Literature DB >> 32841283

Simulating the progression of the COVID-19 disease in Cameroon using SIR models.

Ulrich Nguemdjo1,2, Freeman Meno3, Audric Dongfack4, Bruno Ventelou1.   

Abstract

This paper analyses the evolution of COVID-19 in Cameroon over the period March 6-April 2020 using SIR models. Specifically, we 1) evaluate the basic reproduction number of the virus, 2) determine the peak of the infection and the spread-out period of the disease, and 3) simulate the interventions of public health authorities. Data used in this study is obtained from the Cameroonian Public Health Ministry. The results suggest that over the identified period, the reproduction number of COVID-19 in Cameroon is about 1.5, and the peak of the infection should have occurred at the end of May 2020 with about 7.7% of the population infected. Furthermore, the implementation of efficient public health policies could help flatten the epidemic curve.

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Year:  2020        PMID: 32841283      PMCID: PMC7447022          DOI: 10.1371/journal.pone.0237832

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


1. Introduction

The new coronavirus (COVID-19) started in Wuhan, China last November, presenting pneumonia-like symptoms in patients. The first cases examined in China indicated that it was a new respiratory disease. However, The World Health Organization (WHO) began delivering the most recent discoveries related to this virus on January 7, 2020. By the end of January 2020, with the virus already spread to several countries, the WHO alerted the world, announcing that COVID-19 was an international sanitary crisis. On February 14, 2020, the WHO [1] reported the first confirmed case on the African continent in Egypt, and the Ministry of Public Health of Cameroon announced their first confirmed case on March 6, 2020 [2]. Following this announcement, the spread of the disease gradually increased within the population of Cameroon. Based on the current situation, there is a need to study the evolution of this virus and the efficiency of the measures adopted by local authorities to curb the spread of COVID-19 in Cameroon. The core of the article will give details on the successive steps that we followed for the forecasting exercise: collecting data from the Cameroonian Ministry of Public Health, designing and applying the model, performing simulations for varying rates of exposure and transmittance, and evaluating the results obtained.

2. Data

To explore the evolution of the coronavirus disease in Cameroon, the present paper uses data collected from the Cameroonian Ministry of Public Health. According to the government, the first confirmed case of COVID-19 was detected on March 6, 2020, in the capital, Yaoundé. The government decided to publish daily reports regarding the evolution of the disease including the number of confirmed cases of COVID-19, the number of deaths due to the virus, and the number of recoveries via public declaration. These daily declarations ended on April 10, 2020, which is why our dataset covers from March 6 to April 10. Fig 1 displays an overview of the evolution of the coronavirus disease in Cameroon during our period of study. It shows an exponential increase in the number of confirmed cases. The total number of confirmed cases increases from 10 on March 17 to 820 on April 10, multiplying the total number of cases by 82 in less than a month. Moreover, the figure shows a slight increase in the total number of deaths due to COVID-19 in the country, from 1 on March 25 (the first death) to 12 on April 10. On the last day of our period of observation, the figure shows that the total number of recoveries from COVID-19 in Cameroon is 98, around 8 times more than the total number of deaths observed on the same date.
Fig 1

Number of observed cases of COVID-19 in Cameroon.

