Skip to main content
  • Research article
  • Open access
  • Published:

Importations of COVID-19 into African countries and risk of onward spread

Abstract

Background

The emergence of a novel coronavirus (SARS-CoV-2) in Wuhan, China, at the end of 2019 has caused widespread transmission around the world. As new epicentres in Europe and America have arisen, of particular concern is the increased number of imported coronavirus disease 2019 (COVID-19) cases in Africa, where the impact of the pandemic could be more severe. We aim to estimate the number of COVID-19 cases imported from 12 major epicentres in Europe and America to each African country, as well as the probability of reaching 10,000 cases in total by the end of March, April, May, and June following viral introduction.

Methods

We used the reported number of cases imported from the 12 major epicentres in Europe and America to Singapore, as well as flight data, to estimate the number of imported cases in each African country. Under the assumption that Singapore has detected all the imported cases, the estimates for Africa were thus conservative. We then propagated the uncertainty in the imported case count estimates to simulate the onward spread of the virus, until 10,000 cases are reached or the end of June, whichever is earlier. Specifically, 1,000 simulations were run separately under four different combinations of parameter values to test the sensitivity of our results.

Results

We estimated Morocco, Algeria, South Africa, Egypt, Tunisia, and Nigeria as having the largest number of COVID-19 cases imported from the 12 major epicentres. Based on our 1,000 simulation runs, Morocco and Algeria’s estimated probability of reaching 10,000 cases by end of March was close to 100% under all scenarios. In particular, we identified countries with less than 1,000 cases in total reported by end of June whilst the estimated probability of reaching 10,000 cases by then was higher than 50% even under the most optimistic scenario.

Conclusions

Our study highlights particular countries that are likely to reach (or have reached) 10,000 cases far earlier than the reported data suggest, calling for the prioritization of resources to mitigate the further spread of the epidemic.

Peer Review reports

Background

In late December 2019, a novel coronavirus (SARS-CoV-2) was identified among patients presenting with viral pneumonia in Wuhan city, China [1]. Since then the number of coronavirus disease 2019 (COVID-19) cases and deaths increased rapidly [2, 3], and the city was locked down by the Chinese government on 23rd January 2020. By late February, there had only been limited importations from and to places outside China [4]. However, new epicentres in Europe and America emerged shortly thereafter, causing a second wave of importations that further accelerated the spread of the pandemic [4]. Most countries have since then imposed travel restrictions to prevent further importation of COVID-19 cases [5]. By 15th July 2020, over 13 million cases and 574,000 deaths had been confirmed worldwide [4].

A particular area of focus has been on countries in Africa, with worries about missed imported cases and what the impact will be of widespread transmission given the other heavy health burdens in these countries. The first confirmed case in Africa was reported in Egypt on 14th February 2020, and two weeks later, the virus was found in sub-Saharan Africa with a reported case in Nigeria [4]. By 15th July, over 600,000 cases had been reported in the whole of Africa, with substantial variation in the reported cumulative incidence across different countries [4]. This inter-country heterogeneity can be due to a wide range of factors, such as the number of imported cases, the capacity to conduct tests for COVID-19, surveillance efforts, as well as travel and movement restrictions which vary widely from country to country depending on the local context [5]. The reported data alone thus do not provide a clear depiction of the outbreak situation especially in countries with very limited surveillance capacities, and additional studies are needed to narrow the knowledge gap between the reported data and the real disease burdens.

Previous work has estimated the risk of importation from China at the early stage of the pandemic [6], assessed each African country’s capacity to respond to outbreaks [6], systematically collated information on the importation events reported by the sub-Saharan countries [7], and projected the spread of the epidemic seeded by the early cases represented in the World Health Organization Situation Reports [8]. It is still unclear how many cases may have been introduced to Africa from the new epicentres in Europe and America, although the reported case data do suggest that the size of this second wave of importations has been much larger than the first wave of importations from China [7]. In this study, we aim to estimate the number of COVID-19 cases imported from the major epicentres in Europe and America, and the magnitude of onward spread in each African country. This method is insensitive to the different testing and reporting systems that are in place in different countries.

