Persistence of Respiratory Syncytial Virus Genome and Protein After Acute Bronchiolitis in Guinea Pigs

CHEST Journal ◽  
1994 ◽  
Vol 105 (6) ◽  
pp. 1848-1854 ◽  
Author(s):  
Richard G. Hegele ◽  
Shizu Hayashi ◽  
Andrew M. Bramley ◽  
James C. Hogg
2009 ◽  
Vol 16 (6) ◽  
pp. 816-823 ◽  
Author(s):  
Carolina Scagnolari ◽  
Fabio Midulla ◽  
Alessandra Pierangeli ◽  
Corrado Moretti ◽  
Enea Bonci ◽  
...  

ABSTRACT Given the critical role of pattern recognition receptors (PRRs) in acid nucleic recognition in the initiation of innate immunity and the orchestration of adaptive immunity, the aim of this study was to determine whether any heterogeneity of PRR expression in the airway tracts of infants with respiratory syncytial virus (RSV) infection might explain the broad clinical spectrum of RSV-associated bronchiolitis in infants. For this purpose, the levels of melanoma differentiation-associated protein-5 (MDA-5), retinoic acid inducible gene-1 (RIG-1), and Toll-like receptor 3 (TLR-3), TLR-7, TLR-8, and TLR-9 mRNAs were evaluated, using TaqMan quantitative reverse transcription-PCR, in cells from nasopharyngeal washes collected from 157 infants suffering from acute bronchiolitis whether or not they were associated with respiratory viruses. High interindividual variability was observed in both virus-positive and -negative infants; however, the relative gene expression levels of MDA-5, RIG-1, TLR-7, and TLR-8 were significantly higher in the virus-infected group, whereas the expression levels of TLR-3 and TLR-9 were not significantly different. The differences in the gene expression of MDA-5, RIG-1, TLR-7, and TLR-8 were more evident in infants with RSV infection than in those with bocavirus or rhinovirus infection. In RSV-infected infants, PRR-mRNA levels also were analyzed in relation to interferon protein levels, viral load, clinical severity, days of hospitalization, age, and body weight. A significant positive correlation was observed only between RSV viral load and RIG-1 mRNA levels. These findings provide the first direct evidence that, in infants with respiratory virus-associated bronchiolitis, especially RSV, there are substantial changes in PRR gene expression; this likely is an important determinant of the clinical outcome of bronchiolitis.


2004 ◽  
Vol 98 (9) ◽  
pp. 879-882 ◽  
Author(s):  
Nikolaos G Papadopoulos ◽  
Dimitrios Gourgiotis ◽  
Artem Javadyan ◽  
Apostolos Bossios ◽  
Konstantina Kallergi ◽  
...  

BMJ ◽  
1982 ◽  
Vol 284 (6322) ◽  
pp. 1070-1072 ◽  
Author(s):  
I Laing ◽  
F Reidel ◽  
P L Yap ◽  
H Simpson

1994 ◽  
Vol 36 (4) ◽  
pp. 371-374 ◽  
Author(s):  
MASAYUKI SAIJO ◽  
SATORU TAKAHASHI ◽  
MASAYO KOKUBO ◽  
TOMOYUKI SAINO ◽  
TAKUMA ISHII ◽  
...  

2006 ◽  
Vol 17 (1) ◽  
pp. 29-36 ◽  
Author(s):  
Yoko Nagayama ◽  
Toshikazu Tsubaki ◽  
Shigeru Nakayama ◽  
Kyoko Sawada ◽  
Kazuko Taguchi ◽  
...  

2006 ◽  
Vol 87 (7) ◽  
pp. 1805-1821 ◽  
Author(s):  
Vanessa M. Cowton ◽  
David R. McGivern ◽  
Rachel Fearns

Human respiratory syncytial virus (RSV) is the leading cause of paediatric respiratory disease and is the focus of antiviral- and vaccine-development programmes. These goals have been aided by an understanding of the virus genome architecture and the mechanisms by which it is expressed and replicated. RSV is a member of the order Mononegavirales and, as such, has a genome consisting of a single strand of negative-sense RNA. At first glance, transcription and genome replication appear straightforward, requiring self-contained promoter regions at the 3′ ends of the genome and antigenome RNAs, short cis-acting elements flanking each of the genes and one polymerase. However, from these minimal elements, the virus is able to generate an array of capped, methylated and polyadenylated mRNAs and encapsidated antigenome and genome RNAs, all in the appropriate ratios to facilitate virus replication. The apparent simplicity of genome expression and replication is a consequence of considerable complexity in the polymerase structure and its cognate cis-acting sequences; here, our understanding of mechanisms by which the RSV polymerase proteins interact with signals in the RNA template to produce different RNA products is reviewed.


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