3. The SIR model

To explore the evolution of the coronavirus disease in Cameroon, this paper uses a simple SIR (susceptible (S)–infectious (I)–recovered (R)) model known as a general stochastic epidemic model [3-6]. This model is particularly suitable when dealing with a large population [7]. The initial model considers that individuals are at first Susceptible. If they are infected by the virus, they become immediately Infectious, and they remain infectious until they Recover, assuming immunity during the rest of the outbreak. In our paper, the last group was modified to “Removed” in order to account for the individuals who can no longer transmit the disease for reasons other than recovery, such as placement in quarantine, hospitalization, or dying from the virus [8]. To date (April 10, 2020), it is not certain whether, in the case of COVID-19, the recovered will be immunized for a very long period. In this paper, we assume that recovery confers immunity during the rest of the outbreak. We also assume that the population in our study is closed and that individuals mix uniformly in the community. Following Britton and Giardina [9], we also assume that all individuals are equally susceptible to the disease and equally infectious if they get infected. Supposing a closed population of size N, an individual who gets infected by the coronavirus becomes immediately infectious and remains so for a time determined exponentially with a decay rate of γ (the removal rate). Thus, γ−1 refers to the average number of infectious days that an infected individual has to transmit the virus before being removed from the Infectious group (placed in quarantine, hospitalized, recovered, or died). During the infectious period, an individual has close contact with the rest of the population over the remaining time at a rate determined by the parameter β (also known as effective contact rate), which is the product of the average number of exposures per unit of time (τ) and the likelihood of infection at each occasion of exposure (μ) [3]. S(t), I(t), and R(t) respectively represent the number of susceptible, infectious, and removed individuals in the population at time t. Assuming that we have a closed population, the total population at time t is given as follows: Let’s assume that at the beginning of the epidemic (S(0), I(0), R(0)) = (N-1, 1, 0) meaning that there is initially one infectious individual in the population and no removal. All other things being equal, the number of susceptible individuals decreases symmetrically by: Also, the variation in the number of people infected according to this measure is given by: The result is the following dynamic system, reflecting the generalized SIR Model: The simplicity of this dynamic system gives us rapid information on the rate of spread of the epidemic. Indeed, an epidemic occurs if the number of infected individuals increases continuously, i.e., As highlighted by Jones [3], at the outset of an epidemic, nearly everyone is susceptive. Thus, can be approximated to 1 and the above equation can be written as:

3.1. The parameter R0

The parameter R0 is called the basic reproduction rate. It is the expected number of secondary cases produced by a single infectious individual during the infection period in a completely susceptible population [3, 10]. Regarding the value of the parameter, the severity of the epidemic can be summarized into two cases [11, 9]: R0 > 1: The Supercritical case. The epidemic increases exponentially: one infected individual infects more than one individual on average. R0 ≤ 1: Critical case. No epidemic: the disease will surely die out without affecting a large share of the population Note that an R0 > 1 does not always guarantee an epidemic in the population [12, 9].

4. The results

4.1. Estimating the parameters of the model

To simulate the progression of the coronavirus disease in Cameroon, the next step consists in determining the parameters β and γ that best describe the current evolution of the virus in the country presented in section 2. For this step, knowing the period of observation, we chose to neglect the slight measures adopted by the Cameroonian local government to restrain the spread of the virus. The estimation is done using a Nelder-Mead and maximum likelihood optimization algorithm. The process implies finding β and γ in such a way that when these parameters are substituted in the equations described above, the difference between the data obtained and that recorded on the field is minimized. Computing β and γ using data recorded from March 6 to April 10 and a population of size N = 25,216,237. The results are summarized in Table 1. The confidence intervals presented in the table are built using the distribution of the bootstrap realizations presented in the Appendix (Fig 2, Fig 3, Fig 4, Fig 5 and Fig 6). Simulations conducted with the above parameters yield the results shown in Fig 7.
Table 1

Estimates parameters.

OriginalBiasStd. errorBootstrap normal CI*
InfSup
β0.6157.65e-060.0030.6100.619
γ0.393-3.69e-050.0030.3880.398
R01.5670.0000.0161.5361.597
Maximum Infected2,015,200757.686476,463.731,864,5762,164,309
Number of Days to reach the peak81,06-0.0221.66077.8184.32

*CI = Confidence Interval.

Fig 2

Bootstrap distribution of β.

Fig 3

Bootstrap distribution of γ.

Fig 4

Bootstrap distribution of R0.

Fig 5

Bootstrap distribution of the infected.

Fig 6

Bootstrap distribution of the number of days.

Fig 7

Evolution of the coronavirus disease in Cameroon.