Methods

Data

Case data

We collated data on the daily number of imported cases in Singapore reported by 31st March from the following 12 epicentres: Austria, Belgium, France, Germany, Italy, Netherlands, Portugal, Spain, Switzerland, Turkey, United Kingdom, and United States, which accounted for over 90% of Singapore’s reported number of imported cases from countries outside of Asia [9]. These data will be used later to estimate the number of imported cases in Africa. In addition, we obtained the number of imported cases reported by each sub-Saharan African country by 31st March [7], as well as the total number of confirmed cases in each African country by end of March, April, May, and June respectively [4].

Government response data

For each country, we collated the date on which each of the following policies came into force: [1] banning non-citizens and non-residents from entry (the start date could vary depending on the epicentre country from which a visitor arrived) [2]; mandatory (self-) quarantine for travellers arriving from each of the 12 epicentre countries mentioned earlier [3]; Stay-at-home order for all non-essential workers (hereinafter referred to as “stay-at-home order”). We reviewed the following sources: [1] country-level internal and international restrictions collated by the International SOS [5], [2] Oxford COVID-19 Government Response Tracker [10], [3] international travel restrictions collated by the International Air Transport Association [11], as well as [4] Wikipedia, where a separate page was available for each country containing information regarding the government response. For each Wikipedia page, we manually reviewed the online reports listed in the references to exclude data with unconfirmed or unreliable sources. If stay-at-home order came into force in different states of the same country at different times, only the earliest date was recorded. Since late April, some countries have lifted (and in rare cases, re-imposed) stay-at-home order, and the corresponding dates were taken from the Oxford COVID-19 Government Response Tracker database [10]. The government response data used in this study have been included within the Additional file 1.

Travel data

We obtained the total number of air ticket bookings for each origin-destination route allowing for up to two connections during March 2017 from the Official Airline Guide. This will be used later to estimate the ratio of air passenger volumes between pairs of origin and destination countries, which we assumed to be relatively stable over time.

Statistical analyses

Estimating the number of imported cases

For each African country r, we denote the daily number of air passengers that arrived from an epicentre country e by\( {v}_{e\to r}^{(t)}\ \left(t={t}_e,\kern0.5em {t}_e+1,\dots, {T}_{e\to r}\right) \), where te refers to the start date of the COVID-19 epidemic in the epicentre country e, and Te → r refers to the last day that non-citizens and non-residents travelling from country e were allowed to enter country r. Each day the probability that an air passenger travelling from country e to country r was an imported case is denoted by\( {p}_e^{(t)} \), which we assume to be dependent on both the origin country e and time t, but independent from the destination country r. In other words, the destination location was assumed to have a negligible impact on the risk of a traveller being an imported case, controlling for the origin location and travel date. Hence, the total number of COVID-19 cases imported from an epicentre country e to an African country r by the time the travel ban came into force (denoted by Me → r below) can be approximated using a Poisson distribution (Refer to the Additional file 2 for the derivation details):

$$ {M}_{e\to r}\ \dot{\sim}\ Po\left(\sum \limits_{t={t}_e}^{T_{e\to r}}{v}_{e\to r}^{(t)}\bullet {p}_e^{(t)}\right). $$

We used the imported COVID-19 case data reported by Singapore as well as flight data to provide a conservative estimate for Me → r, under the assumption that Singapore, being one of the countries with the highest surveillance capacity [12], has detected all the imported cases. Owing to the delay from infection to hospital admission, we considered all cases imported from country e to Singapore that were reported by date (Te → r + 9) (hereinafter denoted as SGe, r) based on Linton et al.’s estimated mean incubation period and time from illness onset to hospital admission [13]. We assumed that the ratio between the daily number of air travellers from epicentre e to country r and to Singapore remained stable in the presence of the changes in flight pattern in response to the COVID-19 pandemic (i.e. the percentage change in air passenger volumes was consistent across the two country pairs). This allows us to model Me → r (and SGe, r) as Poisson random variables with mean parameters proportional to the numbers of air passengers travelling from epicentre e to country r (and to Singapore) using the March 2017 flight data (Refer to the Additional file 2 for the derivation details):

