References: Arenaviridae
Abba, Y., Hassim, H., Hamzah, H., Ibrahim, O. E., Ilyasu, Y., Bande, F., Mohd Lila, M. A. & Noordin, M. M. (2016). In vitro isolation and molecular identification of reptarenavirus in Malaysia. Virus Genes 52, 640-650. [PubMed]
Abba, Y., Hassim, H., Hamzah, H., Ibrahim, O. E., Mohd Lila, M. A. & Noordin, M. M. (2017). Pathological vicissitudes and oxidative stress enzyme responses in mice experimentally infected with reptarenavirus (isolate UPM/MY01). Microb Pathog 104, 17-27. [PubMed]
Alfaro-Alarcón, A., Hetzel, U., Smura, T., Baggio, F., Morales, J. A., Kipar, A. & Hepojoki, J. (2022). Boid inclusion body disease is also a disease of wild boa constrictors. Microbiol Spectr 10, e0170522. [PubMed]
Aqrawi, T., Stöhr, A. C., Knauf-Witzens, T., Krengel, A., Heckers, K. O. & Marschang, R. E. (2015). Identification of snake arenaviruses in live boas and pythons in a zoo in Germany. Tierarztliche Praxis Ausgabe K, Kleintiere/Heimtiere 43, 239-247. [PubMed]
Auperin, D., Dimock, K., Cash, P., Rawls, W. E., Leung, W.-C. & Bishop, D. H. L. (1982a). Analyses of the genomes of prototype Pichinde arenavirus and a virulent derivative of Pichinde Munchique: evidence for sequence conservation at the 3' termini of their viral RNA species. Virology 116, 363-367. [PubMed]
Auperin, D. D., Compans, R. W. & Bishop, D. H. L. (1982b). Nucleotide sequence conservation at the 3' termini of the virion RNA species of New World and Old World arenaviruses. Virology 121, 200-203. [PubMed]
Auperin, D. D., Galinski, M. & Bishop, D. H. L. (1984a). The sequences of the N protein gene and intergenic region of the S RNA of Pichinde arenavirus. Virology 134, 208-219. [PubMed]
Auperin, D. D., Romanowski, V., Galinski, M. & Bishop, D. H. L. (1984b). Sequencing studies of Pichinde arenavirus S RNA indicate a novel coding strategy, an ambisense viral S RNA. J Virol 52, 897-904. [PubMed]
Baggio, F., Hetzel, U., Nufer, L., Kipar, A. & Hepojoki, J. (2021). A subpopulation of arenavirus nucleoprotein localizes to mitochondria. Sci Rep 11, 21048. [PubMed]
Bakkers, M. J. G., Moon-Walker, A., Herlo, R., Brusic, V., Stubbs, S. H., Hastie, K. M., Saphire, E. O., Kirchhausen, T. L. & Whelan, S. P. J. (2022). CD164 is a host factor for lymphocytic choriomeningitis virus entry. Proc Natl Acad Sci U S A 119, e2119676119. [PubMed]
Bederka, L. H., Bonhomme, C. J., Ling, E. L. & Buchmeier, M. J. (2014). Arenavirus stable signal peptide is the keystone subunit for glycoprotein complex organization. MBio 5, e02063. [PubMed]
Bentim Góes, L. G., Fischer, C., Almeida Campos, A. C., de Carvalho, C., Moreira-Soto, A., Ambar, G., Ruckert da Rosa, A., de Oliveira, D. C., Jo, W. K., Cruz-Neto, A. P., Pedro, W. A., Queiroz, L. H., Minoprio, P., Durigon, E. L. & Drexler, J. F. (2022). Highly diverse arenaviruses in neotropical bats, Brazil. Emerg Infect Dis 28, 2528-2533. [PubMed]
Bonhomme, C. J., Capul, A. A., Lauron, E. J., Bederka, L. H., Knopp, K. A. & Buchmeier, M. J. (2011). Glycosylation modulates arenavirus glycoprotein expression and function. Virology 409, 223-233. [PubMed]
Borrow, P. & Oldstone, M. B. A. (1994). Mechanism of lymphocytic choriomeningitis virus entry into cells. Virology 198, 1-9. [PubMed]
Bowen, M. D., Peters, C. J. & Nichol, S. T. (1997). Phylogenetic analysis of the Arenaviridae: patterns of virus evolution and evidence for cospeciation between arenaviruses and their rodent hosts. Mol Phylogenet Evol 8, 301-316. [PubMed]
Brouillette, R. B., Phillips, E. K., Patel, R., Mahauad-Fernandez, W., Moller-Tank, S., Rogers, K. J., Dillard, J. A., Cooney, A. L., Martinez-Sobrido, L., Okeoma, C. & Maury, W. (2018). TIM-1 mediates dystroglycan-independent entry of Lassa virus. J Virol 92, e00093-00018. [PubMed]
Brunotte, L., Kerber, R., Shang, W., Hauer, F., Hass, M., Gabriel, M., Lelke, M., Busch, C., Stark, H., Svergun, D. I., Betzel, C., Perbandt, M. & Günther, S. (2011). Structure of the Lassa virus nucleoprotein revealed by X-ray crystallography, small-angle X-ray scattering, and electron microscopy. J Biol Chem 286, 38748-38756. [PubMed]
Buchmeier, M., Adam, E. & Rawls, W. E. (1974). Serological evidence of infection by Pichinde virus among laboratory workers. Infect Immun 9, 821-823. [PubMed]
Buchmeier, M. J. (2002). Arenaviruses: protein structure and function. Curr Top Microbiol Immunol 262, 159-173. [PubMed]
Buchmeier, M. J., Lewicki, H. A., Tomori, O. & Johnson, K. M. (1980). Monoclonal antibodies to lymphocytic choriomeningitis virus react with pathogenic arenaviruses. Nature 288, 486-487. [PubMed]