*CI = Confidence Interval. All else unchanged, the evolution presented in Fig 7 should be a plausible scenario if no action is taken to reduce the spread of the virus. More precisely, the figure reveals that, if the situation remains as during the observed period (from March 6 to April 10), about 7.7% of the Cameroonian population might have ended up being infected, which is close to 2,015,200 individuals. In this case, the peak of the infection will occur between day number 78 and day number 85 starting from March 6, which is between 23th and 29th May. Additionally, assuming a rate of 15.8% of serious complications of the disease [13] approximately 318,402 Cameroonians might find themselves hospitalized in critical conditions. While considering a mortality rate of 3.4% (the overall mortality rate of COVID-19 announced by the WHO on March 3, 2020 [14], the expected number of deaths due to coronavirus could be close to 68,517. Though these results might not be accurate, the approach gives a simple and quick means to figure out the evolution of the spread of the virus and paves the way for a better approach. Our model also suggests that the basic reproduction rate (R0) of COVID-19 in Cameroon up to April 10 is about 1.567 persons, meaning that on average an infectious individual infects 1.567 susceptible individuals during his infection period. The question now is how can we flatten the infectious curve? What has been recommended since the beginning of this epidemic is to apply public health measures.

4.2. Flattening the epidemic curve with public health interventions

Until an efficient medical treatment or vaccine for COVID-19 is available, prevention and control strategies to reduce or stop the transmission of the disease only rely on measures adopted by public health officials. In this section, we model the effect of different public health interventions on the spread of the coronavirus disease in Cameroon.

4.2.1 Physical distancing

Physical or social distancing–keeping space between yourself and other people outside your home–plays a major role in public health interventions. Its objective is to reduce the probability of contact between infected individuals and susceptible ones to minimize the transmission of the disease. In practice, physical distancing [15] can be implemented by adopting the following habits: Stay at least 1 meter (3 feet) from others Do not gather in groups Stay out of crowded places Avoid mass gatherings

4.2.2. Hygiene measures

In addition to physical distancing, public health interventions also incorporate hygiene measures to reduce transmission of the coronavirus between individuals, from individuals to surfaces, and from surfaces to other individuals. These hygiene measures include: Frequent hand washing Avoiding touching eyes, nose, and mouth Practicing respiratory hygiene: cover the mouth and the nose with the bent elbow or tissue when coughing or sneezing Wearing surgical masks Cleaning or disinfection of fomites

4.2.3. Simulating public health interventions

The main concern of public health interventions is to flatten the infectious curve. The shape of the infectious curve is a function of the effective contact rate β, which depends on the average number of exposures per unit of time (τ) and the likelihood of infection at each occasion of exposure (μ) (see section 3). Thus, adjusting τ and μ will influence the kinetics of the flattening curve [16]. More precisely, to simulate an increase in social or physical distancing, we can reduce the average number of exposures per day (τ), whereas, taking into consideration the hygiene measures, we can reduce the probability of infection at each occasion of exposure (μ). According to some studies on COVID-19, the probability of infection at each exposure varies from 1% to 5% [17]. In this paper, 5% is selected as the initial infection probability. As our parameter β = 0.6, we can estimate the initial average number of exposures per day to 12 exposures. Therefore, the goal of the public health interventions in Cameroon will be to progressively reduce the number of exposures (we will simulate using 12, 6, and 2 exposures per day) and the probability of infection (we will simulate using 5%, 2.5%, and 1%). The simulation was done using the R EpiModel package with a population of size N = 1,000 for computational matters [18]. Fig 8 gives the results.
Fig 8

Simulating new cases of COVID-19 with public health interventions.

As we can see, a decrease in the number of exposures per day (from the left to the right on Fig 8) and a decrease in the likelihood of infection (from the top to the bottom of Fig 8) is associated with a flattening in the coronavirus epidemic curve. Furthermore, as the curve flattens, we can observe a decrease in the percentage of the population infected by the virus. Also, decreasing exposures per day or the infection probability prolongs the epidemic overall while slowing down the incidence rate.