$$ {\displaystyle \begin{array}{c}{M}_{e\to r}\dot{\sim}\ Po\left({\beta}_{e,r}\bullet {\sum}_{t\ \mathrm{in}\ \mathrm{Mar}\ 17}{v}_{e\to r}^{(t)}\right),\\ {}{SG}_{e,r}\dot{\sim}\ Po\left({\beta}_{e,r}\bullet {\sum}_{t\ \mathrm{in}\ \mathrm{Mar}\ 17}{v}_{e\to SG}^{(t)}\right).\end{array}} $$

Here, βe, r refers to the proportionality constant to be estimated using the reported value of SGe, r and flight data, and was assigned a uniform prior with support (0, 1). We performed Markov Chain Monte Carlo to sample from the posterior distribution of βe, r using the JAGS software [14]. A total of 10 chains were run in parallel, each with 2,000 iterations burn-in and 15,000 iterations thinned and subsequently merged to obtain a posterior sample of size 5,000. Both Geweke’s statistic and Brooks & Gelman’s potential scale reduction factors were derived to assess convergence (Refer to the Additional file 2 for more details) [15, 16]. The posterior sample for all the model parameters was then used to estimate the uncertainty distribution of the total number of COVID-19 cases imported from the 12 major epicentres to each country.

In March 2020, a spike in the number of cases imported from United Kingdom and United States was observed in Singapore, which was partly due to the increase in the number of returning Singaporean students studying overseas [17]. This change in flight patterns, however, may not be applicable to all African countries. Therefore, to be even more conservative, we also derived the imported case count estimates excluding United Kingdom and United States from the 12 epicentre countries previously considered. The resulting estimates were subsequently used in the simulations of the onward spread of SARS-CoV-2 to get our estimates of case numbers over time.

Simulating the onward transmission following importation

We performed 1,000 simulations drawing from our estimated distribution of the number of imported cases to project the onward spread of SARS-CoV-2 in each country up to 30th June 2020 or the date when we estimate 10,000 cases was reached, whichever was earlier. The time of infection for the cases imported from country e to country r was simulated via resampling from the reporting dates of the SGe, r cases, which was then shifted backwards by 9 days to account for the delay from infection to hospital admission based on Linton et al.’s estimates [13]. To account for the effect of quarantine measures on the onward transmission, we only included the estimated imported cases who had acquired the infection prior to the mandatory quarantine of travellers coming into force, so that the estimation of local SARS-CoV-2 spread is conservative. For each country and each day, we followed Cori et al. and expressed the total infectiousness of the infected individuals as the weighted sum of the past incident cases [18], where the weight parameters were derived from the cumulative distribution function of COVID-19’s serial interval based on Nishiura et al.’s estimate [19]. We assumed the offspring distribution to follow a negative binomial distribution with mean μ = 2 in the absence of stay-at-home order, and mean μ = 1.0 or 1.5 once the stay-at-home order came into force, where we created two scenarios for the value of μ′. The over-dispersion parameter (denoted by k) of the offspring distribution was assumed to be time-invariant, and we tested the sensitivity of our simulation results with respect to the estimated value of k obtained from previous studies, namely, 0.10 by Endo et al [20], and 0.58 by Bi et al [21]. Hence, there are a total of four combinations of parameter values of μ′ and k, and under each combination, we ran the simulation algorithm following Churcher et al. [22] and derived the estimated probability of reaching 10,000 cases by the end of March, April, May, and June respectively for each country. (Refer to Figure 1 for the schematic overview of the methods, the Additional file 2 for the implementation details, and the Additional file 4 for the R code)

Fig. 1
figure 1

Schematic overview of the methods. Blue boxes denote input data, and orange boxes output estimates. Brown boxes are used to show the model parameters for which more than one possible value was specified to test the sensitivity of our simulation results.