Buchmeier, M. J. & Rawls, W. E. (1977). Variation between strains of hamsters in the lethality of Pichinde virus infections. Infect Immun 16, 413-421. [PubMed]
Buchmeier, M. J., Southern, P. J., Parekh, B. S., Wooddell, M. K. & Oldstone, M. B. A. (1987). Site-specific antibodies define a cleavage site conserved among arenavirus GP-C glycoproteins. J Virol 61, 982-985. [PubMed]
Cajimat, M. N., Milazzo, M. L., Bradley, R. D. & Fulhorst, C. F. (2012). Ocozocoautla de Espinosa virus and hemorrhagic fever, Mexico. Emerg Infect Dis 18, 401-405. [PubMed]
Cajimat, M. N., Milazzo, M. L., Haynie, M. L., Hanson, J. D., Bradley, R. D. & Fulhorst, C. F. (2011). Diversity and phylogenetic relationships among the North American Tacaribe serocomplex viruses (family Arenaviridae). Virology 421, 87-95. [PubMed]
Cajimat, M. N., Milazzo, M. L., Mauldin, M. R., Bradley, R. D. & Fulhorst, C. F. (2013). Diversity among Tacaribe serocomplex viruses (family Arenaviridae) associated with the southern plains woodrat (Neotoma micropus). Virus Res 178, 486-494. [PubMed]
Cao, W., Henry, M. D., Borrow, P., Yamada, H., Elder, J. H., Ravkov, E. V., Nichol, S. T., Compans, R. W., Campbell, K. P. & Oldstone, M. B. A. (1998). Identification of α-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus. Science 282, 2079-2081. [PubMed]
Capul, A. A., Perez, M., Burke, E., Kunz, S., Buchmeier, M. J. & de la Torre, J. C. (2007). Arenavirus Z-glycoprotein association requires Z myristoylation but not functional RING or late domains. J Virol 81, 9451-9460. [PubMed]
Carballal, G., Videla, C., Dulout, F., Cossio, P. M., Acuña, A. M. & Bianchi, N. O. (1986). Experimental infection of Akodon molinae (Rodentia, Cricetidae) with Junín virus. J Med Virol 19, 47-54. [PubMed]
Carella, F., Villari, G., Maio, N. & De Vico, G. (2016). Disease and disorders of freshwater unionid mussels: a brief overview of recent studies. Front Physiol 7, 489. [PubMed]
Charrel, R. N. & de Lamballerie, X. (2003). Arenaviruses other than Lassa virus. Antiviral Res 57, 89-100. [PubMed]
Chen, Y.-M., Sadiq, S., Tian, J.-H., Chen, X., Lin, X.-D., Shen, J.-J., Chen, H., Hao, Z.-Y., Yang, W.-D., Zhou, Z.-C., Wu, J., Li, F., Wang, H.-W., Xu, Q.-Y., Wang, W., Gao, W.-H. & Holmes, E. C. Z., Yong (2021). RNA virome composition is shaped by sampling ecotype.
Childs, J. E. (1993). Ecology and epidemiology of arenaviruses and their hosts In The Arenaviridae, pp. 331-401. Edited by M. S. Salvato. New York, USA: Plenum Press.
Cogswell-Hawkinson, A., Bowen, R., James, S., Gardiner, D., Calisher, C. H., Adams, R. & Schountz, T. (2012). Tacaribe virus causes fatal infection of an ostensible reservoir host, the Jamaican fruit bat. J Virol 86, 5791-5799. [PubMed]
Costa, V. A., Mifsud, J. C. O., Gilligan, D., Williamson, J. E., Holmes, E. C. & Geoghegan, J. L. (2021). Metagenomic sequencing reveals a lack of virus exchange between native and invasive freshwater fish across the Murray-Darling Basin, Australia. Virus Evol 7, veab034. [PubMed]
Coulibaly-N'Golo, D., Allali, B., Kouassi, S. K., Fichet-Calvet, E., Becker-Ziaja, B., Rieger, T., Olschläger, S., Dosso, H., Denys, C., Ter Meulen, J., Akoua-Koffi, C. & Günther, S. (2011). Novel arenavirus sequences in Hylomyscus sp. and Mus (Nannomys) setulosus from Côte d'Ivoire: implications for evolution of arenaviruses in Africa. PLoS One 6, e20893. [PubMed]
Cui, X., Fan, K., Liang, X., Gong, W., Chen, W., He, B., Chen, X., Wang, H., Wang, X., Zhang, P., Lu, X., Chen, R., Lin, K., Liu, J., Zhai, J., Liu, D. X., Shan, F., Li, Y., Chen, R. A., Meng, H., Li, X., Mi, S., Jiang, J., Zhou, N., Chen, Z., Zou, J. J., Ge, D., Yang, Q., He, K., Chen, T., Wu, Y. J., Lu, H., Irwin, D. M., Shen, X., Hu, Y., Lu, X., Ding, C., Guan, Y., Tu, C. & Shen, Y. (2023). Virus diversity, wildlife-domestic animal circulation and potential zoonotic viruses of small mammals, pangolins and zoo animals. Nat Commun 14, 2488. [PubMed]
Cuypers, L. N., Gryseels, S., Van Houtte, N., Baird, S. J. E., Sabuni, C. A., Katakweba, A. S., van den Burg, S. R. M., Bryja, J., Leirs, H. & Goüy de Bellocq, J. (2023). Subspecific rodent taxa as the relevant host taxonomic level for mammarenavirus host specificity. Virology 581, 116-127. [PubMed]
Dalton, A. J., Rowe, W. P., Smith, G. H., Wilsnack, R. E. & Pugh, W. E. (1968). Morphological and cytochemical studies on lymphocytic choriomeningitis virus. J Virol 2, 1465-1478. [PubMed]