5. Conclusion

The present paper aims to analyze the evolution of the coronavirus disease in Cameroon. The study uses data collected by the Cameroonian health ministry between March 6 (date of the first confirmed case in the country) to April 10, 2020. Descriptive statistics show an exponential increase in the total number of infectious individuals. This gives a first idea of how the virus is spreading out in Cameroon. Starting from the natural evolution of the epidemic in the first days of propagation in the country, a SIR model was applied to the observed data. The results of the calibration show that, if actions undertaken by Cameroonians to fight against the coronavirus do not improve, the peak of the infection would occur at the end of May 2020, with about 7.7% of the Cameroonian population infected. Using the WHO mortality rate associated with COVID-19, the expected number of deaths due to the virus in Cameroon could be close to 70,000. At this time, and using the most recent information available for Cameroon to verify the accuracy of the modeling, one can observe that the epidemic indeed reached its peak at the end of May 2020, as suggested by the public health minister in an alarmist tweet on May 25th [19]. For the first time on Twitter, the minister warned that the country was entering a complicated phase of the epidemic, and encourage preventive measures such as handwashing and wearing mask when going out. In later comments related to this tweet, he stated the peak was soon approaching [20]. However, by intensifying public health interventions, the epidemic curve could have flattened more, as suggested in the simulation. The results of the modeling seem to underline the value of appropriate communication campaigns from the government and the importance of the population’s compliance with the public health measures recommended by the WHO to limit and stop the spread of the coronavirus disease, at least while waiting for possible preventive and/or curative treatments to be found. To date, some public measures have been taken by the Cameroonian government such as sensibilization through public media, shutting down schools, and the closing of public spaces and of some informal/formal businesses. However, these measures were relaxed just a few weeks after their execution due to their negative economic impact on most Cameroonian households. This quick renouncement to the measures may explain why the alarmist tweet of the health minister occurred exactly when the model predicted the peak without any intervention, precisely at the end of May [19]. Even though the paper has some limitations, such as the ‘closed population’ assumptions or the homogeneous mixture of the population (particularly across the geography of Cameroon), our model is particularly suitable while dealing with a large population of subjects, such as a human population observed at a country level [3]. We should also note that the basic reproduction rate, which is constant in this paper, may change depending on several variables (awareness of the population, intensity of trade, movement of people), and thus, create a time-varying basic reproduction rate [21, 22]. In all cases, knowing the paucity of the literature available for African countries, this paper enriches the knowledge by providing some quantitative evidence in support of the Cameroonian government’s actions attempting to fight against the coronavirus. As an extension of this paper, studies with more sophisticated assumptions on the contact-matrix could be carried out (the matrix that accounts for the different interactions between the susceptible), as well as simulations showing, in parallel of the disease propagation, the economic impact of the coronavirus epidemic on the Cameroonian population.

