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1.
J Theor Biol ; 508: 110453, 2021 01 07.
Artigo em Inglês | MEDLINE | ID: mdl-32949588

RESUMO

Tuberculosis (TB) is still an important public health issue in Jiangsu province, China. In this study, based on the TB transmission routes and the statistical data of TB cases, we formulate a novel TB epidemic model accounting for the effects of the contaminated environments on TB transmission dynamics. The value of this study lies in two aspects. Mathematically, we define the basic reproduction number, R0, and prove that R0 can be used to govern the threshold dynamics of the model. Epidemiologically, we find that the annual average R0 is 1.13,>1 and TB in Jiangsu is an endemic disease. Therefore, in order to control the TB in Jiangsu efficiently, we must decrease the virus shedding rate or increase the recovery rates, and increase the environmental clearance rate.


Assuntos
Epidemias , Tuberculose , Número Básico de Reprodução , China/epidemiologia , Humanos , Tuberculose/epidemiologia
2.
Virology ; 474: 1-9, 2015 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-25463598

RESUMO

During HIV type 1 (HIV-1) entry, trimers of gp120 bind to CD4 and either the CCR5 or CXCR4 coreceptor on the target cell. The stoichiometric parameters associated with HIV-1 entry remain unclear. Important unanswered questions include: how many trimers must attach to CD4 molecules, how many must bind coreceptors, and how many functional gp120 subunits per trimer are required for entry? We performed single round infectivity assays with chimeric viruses and compared the experimental relative infectivity curves with curves generated by mathematical models. Our results indicate that HIV-1 entry requires only a small number of functional spikes (one or two), that Env trimers may function with fewer than three active subunits, and that there is no major difference in the stoichiometric requirements for CCR5 vs. CXCR4 mediated HIV-1 entry into host cells.


Assuntos
HIV-1/fisiologia , Internalização do Vírus , Antígenos CD4/genética , Antígenos CD4/fisiologia , Genes Virais , Células HEK293 , Proteína gp120 do Envelope de HIV/biossíntese , Proteína gp120 do Envelope de HIV/química , Proteína gp120 do Envelope de HIV/genética , HIV-1/genética , Interações Hospedeiro-Patógeno/genética , Interações Hospedeiro-Patógeno/fisiologia , Proteínas do Vírus da Imunodeficiência Humana/biossíntese , Proteínas do Vírus da Imunodeficiência Humana/química , Proteínas do Vírus da Imunodeficiência Humana/genética , Humanos , Modelos Biológicos , Mutação , Receptores de HIV/genética , Receptores de HIV/fisiologia
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