Results

We estimated Morocco, Algeria, South Africa, Egypt, Tunisia, and Nigeria as having the largest number of COVID-19 cases imported from the 12 new epicentres in Europe and America (Table 1 and Figure 2). All of these countries had their lower bound estimate of the imported case count exceeding 100 (Table 1). By contrast, nine countries (e.g. Lesotho, Eswatini, and South Sudan) were found to have a very low risk of importation, with the upper bound estimate of the imported case count below 10 (Table 1). For some countries such as Angola, the reported number of imported cases was substantially lower than our posterior median estimate (Figure 2). In a more conservative scenario where United Kingdom and United States were excluded from the list of epicentre countries, the estimated number of imported cases did not change drastically for most countries, albeit with some exceptions such as Kenya, whose estimate decreased from 97 (95% CI: 75–120) to 27 (95% CI: 16–41) (Table 1). The data file for Table 1 has been included within Additional file 3.

Table 1 Estimated number of COVID-19 cases (with 95% credible interval) imported from the 12 new epicentres in Europe and America (second column), and after excluding United Kingdom and United States from the list of epicentre countries (third column) to create a more conservative estimate (refer to Methods for more details). Note that in our estimates we only considered imported cases who had acquired infections prior to the travel ban coming into force
Fig. 2
figure 2

Estimated and reported number of imported COVID-19 cases. The first two subplots show the posterior median estimates of the number of COVID-19 cases imported from (a) all the 12 major epicentres in Europe and America, and (b) 10 epicentres only, after excluding United Kingdom and United States to create a more conservative estimate (Refer to Methods for more details). Note that in our estimates we only considered imported cases who had acquired infections prior to the travel ban coming into force. Subplot (c) shows the number of imported cases in each sub-Saharan African country that were reported by 31st March 2020 based on data collated by Skrip et al. (Countries not included in Skrip et al. were coloured in grey).

Based on our 1,000 simulations of the onward SARS-CoV-2 spread, both Morocco and Algeria’s estimated probability of reaching 10,000 cases by end of March was close to 100% under all the four scenarios that we considered, whilst the reported total number of cases in each country by end of March was ~500 (Figures 3 and 4). We found the numbers of countries with a higher-than-50% estimated probability of reaching 10,000 cases by end of March, April, May, and June to be 2, 13, 22, and 24 respectively (Figure 3) under the assumption that reproduction number is reduced to 1.0 by stay-at-home order and the offspring distribution is highly over-dispersed (i.e. k = 0.10). This scenario is considered to be the most conservative in terms of the estimated risk of reaching 10,000 cases in general (Figures 3 and 4), and yet the total numbers of countries that had reported over 10,000 cases by end of March, April, May, and June were only 0, 0, 2, and 7 respectively. Moreover, six countries (Angola, Gambia, Mauritius, Mozambique, Sao Tome and Principe, and Tanzania) were found to have reported less than 1,000 cases by end of June whilst the estimated probability of reaching 10,000 cases by then was higher than 50% even under the most optimistic scenario (Figure 3), suggesting that a very substantial number of cases may have been undetected. It should be noted that when the over-dispersion parameter k was changed from 0.10 to 0.58 there was a significant increase in our risk estimates in the later months (i.e. May and June) (Figures 3 and 4), and the 95% credible interval for the date at which 10,000 cases are reached in each country was also narrower in general under a less over-dispersed offspring distribution (i.e. k = 0.58) (Tables 2 and 3). Nonetheless, the ranking of the estimated risk of reaching 10,000 cases in each country was largely consistent across different combinations of model parameter values (Figures 3 and 4).

Fig. 3
figure 3

Estimated probability of reaching 10,000 cases as well as the reported total number of cases by each country (Stay-at-home order was assumed to reduce the reproduction number to 1.0). Reproduction number in the absence of stay-at-home order in each country was assumed to be 2. The over-dispersion parameter of the offspring distribution was (ad) 0.10 and (eh) 0.58 respectively. Reported total number of cases (il) were extracted from the World Health Organization’s situation reports.