Transfer Alert

This paper was transferred from another journal. As a result, its full editorial history (including decision letters, peer reviews and author responses) may not be present. 16 Jun 2020 PONE-D-20-14463 Simulating the progression of the COVID-19 disease in Cameroon using SIR models PLOS ONE Dear Dr. NGUEMDJO, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. Your manuscript was reviewed by 2 experts in the field. Both identified many important problems in your submission, which require your careful attention. Please review the attached comments and provide point-by-point responses. Please submit your revised manuscript by Jul 31 2020 11:59PM. 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Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: No ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: PLOS ONE Manuscript number: PONE-D-20-14463 Title: Simulating the progression of the COVID-19 disease in Cameroon using SIR models Nguemdjo et al. apply a modified “Susceptible-Infected-Recovered” epidemiological model to COVID-19 data collected from the Cameroonian Ministry of Health. They generate models with various degrees of infectiousness and infer upon to which level the implemented measures of public heatlh intervention would successfully contain the epidemic. General comments: The paper is confirming the validity of a globally applied epidemic model within the settings of Cameroon and providing valuable statistical information regarding the resolution of the pandemic crisis at a national level. The authors may also wish to consider the following: 1. A general revision of English language, syntax and grammar is necessary. 2. Footnotes must instead be incorporated into the text or properly added as references following the journal’s citation style. 3. Figures should have captions in a style as dictated by the journal, with a more extensive legend. 4. Gallicisms, such as using the French spelling of the name of the Republic of Cameroon, should be corrected. 5. The Authors analyse data available until April 10th, and its association with public health interventions. Given that more than one month has passed after this date, the Authors can comment and provide more information on the current situation and the impact of the measures taken. Specific comments: 1. “The rest of the study is organized…” - this details the structure of the paper (which is unnecessary), not the study itself. That would be collecting data from the Cameroonian ministry of health, applying the model, performing simulations for varying rates of exposure and transmittance and evaluating the data. 2. “The political capital, Yaoundé” 3. Line 41/54: The headings “The Model” and “The SIR Model” are redundant with each other. The sections should be merged. 4. Line 45: Provide a source for the sentence “This model..... a large population”. 5. Lines 45-46: When first explaining the model, names of the population fractions shouldn’t be capitalized (“Susceptible”, “Infectious”, “Recovered”), instead the abbreviation should be put in brackets: “susceptible (S)”, “infectious (I)”, “recovered (R)”. 6. Lines 47-48: “the last group was modified to “Removed”” - here a clearer explanation is needed, for example “was modified to “Removed” in order to cover/account for individuals who can no longer transmit the disease for reasons other than acquired immunity, such as being placed in quarantine, hospitalized, or dying”. 7. Line 56: “an exponentially distributed time” - Time is not distributed, but determined exponentially with a decay rate of γ. 8. Line 60: Why does ”close contact” need to be in quotes? Also, it should be merged with the next sentence: “… an individual has close contact with the rest of the population over the remaining time at a rate determined by the parameter β (also known as effective contact rate), which is the product of the average number of exposures per unit of time (τ) and the likelihood of infection at each occasion of exposure (μ).” The equation (β = τ × μ) should be included in its own paragraph below. 9. Line 107: Consider substituting “if nothing is done indeed” by “if no action is taken”. 10. Line 150-155: There lacks a clear, mathematical expression of the relationship between hygienic measures and the probability of infection upon contact. It needs to be framed in terms of the removal rate and its connection to flattened curve kinetics. 11. “Besides, we can observe a decrease in the percentage of the population infected by the virus” A direct link between a flatter curve, a greater proportion of Removed individuals and total population infected is not sufficiently made clear. 12. “and the disease lasts for a shorter period” - from my understanding decreasing exposures per day prolongs the epidemic overall while slowing down the incidence rate. 13. “a SIR model was calibrated” : “calibration” is usually understood as the preparation of a model or device for accurate measurements by adjusting it to known standards. In this case, “applied”, “simulated” or “fitted” would be suitable to use. 14. Line 190: “contact-matrix (between susceptible)” – upon introducing a new term, provide more detailed information about it. 15. Footnote number 10 should be incorporated in the methods section. Minor spelling, grammar and punctuation issues: 1. Line 9 : “could help flattens the epidemic curve”, remove the “s” in flattens. 2. Line 16: The WHO alerted, instead of “alleged”. 3. Line 21 : “there is a need to study” 4. Line 22: “Covid-19 diseases” is redundant, remove the word diseases. 5. Line 29 : “The government decided to publish daily reports” 6. Line 30 : “the number of deaths 7. Line 31 : “These declarations ended on April 10, 2020, that which is why…”. Remove “that”. 8. Line 44 : Remove “while” in “suitable while when dealing” 9. Line 48: “Thus, the individual is Infectious until he is” - “Thus, the individual is infectious until they are…”; Also line 121. 10. Line 55 : “Supposed” instead of “Supposing a closed population…” 11. Line 59 : Substitute word infectious by infection in “During the infectious period ”; Also line 80, 122. 