Damonte, E. B., Mersich, S. E., Candurra, N. A. & Coto, C. E. (1986). Cross reactivity between Junin and Tacaribe viruses as determined by neutralization test and immunoprecipitation. Med Microbiol Immunol 175, 85-88. [PubMed]
Downs, W. G., Anderson, C. R., Spence, L., Aitken, T. H. K. & Greenhall, A. H. (1963). Tacaribe virus, a new agent isolated from Artibeus bats and mosquitoes in Trinidad, West Indies. Am J Trop Med Hyg 12, 640-646. [PubMed]
Eichler, R., Lenz, O., Strecker, T., Eickmann, M., Klenk, H.-D. & Garten, W. (2003). Identification of Lassa virus glycoprotein signal peptide as a trans-acting maturation factor. EMBO Rep 4, 1084-1088. [PubMed]
Eichler, R., Strecker, T., Kolesnikova, L., ter Meulen, J., Weissenhorn, W., Becker, S., Klenk, H. D., Garten, W. & Lenz, O. (2004). Characterization of the Lassa virus matrix protein Z: electron microscopic study of virus-like particles and interaction with the nucleoprotein (NP). Virus Res 100, 249-255. [PubMed]
Elliott, L. H., McCormick, J. B. & Johnson, K. M. (1982). Inactivation of Lassa, Marburg, and Ebola viruses by gamma irradiation. J Clin Microbiol 16, 704-708. [PubMed]
Fehling, S. K., Lennartz, F. & Strecker, T. (2012). Multifunctional nature of the arenavirus RING finger protein Z. Viruses 4, 2973-3011. [PubMed]
Fisher-Hoch, S. P., Tomori, O., Nasidi, A., Perez-Oronoz, G. I., Fakile, Y., Hutwagner, L. & McCormick, J. B. (1995). Review of cases of nosocomial Lassa fever in Nigeria: the high price of poor medical practice. BMJ 311, 857-859. [PubMed]
Gaidamovich, S. Y., Butenko, A. M. & Leschinskaya, H. V. (2000). Human laboratory acquired arbo-, arena-, and hantavirus infections. J Am Biol Safety Assoc 5, 5-11.
Gajdamovič, S. J., Klisenko, G. A., Kočerovskaja, M. J. & Šanojan, N. K. (1975). Antigenic relationships of lymphocytic choriomeningitis virus and Tacaribe virus in the indirect haemagglutination test. Bull World Health Organ 52, 437-439. [PubMed]
Garcin, D. & Kolakofsky, D. (1990). A novel mechanism for the initiation of Tacaribe arenavirus genome replication. J Virol 64, 6196-6203. [PubMed]
Garcin, D. & Kolakofsky, D. (1992). Tacaribe arenavirus RNA synthesis in vitro is primer dependent and suggests an unusual model for the initiation of genome replication. J Virol 66, 1370-1376. [PubMed]
Geoghegan, J. L., Di Giallonardo, F., Wille, M., Ortiz-Baez, A. S., Costa, V. A., Ghaly, T., Mifsud, J. C. O., Turnbull, O. M. H., Bellwood, D. R., Williamson, J. E. & Holmes, E. C. (2021). Virome composition in marine fish revealed by meta-transcriptomics. Virus Evol 7, veab005. [PubMed]
Glushakova, S. E. & Lukashevich, I. S. (1989). Early events in arenavirus replication are sensitive to lysosomotropic compounds. Arch Virol 104, 157-161. [PubMed]
Golden, J. W., Hammerbeck, C. D., Mucker, E. M. & Brocato, R. L. (2015). Animal models for the study of rodent-borne hemorrhagic fever viruses: arenaviruses and hantaviruses. Biomed Res Int 2015, 793257. [PubMed]
Gonzalez, J. P., Emonet, S., de Lamballerie, X. & Charrel, R. (2007). Arenaviruses. Curr Top Microbiol Immunol 315, 253-288. [PubMed]
González, P. H., Cossio, P. M., Arana, R., Maiztegui, J. I. & Laguens, R. P. (1980). Lymphatic tissue in Argentine hemorrhagic fever. Pathologic features. Arch Pathol Lab Med 104, 250-254. [PubMed]
Granzow, H., Fichtner, D., Schütze, H., Lenk, M., Dresenkamp, B., Nieper, H. & Mettenleiter, T. C. (2014). Isolation and partial characterization of a novel virus from different carp species suffering gill necrosis - ultrastructure and morphogenesis. J Fish Dis 37, 559-569. [PubMed]
Grimwood, R. M., Fortune-Kelly, G., Holmes, E. C., Ingram, T. & Geoghegan, J. L. (2023). Host specificity shapes fish viromes across lakes on an isolated remote island. bioRxiv, doi: 10.1101/2023.1107.1103.547585.
Grimwood, R. M., Holmes, E. C. & Geoghegan, J. L. (2021). A novel rubi-like virus in the Pacific electric ray (Tetronarce californica) reveals the complex evolutionary history of the Matonaviridae. Viruses 13. [PubMed]
Grutadauria, S., Castilla, V., Zapata, M. & Mersich, S. (1999). Analysis of viral glycoproteins by glycosidic digestion inside a polyacrylamide gel. J Virol Methods 80, 217-221. [PubMed]
Harding, E. F., Russo, A. G., Yan, G. J., Mercer, L. K. & White, P. A. (2022). Revealing the uncharacterised diversity of amphibian and reptile viruses. ISME Communications 2, 95.
Harnish, D. G., Polyak, S. J. & Rawls, W. E. (1993). Arenavirus replication: molecular dissection of the role of protein and RNA. In The Arenaviridae, pp. 157-174. Edited by M. S. Salvato. New York, USA: Plenum Press.