Fig. 4
figure 4

Estimated probability of reaching 10,000 cases as well as the reported total number of cases by each country (Stay-at-home order was assumed to reduce the reproduction number to 1.5). Reproduction number in the absence of stay-at-home order in each country was assumed to be 2. The over-dispersion parameter of the offspring distribution was (ad) 0.10 and (eh) 0.58 respectively. Reported total number of cases (il) were extracted from the World Health Organization’s situation reports.

Table 2 Summary statistics for the estimated date by which 10,000 cases are reached in each African country. Reproduction numbers used for the simulation were 2.0 before and 1.0 after stay-at-home order came into force in each country. Estimates were derived under two scenarios, where the over-dispersion parameter of the offspring distribution was set at 0.10 (higher over-dispersion) and 0.58 (lower over-dispersion) respectively. Simulations were performed until 30th June, or 10,000 cases are reached, whichever is earlier, based on 1,000 model runs
Table 3 Summary statistics for the estimated date by which 10,000 cases are reached in each African country. Reproduction numbers used for the simulation were 2.0 before and 1.5 after stay-at-home order came into force in each country. Estimates were derived under two scenarios, where the over-dispersion parameter of the offspring distribution was set at 0.10 (higher over-dispersion) and 0.58 (lower over-dispersion) respectively. Simulations were performed until 30th June, or 10,000 cases are reached, whichever is earlier, based on 1,000 model runs

Discussion

Our study has estimated the size of the second wave of COVID-19 importations in each African country from the 12 major epicentres in Europe and America. This allows us to narrow the knowledge gap between the observed and actual number of importations, so that the unfolding of the epidemic seeded by the imported cases can be better projected especially in countries with very low testing capacities.

In the first wave of importations of cases from Wuhan, China, to other places outside China we estimated that most places at risk were in Asia, Europe and USA [23]. Though there were links between China and African countries, these were fewer than those between China and the rest of Asia, Europe and USA [23]. The shut down in China severely curtailed continuing importations out of China and so these importations rapidly stopped.

Lower initial importations into Africa compared to Asia and Europe certainly tallies with what has been seen. There have been very few reported cases in Africa in the first wave of importations, and no reports of onward transmission. There was much discussion at the time whether the lack of reported imported cases in Africa was because imported cases were not being picked up. This may be some of the story, but our analysis would suggest that this was not the whole story, and it was more that the early risk of importation into Africa was lower than other places [23]. However the results we present in this paper estimate that this risk has dramatically increased with the spread of the virus in Europe and the USA. This also tallies with what we have seen, as countries in Africa started to report their first imported cases from Europe and the USA [4]. As of July 15th 2020, South Africa had reported the highest number of cases at 298,292 [4], and we estimated South Africa to have had one of the highest numbers of imported cases from the new epi-centres, although it was also rated highest at risk in Africa of importations from China in previous analysis [6]. Senegal is one of the countries for whom the risk has notably increased from the risk of importation from China as estimated in previous analyses [6, 23]. We only considered importations from the major epicentres in Europe and America, and so the number of importations from all countries will be even higher. Hence, countries whose reported total number of imported cases was substantially lower than our estimates were likely to have severely under-detected COVID-19 cases imported from the new epi-centres. However it could also be that the difference between the reported and estimated numbers was due to missing travel history information among the reported cases.

Our study provides countries with information on the estimated timing of reaching 10,000 cases, which complements previous work by Pearson et al. [8] Our analyses further accounted for the estimated number and timing of imported cases, both being insensitive to the case reporting rates that vary across different countries. We also incorporated the effects of quarantine and stay-at-home order on the onward transmission, as well as the impact of different input parameter values on the simulation results. Notably, we found that a highly over-dispersed offspring distribution would lead to a relatively lower estimated magnitude of onward transmission, as well as higher uncertainty in the timing of reaching 10,000 cases. The former can be explained by a larger probability of producing zero offspring per COVID-19 case albeit a higher occurrence of super-spreading events. Whilst it is challenging to produce accurate estimates of the over-dispersion parameter and reproduction number in each country, the different scenarios created in our sensitivity analysis overall reflect our current understanding of the possible range of parameter values based on the data available [20, 21, 24]. Importantly, our results highlight countries whose reported numbers of cases remained substantially lower than the model estimates under all the scenarios that we considered, including some (e.g. Tanzania) where stringent measures such as stay-at-home order have yet to be implemented at the time of writing.