12. Line 60 : “at a rate β” 13. Line 99 : “Marche 6”. Remove “e” 14. Line 157: “to progressively reduce instead of to reduce progressively” 15. Figure 1: “recovery” should be replaced by “recovered” or “recoveries”. 16. Figure 2: “total population” 17. Appendix: The “the” before letters denoting parameters should be removed (“distribution of the β”). Reviewer #2: Summary: This is an interesting article on how to use SIR models to make forward decisions on COVID-19. The authors use data from Cameroon to fit the model parameters and then make predictions on how different control strategies will impact the dynamics. Recommendations: 1. The citations are low and there are nearly daily publications on COVID-19 SIR models. Two are in NEJM and JAMA. The authors should cite these to let readers know this is standard. 2. The SIR model is the Kermack and McKendrick model not Kendrick “model known as a general stochastic epidemic model (Kendrick and Kermarck 1927; Jones 2007)”. 3. Make a table of parameter meanings, description of how they are estimated and their units. The parameters all have standard names like effective contact rate etc. The authors should rely on these standards. 4. The model doesn’t include any time lag and relies on those who were tested. Were these symptomatic cases? If so, the authors should point out their model does not include asymptomatic cases that were infectious and thus represents an underestimate. 5. The calculation of R0 can be done in different methods. The authors make an assumption which helps their calculation. They should cite Pauline van den Dreissche’s work on calculating R0. Also, R0 may change based on controls and thus create a time-varying R0. This should be noted in the discussion. A constant R0 is based on the assumptions behind the model. If these assumptions change, then the R0 changes. 6. There is no data sharing plan or information. 7. There are some places the language can be tightened up. The authors should review a few times to clean up the writing. ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No Reviewer #2: Yes: Diana Thomas [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 6 Jul 2020 Dear Editor, Thank you for giving us the opportunity to revise our paper on “Simulating the progression of the COVID-19 disease in Cameroon using SIR models” The suggestions offered by the reviewers have been helpful and we also appreciate your insightful comments on revising some aspects of the paper. We have included the reviewers’ comments immediately after this letter and responded to them individually, indicating how we addressed each concern and describing the changes we have made. Best regards, Ulrich NGUEMDJO Freeman MENO Audric DONGFACK Bruno VENTELOU Submitted filename: Response to Reviewers.pdf Click here for additional data file. 23 Jul 2020 PONE-D-20-14463R1 Simulating the progression of the COVID-19 disease in Cameroon using SIR models PLOS ONE Dear Dr. NGUEMDJO, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. ============================== Your manuscript was reviewed by one of the original reviewers. There are  still problems that require your attention. Please note comments on careful spell checking your manuscript and using references. ============================== Please submit your revised manuscript by Sep 06 2020 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript: A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'. An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter. If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols We look forward to receiving your revised manuscript. Kind regards, Yury E Khudyakov, PhD Academic Editor PLOS ONE [Note: HTML markup is below. Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #2: (No Response) ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #2: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #2: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #2: Yes ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #2: No ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #2: There are still spelling errors for example on page 38, acute should be accurate. The time varying reproductive rate reference is not Pauline van den Dreissche's. Her article discusses ways to compute R0. This article discusses time varying R0: Massad E, Burattini MN, Lopez LF, Coutinho FA. Forecasting versus projection models in epidemiology: the case of the SARS epidemics. Med Hypotheses. 2005;65(1):17-22. Epub 2005/05/17. doi: 10.1016/j.mehy.2004.09.029. PubMed PMID: 15893110; PubMed Central PMCID: PMCPMC7116954. ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #2: Yes: Diana Thomas [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 31 Jul 2020 Reviewer #2: 1. There are still spelling errors for example on page 38, acute should be accurate. Response: Thank you for the comment, the paper has been sent for editing. It is now OK. 2. The time varying reproductive rate reference is not Pauline van den Dreissche's. Her article discusses ways to compute R0. This article discusses time varying R0: Massad E, Burattini MN, Lopez LF, Coutinho FA. Forecasting versus projection models in epidemiology: the case of the SARS epidemics. Med Hypotheses. 2005;65(1):17-22. Epub 2005/05/17. doi: 10.1016/j.mehy.2004.09.029. PubMed PMID: 15893110; PubMed Central PMCID: PMCPMC7116954. Response: Thank you for the comment. We added the reference in the manuscript. Submitted filename: Response to Reviewers.pdf Click here for additional data file. 5 Aug 2020 Simulating the progression of the COVID-19 disease in Cameroon using SIR models PONE-D-20-14463R2 Dear Dr. NGUEMDJO, We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. Kind regards, Yury E Khudyakov, PhD Academic Editor PLOS ONE Additional Editor Comments (optional): Reviewers' comments: 7 Aug 2020 PONE-D-20-14463R2 Simulating the progression of the COVID-19 disease in Cameroon using SIR models Dear Dr. Nguemdjo: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Yury E Khudyakov Academic Editor PLOS ONE
  8 in total