Hass, M., Westerkofsky, M., Müller, S., Becker-Ziaja, B., Busch, C. & Günther, S. (2006). Mutational analysis of the lassa virus promoter. J Virol 80, 12414-12419. [PubMed]
Hastie, K. M., Kimberlin, C. R., Zandonatti, M. A., MacRae, I. J. & Saphire, E. O. (2011a). Structure of the Lassa virus nucleoprotein reveals a dsRNA-specific 3' to 5' exonuclease activity essential for immune suppression. Proc Natl Acad Sci USA 108, 2396-2401. [PubMed]
Hastie, K. M., Liu, T., Li, S., King, L. B., Ngo, N., Zandonatti, M. A., Woods, V. L., Jr., de la Torre, J. C. & Saphire, E. O. (2011b). Crystal structure of the Lassa virus nucleoprotein-RNA complex reveals a gating mechanism for RNA binding. Proc Natl Acad Sci USA 108, 19365-19370. [PubMed]
Hastie, K. M., Zandonatti, M., Liu, T., Li, S., Woods, V. L., Jr. & Saphire, E. O. (2016). Crystal Structure of the Oligomeric Form of Lassa Virus Matrix Protein Z. J Virol 90, 4556-4562. [PubMed]
Hastie, K. M., Zandonatti, M. A., Kleinfelter, L. M., Heinrich, M. L., Rowland, M. M., Chandran, K., Branco, L. M., Robinson, J. E., Garry, R. F. & Saphire, E. O. (2017). Structural basis for antibody-mediated neutralization of Lassa virus. Science 356, 923-928. [PubMed]
Hensley, L. E., Smith, M. A., Geisbert, J. B., Fritz, E. A., Daddario-DiCaprio, K. M., Larsen, T. & Geisbert, T. W. (2011). Pathogenesis of Lassa fever in cynomolgus macaques. Virol J 8, 205. [PubMed]
Hepojoki, J., Hepojoki, S., Smura, T., Szirovicza, L., Dervas, E., Prähauser, B., Nufer, L., Schraner, E. M., Vapalahti, O., Kipar, A. & Hetzel, U. (2018). Characterization of Haartman Institute snake virus 1 (HISV-1) and HISV-like viruses - the representatives of genus Hartmanivirus, family Arenaviridae. PLoS Pathog 14, e1007415. [PubMed]
Hepojoki, J., Salmenperä, P., Sironen, T., Hetzel, U., Korzyukov, Y., Kipar, A. & Vapalahti, O. (2015). Arenavirus Coinfections Are Common in Snakes with Boid Inclusion Body Disease. J Virol 89, 8657-8660. [PubMed]
Hetzel, U., Sironen, T., Laurinmäki, P., Liljeroos, L., Patjas, A., Henttonen, H., Vaheri, A., Artelt, A., Kipar, A., Butcher, S. J., Vapalahti, O. & Hepojoki, J. (2013). Isolation, identification, and characterization of novel arenaviruses, the etiological agents of boid inclusion body disease. J Virol 87, 10918-10935. [PubMed]
Hirsch, M. S., Moellering, R. C., Jr., Pope, H. G. & Poskanzer, D. C. (1974). Lymphocytic-choriomeningitis-virus infection traced to a pet hamster. New Engl J Med 291, 610-612. [PubMed]
Hugot, J. P., Gonzalez, J. P. & Denys, C. (2001). Evolution of the Old World Arenaviridae and their rodent hosts: generalized host-transfer or association by descent? Infect Genet Evol 1, 13-20. [PubMed]
Hyndman, T. H., Marschang, R. E., Bruce, M., Clark, P. & Vitali, S. D. (2019). Reptarenaviruses in apparently healthy snakes in an Australian zoological collection. Aust Vet J 97, 93-102. [PubMed]
Jae, L. T., Raaben, M., Herbert, A. S., Kuehne, A. I., Wirchnianski, A. S., Soh, T. K., Stubbs, S. H., Janssen, H., Damme, M., Saftig, P., Whelan, S. P., Dye, J. M. & Brummelkamp, T. R. (2014). Virus entry. Lassa virus entry requires a trigger-induced receptor switch. Science 344, 1506-1510. [PubMed]
Jay, M. T., Glaser, C. & Fulhorst, C. F. (2005). The arenaviruses. J Am Vet Med Assoc 227, 904-915. [PubMed]
Johnson, K. M. (1965). Epidemiology of Machupo virus infection. III. Significance of virological observations in man and animals. Am J Trop Med Hyg 14, 816-818. [PubMed]
Justines, G. & Johnson, K. M. (1969). Immune tolerance in Calomys callosus infected with Machupo virus. Nature 222, 1090-1091. [PubMed]
Katoh, K. & Standley, D. M. (2013). MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol 30, 772-780. [PubMed]
Katz, M., Weinstein, J., Eilon-Ashkenazy, M., Gehring, K., Cohen-Dvashi, H., Elad, N., Fleishman, S. J. & Diskin, R. (2022). Structure and receptor recognition by the Lassa virus spike complex. Nature 603, 174-179. [PubMed]
Keenlyside, R. A., McCormick, J. B., Webb, P. A., Smith, E., Elliott, L. & Johnson, K. M. (1983). Case-control study of Mastomys natalensis and humans in Lassa virus-infected households in Sierra Leone. Am J Trop Med Hyg 32, 829-837. [PubMed]
Keller, S., Hetzel, U., Sironen, T., Korzyukov, Y., Vapalahti, O., Kipar, A. & Hepojoki, J. (2017). Co-infecting reptarenaviruses can be vertically transmitted in Boa Constrictor. PLoS Pathog 13, e1006179. [PubMed]
Koellhoffer, J. F., Dai, Z., Malashkevich, V. N., Stenglein, M. D., Liu, Y., Toro, R., J, S. H., Chandran, K., DeRisi, J. L., Almo, S. C. & Lai, J. R. (2014). Structural characterization of the glycoprotein GP2 core domain from the CAS virus, a novel arenavirus-like species. J Mol Biol 426, 1452-1468. [PubMed]
Korzyukov, Y., Hetzel, U., Kipar, A., Vapalahti, O. & Hepojoki, J. (2016). Generation of anti-boa immunoglobulin antibodies for serodiagnostic applications, and their use to detect anti-reptarenavirus antibodies in Boa constrictor. PLoS One 11, e0158417. [PubMed]
Kouba, T., Vogel, D., Thorkelsson, S. R., Quemin, E. R. J., Williams, H. M., Milewski, M., Busch, C., Günther, S., Grünewald, K., Rosenthal, M. & Cusack, S. (2021). Conformational changes in Lassa virus L protein associated with promoter binding and RNA synthesis activity. Nat Commun 12, 7018. [PubMed]
