Topley &Amp; Wilson's Microbiology and Microbial Infections 2010
DOI: 10.1002/9780470688618.taw0243
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Pneumovirus and Metapneumovirus: Respiratory Syncytial Virus and Human Metapneumovirus

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Cited by 3 publications
(3 citation statements)
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“…The RSV genome encodes a total of 11 proteins, many which are under investigation as possible drug targets (Figure 1; Table 1)[21-23]. There are two major antigenic subgroups, A and B, which are defined by different envelope proteins and co-circulate each year.…”
Section: Viral Drug Targetsmentioning
confidence: 99%
“…The RSV genome encodes a total of 11 proteins, many which are under investigation as possible drug targets (Figure 1; Table 1)[21-23]. There are two major antigenic subgroups, A and B, which are defined by different envelope proteins and co-circulate each year.…”
Section: Viral Drug Targetsmentioning
confidence: 99%
“…RSV, classified in the Pneumovirus genus of the Paramyxoviridae family is an enveloped virus with a negative‐sense single‐stranded RNA genome that encodes 11 proteins [Tripp, ]. Based on reaction with monoclonal antibodies against the G and F glycoproteins and genetic differences, RSV has been classified into two major groups A and B [Anderson et al, ; Mufson et al, ; Cane, ].…”
Section: Introductionmentioning
confidence: 99%
“…Respiratory syncytial virus (RSV), a member of the Pneumovirus genus within the family Paramyxoviridae , is the single most important viral respiratory pathogen infecting infants and young children worldwide, as well as an important cause of respiratory tract illness in the elderly, transplant patients, and immune suppressed [ 12 , 22 , 33 , 48 , 51 ]. The RSV genome (15 kb) is single-stranded, negative-sense RNA that contains 10 transcription units which are sequentially transcribed to produce 11 proteins in the following order: NS1, NS2, N, P, M, SH, G, F, M2-1, M2-2, and L [ 52 ]. The NS1 and NS2 non-structural proteins are not expressed on the virion but are two of the most abundantly expressed RNAs in RSV-infected cells due to their promoter-proximal location [ 5 , 11 , 15 ] These accessory proteins have been shown to act cooperatively to suppress the activation and nuclear translocation of the IFN-regulatory factor IRF-3 [ 4 , 47 ], and inhibit the type I IFN signaling cascade by mediating proteosome degradation of signal transducer and activator of transcription 2 (STAT2) with Elongin-Cullin E3 ligase [ 10 , 29 ].…”
Section: Introductionmentioning
confidence: 99%