clinical Infectious Diseases. 2020;71(12):3163–3167. doi: 10.1093/cid/ciaa790. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yamagishi T., Ohnishi M., Matsunaga N., Kakimoto K., Kamiya H., Okamoto K., et al. Environmental sampling for severe acute respiratory syndrome coronavirus 2 during a COVID-19 outbreak on the diamond princess cruise ship. The Journal of Infectious Diseases. 2020;222(7):1098–1102. doi: 10.1093/infdis/jiaa437. [DOI] [PMC free article] [PubMed] [Google Scholar]
- You C., Deng Y., Hu W., Sun J., Lin Q., Zhou F., et al. Estimation of the time-varying reproduction number of COVID-19 outbreak in China. medRxiv. 2020;2020 doi: 10.1016/j.ijheh.2020.113555. 02.08.20021253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang S., Diao M., Yu W., Pei L., Lin Z., Chen D. Estimation of the reproductive number of novel coronavirus (COVID-19) and the probable outbreak size on the diamond princess cruise ship: A data-driven analysis. International Journal of Infectious Diseases. 2020;93:201–204. doi: 10.1016/j.ijid.2020.02.033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhao S. Estimating the time interval between transmission generations when negative values occur in the serial interval data: Using COVID-19 as an example. Mathematical Biosciences and Engineering. 2020;17(4):3512–3519. doi: 10.3934/mbe.2020198. [DOI] [PubMed] [Google Scholar]
- Zhao S., Cao P., Gao D., Zhuang Z., Cai Y., Ran J., et al. Serial interval in determining the estimation of reproduction number of the novel coronavirus disease (COVID-19) during the early outbreak. Journal of Travel Medicine. 2020;27(3) doi: 10.1093/jtm/taaa033. taaa033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhao S., Gao D.Z., Zhuang Z., Chong M.K.C., Cai Y.L., Ran J.J., et al. Estimating the serial interval of the novel coronavirus disease (COVID-19): A statistical analysis using the public data in Hong Kong from January 16 to February 15, 2020. Frontiers in Physics. 2020;8:347. [Google Scholar]
- Zhao S., Gao D., Zhuang Z., Chong M., Cai Y., Ran J., et al. Estimating the serial interval of the novel coronavirus disease (COVID-19): A statistical analysis using the public data in Hong Kong from January 16 to February 15, 2020. medRxiv. 2020;2020 02.21.20026559. [Google Scholar]
- Zhao S., Lin Q., Ran J., Musa S.S., Yang G., Wang W., et al. Preliminary estimation of the basic reproduction number of novel coronavirus (2019-nCoV) in China, from 2019 to 2020: A data-driven analysis in the early phase of the outbreak. Int J Infect Dis. 2020;92:214–217. doi: 10.1016/j.ijid.2020.01.050. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhao S., Shen M., Musa S.S., Guo Z., Ran J., Peng Z., et al. Inferencing superspreading potential using zero-truncated negative binomial model: Exemplification with COVID-19. BMC Med Res Methodol. 2021;21(1):1–8. doi: 10.1186/s12874-021-01225-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhao S., Tang B., Musa S.S., Ma S., Zhang J., Zeng M., et al. Estimating the generation interval and inferring the latent period of COVID-19 from the contact tracing data. Epidemics. 2021;36 doi: 10.1016/j.epidem.2021.100482. [DOI] [PMC free article] [PubMed] [Google Scholar]
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