Prechtel, Alexander T., Turza, Nadine M., Kobelt, Dieter J., Eisemann, Jutta I., Coffin, Robert S., McGrath, Yvonne, Hacker, Christine, Ju, Xinsheng et al.

p. 1645 https://doi.org/10.1099/vir.0.80852-0

Koi herpesvirus represents a third cyprinid herpesvirus (CyHV-3) in the family Herpesviridae

Waltzek, Thomas B., Kelley, Garry O., Stone, David M., Way, Keith, Hanson, Larry, Fukuda, Hideo, Hirono, Ikuo, Aoki, Takashi et al.

p. 1659 https://doi.org/10.1099/vir.0.80982-0

Susceptibility of B lymphocytes to adenovirus type 5 infection is dependent upon both coxsackie-adenovirus receptor and {alpha}v{beta}5 integrin expression

Richardson, Ciaran, Brennan, Paul, Powell, Martin, Prince, Stuart, Chen, Yun-Hsiang, Spiller, O. Brad, Rowe, Martin

p. 1669 https://doi.org/10.1099/vir.0.80806-0

Complete genome sequence of simian adenovirus 1: an Old World monkey adenovirus with two fiber genes

Kovacs, Gabor M., Harrach, Balazs, Zakhartchouk, Alexander N., Davison, Andrew J.

p. 1681 https://doi.org/10.1099/vir.0.80757-0

A quasi-monoclonal anti-HBs response can lead to immune escape of 'wild-type' hepatitis B virus

Margeridon, Severine, Lachaux, Alain, Trepo, Christian, Zoulim, Fabien, Kay, Alan

p. 1687 https://doi.org/10.1099/vir.0.80810-0

Human papillomavirus, viral load and proliferation rate in recurrent respiratory papillomatosis in response to alpha interferon treatment

Szeps, Michael, Dahlgren, Liselotte, Aaltonen, Leena-Maija, Ohd, John, Kanter-Lewenshon, Lena, Dahlstrand, Hanna, Munck-Wikland, Eva, Grander, Dan et al.

p. 1695 https://doi.org/10.1099/vir.0.80849-0

Prevalence and stability of human serum antibodies to simian virus 40 VP1 virus-like particles

Lundstig, Annika, Eliasson, Linda, Lehtinen, Matti, Sasnauskas, Kestutis, Koskela, Pentti, Dillner, Joakim

p. 1703 https://doi.org/10.1099/vir.0.80783-0

Chimeric monoclonal antibodies to hypervariable region 1 of hepatitis C virus

Li, Chengyao, Allain, Jean-Pierre

p. 1709 https://doi.org/10.1099/vir.0.80912-0

Continuous release of hepatitis C virus (HCV) by peripheral blood mononuclear cells and B-lymphoblastoid cell-line cultures derived from HCV-infected patients

Bare, Patricia, Massud, Ivana, Parodi, Cecilia, Belmonte, Liliana, Garcia, Gabriel, Nebel, Marcelo Campos, Corti, Marcelo, Pinto, Miguel Tezanos et al.

p. 1717 https://doi.org/10.1099/vir.0.80882-0

African origin of GB virus C determined by phylogenetic analysis of a complete genotype 5 genome from South Africa

Muerhoff, A. Scott, Leary, Thomas P., Sathar, Mahomed A., Dawson, George J., Desai, Suresh M.

p. 1729 https://doi.org/10.1099/vir.0.80854-0

Stable human lymphoblastoid cell lines constitutively expressing hepatitis C virus proteins

Wolk, Benno, Gremion, Christel, Ivashkina, Natalia, Engler, Olivier B., Grabscheid, Benno, Bieck, Elke, Blum, Hubert E., Cerny, Andreas et al.

p. 1737 https://doi.org/10.1099/vir.0.80853-0

Characterization of an infectious clone of the wild-type yellow fever virus Asibi strain that is able to infect and disseminate in mosquitoes

McElroy, Kate L., Tsetsarkin, Konstantin A., Vanlandingham, Dana L., Higgs, Stephen

p. 1747 https://doi.org/10.1099/vir.0.80746-0

Wild-type Rinderpest virus uses SLAM (CD150) as its receptor

Baron, Michael D.

