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• We measure infection of human (A549-ACE2) and animal (Vero-E6) cells by SARS-CoV-2. • We use mathematical modelling to estimate SARS-CoV-2 infection parameters. • SARS-CoV-2 infection rate of A549-ACE2 cells is lower than that of Vero E6 cells. • Latent phase of infected A549-ACE2 cells is longer than that of Vero E6 cells. • We conclude that Vero-E6 cells are not suitable for long-term drug screening assays. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV -2), a causative agent of COVID-19 disease, poses a significant threat to public health. Since its outbreak in December 2019, Wuhan, China, extensive collection of diverse data from cell culture and animal infections as well as population level data from an ongoing pandemic, has been vital in assessing strategies to battle its spread. Mathematical modelling plays a key role in quantifying determinants that drive virus infection dynamics, especially those relevant for epidemiological investigations and predictions as well as for proposing efficient mitigation strategies. We utilized a simple mathematical model to describe and explain experimental results on viral replication cycle kinetics during SARS-CoV-2 infection of animal and human derived cell lines, green monkey kidney cells, Vero-E6, and human lung epithelium cells, A549-ACE2, respectively. We conducted cell infections using two distinct initial viral concentrations and quantified viral loads over time. We then fitted the model to our experimental data and quantified the viral parameters. We showed that such cellular tropism generates significant differences in the infection rates and incubation times of SARS-CoV-2, that is, the times to the first release of newly synthesised viral progeny by SARS-CoV-2-infected cells. Specifically, the rate at which A549-ACE2 cells were infected by SARS-CoV-2 was 15 times lower than that in the case of Vero-E6 cell infection and the duration of latent phase of A549-ACE2 cells was 1.6 times longer than that of Vero-E6 cells. On the other hand, we found no statistically significant differences in other viral parameters, such as viral production rate or infected cell death rate. Since in vitro infection assays represent the first stage in the development of antiviral treatments against SARS-CoV-2, discrepancies in the viral parameter values across different cell hosts have to be identified and quantified to better target vaccine and antiviral research. [ABSTRACT FROM AUTHOR]

• COVID-19 outbreak situation in India is considered. • A deterministic compartmental model is proposed. • Basic reproduction number and effective reproduction number are estimated. • Impact of intervention on disease spread is studied. The outbreak of coronavirus disease 2019 (COVID-19), caused by the virus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has already created emergency situations in almost every country of the world. The disease spreads all over the world within a very short period of time after its first identification in Wuhan, China in December, 2019. In India, the outbreak, starts on 2 nd March, 2020 and after that the cases are increasing exponentially. Very high population density, the unavailability of specific medicines or vaccines, insufficient evidences regarding the transmission mechanism of the disease also make it more difficult to fight against the disease properly in India. Mathematical models have been used to predict the disease dynamics and also to assess the efficiency of the intervention strategies in reducing the disease burden. In this work, we propose a mathematical model to describe the disease transmission mechanism between the individuals. Our proposed model is fitted to the daily new reported cases in India during the period 2 nd March, 2020 to 12 th November, 2020. We estimate the basic reproduction number, effective reproduction number and epidemic doubling time from the incidence data for the above-mentioned period. We further assess the effect of implementing preventive measures in reducing the new cases. Our model projects the daily new COVID-19 cases in India during 13 th November, 2020 to 25 th February, 2021 for a range of intervention strength. We also investigate that higher intervention effort is required to control the disease outbreak within a shorter period of time in India. Moreover, our analysis reveals that the strength of the intervention should be increased over the time to eradicate the disease effectively. [ABSTRACT FROM AUTHOR]