Kranzusch, P. J., Schenk, A. D., Rahmeh, A. A., Radoshitzky, S. R., Bavari, S., Walz, T. & Whelan, S. P. J. (2010). Assembly of a functional Machupo virus polymerase complex. Proc Natl Acad Sci USA 107, 20069-20074. [PubMed]
Kronmann, K. C., Nimo-Paintsil, S., Guirguis, F., Kronmann, L. C., Bonney, K., Obiri-Danso, K., Ampofo, W. & Fichet-Calvet, E. (2013). Two novel arenaviruses detected in pygmy mice, Ghana. Emerg Infect Dis 19, 1832-1835. [PubMed]
Kunz, S., Edelmann, K. H., de la Torre, J.-C., Gorney, R. & Oldstone, M. B. A. (2003). Mechanisms for lymphocytic choriomeningitis virus glycoprotein cleavage, transport, and incorporation into virions. Virology 314, 168-178. [PubMed]
Lampuri, J. S., Vidal, M. D. & Coto, C. E. (1982). Respuesta del Calomys musculinus a la infección experimental con virus Junín. Medicina 42, 61-66. [PubMed]
Lavergne, A., de Thoisy, B., Donato, D., Guidez, A., Matheus, S., Catzeflis, F. & Lacoste, V. (2015). Patawa virus, a new arenavirus hosted by forest rodents in French Guiana. EcoHealth 12, 339-346. [PubMed]
Lecompte, E., ter Meulen, J., Emonet, S., Daffis, S. & Charrel, R. N. (2007). Genetic identification of Kodoko virus, a novel arenavirus of the African pigmy mouse (Mus Nannomys minutoides) in West Africa. Virology 364, 178-183. [PubMed]
Leifer, E., Gocke, D. J. & Bourne, H. (1970). Lassa fever, a new virus disease of man from West Africa. II. Report of a laboratory-acquired infection treated with plasma from a person recently recovered from the disease. Am J Trop Med Hyg 19, 677-679. [PubMed]
Lenz, O., ter Meulen, J., Klenk, H.-D., Seidah, N. G. & Garten, W. (2001). The Lassa virus glycoprotein precursor GP-C is proteolytically processed by subtilase SKI-1/S1P. Proc Natl Acad Sci USA 98, 12701-12705. [PubMed]
Leung, W.-C., Ghosh, H. P. & Rawls, W. E. (1977). Strandedness of Pichinde virus RNA. J Virol 22, 235-237. [PubMed]
Leung, W.-C. & Rawls, W. E. (1977). Virion-associated ribosomes are not required for the replication of Pichinde virus. Virology 81, 174-176. [PubMed]
Li, S., Sun, Z., Pryce, R., Parsy, M.-L., Fehling, S. K., Schlie, K., Siebert, C. A., Garten, W., Bowden, T. A., Strecker, T. & Huiskonen, J. T. (2016). Acidic pH-induced conformations and LAMP1 binding of the Lassa virus glycoprotein spike. PLoS Pathog 12, e1005418. [PubMed]
Lukashevich, I. S. (1992). Generation of reassortants between African arenaviruses. Virology 188, 600-605. [PubMed]
Lukashevich, I. S., Maryankova, R. F. & Fidarov, F. M. (1983). Reproduction of Lassa virus in different cell cultures. Acta Virol 27, 282-285. [PubMed]
Luo, X. L., Lu, S., Qin, C., Shi, M., Lu, X. B., Wang, L., Ga, S., Jin, D., Ma, X. L., Yang, J., Dai, Y., Bao, L. L., Cheng, Y. P., Ge, Y. J., Bai, Y. B., Zhu, W. T., Pu, J., Sun, H., Huang, Y. Y., Xu, M. C., Lei, W. J., Dong, K., Yang, C. X., Jiao, Y. F., Lv, Q., Li, F. D. & Xu, J. (2023). Emergence of an ancient and pathogenic mammarenavirus. Emerg Microbes Infect 12, e2192816. [PubMed]
MacNeil, A., Ströher, U., Farnon, E., Campbell, S., Cannon, D., Paddock, C. D., Drew, C. P., Kuehnert, M., Knust, B., Gruenenfelder, R., Zaki, S. R., Rollin, P. E., Nichol, S. T. & LCMV Transplant Investigation Team (2012). Solid organ transplant-associated lymphocytic choriomeningitis, United States, 2011. Emerg Infect Dis 18, 1256-1262. [PubMed]
Maiztegui, J. I. (1975). Clinical and epidemiological patterns of Argentine haemorrhagic fever. Bull World Health Organ 52, 567-575. [PubMed]
Martínez-Sobrido, L., Zúñiga, E. I., Rosario, D., García-Sastre, A. & de la Torre, J. C. (2006). Inhibition of the type I interferon response by the nucleoprotein of the prototypic arenavirus lymphocytic choriomeningitis virus. J Virol 80, 9192-9199. [PubMed]
Martinez, M. G., Cordo, S. M. & Candurra, N. A. (2007). Characterization of Junín arenavirus cell entry. J Gen Virol 88, 1776-1784. [PubMed]
Meyer, B. J., de la Torre, J. C. & Southern, P. J. (2002). Arenaviruses: genomic RNAs, transcription, and replication. Curr Top Microbiol Immunol 262, 139-157. [PubMed]
Meyer, B. J. & Southern, P. J. (1993). Concurrent sequence analysis of 5' and 3' RNA termini by intramolecular circularization reveals 5' nontemplated bases and 3' terminal heterogeneity for lymphocytic choriomeningitis virus mRNAs. J Virol 67, 2621-2627. [PubMed]
Meyer, B. J. & Southern, P. J. (1994). Sequence heterogeneity in the termini of lymphocytic choriomeningitis virus genomic and antigenomic RNAs. J Virol 68, 7659-7664. [PubMed]
Milazzo, M. L., Cajimat, M. N. B., Mauldin, M. R., Bennett, S. G., Hess, B. D., Rood, M. P., Conlan, C. A., Nguyen, K., Wekesa, J. W., Ramos, R. D., Bradley, R. D. & Fulhorst, C. F. (2015). Epizootiology of Tacaribe serocomplex viruses (Arenaviridae) associated with neotomine rodents (Cricetidae, Neotominae) in southern California. Vector Borne Zoonotic Dis 15, 156-166. [PubMed]
Mills, J. N., Ellis, B. A., McKee, K. T., Jr., Calderon, G. E., Maiztegui, J. I., Nelson, G. O., Ksiazek, T. G., Peters, C. J. & Childs, J. E. (1992). A longitudinal study of Junin virus activity in the rodent reservoir of Argentine hemorrhagic fever. Am J Trop Med Hyg 47, 749-763. [PubMed]
Milzer, A. & Levinson, S. O. (1942). Laboratory infection with the virus of lymphocytic choriomeningitis. A two year study of antibody response. J Am Med Assoc 120, 27-30.