p. 1753 https://doi.org/10.1099/vir.0.80836-0

Virulence of Newcastle disease virus is determined by the cleavage site of the fusion protein and by both the stem region and globular head of the haemagglutinin-neuraminidase protein

de Leeuw, Olav S., Koch, Guus, Hartog, Leo, Ravenshorst, Niek, Peeters, Ben P. H.

p. 1759 https://doi.org/10.1099/vir.0.80822-0

Measles virus nucleoprotein induces cell-proliferation arrest and apoptosis through NTAIL-NR and NCORE-Fc{gamma}RIIB1 interactions, respectively

Laine, D., Bourhis, J. M., Longhi, S., Flacher, M., Cassard, L., Canard, B., Sautes-Fridman, C., Rabourdin-Combe, C. et al.

p. 1771 https://doi.org/10.1099/vir.0.80791-0

PRA1 co-localizes with envelope but does not influence primate lentivirus production, infectivity or envelope incorporation

Blancou, Philippe, Evans, David T., Desrosiers, Ronald C.

p. 1785 https://doi.org/10.1099/vir.0.80873-0

RNA Viruses

Analysis of a 17-amino acid residue, virus-neutralizing microantibody

Caroline J. Heap, Yuqin Wang, Teresa J. T. Pinheiro, Steven A. Reading, Keith R. Jennings, Nigel J. Dimmock

p. 1791–1800 https://doi.org/10.1099/vir.0.80812-0

Full restoration of viral fitness by multiple compensatory co-mutations in the nucleoprotein of influenza A virus cytotoxic T-lymphocyte escape mutants

Rimmelzwaan, G. F., Berkhoff, E. G. M., Nieuwkoop, N. J., Smith, D. J., Fouchier, R. A. M., Osterhaus, A. D. M. E.

p. 1801 https://doi.org/10.1099/vir.0.80867-0

Correlation between positivity for immunoglobulin A antibodies and viraemia of swine hepatitis E virus observed among farm pigs in Japan

Takahashi, Masaharu, Nishizawa, Tsutomu, Tanaka, Toshinori, Tsatsralt-Od, Bira, Inoue, Jun, Okamoto, Hiroaki

p. 1807 https://doi.org/10.1099/vir.0.80909-0

Coat proteins of Rice tungro bacilliform virus and Mungbean yellow mosaic virus contain multiple nuclear-localization signals and interact with importin {alpha}

Guerra-Peraza, O., Kirk, D., Seltzer, V., Veluthambi, K., Schmit, A. C., Hohn, T., Herzog, E.

p. 1815 https://doi.org/10.1099/vir.0.80920-0

Nemesia ring necrosis virus: a new tymovirus with a genomic RNA having a histidylatable tobamovirus-like 3' end

Koenig, R., Barends, S., Gultyaev, A. P., Lesemann, D.-E., Vetten, H. J., Loss, S., Pleij, C. W. A.

p. 1827 https://doi.org/10.1099/vir.0.80916-0

Mutational analysis does not support the existence of a putative tertiary structural element in the left terminal domain of Potato spindle tuber viroid

Owens, Robert A., Thompson, Susan M.

p. 1835 https://doi.org/10.1099/vir.0.80869-0

Coat protein enhances translational efficiency of Alfalfa mosaic virus RNAs and interacts with the eIF4G component of initiation factor eIF4F

Krab, Ivo M., Caldwell, Christian, Gallie, Daniel R., Bol, John F.

p. 1841 https://doi.org/10.1099/vir.0.80796-0

Characteristics of the promoters derived from the single-stranded DNA components of Milk vetch dwarf virus in transgenic tobacco

Shirasawa-Seo, Naomi, Sano, Yoshitaka, Nakamura, Shigeo, Murakami, Taka, Seo, Shigemi, Ohashi, Yuko, Hashimoto, Yoshifumi, Matsumoto, Tsuguo

p. 1851 https://doi.org/10.1099/vir.0.80790-0

No influence of amyloid-{beta}-degrading neprilysin activity on prion pathogenesis

Glatzel, Markus, Mohajeri, M. Hasan, Poirier, Raphael, Nitsch, Roger M., Schwarz, Petra, Lu, Bao, Aguzzi, Adriano

p. 1861 https://doi.org/10.1099/vir.0.80811-0