Many countries in Africa have considerable experience in dealing with other infectious disease outbreaks, most notably Ebola, and will be able to call upon that experience for COVID-19. Countries hit in this third wave of transmission, including those in Africa have some advantage as there have been a variety of responses from around the world from which to assess what to do or not to do. However there will need to be consideration of how effective measures can be adapted to different settings [25]. Issues such as high HIV prevalence in some countries, and a younger demographic may both affect the cases and deaths observed in different ways. Recent work has yielded important insights into the age-dependent susceptibility to infection as well as symptomatic rates [26], and more studies are urgently needed from different locations to parameterise this in models for different countries and to inform how best to respond in each local context.

Many countries in Africa are on high alert for incoming cases from Europe and USA, taking measures such as quarantine of arrivals or shutting down travel from affected countries. However as travel is either maintained or reopened between countries closer by, risk of importations from other countries should continue to be considered. Close attention should therefore be paid to where will be the next epicentre, perhaps within Africa, and how this could translate into imported cases for each country, particularly for those countries that we estimate to have experienced lower numbers of imported cases previously and therefore lower onward transmission.

Not accounted for in our study currently is the impact of less stringent interventions on the local SARS-CoV-2 spread, such as the effect of prohibiting large public gatherings, closure of social venues and schools, and restrictions on inter-district travels. It is still unclear as to whether and to what extent these interventions were effective in their local context, and hence in our simulations we only considered stay-at-home order for all non-essential workers as an effective intervention to reduce local transmission. Future modelling work considering the impact of different interventions in different places will be vital for determining how each country can continue to respond.

In addition, we have made simplifying assumptions about the change in travel patterns in response to the pandemic in each African country relative to that in Singapore, due to the unavailability of 2020 flight data. We were also unable to account for the complex effects of population structure on the onward transmission of the virus in each country. Despite these limitations, most of our model assumptions throughout the analyses have been fairly conservative to avoid inflating the projections of the SARS-CoV-2 spread. For example, the reported number of imported cases in Singapore was assumed to be complete, and the risk of returning citizens carrying SARS-CoV-2 after travel restrictions came into force in each African country was also not included. Simulations of the onward spread of the virus were based on the estimated number of imported cases from the selected 10 epicentre countries, and stay-at-home order was assumed to be effective (reproduction numbers being 1.5 and 1.0 in the two scenarios we considered). In light of these conservative assumptions, any countries found to have a high probability of reaching 10,000 cases by end May or June under the most optimistic scenario—especially those with very limited cases detected—need urgent actions.

Conclusions

In conclusion, our study provides model estimates of the number of COVID-19 cases imported from major epicentres in Europe and America to each country in Africa, as well as simulation results of the onward epidemic spread. Our results highlight particular countries that are likely to reach (or have reached) 10,000 cases far earlier than the reported data suggest, calling for the prioritization of resources to mitigate the further spread of the epidemic.

Availability of data and materials

Data on the reported number of imported cases in Singapore are available from https://www.moh.gov.sg/covid-19/past-updates

Flight data used in this study were purchased from the Official Airline Guide.

Government response data used in this study have been included within the Additional file 1.

Supporting information has been included within the Additional file 2.

Data file for Table 1 has been included within Additional file 3.

R code has been included within Additional file 4.

Abbreviations

COVID-19:

Coronavirus disease 2019

SARS-CoV-2:

Severe acute respiratory syndrome coronavirus 2

References

  1. Lu R, Zhao X, Li J, Niu P, Yang B, Wu H, et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet (London, England). 2020;395(10224):P565-74.

