1984
DOI: 10.1099/0022-1317-65-1-165
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Studies of a Recombinant which Inherited the Haemagglutinin from the Human Influenza Virus A/Hong Kong/1/68 (H3N2) and Other Genes from Influenza Virus A/duck/Ukraine/1/63 (H3N8)

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Cited by 4 publications
(4 citation statements)
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“…b 3H-labelled RNA of A/Duck/Hoshimin/014/78 (1 and 6), reassortants R 1 (2) (2 and 9), R 2 (6) 3 (3 and 8) and R (8) (4 and 7), and A/USSR/90/ 77 (5 and 10) was annealed with an excess of virion RNA of A/USSR/90/77 (1, 2, 3, 4, and 5) or A/Duck/Hoshimin/014/78 (6, 7, 8, 9, and 10). Triangles indicate the position of homoduplexes in reassortant RNA samples (1,3,5,7,9, and 11) and 48 hours (2,4,6,8, and 10) post infection thesis can be revealed no sooner than the majority (or, at least, a large part) of the cell population is infected. At 31 °C this condition was achieved by 48 h post infection with A/USSR/90/77, R 3 or R (8); in the cells infected with R 1 (2) or R 2 (6) 3, only the synthesis of cell proteins was registered (Fig.…”
Section: Resultsmentioning
confidence: 97%
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“…b 3H-labelled RNA of A/Duck/Hoshimin/014/78 (1 and 6), reassortants R 1 (2) (2 and 9), R 2 (6) 3 (3 and 8) and R (8) (4 and 7), and A/USSR/90/ 77 (5 and 10) was annealed with an excess of virion RNA of A/USSR/90/77 (1, 2, 3, 4, and 5) or A/Duck/Hoshimin/014/78 (6, 7, 8, 9, and 10). Triangles indicate the position of homoduplexes in reassortant RNA samples (1,3,5,7,9, and 11) and 48 hours (2,4,6,8, and 10) post infection thesis can be revealed no sooner than the majority (or, at least, a large part) of the cell population is infected. At 31 °C this condition was achieved by 48 h post infection with A/USSR/90/77, R 3 or R (8); in the cells infected with R 1 (2) or R 2 (6) 3, only the synthesis of cell proteins was registered (Fig.…”
Section: Resultsmentioning
confidence: 97%
“…The properties of the hemagglutinin also seem to be of importance. The hemagglutinins of avian and human viruses recognize different kinds of cell receptors [1,11]; the substitution of HA gene suppresses the ability of avian viruses to replicate in the avian host [3,9].…”
Section: Discussionmentioning
confidence: 99%
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“…In these studies, adapted virus often showed a change in receptor-binding preference and a reduction in NA stalk length, consistent with what we observed in Quail/CA12. The higher binding preference for α2,6-linked sialic acids in the HA of Quail/CA12 likely altered its ability to infect duck-origin cells, and enhanced its ability to infect chickens [20, 27, 28]. Other molecular changes such as the K151T mutation (which results in the introduction of a putative glycosylation sequon in the 130-loop) [29, 30], and the DG156/157GE and A158E on the top and the edge of the globular head, respectively [24, 25] were also observed in laboratory -adaptation experiments and could have occurred to compensate for the reduced NA activity due to a shorter stalk [29–31].…”
Section: Discussionmentioning
confidence: 99%