Id |
Subject |
Object |
Predicate |
Lexical cue |
T202 |
0-6 |
Sentence |
denotes |
3.2.6. |
T203 |
7-18 |
Sentence |
denotes |
South Korea |
T204 |
19-220 |
Sentence |
denotes |
The first active IAV infection in the Korean swine was identified in December 1998 when three H3N2 virus isolates were recovered from the swine experiencing an acute influenza-like respiratory disease. |
T205 |
221-395 |
Sentence |
denotes |
The close relatedness of these Korean swine H3N2 isolates with human-origin H3N2 viruses reported from Korea between 1987–1999 suggested the events of reverse zoonosis [127]. |
T206 |
396-615 |
Sentence |
denotes |
One unique H7N2 virus isolate was detected in swine which had seven gene segments originated from Hong Kong avian-origin H7N2 virus isolated in 1978 and the NS gene originated from Hong Kong H5N3 virus isolated in 1977. |
T207 |
616-703 |
Sentence |
denotes |
Additionally, four typical swine influenza H1N1 viruses were identified in swine [128]. |
T208 |
704-826 |
Sentence |
denotes |
Several H1N1, H1N2, and H3N2 viruses were detected in symptomatic South Korean swine after 2000 [129,130,131,132,133,134]. |
T209 |
827-918 |
Sentence |
denotes |
The IAV localization in the swine lung tissues was confirmed by immunohistochemistry [130]. |
T210 |
919-1115 |
Sentence |
denotes |
Total 35 avian-origin H5N2 viruses of Eurasian lineage were identified in swine in different South Korean provinces during 2004–2008 which suggested cross-species transmission of H5N2 virus [135]. |
T211 |
1116-1244 |
Sentence |
denotes |
Three H1N1 virus isolates closely related to US isolates of H1N1 were obtained from 45-day-old piglets in Korea in January 2005. |
T212 |
1245-1342 |
Sentence |
denotes |
The other swine farms in the proximity of this index farm were negative for the H1N1 virus [136]. |
T213 |
1343-1677 |
Sentence |
denotes |
Further, one H1N1, two H1N2, and one H3N2 subtypes of IAV identical to the American strains based on their HA and NA gene sequences were obtained from swine nasal swab, lung, and thoracic fluid samples during 2005–2006 which suggested that there was no probability of arising of these IAV strains in Korea through recombination [137]. |
T214 |
1678-1895 |
Sentence |
denotes |
Two novel isolates of swine H3N1 virus with high genomic similarity to each other were retrieved from two different swine farms in Korea during March–April 2006 which would be due to a common origin of these isolates. |
T215 |
1896-2012 |
Sentence |
denotes |
These viruses had human-like H3 gene while other gene segments originated from swine influenza viruses within Korea. |
T216 |
2013-2184 |
Sentence |
denotes |
High reactivity of the 52 swine sera samples to H3N1 virus antibodies suggested a previous exposure and probability of the swine to swine transmission of H3N1 virus [138]. |
T217 |
2185-2355 |
Sentence |
denotes |
The human to swine transmission of A(H1N1)pdm09 virus was reported in Chungbuk province where 42 A(H1N1)pdm09 virus isolates were recovered from swine lung tissues [139]. |
T218 |
2356-2476 |
Sentence |
denotes |
The reassortment between A(H1N1)pdm09 and swine H1N2 viruses emerged into a novel reassortant H1N2 virus in swine [140]. |
T219 |
2477-2639 |
Sentence |
denotes |
A triple-reassortant H3N2 virus was identified in swine during December 2011–May 2012 which indicated the IAV reassortment was taking place in Korean swine [141]. |
T220 |
2640-2821 |
Sentence |
denotes |
A swine fever eradication campaign identified nine A(H1N1)pdm09, two classical H1N1 and one H1N2 viruses in wild boars which were hunted and killed in South Korea during 2012 [142]. |
T221 |
2822-2936 |
Sentence |
denotes |
More recently, a complete genome sequence of H1N1 virus was reported from a domestic swine in Korea in 2016 [143]. |