  2. 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. N Engl J Med. 2020. https://doi.org/10.1056/NEJMoa2001316.

  3. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet (London, England). 2020;395(10223)P497-506.

  4. World Health Organization. Coronavirus disease (COVID-2019) situation reports. 2020. Available from: https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports.

    Google Scholar 

  5. International SOS. TRAVEL RESTRICTIONS, FLIGHT OPERATIONS AND SCREENING. 2020. Available from: https://pandemic.internationalsos.com/2019-ncov/ncov-travel-restrictions-flight-operations-and-screening. [cited 2020 Apr 27].

    Google Scholar 

  6. Gilbert M, Pullano G, Pinotti F, Valdano E, Poletto C, Boëlle P-Y, et al. Preparedness and vulnerability of African countries against importations of COVID-19: a modelling study. Lancet (London, England). 2020;395(10227):871–7.

    Article  CAS  Google Scholar 

  7. Skrip LA, Selvaraj P, Hagedorn B, Ouédraogo AL, Noori N, Mistry D, et al. Seeding COVID-19 across sub-Saharan Africa: an analysis of reported importation events across 40 countries. MedRxiv. 2020; Available from: http://medrxiv.org/content/early/2020/04/06/2020.04.01.20050203.abstract. 2020.04.01.20050203.

  8. Pearson CAB, Schalkwyk C Van, Foss A, O’Reilly K, SACEMA’s Modelling and Analysis Response Team, CMMID COVID­19 working group, et al. Projection of early spread of COVID­19 in Africa as of 25 March 2020. 2020. Available from: https://cmmid.github.io/topics/covid19/current-patterns-transmission/reports/COVID10k_Africa.pdf.

    Google Scholar 

  9. Ministry of Health Singapore. UPDATES ON COVID-19 (CORONAVIRUS DISEASE 2019) LOCAL SITUATION. 2020. Available from: https://www.moh.gov.sg/covid-19. [cited 2020 Apr 1].

    Google Scholar 

  10. Hale T, Webster S, Petherick A, Phillips T, Kira B. Oxford COVID-19 Government Response Tracker [Internet]. 2020. Available from: https://covidtracker.bsg.ox.ac.uk/.

    Google Scholar 

  11. IATA. CORONAVIRUS OUTBREAK - UPDATE [Internet]. 2020. Available from: https://www.iatatravelcentre.com/international-travel-document-news/1580226297.htm. [cited 2020 Apr 11].

    Google Scholar 

  12. Niehus R, De Salazar PM, Taylor A, Lipsitch M. Quantifying bias of COVID-19 prevalence and severity estimates in Wuhan, China that depend on reported cases in international travelers. MedRxiv. 2020.

  13. Linton NM, Kobayashi T, Yang Y, Hayashi K, Akhmetzhanov AR, Jung S, et al. Incubation Period and Other Epidemiological Characteristics of 2019 Novel Coronavirus Infections with Right Truncation: A Statistical Analysis of Publicly Available Case Data. J Clin Med. 2020;9(2):538 Available from: https://www.mdpi.com/2077-0383/9/2/538.

    Article  Google Scholar 

  14. Plummer M. JAGS : A program for analysis of Bayesian graphical models using Gibbs sampling. 2003.Available from: http://www.ci.tuwien.ac.at/Conferences/DSC-2003/.

    Google Scholar 

  15. Geweke J. Evaluating the accuracy of sampling-based approaches to calculating posterior moments. In: Bayesian Statistics 4. Oxford: Clarendon Press; 1992. p. 169–93.

    Google Scholar 

  16. Brooks SP, Gelman A. General methods for monitoring convergence of iterative simulations. J Comput Graph Stat. 1998;7:434–55.

    Google Scholar 

  17. Elangovan N, Lim J. Covid-19: S’porean students abroad heading home after government advisory but a few plan to stay put. TODAY. 2020; Available from: https://www.todayonline.com/singapore/covid-19-sporean-students-overseas-prepare-head-home-after-government-advisory-few-vow. [cited 2020 Apr 11].

