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During the epidemics of respiratory infectious diseases, the use of public transportation increases the risk of disease transmission. Therefore, we established a dynamic model to provide an in-depth understanding of the mechanism of epidemic spread via this route. We designed a computer program to model a rail transit system including four transit lines in a small town in which assumed 70% of the residents commute via these trams in weekdays and the remaining residents take the tram at random. The model could identify the best travel route for each passenger and the specific passengers onboard when the tram passed through each station, and simulate the dynamic spread of a respiratory pathogen as the passengers used the rail transit system. Based on the program operating, we estimated that all residents in the town were ultimately infected, including 86.6% who were infected due to the public transportation system. The remaining individuals were infected at home. As the infection rate increased, the number of infected individuals increased more rapidly. Reducing the frequency of trams, driving private cars or riding bicycles, showing nucleic acid certificates and wearing masks for passengers, etc., are effective measures for the prevention of the spread of epidemic diseases.

The combination of histone deacetylase inhibitor and BRAF inhibitor (BRAFi) has been shown to enhance the antineoplastic effect and reduce the progress of BRAFi resistance. In this study, a series of (thiazol-5-yl)pyrimidin-2-yl)amino)-N-hydroxyalkanamide derivatives were designed and synthesized as novel dual inhibitors of BRAF and HDACs using a pharmacophore hybrid strategy. In particular, compound 14b possessed potent activities against BRAF, HDAC1, and HDAC6 enzymes. It potently suppressed the proliferation of HT-29 cells harboring BRAFV600E mutation as well as HCT116 cells with wild-type BRAF. The dual inhibition against BRAF and HDAC downstream proteins was validated in both cells. Collectively, the results support 14b as a promising lead molecule for further development and a useful tool for studying the effects of BRAF/HDAC dual inhibitors.

Abstract Background Outbreaks of respiratory infectious diseases often occur in crowded places. To understand the pattern of spread of an outbreak of a respiratory infectious disease and provide a theoretical basis for targeted implementation of scientific prevention and control, we attempted to establish a stochastic model to simulate an outbreak of a respiratory infectious disease at a military camp. This model fits the general pattern of disease transmission and further enriches theories on the transmission dynamics of infectious diseases. Methods We established an enclosed system of 500 people exposed to adenovirus type 7 (ADV 7) in a military camp. During the infection period, the patients transmitted the virus randomly to susceptible people. The spread of the epidemic under militarized management mode was simulated using a computer model named “the random collision model”, and the effects of factors such as the basic reproductive number (R 0), time of isolation of the patients (TOI), interval between onset and isolation (IOI), and immunization rates (IR) on the developmental trend of the epidemic were quantitatively analysed. Results Once the R 0 exceeded 1.5, the median attack rate increased sharply; when R 0 = 3, with a delay in the TOI, the attack rate increased gradually and eventually remained stable. When the IOI exceeded 2.3 days, the median attack rate also increased dramatically. When the IR exceeded 0.5, the median attack rate approached zero. The median generation time was 8.26 days, (95% confidence interval [CI]: 7.84–8.69 days). The partial rank correlation coefficients between the attack rate of the epidemic and R 0, TOI, IOI, and IR were 0.61, 0.17, 0.45, and − 0.27, respectively. Conclusions The random collision model not only simulates how an epidemic spreads with superior precision but also allows greater flexibility in setting the activities of the exposure population and different types of infectious diseases, which is conducive to furthering exploration of the epidemiological characteristics of epidemic outbreaks.