Mitchell, S. W. & McCormick, J. B. (1984). Physicochemical inactivation of Lassa, Ebola, and Marburg viruses and effect on clinical laboratory analyses. J Clin Microbiol 20, 486-489. [PubMed]
Montali, R. J., Scanga, C. A., Pernikoff, D., Wessner, D. R., Ward, R. & Holmes, K. V. (1993). A common-source outbreak of callitrichid hepatitis in captive tamarins and marmosets. J Infect Dis 167, 946-950. [PubMed]
Mordecai, G. J., Miller, K. M., Di Cicco, E., Schulze, A. D., Kaukinen, K. H., Ming, T. J., Li, S., Tabata, A., Teffer, A., Patterson, D. A., Ferguson, H. W. & Suttle, C. A. (2019). Endangered wild salmon infected by newly discovered viruses. Elife 8, e47615. [PubMed]
Neuman, B. W., Adair, B. D., Burns, J. W., Milligan, R. A., Buchmeier, M. J. & Yeager, M. (2005). Complementarity in the supramolecular design of arenaviruses and retroviruses revealed by electron cryomicroscopy and image analysis. J Virol 79, 3822-3830. [PubMed]
Paweska, J. T., Sewlall, N. H., Ksiazek, T. G., Blumberg, L. H., Hale, M. J., Lipkin, W. I., Weyer, J., Nichol, S. T., Rollin, P. E., McMullan, L. K., Paddock, C. D., Briese, T., Mnyaluza, J., Dinh, T.-H., Mukonka, V., Ching, P., Duse, A., Richards, G., de Jong, G., Cohen, C., Ikalafeng, B., Mugero, C., Asomugha, C., Malotle, M. M., Nteo, D. M., Misiani, E., Swanepoel, R. & Zaki, S. R. (2009). Nosocomial outbreak of novel arenavirus infection, southern Africa. Emerg Infect Dis 15, 1598-1602. [PubMed]
Peng, R., Xu, X., Jing, J., Wang, M., Peng, Q., Liu, S., Wu, Y., Bao, X., Wang, P., Qi, J., Gao, G. F. & Shi, Y. (2020). Structural insight into arenavirus replication machinery. Nature 579, 615-619. [PubMed]
Perez, M., Craven, R. C. & de la Torre, J. C. (2003). The small RING finger protein Z drives arenavirus budding: implications for antiviral strategies. Proc Natl Acad Sci USA 100, 12978-12983. [PubMed]
Perez, M., Greenwald, D. L. & de la Torre, J. C. (2004). Myristoylation of the RING finger Z protein is essential for arenavirus budding. J Virol 78, 11443-11448. [PubMed]
Peters, C. J., Jahrling, P. B., Liu, C. T., Kenyon, R. H., McKee, K. T., Jr. & Barrera Oro, J. G. (1987). Experimental studies of arenaviral hemorrhagic fevers. Curr Top Microbiol Immunol 134, 5-68. [PubMed]
Pfau, C. J. (1965). Biophysical and biochemical characterization of lymphocytic choriomeningitis virus. 2. Partial purification by differential centrifugation and fluorocarbon techniques. Acta Pathol Microbiol Scand 63, 198-205. [PubMed]
Pinschewer, D. D., Perez, M. & de la Torre, J. C. (2005). Dual role of the lymphocytic choriomeningitis virus intergenic region in transcription termination and virus propagation. J Virol 79, 4519-4526. [PubMed]
Raaben, M., Jae, L. T., Herbert, A. S., Kuehne, A. I., Stubbs, S. H., Chou, Y.-Y., Blomen, V. A., Kirchhausen, T., Dye, J. M., Brummelkamp, T. R. & Whelan, S. P. (2017). NRP2 and CD63 are host factors for Lujo virus cell entry. Cell Host Microbe 22, 688-696 e685. [PubMed]
Radoshitzky, S. R., Abraham, J., Spiropoulou, C. F., Kuhn, J. H., Nguyen, D., Li, W., Nagel, J., Schmidt, P. J., Nunberg, J. H., Andrews, N. C., Farzan, M. & Choe, H. (2007). Transferrin receptor 1 is a cellular receptor for New World haemorrhagic fever arenaviruses. Nature 446, 92-96. [PubMed]
Radoshitzky, S. R., Bào, Y., Buchmeier, M. J., Charrel, R. N., Clawson, A. N., Clegg, C. S., DeRisi, J. L., Emonet, S., Gonzalez, J.-P., Kuhn, J. H., Lukashevich, I. S., Peters, C. J., Romanowski, V., Salvato, M. S., Stenglein, M. D. & de la Torre, J. C. (2015). Past, present, and future of arenavirus taxonomy. Arch Virol 160, 1851-1874. [PubMed]
Radoshitzky, S. R., Buchmeier, M. & de la Torre, J. C. (2020). Arenaviridae: the viruses and their replication. In Fields Virology, 7th edn, pp. 784-809. Edited by P. M. Howley, D. M. Knipe & S. P. J. Whelan. Philadelphia, Pennsylvania, USA: Wolters Kluwer/Lippincott Williams & Wilkins.
