scholarly journals Detection and genetic characterization of African swine fever virus (ASFV) in clinically infected pigs in two districts in South Kivu province, Democratic Republic Congo

Heliyon ◽  
2021 ◽  
Vol 7 (3) ◽  
pp. e06419
Author(s):  
Patrick N. Bisimwa ◽  
Lionel K. Ishara ◽  
Dieudonné S. Wasso ◽  
Fabrice Bantuzeko ◽  
Ronald Tonui ◽  
...  
2019 ◽  
Vol 57 (4) ◽  
pp. 316-324 ◽  
Author(s):  
Abel Wade ◽  
Jenna Elizabeth Achenbach ◽  
Carmina Gallardo ◽  
Tirumala Bharani K. Settypalli ◽  
Abdoulkadiri Souley ◽  
...  

2020 ◽  
Vol 285 ◽  
pp. 113946
Author(s):  
David A. Meekins ◽  
Jessie D. Trujillo ◽  
Natasha N. Gaudreault ◽  
Igor Morozov ◽  
Daniel Pérez-Núñez ◽  
...  

Author(s):  
Katherukamem Rajukumar ◽  
Dhanapal Senthilkumar ◽  
Govindarajulu Venkatesh ◽  
Fateh Singh ◽  
Vishnu P. Patil ◽  
...  

2019 ◽  
Vol 58 (1) ◽  
Author(s):  
Vivian K. O’Donnell ◽  
Frederic R. Grau ◽  
Gregory A. Mayr ◽  
Tracy L. Sturgill Samayoa ◽  
Kimberly A. Dodd ◽  
...  

ABSTRACT African swine fever virus (ASFV) is the causative agent of a severe and highly contagious viral disease of pigs that poses serious economic consequences to the swine industry due to the high mortality rate and impact on international trade. There is no effective vaccine to control African swine fever (ASF), and therefore, efficient disease control is dependent on early detection and diagnosis of ASFV. The large size of the ASFV genome (∼180 kb) has historically hindered efforts to rapidly obtain a full-genome sequence. Rapid acquisition of data is critical for characterization of the isolate and to support epidemiological efforts. Here, we investigated the capacity of the Oxford Nanopore MinION sequence sensing device to act as a rapid sequencing tool. When coupled with our novel companion software script, the African swine fever fast analysis sequencing tool (ASF-FAST), the analysis of output data was performed in real time. Complete ASFV genome sequences were generated from cell culture isolates and blood samples obtained from experimentally infected pigs. Removal of the host-methylated DNA from the extracted nucleic acid facilitated rapid ASFV sequence identification, with reads specific to ASFV detected within 6 min after the initiation of sequencing. Regardless of the starting material, sufficient sequence was available for complete genome resolution (up to 100%) within 10 min. Overall, this paper highlights the use of Nanopore sequencing technology in combination with the ASF-FAST software for the purpose of rapid and real-time resolution of the full ASFV genome from a diagnostic sample.


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