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1.
Pathog Dis ; 79(1)2021 01 09.
Artigo em Inglês | MEDLINE | ID: mdl-33289808

RESUMO

A vast proportion of coronavirus disease 2019 (COVID-19) individuals remain asymptomatic and can shed severe acute respiratory syndrome (SARS-CoV) type 2 virus to transmit the infection, which also explains the exponential increase in the number of COVID-19 cases globally. Furthermore, the rate of recovery from clinical COVID-19 in certain pockets of the globe is surprisingly high. Based on published reports and available literature, here, we speculated a few immunovirological mechanisms as to why a vast majority of individuals remain asymptomatic similar to exotic animal (bats and pangolins) reservoirs that remain refractile to disease development despite carrying a huge load of diverse insidious viral species, and whether such evolutionary advantage would unveil therapeutic strategies against COVID-19 infection in humans. Understanding the unique mechanisms that exotic animal species employ to achieve viral control, as well as inflammatory regulation, appears to hold key clues to the development of therapeutic versatility against COVID-19.


Assuntos
COVID-19/imunologia , Síndrome da Liberação de Citocina/imunologia , Proteína 3 que Contém Domínio de Pirina da Família NLR/imunologia , Receptores KIR/imunologia , Receptores Semelhantes a Lectina de Células NK/imunologia , Zoonoses/imunologia , Animais , Animais Exóticos/virologia , Doenças Assintomáticas , COVID-19/genética , COVID-19/transmissão , COVID-19/virologia , Quirópteros/virologia , Síndrome da Liberação de Citocina/genética , Síndrome da Liberação de Citocina/prevenção & controle , Síndrome da Liberação de Citocina/virologia , Reservatórios de Doenças , Eutérios/virologia , Expressão Gênica , Especificidade de Hospedeiro , Humanos , Tolerância Imunológica , Imunidade Inata , Interferon beta/deficiência , Interferon beta/genética , Interferon beta/imunologia , Células Matadoras Naturais/imunologia , Células Matadoras Naturais/virologia , Monócitos/imunologia , Monócitos/virologia , Proteína 3 que Contém Domínio de Pirina da Família NLR/deficiência , Proteína 3 que Contém Domínio de Pirina da Família NLR/genética , Receptores KIR/deficiência , Receptores KIR/genética , Receptores Semelhantes a Lectina de Células NK/deficiência , Receptores Semelhantes a Lectina de Células NK/genética , SARS-CoV-2/patogenicidade , Fator de Necrose Tumoral alfa/deficiência , Fator de Necrose Tumoral alfa/genética , Fator de Necrose Tumoral alfa/imunologia , Zoonoses/genética , Zoonoses/transmissão , Zoonoses/virologia
2.
Front Immunol ; 11: 939, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32574256

RESUMO

Zoonotic infections are an imminent threat to human health. Pangolins were recently identified as carriers and intermediate hosts of coronaviruses. Previous research has shown that infection with coronaviruses activates an innate immune response upon sensing of viral RNA by interferon-induced with helicase C domain 1 (IFIH1), also known as MDA5. Here, we performed a comparative genomics study of RNA sensor genes in three species of pangolins. DDX58/RIG-I, a sensor of cytoplasmic viral RNA and toll-like receptors (TLR) 3, 7, and 8, which bind RNA in endosomes, are conserved in pangolins. By contrast, IFIH1 a sensor of intracellular double-stranded RNA, has been inactivated by mutations in pangolins. Likewise, Z-DNA-binding protein (ZBP1), which senses both Z-DNA and Z-RNA, has been lost during the evolution of pangolins. These results suggest that the innate immune response to viruses differs significantly between pangolins and other mammals, including humans. We put forward the hypothesis that loss of IFIH1 and ZBP1 provided an evolutionary advantage by reducing inflammation-induced damage to host tissues and thereby contributed to a switch from resistance to tolerance of viral infections in pangolins.


Assuntos
Infecções por Coronavirus/imunologia , Eutérios/virologia , Imunidade Inata/genética , Helicase IFIH1 Induzida por Interferon/genética , Animais , Coronavirus/imunologia , Proteína DEAD-box 58/genética , Deleção de Genes , Humanos , Imunidade Inata/imunologia , RNA Viral/imunologia , Proteínas de Ligação a RNA/genética , Zoonoses/virologia
3.
Biomed Res Int ; 2020: 4389089, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32596311

RESUMO

The Coronavirus Disease 2019 (COVID-19) is a new viral infection caused by the severe acute respiratory coronavirus 2 (SARS-CoV-2). Genomic analyses have revealed that SARS-CoV-2 is related to Pangolin and Bat coronaviruses. In this report, a structural comparison between the Sars-CoV-2 Envelope and Membrane proteins from different human isolates with homologous proteins from closely related viruses is described. The analyses here reported show the high structural similarity of Envelope and Membrane proteins to the counterparts from Pangolin and Bat coronavirus isolates. However, the comparisons have also highlighted structural differences specific of Sars-CoV-2 proteins which may be correlated to the cross-species transmission and/or to the properties of the virus. Structural modelling has been applied to map the variant sites onto the predicted three-dimensional structure of the Envelope and Membrane proteins.


