scholarly journals Secondary structure of the segment 5 genomic RNA of influenza A virus and its application for designing antisense oligonucleotides

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Paula Michalak ◽  
Marta Soszynska-Jozwiak ◽  
Ewa Biala ◽  
Walter N. Moss ◽  
Julita Kesy ◽  
...  
Pathogens ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. 925 ◽  
Author(s):  
Marta Szabat ◽  
Dagny Lorent ◽  
Tomasz Czapik ◽  
Maria Tomaszewska ◽  
Elzbieta Kierzek ◽  
...  

Influenza is an important research subject around the world because of its threat to humanity. Influenza A virus (IAV) causes seasonal epidemics and sporadic, but dangerous pandemics. A rapid antigen changes and recombination of the viral RNA genome contribute to the reduced effectiveness of vaccination and anti-influenza drugs. Hence, there is a necessity to develop new antiviral drugs and strategies to limit the influenza spread. IAV is a single-stranded negative sense RNA virus with a genome (viral RNA—vRNA) consisting of eight segments. Segments within influenza virion are assembled into viral ribonucleoprotein (vRNP) complexes that are independent transcription-replication units. Each step in the influenza life cycle is regulated by the RNA and is dependent on its interplay and dynamics. Therefore, viral RNA can be a proper target to design novel therapeutics. Here, we briefly described examples of anti-influenza strategies based on the antisense oligonucleotide (ASO), small interfering RNA (siRNA), microRNA (miRNA) and catalytic nucleic acids. In particular we focused on the vRNA structure-function relationship as well as presented the advantages of using secondary structure information in predicting therapeutic targets and the potential future of this field.


2016 ◽  
Vol 26 (5) ◽  
pp. 277-285 ◽  
Author(s):  
Elzbieta Lenartowicz ◽  
Aitor Nogales ◽  
Elzbieta Kierzek ◽  
Ryszard Kierzek ◽  
Luis Martínez-Sobrido ◽  
...  

1998 ◽  
Vol 76 ◽  
pp. 286
Author(s):  
Tadashi Mizuta ◽  
Masatoshi Fujiwara ◽  
Tomoyuki Yokota ◽  
Shiro Shigeta ◽  
Toshifumi Hatta ◽  
...  

2020 ◽  
Vol 14 (1) ◽  
pp. 157-161
Author(s):  
Jolyon K. Claridge ◽  
Faiz Mohd-Kipli ◽  
Andrei Florea ◽  
Thomas Gate ◽  
Jason R. Schnell

Vaccine ◽  
2012 ◽  
Vol 30 (51) ◽  
pp. 7359-7367 ◽  
Author(s):  
Emilie Fournier ◽  
Vincent Moules ◽  
Boris Essere ◽  
Jean-Christophe Paillart ◽  
Jean-Daniel Sirbat ◽  
...  

2021 ◽  
pp. 101245
Author(s):  
Marta Soszynska-Jozwiak ◽  
Maciej Pszczola ◽  
Julita Piasecka ◽  
Jake M. Peterson ◽  
Walter N. Moss ◽  
...  

2006 ◽  
Vol 80 (1) ◽  
pp. 252-261 ◽  
Author(s):  
John F. Regan ◽  
Yuying Liang ◽  
Tristram G. Parslow

ABSTRACT The RNA-dependent RNA polymerase of influenza A virus is composed of three subunits that together synthesize all viral mRNAs and also replicate the viral genomic RNA segments (vRNAs) through intermediates known as cRNAs. Here we describe functional characterization of 16 site-directed mutants of one polymerase subunit, termed PA. In accord with earlier studies, these mutants exhibited diverse, mainly quantitative impairments in expressing one or more classes of viral RNA, with associated infectivity defects of varying severity. One PA mutant, however, targeting residues 507 and 508, caused only modest perturbations of RNA expression yet completely eliminated the formation of plaque-forming virus. Polymerases incorporating this mutant, designated J10, proved capable of synthesizing translationally active mRNAs and of replicating diverse cRNA or vRNA templates at levels compatible with viral infectivity. Both the mutant protein and its RNA products were appropriately localized in the cytoplasm, where influenza virus assembly occurs. Nevertheless, J10 failed to generate infectious particles from cells in a plasmid-based influenza virus assembly assay, and hemagglutinating material from the supernatants of such cells contained little or no nuclease-resistant genomic RNA. These findings suggest that PA has a previously unrecognized role in assembly or release of influenza virus virions, perhaps influencing core structure or the packaging of vRNAs or other essential components into nascent influenza virus particles.


2004 ◽  
Vol 78 (12) ◽  
pp. 6263-6270 ◽  
Author(s):  
Mandy Crow ◽  
Tao Deng ◽  
Mark Addley ◽  
George G. Brownlee

ABSTRACT Replication of the influenza A virus virion RNA (vRNA) requires the synthesis of full-length cRNA, which in turn is used as a template for the synthesis of more vRNA. A “corkscrew” secondary-structure model of the cRNA promoter has been proposed recently. However the data in support of that model were indirect, since they were derived from measurement, by use of a chloramphenicol acetyltransferase (CAT) reporter in 293T cells, of mRNA levels from a modified cRNA promoter rather than the authentic cRNA promoter found in influenza A viruses. Here we measured steady-state cRNA and vRNA levels from a CAT reporter in 293T cells, directly measuring the replication of the authentic influenza A virus wild-type cRNA promoter. We found that (i) base pairing between the 5′ and 3′ ends and (ii) base pairing in the stems of both the 5′ and 3′ hairpin loops of the cRNA promoter were required for in vivo replication. Moreover, nucleotides in the tetraloop at positions 4, 5, and 7 and nucleotides forming the 2-9 base pair of the 3′ hairpin loop were crucial for promoter activity in vivo. However, the 3′ hairpin loop was not required for polymerase binding in vitro. Overall, our results suggest that the corkscrew secondary-structure model is required for authentic cRNA promoter activity in vivo, although the precise role of the 3′ hairpin loop remains unknown.


2016 ◽  
Vol 473 (23) ◽  
pp. 4327-4348 ◽  
Author(s):  
Agnieszka Ruszkowska ◽  
Elzbieta Lenartowicz ◽  
Walter N. Moss ◽  
Ryszard Kierzek ◽  
Elzbieta Kierzek

The influenza A virus (IAV) genome comprises eight negative-sense viral (v)RNA segments. The seventh segment of the genome encodes two essential viral proteins and is specifically packaged alongside the other seven vRNAs. To gain insights into the possible roles of RNA structure both within and without virions, a secondary structure model of a naked (protein-free) segment 7 vRNA (vRNA7) has been determined using chemical mapping and thermodynamic energy minimization. The proposed structure model was validated using microarray mapping, RNase H cleavage and comparative sequence analysis. Additionally, the detailed structures of three vRNA7 fragment constructs — comprising independently folded subdomains — were determined. Much of the proposed vRNA7 structure is preserved between IAV strains, suggesting their importance in the influenza replication cycle. Possible structure rearrangements, which allow or preclude long-range RNA interactions, are also proposed.


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