  18. Cori A, Ferguson NM, Fraser C, Cauchemez S. A New Framework and Software to Estimate Time-Varying Reproduction Numbers During Epidemics. Am J Epidemiol. 2013;178(9):1505–12 Available from: https://academic.oup.com/aje/article-lookup/doi/10.1093/aje/kwt133.

    Article  Google Scholar 

  19. Nishiura H, Linton NM, Akhmetzhanov AR. Serial interval of novel coronavirus (COVID-19) infections. Int J Infect Dis [Internet]. 2020;93:284–6 Available from: https://linkinghub.elsevier.com/retrieve/pii/S1201971220301193.

    Article  CAS  Google Scholar 

  20. Endo A, Abbott S, Kucharski AJ, Funk S. Estimating the overdispersion in COVID-19 transmission using outbreak sizes outside China. Wellcome Open Res. 2020;5:67 Available from: https://wellcomeopenresearch.org/articles/5-67/v3.

    Article  Google Scholar 

  21. Bi Q, Wu Y, Mei S, Ye C, Zou X, Zhang Z, et al. Epidemiology and transmission of COVID-19 in 391 cases and 1286 of their close contacts in Shenzhen, China: a retrospective cohort study. Lancet Infect Dis. 2020; Available from: https://linkinghub.elsevier.com/retrieve/pii/S1473309920302875.

  22. Churcher TS, Cohen JM, Novotny J, Ntshalintshali N, Kunene S. Cauchemez S. Measuring the path toward malaria elimination. Science. 2014;344(6189):1230–2. https://doi.org/10.1126/science.1251449.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Sun H, Dickens BL, Chen M, Cook AR, Clapham HE. Estimating number of global importations of COVID-19 from Wuhan, risk of transmission outside mainland China and COVID-19 introduction index between countries outside mainland China. medRxiv. 2020; 2020.02.17.20024075.

  24. Abbott S, Hellewell J, Thompson RN, Sherratt K, Gibbs HP, Bosse NI, et al. Estimating the time-varying reproduction number of SARS-CoV-2 using national and subnational case counts. Wellcome Open Res. 2020;5:112 Available from: https://wellcomeopenresearch.org/articles/5-112/v1.

    Article  Google Scholar 

  25. Mehtar S, Preiser W, Lakhe NA, Bousso A, TamFum J-JM, Kallay O, et al. Limiting the spread of COVID-19 in Africa: one size mitigation strategies do not fit all countries. Lancet Glob Heal. 2020; Available from: https://linkinghub.elsevier.com/retrieve/pii/S2214109X20302126.

  26. Davies NG, Klepac P, Liu Y, et al. Age-dependent effects in the transmission and control of COVID-19 epidemics. Nat Med. 2020;26:1205–11. https://doi.org/10.1038/s41591-020-0962-9.

Download references

Acknowledgements

Not applicable.

Funding

This research is supported by the Singapore Ministry of Health’s National Medical Research Council under the Centre Grant Programme - Singapore Population Health Improvement Centre (NMRC/CG/C026/2017_NUHS) and grant COVID19RF-004. The funders had no role in the design of the study, the collection, analysis and interpretation of data, or in writing the manuscript.

Author information

Authors and Affiliations

Authors

Contributions

HS and HC designed the study and HS carried out the analysis. HS, BD, AC, and HC contributed to the results interpretation, writing of the manuscript and approved it before submission.

Corresponding authors

Correspondence to Haoyang Sun or Hannah E. Clapham.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1.

Start dates of travel/internal restrictions in each African country.

Additional file 2.

Supporting information.

Additional file 3.

Data file for Table 1.

Additional file 4.

R code.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sun, H., Dickens, B.L., Cook, A.R. et al. Importations of COVID-19 into African countries and risk of onward spread. BMC Infect Dis 20, 598 (2020). https://doi.org/10.1186/s12879-020-05323-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12879-020-05323-w

Keywords