Assuntos
Betacoronavirus/química , Infecções por Coronavirus/virologia , Pneumonia Viral/virologia , Proteínas do Envelope Viral/química , Proteínas da Matriz Viral/química , Alphacoronavirus/química , Alphacoronavirus/classificação , Alphacoronavirus/genética , Sequência de Aminoácidos , Animais , Betacoronavirus/classificação , Betacoronavirus/genética , COVID-19 , Quirópteros/virologia , Coronaviridae/química , Coronaviridae/classificação , Coronaviridae/genética , Proteínas do Envelope de Coronavírus , Eutérios/virologia , Humanos , Modelos Moleculares , Pandemias , Conformação Proteica , SARS-CoV-2 , Homologia de Sequência de Aminoácidos , Especificidade da Espécie , Homologia Estrutural de Proteína , Proteínas do Envelope Viral/genética , Proteínas da Matriz Viral/genética
4.
Genomics ; 112(5): 3226-3237, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32540495

RESUMO

A global emergency due to the COVID-19 pandemic demands various studies related to genes and genomes of the SARS-CoV2. Among other important proteins, the role of accessory proteins are of immense importance in replication, regulation of infections of the coronavirus in the hosts. The largest accessory protein in the SARS-CoV2 genome is ORF3a which modulates the host response to the virus infection and consequently it plays an important role in pathogenesis. In this study, an attempt is made to decipher the conservation of nucleotides, dimers, codons and amino acids in the ORF3a genes across thirty-two genomes of Indian patients. ORF3a gene possesses single and double point mutations in Indian SARS-CoV2 genomes suggesting the change of SARS-CoV2's virulence property in Indian patients. We find that the parental origin of the ORF3a gene over the genomes of SARS-CoV2 and Pangolin-CoV is same from the phylogenetic analysis based on conservation of nucleotides and so on. This study highlights the accumulation of mutation on ORF3a in Indian SARS-CoV2 genomes which may provide the designing therapeutic approach against SARS-CoV2.


Assuntos
Betacoronavirus/genética , Sequência Conservada , Infecções por Coronavirus/virologia , Mutação , Pneumonia Viral/virologia , Proteínas Virais Reguladoras e Acessórias/genética , Animais , Sequência de Bases , Evolução Biológica , COVID-19 , Quirópteros/virologia , Infecções por Coronavirus/veterinária , Eutérios/virologia , Genoma Viral , Genômica , Humanos , Índia , Pandemias , Filogenia , SARS-CoV-2 , Proteínas Virais Reguladoras e Acessórias/química , Proteínas Estruturais Virais/química , Proteínas Estruturais Virais/genética , Proteínas Viroporinas
5.
Nature ; 583(7815): 286-289, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32380510

RESUMO

The current outbreak of coronavirus disease-2019 (COVID-19) poses unprecedented challenges to global health1. The new coronavirus responsible for this outbreak-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-shares high sequence identity to SARS-CoV and a bat coronavirus, RaTG132. Although bats may be the reservoir host for a variety of coronaviruses3,4, it remains unknown whether SARS-CoV-2 has additional host species. Here we show that a coronavirus, which we name pangolin-CoV, isolated from a Malayan pangolin has 100%, 98.6%, 97.8% and 90.7% amino acid identity with SARS-CoV-2 in the E, M, N and S proteins, respectively. In particular, the receptor-binding domain of the S protein of pangolin-CoV is almost identical to that of SARS-CoV-2, with one difference in a noncritical amino acid. Our comparative genomic analysis suggests that SARS-CoV-2 may have originated in the recombination of a virus similar to pangolin-CoV with one similar to RaTG13. Pangolin-CoV was detected in 17 out of the 25 Malayan pangolins that we analysed. Infected pangolins showed clinical signs and histological changes, and circulating antibodies against pangolin-CoV reacted with the S protein of SARS-CoV-2. The isolation of a coronavirus from pangolins that is closely related to SARS-CoV-2 suggests that these animals have the potential to act as an intermediate host of SARS-CoV-2. This newly identified coronavirus from pangolins-the most-trafficked mammal in the illegal wildlife trade-could represent a future threat to public health if wildlife trade is not effectively controlled.


Assuntos
Betacoronavirus/genética , Betacoronavirus/isolamento & purificação , Eutérios/virologia , Evolução Molecular , Genoma Viral/genética , Homologia de Sequência do Ácido Nucleico , Animais , Betacoronavirus/classificação , COVID-19 , China , Quirópteros/virologia , Chlorocebus aethiops , Proteínas do Envelope de Coronavírus , Infecções por Coronavirus/epidemiologia , Infecções por Coronavirus/patologia , Infecções por Coronavirus/transmissão , Infecções por Coronavirus/veterinária , Infecções por Coronavirus/virologia , Proteínas M de Coronavírus , Proteínas do Nucleocapsídeo de Coronavírus , Reservatórios de Doenças/virologia , Genômica , Especificidade de Hospedeiro , Humanos , Pulmão/patologia , Pulmão/virologia , Malásia , Proteínas do Nucleocapsídeo/genética , Pandemias , Fosfoproteínas , Filogenia , Pneumonia Viral/epidemiologia , Pneumonia Viral/transmissão , Pneumonia Viral/virologia , Reação em Cadeia da Polimerase , Recombinação Genética , SARS-CoV-2 , Alinhamento de Sequência , Análise de Sequência de RNA , Glicoproteína da Espícula de Coronavírus/genética , Células Vero , Proteínas do Envelope Viral/genética , Proteínas da Matriz Viral/genética , Zoonoses/transmissão , Zoonoses/virologia
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