1.  EpiModel: An R Package for Mathematical Modeling of Infectious Disease over Networks.

Authors:  Samuel M Jenness; Steven M Goodreau; Martina Morris
Journal:  J Stat Softw       Date:  2018-04-20       Impact factor: 6.440

2.  Deterministic SIR (Susceptible-Infected-Removed) models applied to varicella outbreaks.

Authors:  J Ospina Giraldo; D Hincapié Palacio
Journal:  Epidemiol Infect       Date:  2007-07-26       Impact factor: 2.451

3.  The spread of HIV-1 in Africa: sexual contact patterns and the predicted demographic impact of AIDS.

Authors:  R M Anderson; R M May; M C Boily; G P Garnett; J T Rowley
Journal:  Nature       Date:  1991-08-15       Impact factor: 49.962

4.  Modeling Epidemics With Compartmental Models.

Authors:  Juliana Tolles; ThaiBinh Luong
Journal:  JAMA       Date:  2020-06-23       Impact factor: 56.272

Review 5.  Reproduction numbers of infectious disease models.

Authors:  Pauline van den Driessche
Journal:  Infect Dis Model       Date:  2017-06-29

6.  Forecasting versus projection models in epidemiology: the case of the SARS epidemics.

Authors:  Eduardo Massad; Marcelo N Burattini; Luis F Lopez; Francisco A B Coutinho
Journal:  Med Hypotheses       Date:  2005       Impact factor: 1.538

7.  Estimation of time-varying reproduction numbers underlying epidemiological processes: A new statistical tool for the COVID-19 pandemic.

Authors:  Hyokyoung G Hong; Yi Li
Journal:  PLoS One       Date:  2020-07-21       Impact factor: 3.240

8.  Why is it difficult to accurately predict the COVID-19 epidemic?

Authors:  Weston C Roda; Marie B Varughese; Donglin Han; Michael Y Li
Journal:  Infect Dis Model       Date:  2020-03-25
  8 in total
  6 in total

1.  Understanding Dynamics of Pandemic Models to Support Predictions of COVID-19 Transmission: Parameter Sensitivity Analysis of SIR-Type Models.

Authors:  Chunfeng Ma; Xin Li; Zebin Zhao; Feng Liu; Kun Zhang; Adan Wu; Xiaowei Nie
Journal:  IEEE J Biomed Health Inform       Date:  2022-06-03       Impact factor: 7.021

2.  Bistability in deterministic and stochastic SLIAR-type models with imperfect and waning vaccine protection.

Authors:  Julien Arino; Evan Milliken
Journal:  J Math Biol       Date:  2022-06-23       Impact factor: 2.164

3.  Analytical Parameter Estimation of the SIR Epidemic Model. Applications to the COVID-19 Pandemic.

Authors:  Dimiter Prodanov
Journal:  Entropy (Basel)       Date:  2020-12-31       Impact factor: 2.524

4.  A proposed fractional dynamic system and Monte Carlo-based back analysis for simulating the spreading profile of COVID-19.

Authors:  Arash Sioofy Khoojine; Mojtaba Mahsuli; Mahdi Shadabfar; Vahid Reza Hosseini; Hadi Kordestani
Journal:  Eur Phys J Spec Top       Date:  2022-03-30       Impact factor: 2.707

5.  Gauging the Impact of Artificial Intelligence and Mathematical Modeling in Response to the COVID-19 Pandemic: A Systematic Review.

Authors:  Afshan Hassan; Devendra Prasad; Shalli Rani; Musah Alhassan
Journal:  Biomed Res Int       Date:  2022-03-14       Impact factor: 3.411

6.  Association of anti-contagion policies with the spread of COVID-19 in United States.

Authors:  Ali Faghani; M Courtney Hughes; Mahdi Vaezi
Journal:  J Public Health Res       Date:  2022-03-25
  6 in total

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