2021
DOI: 10.1016/j.virol.2020.11.006
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Characterization of contemporary 2010.1 H3N2 swine influenza A viruses circulating in United States pigs

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Cited by 19 publications
(23 citation statements)
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“…In addition, the 2WF10:6pH1N1 virus was also able to transmit by airborne route, although with delayed replication kinetics, whereas no evidence of airborne transmission with 1WF10:7pH1N1 was observed, suggesting that compatibility and balance between the HA and NA is also important (Figure 2B). It is tempting to speculate that the pH1N1 backbone is more flexible to accept reassortment with diverse surface genes and does provide a replicative advantage in mammals, as has been observed in multiple examples of reassortant H1N1 and H3N2 viruses in swine [127][128][129][130]. Sequencing information showed a S261N mutation in PB1 and V104A in HA in the viruses isolated from respiratory contact animals (Table 1); however, the role of those positions in airborne transmission remains unknown [88].…”
Section: Experimental Infections/transmission Of H9n2 Iav In Mammalian Modelsmentioning
confidence: 94%
“…In addition, the 2WF10:6pH1N1 virus was also able to transmit by airborne route, although with delayed replication kinetics, whereas no evidence of airborne transmission with 1WF10:7pH1N1 was observed, suggesting that compatibility and balance between the HA and NA is also important (Figure 2B). It is tempting to speculate that the pH1N1 backbone is more flexible to accept reassortment with diverse surface genes and does provide a replicative advantage in mammals, as has been observed in multiple examples of reassortant H1N1 and H3N2 viruses in swine [127][128][129][130]. Sequencing information showed a S261N mutation in PB1 and V104A in HA in the viruses isolated from respiratory contact animals (Table 1); however, the role of those positions in airborne transmission remains unknown [88].…”
Section: Experimental Infections/transmission Of H9n2 Iav In Mammalian Modelsmentioning
confidence: 94%
“…In addition, the 2WF10:6pH1N1 virus was also able to transmit by airborne route, although with delayed replication kinetics, whereas no evidence of airborne transmission with 1WF10:7pH1N1 was observed, suggesting that compatibility and balance between the HA and NA is also important (Fig 2B). It is tempting to speculate that the pH1N1 backbone is more flexible to accept reassortment with diverse surface genes and does provide a replicative advantage in mammals, as has been observed in multiple examples of reassortant H1N1 and H3N2 viruses in swine (Everett et al 2020, Powell et al 2021, Ryt-Hansen et al 2020, Zell et al 2020). Sequencing information showed a S261N mutation in PB1 and V104A in HA in the viruses isolated from respiratory contact animals (Table 1); however, the role of those positions in airborne transmission remains unknown (Kimble et al 2011).…”
Section: Experimental Infections/transmission Of H9n2 Iav In Mammalian Modelsmentioning
confidence: 96%
“…Though there is little experimental work in swine IAV (but see examples in human IAV White and Lowen, 2018; White et al ., 2019 and review by Lowen, 2017), there is observational evidence that certain gene combinations provide fitness advantages and disadvantages. This is evident from the presence of extensive reassortment of IAV in swine (Gao et al ., 2017; Rajão et al ., 2017; Diaz et al ., 2017; Henritzi et al ., 2020) with more than 100 distinct genome constellations, but only a small fraction of these constellations are frequently detected, suggesting that the majority of these reassorted viruses may have little epidemiological relevance (Powell et al ., 2020).…”
Section: Empirical Studymentioning
confidence: 99%
“…In this empirical example, we focus on an H3.2010.1 swine IAV lineage derived from a human-seasonal H3 introduction to swine (Anderson et al ., 2020; Rajão et al ., 2015). Generally, human IAV infection in swine results in low replication and rare pig-to-pig transmission, but some human-origin IAV become endemic, and this is typically associated with genetic differences from the precursor strain (Lewis et al ., 2016; Rajão et al ., 2018; Powell et al ., 2020), or reassortment with endemic host-adapted viruses. The H3.2010.1 lineage follows this paradigm, and assessing reassortment in this lineage allows us to generate testable hypotheses on how expansion in the genomic diversity of IAV in swine populations may facilitate IAV capable of spillover from swine to humans.…”
Section: Empirical Studymentioning
confidence: 99%
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