Long-term persistence of neutralising antibodies against bluetongue virus serotype 8 in naturally infected cattle

Vaccine ◽  
2012 ◽  
Vol 30 (50) ◽  
pp. 7142-7143 ◽  
Author(s):  
Michael Eschbaumer ◽  
Josef Eschweiler ◽  
Bernd Hoffmann
2013 ◽  
Vol 166 (1-2) ◽  
pp. 165-173 ◽  
Author(s):  
Andrea Vögtlin ◽  
Martin A. Hofmann ◽  
Christoph Nenniger ◽  
Sandra Renzullo ◽  
Adolf Steinrigl ◽  
...  

1991 ◽  
Vol 180 (2) ◽  
pp. 994-1001 ◽  
Author(s):  
Xiao-Song He ◽  
Lin-Fa Wang ◽  
Roy H. Doi ◽  
Maurecio Maia ◽  
Bennie I. Osburn ◽  
...  

2012 ◽  
Vol 24 (3) ◽  
pp. 469-478 ◽  
Author(s):  
Piet A. van Rijn ◽  
René G. Heutink ◽  
Jan Boonstra ◽  
Hans A. Kramps ◽  
René G. P. van Gennip

Vaccine ◽  
2014 ◽  
Vol 32 (49) ◽  
pp. 6614-6621 ◽  
Author(s):  
Jenna Anderson ◽  
Sara Hägglund ◽  
Emmanuel Bréard ◽  
Mickaël Riou ◽  
Siamak Zohari ◽  
...  

2008 ◽  
Vol 14 (9) ◽  
pp. 1421-1423 ◽  
Author(s):  
Bernd Hoffmann ◽  
Michael Saßerath ◽  
Sabine Thalheim ◽  
Claudia Bunzenthal ◽  
Günter Strebelow ◽  
...  

2011 ◽  
Vol 101 (1-2) ◽  
pp. 42-50 ◽  
Author(s):  
Simon Nusinovici ◽  
Henri Seegers ◽  
Alain Joly ◽  
François Beaudeau ◽  
Christine Fourichon

2017 ◽  
Vol 65 (2) ◽  
pp. e243-e250 ◽  
Author(s):  
C. Schulz ◽  
C. Sailleau ◽  
E. Bréard ◽  
J. Flannery ◽  
C. Viarouge ◽  
...  

2015 ◽  
Vol 27 (4) ◽  
pp. 442-448 ◽  
Author(s):  
Natasha N. Gaudreault ◽  
Dane C. Jasperson ◽  
Edward J. Dubovi ◽  
Donna J. Johnson ◽  
Eileen N. Ostlund ◽  
...  

Bluetongue virus (BTV) is a vector-transmitted pathogen that typically infects and causes disease in domestic and wild ruminants. BTV is also known to infect domestic canines as discovered when dogs were vaccinated with a BTV-contaminated vaccine. Canine BTV infections have been documented through serological surveys, and natural infection by the Culicoides vector has been suggested. The report of isolation of BTV serotype 11 (BTV-11) from 2 separate domestic canine abortion cases in the states of Texas in 2011 and Kansas in 2012, were apparently unrelated to BTV-contaminated vaccination or consumption of BTV-contaminated raw meat as had been previously speculated. To elucidate the origin and relationship of these 2 domestic canine BTV-11 isolates, whole genome sequencing was performed. Six additional BTV-11 field isolates from Texas, Florida, and Washington, submitted for diagnostic investigation during 2011 and 2013, were also fully sequenced and analyzed. The phylogenetic analysis indicates that the BTV-11 domestic canine isolates are virtually identical, and both share high identity with 2 BTV-11 isolates identified from white-tailed deer in Texas in 2011. The results of the current study further support the hypothesis that a BTV-11 strain circulating in the Midwestern states could have been transmitted to the dogs by the infected Culicoides vector. Our study also expands the short list of available BTV-11 sequences, which may aid BTV surveillance and epidemiology.


2021 ◽  
Vol 14 ◽  
Author(s):  
Emilie Audouard ◽  
Valentin Oger ◽  
Béatrix Meha ◽  
Nathalie Cartier ◽  
Caroline Sevin ◽  
...  

Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder characterized by accumulation of sulfatides in both glial cells and neurons. MLD results from an inherited deficiency of arylsulfatase A (ARSA) and myelin degeneration in the central and peripheral nervous systems. Currently, no effective treatment is available for the most frequent late infantile (LI) form of MLD after symptom onset. The LI form results in rapid neurological degradation and early death. ARSA enzyme must be rapidly and efficiently delivered to brain and spinal cord oligodendrocytes of patients with LI MLD in order to potentially stop the progression of the disease. We previously showed that brain gene therapy with adeno-associated virus serotype rh10 (AAVrh10) driving the expression of human ARSA cDNA alleviated most long-term disease manifestations in MLD mice but was not sufficient in MLD patient to improve disease progression. Herein, we evaluated the short-term effects of intravenous AAVPHP.eB delivery driving the expression of human ARSA cDNA under the control of the cytomegalovirus/b-actin hybrid (CAG) promoter in 6-month-old MLD mice that already show marked sulfatide accumulation and brain pathology. Within 3 months, a single intravenous injection of AAVPHP.eB-hARSA-HA resulted in correction of brain and spinal cord sulfatide storage, and improvement of astrogliosis and microgliosis in brain and spinal cord of treated animals. These results strongly support to consider the use of AAVPHP.eB-hARSA vector for intravenous gene therapy in symptomatic rapidly progressing forms of MLD.


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