Radoshitzky, S. R., Kuhn, J. H., Jahrling, P. B. & Bavari, S. (2018). Hemorrhagic fever-causing mammarenaviruses. In Medical aspects of biological warfare, pp. 517-545. Edited by J. Bozue, C. K. Cote & P. J. Glass. Fort Sam Houston, USA: Borden Institute, US Army Medical Department Center and School, Health Readiness Center of Excellence.
Raju, R., Raju, L., Hacker, D., Garcin, D., Compans, R. & Kolakofsky, D. (1990). Nontemplated bases at the 5' ends of Tacaribe virus mRNAs. Virology 174, 53-59. [PubMed]
Rawls, W. E. & Buchmeier, M. (1975). Arenaviruses: purification and physicochemical nature. Bull World Health Organ 52, 393-401. [PubMed]
Reguera, J., Gerlach, P. & Cusack, S. (2016). Towards a structural understanding of RNA synthesis by negative strand RNA viral polymerases. Curr Opin Struct Biol 36, 75-84. [PubMed]
Reuter, G., Boros, Á., Takáts, K., Mátics, R. & Pankovics, P. (2023). A novel mammarenavirus (family Arenaviridae) in hedgehogs (Erinaceus roumanicus) in Europe. Arch Virol 168, 174. [PubMed]
Romanowski, V. & Bishop, D. H. L. (1983). The formation of arenaviruses that are genetically diploid. Virology 126, 87-95. [PubMed]
Rowe, W. P., Murphy, F. A., Bergold, G. H., Casals, J., Hotchin, J., Johnson, K. M., Lehmann-Grube, F., Mims, C. A., Traub, E. & Webb, P. A. (1970a). Arenoviruses: proposed name for a newly defined virus group. J Virol 5, 651-652. [PubMed]
Rowe, W. P., Pugh, W. E., Webb, P. A. & Peters, C. J. (1970b). Serological relationship of the Tacaribe complex of viruses to lymphocytic choriomeningitis virus. J Virol 5, 289-292. [PubMed]
Rugiero, H. R., Parodi, A. S., Gotta, H., Boxaca, M., Olivari, A. J. & González, E. (1962). Fiebre hemorrágica epidémica. Infección de laboratorio y pasaje interhumano. Rev Asoc Med Argent 76, 413-417.
Saito, T., Hattori, T., Okuya, K., Manzoor, R., Miyamoto, H., Kajihara, M. & Takada, A. (2021). Molecular mechanisms underlying the cellular entry and host range restriction of Lujo virus. MBio 13, e0306021. [PubMed]
Salazar-Bravo, J., Dragoo, J. W., Bowen, M. D., Peters, C. J., Ksiazek, T. G. & Yates, T. L. (2002a). Natural nidality in Bolivian hemorrhagic fever and the systematics of the reservoir species. Infect Genet Evol 1, 191-199. [PubMed]
Salazar-Bravo, J., Ruedas, L. A. & Yates, T. L. (2002b). Mammalian reservoirs of arenaviruses. Curr Top Microbiol Immunol 262, 25-63. [PubMed]
Salvato, M., Shimomaye, E. & Oldstone, M. B. A. (1989). The primary structure of the lymphocytic choriomeningitis virus L gene encodes a putative RNA polymerase. Virology 169, 377-384. [PubMed]
Salvato, M. S. & Shimomaye, E. M. (1989). The completed sequence of lymphocytic choriomeningitis virus reveals a unique RNA structure and a gene for a zinc finger protein. Virology 173, 1-10. [PubMed]
Sanchez, A., Pifat, D. Y., Kenyon, R. H., Peters, C. J., McCormick, J. B. & Kiley, M. P. (1989). Junin virus monoclonal antibodies: characterization and cross-reactivity with other arenaviruses. J Gen Virol 70 ( Pt 5), 1125-1132. [PubMed]
Sarute, N. & Ross, S. R. (2020). CACNA1S haploinsufficiency confers resistance to New World arenavirus infection. Proc Natl Acad Sci USA 117, 19497-19506. [PubMed]
Sayler, K. A., Barbet, A. F., Chamberlain, C., Clapp, W. L., Alleman, R., Loeb, J. C. & Lednicky, J. A. (2014). Isolation of Tacaribe virus, a Caribbean arenavirus, from host-seeking Amblyomma americanum ticks in Florida. PLoS One 9, e115769. [PubMed]
Shao, J., Liang, Y. & Ly, H. (2018). Roles of Arenavirus Z Protein in Mediating Virion Budding, Viral Transcription-Inhibition and Interferon-Beta Suppression. Methods Mol Biol 1604, 217-227. [PubMed]
Shedroff, E., Whitmer, S., Montgomery, J. & Klena, J. D. (2023). Genome sequence of Serodino virus, a novel Oliveros-like clade C mammarenavirus. In APHL 2023. SAFE Credit Union Convention Center, Sacramento, California.
