Expression of an RNase P Ribozyme Against the mRNA Encoding Human Cytomegalovirus Protease Inhibits Viral Capsid Protein Processing and Growth

2003 ◽  
Vol 328 (5) ◽  
pp. 1123-1135 ◽  
Author(s):  
Phong Trang ◽  
Kihoon Kim ◽  
Jiaming Zhu ◽  
Fenyong Liu
2011 ◽  
Vol 86 (6) ◽  
pp. 3318-3326 ◽  
Author(s):  
R. D. Cadena-Nava ◽  
M. Comas-Garcia ◽  
R. F. Garmann ◽  
A. L. N. Rao ◽  
C. M. Knobler ◽  
...  

2006 ◽  
Vol 94 (6) ◽  
pp. 1129-1137 ◽  
Author(s):  
Maggie Y.T. Lee ◽  
Yuanxiang Zhou ◽  
Raymond W.M. Lung ◽  
Mee-Len Chye ◽  
Wing-Kin Yip ◽  
...  

1973 ◽  
Vol 19 (2) ◽  
pp. 299-301 ◽  
Author(s):  
Lorne A. Babiuk ◽  
James B. Hudson

Mouse cells which normally permitted polyoma virus development, and hamster cells which were non-permissive (BHK-21 and polyoma virus-transformed hamster cells), were subjected to cell-fusion techniques, and the resultant cultures were examined for the capacity of heterokaryons to yield polyoma viral capsid protein. Little or no capsid protein was synthesized in the heterokaryons, although individual mouse cells and mouse homokaryons gave normal yields. Furthermore, the hamster cell inhibitory effect manifested itself even when the mouse cells had been infected with the virus before cell fusion.


2012 ◽  
Vol 9 (1) ◽  
pp. 26 ◽  
Author(s):  
Fan Gao ◽  
Yi-Ping Wang ◽  
Qun-Ying Mao ◽  
Xin Yao ◽  
Shuang Liu ◽  
...  

2012 ◽  
Vol 9 (1) ◽  
pp. 155 ◽  
Author(s):  
Wei-Choong Ch’ng ◽  
Eric J Stanbridge ◽  
Kum-Thong Wong ◽  
Kien-Chai Ong ◽  
Khatijah Yusoff ◽  
...  

2001 ◽  
Vol 82 (6) ◽  
pp. 1517-1527 ◽  
Author(s):  
Ewa Sadowy ◽  
Marek Juszczuk ◽  
Chantal David ◽  
Bruno Gronenborn ◽  
M. Danuta Hulanicka

cDNA expression vectors of Potato leafroll virus (PLRV) were used to analyse specific mutations in the proteinase and replicase domains of the proteins encoded by ORF1 and ORF2. Agrobacterium-mediated DNA transfer was used to introduce a PLRV RNA expression unit, controlled by the 35S promoter of Cauliflower mosaic virus, into potato leaf cells. Expression of unmodified PLRV cDNA led to the replication of viral genomic and subgenomic RNAs and accumulation of the viral capsid protein, whereas alteration of amino acids GDD513–515 of the replicase to VHD abolished PLRV replication. Mutations in the presumed H-D-S catalytic triad of the viral proteinase abolished the formation of viral genomic and subgenomic RNAs as well as synthesis of the viral capsid protein. Co-agroinoculation of the GDD mutant along with any of the proteinase mutants restored virus replication in leaf discs, showing that these mutants are able to complement each other. Moreover, mutation of the postulated serine residue of the catalytic triad of the proteinase altered the pattern of proteins synthesized in vitro in comparison to wild-type, further supporting the relevance of the H-D-S motif.


mSphere ◽  
2017 ◽  
Vol 2 (3) ◽  
Author(s):  
Nichole E. Brinkman ◽  
G. Shay Fout ◽  
Scott P. Keely

ABSTRACT Enterovirus infections are often not tracked or reported to health officials. This makes it hard to know how many people in a community are infected with these viruses at any given time. Here, we explored enterovirus in municipal wastewater to look at this issue. We show that enteroviruses are present year-round in municipal wastewater at levels of up to 800,000 genomic copies per liter. We estimate that, on average, 2.8% of the people contributing to the wastewater shed enterovirus daily. Sequence analysis of the viral capsid protein 4 gene shows that 8 enterovirus types are key drivers of seasonal trends. Populations of Enterovirus A members peak in the spring, while Enterovirus B types are most prevalent during the summer and fall months and Enterovirus C members influence the winter months. Enterovirus D was observed sporadically and did not influence seasonal trends. Enteroviruses are RNA viruses that are responsible for both mild gastroenteritis and mild respiratory illnesses as well as debilitating diseases such as meningitis and myocarditis. The disease burden of enteroviruses in the United States is difficult to assess because most infections are not recorded. Since infected individuals shed enterovirus in feces and urine, surveillance of municipal wastewater can reveal the diversity of enteroviruses circulating in human populations. Therefore, monthly municipal wastewater samples were collected for 1 year and enteroviruses were quantified by reverse transcriptase quantitative PCR and identified by next-generation, high-throughput sequencing. Enterovirus concentrations ranged from 3.8 to 5.9 log10 equivalent copies/liter in monthly samples. From the mean monthly concentration, it can be estimated that 2.8% of the contributing population was shedding enterovirus daily. Sequence analysis showed that Enterovirus A and Enterovirus B alternate in predominance, with Enterovirus B comprising over 80% of the reads during the summer and fall months and Enterovirus A accounting for >45% of the reads in spring. Enterovirus C was observed throughout the year, while Enterovirus D was present intermittently. Principal-component analysis further supported the date corresponding to enterovirus seasonal trends as CVA6 (Enterovirus A) was predominant in the spring months; CVB3, CVB5, and E9 (Enterovirus B) were predominant in the summer and fall months; and CVA1, CVA19, and CVA22 (Enterovirus C) and EV97 (Enterovirus B) were predominant in winter. Rhinoviruses were also observed. Wastewater monitoring of human enterovirus provided improved insight into the seasonal patterns of enteroviruses circulating in communities and can contribute to understanding of enterovirus disease burden. IMPORTANCE Enterovirus infections are often not tracked or reported to health officials. This makes it hard to know how many people in a community are infected with these viruses at any given time. Here, we explored enterovirus in municipal wastewater to look at this issue. We show that enteroviruses are present year-round in municipal wastewater at levels of up to 800,000 genomic copies per liter. We estimate that, on average, 2.8% of the people contributing to the wastewater shed enterovirus daily. Sequence analysis of the viral capsid protein 4 gene shows that 8 enterovirus types are key drivers of seasonal trends. Populations of Enterovirus A members peak in the spring, while Enterovirus B types are most prevalent during the summer and fall months and Enterovirus C members influence the winter months. Enterovirus D was observed sporadically and did not influence seasonal trends.


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