In vitro replication of Macrobrachium rosenbergii nodavirus and extra small virus in C6/36 mosquito cell line

2007 ◽  
Vol 146 (1-2) ◽  
pp. 112-118 ◽  
Author(s):  
R. Sudhakaran ◽  
V. Parameswaran ◽  
A.S. Sahul Hameed
2021 ◽  
Author(s):  
S. Santhosh Kumar ◽  
S. Sivakumar ◽  
S. Abdul Majeed ◽  
S. Vimal ◽  
G. Taju ◽  
...  

2011 ◽  
Vol 34 (10) ◽  
pp. 805-810 ◽  
Author(s):  
N Arunrut ◽  
J Phromjai ◽  
W Gangnonngiw ◽  
N Kanthong ◽  
S Sriurairatana ◽  
...  

1984 ◽  
Vol 39 (9-10) ◽  
pp. 993-1002 ◽  
Author(s):  
Herbert G. Miltenburger ◽  
Werner L. Naser ◽  
Jeanne P. Harvey ◽  
Jürg Huber ◽  
Alois M. Huger

Abstract We established more than 200 primary cell lines of Cydia pomonella (codling moth). 81 of them were selected and screened for replication of two baculoviruses (from two different subgroups): the Choristoneura murinana NPV and the Cydia pomonella GV. Although all these cell lines had been derived from the same insect species, they varied largely in their response to challenge with the NPV. Most of them showed CPE or produced different amounts of poly-hedra. Interestingly, we also found a few cell lines that were permissive for GV replication. To our knowledge this is the first time that GV replication in cell lines has been obtained. Our results show that cell line properties are most important for baculovirus in vitro replication.


Author(s):  
M.G.R. Varma ◽  
Mary Pudney ◽  
C.J. Leake ◽  
Christine Wallace

PLoS ONE ◽  
2014 ◽  
Vol 9 (4) ◽  
pp. e96107 ◽  
Author(s):  
Jaime G. Mayoral ◽  
Kayvan Etebari ◽  
Mazhar Hussain ◽  
Alexander A. Khromykh ◽  
Sassan Asgari

2007 ◽  
Vol 77 (2) ◽  
pp. 283-290 ◽  
Author(s):  
Juan Salas-Benito ◽  
Jorge Reyes-Del Valle ◽  
Ivonne Ceballos-Olvera ◽  
Rosa M. del Angel ◽  
Mariana Salas-Benito ◽  
...  

Author(s):  
Mary Pudney ◽  
Z. Marhoul ◽  
M.G.R. Varma ◽  
C.J. Leake

2006 ◽  
Vol 72 (2) ◽  
pp. 1705-1707 ◽  
Author(s):  
Maurício C. Horta ◽  
Marcelo B. Labruna ◽  
Edison L. Durigon ◽  
Teresinha T. S. Schumaker

ABSTRACT We report the isolation and establishment of Rickettsia felis in the C6/36 cell line. Rickettsial growth was intense, always with 90 to 100% of cells being infected after few weeks. The rickettsial isolate was confirmed by testing infected cells by PCR and sequencing fragments of three major Rickettsia genes (gltA, ompB, and the 17-kDa protein gene).


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