Influenza B Virus in Seals

National Influenza Center, Department of Virology, Erasmus University, Doctor Molewaterplein 50, 3015 GE Rotterdam, Netherlands.
Science (Impact Factor: 33.61). 06/2000; 288(5468):1051-3. DOI: 10.1126/science.288.5468.1051
Source: PubMed


Influenza B virus is a human pathogen whose origin and possible reservoir in nature are not known. An influenza B virus was
isolated from a naturally infected harbor seal (Phoca vitulina) and was found to be infectious to seal kidney cells in vitro. Sequence analyses and serology indicated that influenza virus
B/Seal/Netherlands/1/99 is closely related to strains that circulated in humans 4 to 5 years earlier. Retrospective analyses
of sera collected from 971 seals showed a prevalence of antibodies to influenza B virus in 2% of the animals after 1995 and
in none before 1995. This animal reservoir, harboring influenza B viruses that have circulated in the past, may pose a direct
threat to humans.

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    • "IBV epidemics tend to be less severe than H3N2 IAVs but more severe than H1N1 AIVs in adults and the elderly (Ohmit and Monto, 1995; Olson et al., 2007; Thompson et al., 2003; Van Voris et al., 1982) However, IBV infections are associated with excess morbidity and mortality in the pediatric population (Belshe, 2010; Hite et al., 2007; Li et al., 2008; Olson et al., 2007). Contrary to IAVs, which has a broad host reservoir in many avian and mammalian species, IBVs are mainly restricted to humans (Wright et al., 2007), although occasional infections of seals have been documented (Osterhaus et al., 2000). Vaccines and antivirals are available to combat influenza viruses (Baker et al., 2015b; Burnham et al., 2013; Jackson et al., 2011a; Krammer et al., 2015; Nguyen et al., 2010; Seibert et al., 2010). "
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    ABSTRACT: Influenza B viruses (IBVs) cause annual outbreaks of respiratory illness in humans and are increasingly recognized as a major cause of influenza-associated morbidity and mortality. Studying influenza viruses requires the use of secondary methodologies to identify virus-infected cells. To this end, replication-competent influenza A viruses (IAVs) expressing easily traceable fluorescent proteins have been recently developed. In contrast, similar approaches for IBV are mostly lacking. In this report, we describe the generation and characterization of replication-competent influenza B/Brisbane/60/2008 viruses expressing fluorescent mCherry or GFP fused to the C-terminal of the viral non-structural 1 (NS1) protein. Fluorescent-expressing IBVs display similar growth kinetics and plaque phenotype to wild-type IBV, while fluorescent protein expression allows for the easy identification of virus-infected cells. Without the need of secondary approaches to monitor viral infection, fluorescent-expressing IBVs represent an ideal approach to study the biology of IBV and an excellent platform for the rapid identification and characterization of antiviral therapeutics or neutralizing antibodies using high-throughput screening approaches. Lastly, fluorescent-expressing IBVs can be combined with the recently described reporter-expressing IAVs for the identification of novel therapeutics to combat these two important human respiratory pathogens.
    No preview · Article · Nov 2015 · Virus Research
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    • "In fact, in addition to HPV-11, Bordetella pertussis and measles viruses have been reported to be human-specific pathogens [39,40] (Table 2). Moreover, the IBV is restricted to humans with the exception of an infection identified in seals stranded on the Dutch coast [41]. At present, however, the repertoire of peptides bound by each allele is limited in the experimental data. "
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    ABSTRACT: Background Diversity among human leukocyte antigen (HLA) molecules has been maintained by host-pathogen coevolution over a long period of time. Reflecting this diversity, the HLA loci are the most polymorphic in the human genome. One characteristic of HLA diversity is long-term persistence of allelic lineages, which causes trans-species polymorphisms to be shared among closely related species. Modern humans have disseminated across the world after their exodus from Africa, while chimpanzees have remained in Africa since the speciation event between humans and chimpanzees. It is thought that modern humans have recently acquired resistance to novel pathogens outside Africa. In the present study, we investigated HLA alleles that could contribute to this local adaptation in humans and also studied the contribution of natural selection to human evolution by using molecular data. Results Phylogenetic analysis of HLA-DRB1 genes identified two major groups, HLA Groups A and B. Group A formed a monophyletic clade distinct from DRB1 alleles in other Catarrhini, suggesting that Group A is a human-specific allelic group. Our estimates of divergence time suggested that seven HLA-DRB1 Group A allelic lineages in humans have been maintained since before the speciation event between humans and chimpanzees, while chimpanzees possess only one DRB1 allelic lineage (Patr-DRB1*03), which is a sister group to Group A. Experimental data showed that some Group A alleles bound to peptides derived from human-specific pathogens. Of the Group A alleles, three exist at high frequencies in several local populations outside Africa. Conclusions HLA Group A alleles are likely to have been retained in human lineages for a long period of time and have not expanded since the divergence of humans and chimpanzees. On the other hand, most orthologs of HLA Group A alleles may have been lost in the chimpanzee due to differences in selective pressures. The presence of alleles with high frequency outside of Africa suggests these HLA molecules result from the local adaptations of humans. Our study helps elucidate the mechanism by which the human adaptive immune system has coevolved with pathogens over a long period of time.
    Full-text · Article · Jun 2014 · Journal of PHYSIOLOGICAL ANTHROPOLOGY
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    • "reservoir and co - circulation of different multiple lineages in single population increase the chances for reassortment and generating new viruses [ Xu et al . , 2004 ] . In addition , other epidemiological factors , such as multitype interference and accumula - tion of permissive reservoirs may control influenza B virus infection and epidemics [ Osterhaus et al . , 2000 ; Yang et al . , 2012 ] ."
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    ABSTRACT: Influenza viruses are known as continuing threats to human public health every year worldwide. Evolutionary dynamics of influenza B viruses in humans are in a unique progression having two lineages; B/Yam and B/Vic-like viruses, which are circulating simultaneously worldwide. There is a considerable lack of data on influenza B viruses circulating in Saudi Arabia. During the winter-spring season of 2010-2011, 80 nasopharyngeal aspirates were collected from hospitalized patients with flu-like symptoms in Riyadh. Screening of samples by one-step RT-PCR identified three (3.8%) influenza B viruses. Sequencing of hemagglutinin (HA) and neuraminidase (NA) genes was performed to analyze influenza B viruses circulating in Riyadh as compared to the globally circulating strains. Several common and six unique amino acid substitutions were observed for both HA and NA genes of influenza B Saudi strains. Three unique substitutions (T182A, D196N, and K254R) were identified in HA gene of the B/Yam-like Riyadh strains. In NA gene, a unique common substitution (D53G) was found in all Riyadh strains, while two unique substitutions (L38P, G233R) were recognized only in B/Vic-like Riyadh strains. Riyadh strains were also found to contain N-glycosylation site in HA gene of both B/Vic and B/Yam lineages at positions 197-199 (NET) and 196-198 (NNK/DNK), respectively. The significance of these mutations on the antigenicity of both lineages is discussed herein. The unique changes observed in HA and NA genes of influenza B Riyadh strains support strongly the need for continuous surveillance and monitoring of new evolving strains that might pose threat to the Saudi community. J. Med. Virol. © 2013 Wiley Periodicals, Inc.
    Full-text · Article · Jun 2014 · Journal of Medical Virology
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