Shi, M., Lin, X.-D., Chen, X., Tian, J.-H., Chen, L.-J., Li, K., Wang, W., Eden, J.-S., Shen, J.-J., Liu, L., Holmes, E. C. & Zhang, Y.-Z. (2018). The evolutionary history of vertebrate RNA viruses. Nature 556, 197-202. [PubMed]
Shi, M., Lin, X.-D., Tian, J.-H., Chen, L.-J., Chen, X., Li, C.-X., Qin, X.-C., Li, J., Cao, J.-P., Eden, J.-S., Buchmann, J., Wang, W., Xu, J., Holmes, E. C. & Zhang, Y.-Z. (2016). Redefining the invertebrate RNA virosphere. Nature 540, 539-543. [PubMed]
Shimojima, M., Ströher, U., Ebihara, H., Feldmann, H. & Kawaoka, Y. (2012). Identification of cell surface molecules involved in dystroglycan-independent Lassa virus cell entry. J Virol 86, 2067-2078. [PubMed]
Singh, M. K., Fuller-Pace, F. V., Buchmeier, M. J. & Southern, P. J. (1987). Analysis of the genomic L RNA segment from lymphocytic choriomeningitis virus. Virology 161, 448-456. [PubMed]
Sommerstein, R., Flatz, L., Remy, M. M., Malinge, P., Magistrelli, G., Fischer, N., Sahin, M., Bergthaler, A., Igonet, S., Ter Meulen, J., Rigo, D., Meda, P., Rabah, N., Coutard, B., Bowden, T. A., Lambert, P.-H., Siegrist, C.-A. & Pinschewer, D. D. (2015). Arenavirus glycan shield promotes neutralizing antibody evasion and protracted infection. PLoS Pathog 11, e1005276. [PubMed]
Southern, P. J., Singh, M. K., Riviere, Y., Jacoby, D. R., Buchmeier, M. J. & Oldstone, M. B. A. (1987). Molecular characterization of the genomic S RNA segment from lymphocytic choriomeningitis virus. Virology 157, 145-155. [PubMed]
Spiropoulou, C. F., Kunz, S., Rollin, P. E., Campbell, K. P. & Oldstone, M. B. (2002). New World arenavirus clade C, but not clade A and B viruses, utilizes alpha-dystroglycan as its major receptor. J Virol 76, 5140-5146. [PubMed]
Stenglein, M. D., Jacobson, E. R., Chang, L.-W., Sanders, C., Hawkins, M. G., Guzman, D. S.-M., Drazenovich, T., Dunker, F., Kamaka, E. K., Fisher, D., Reavill, D. R., Meola, L. F., Levens, G. & DeRisi, J. L. (2015). Widespread recombination, reassortment, and transmission of unbalanced compound viral genotypes in natural arenavirus infections. PLoS Pathog 11, e1004900. [PubMed]
Stenglein, M. D., Sanchez-Migallon Guzman, D., Garcia, V. E., Layton, M. L., Hoon-Hanks, L. L., Boback, S. M., Keel, M. K., Drazenovich, T., Hawkins, M. G. & DeRisi, J. L. (2017). Differential disease susceptibilities in experimentally reptarenavirus-infected boa constrictors and ball pythons. J Virol 91, e00451-00417. [PubMed]
Stenglein, M. D., Sanders, C., Kistler, A. L., Ruby, J. G., Franco, J. Y., Reavill, D. R., Dunker, F. & Derisi, J. L. (2012). Identification, characterization, and in vitro culture of highly divergent arenaviruses from boa constrictors and annulated tree boas: candidate etiological agents for snake inclusion body disease. MBio 3, e00180-00112. [PubMed]
Strecker, T., Eichler, R., Meulen, J., Weissenhorn, W., Dieter Klenk, H., Garten, W. & Lenz, O. (2003). Lassa virus Z protein is a matrix protein and sufficient for the release of virus-like particles. J Virol 77, 10700-10705. [PubMed]
Strecker, T., Maisa, A., Daffis, S., Eichler, R., Lenz, O. & Garten, W. (2006). The role of myristoylation in the membrane association of the Lassa virus matrix protein Z. Virol J 3, 93. [PubMed]
Terrell, T. G., Stookey, J. L., Spertzel, R. O. & Kuehne, R. W. (1973). Comparative histopathology of two strains of Bolivian hemorrhagic fever virus infections in suckling hamsters. Am J Trop Med Hyg 22, 814-818. [PubMed]
Tortorici, M. A., Albariño, C. G., Posik, D. M., Ghiringhelli, P. D., Lozano, M. E., Rivera Pomar, R. & Romanowski, V. (2001). Arenavirus nucleocapsid protein displays a transcriptional antitermination activity in vivo. Virus Res 73, 41-55. [PubMed]
Trifinopoulos, J., Nguyen, L. T., von Haeseler, A. & Minh, B. Q. (2016). W-IQ-TREE: a fast online phylogenetic tool for maximum likelihood analysis. Nucleic Acids Res 44, W232-235. [PubMed]
Urata, S., Yasuda, J. & de la Torre, J. C. (2009). The z protein of the new world arenavirus tacaribe virus has bona fide budding activity that does not depend on known late domain motifs. J Virol 83, 12651-12655. [PubMed]
Vasconcelos, P. F. d. C., Travassos da Rosa, A. P. d. A., Rodrigues, S. G., Tesh, R., Travassos da Rosa, J. F. S. & Travassos da Rosa, E. S. (1993). Infecção humana adquirida em laboratório causada pelo virus SP H 114202 (Arenavirus: família Arenaviridae): aspectos clínicos e laboratoriais. Revista do Instituto de Medicina Tropical de Sao Paulo 35, 521-525. [PubMed]
Vela, E. (2012). Animal models, prophylaxis, and therapeutics for arenavirus infections. Viruses 4, 1802-1829. [PubMed]
Vela, E. M., Zhang, L., Colpitts, T. M., Davey, R. A. & Aronson, J. F. (2007). Arenavirus entry occurs through a cholesterol-dependent, non-caveolar, clathrin-mediated endocytic mechanism. Virology 369, 1-11. [PubMed]
Wagner, F. S., Eddy, G. A. & Brand, O. M. (1977). The African green monkey as an alternate primate host for studying Machupo virus infection. Am J Trop Med Hyg 26, 159-162. [PubMed]
Walker, D. H., Wulff, H., Lange, J. V. & Murphy, F. A. (1975). Comparative pathology of Lassa virus infection in monkeys, guinea-pigs, and Mastomys natalensis. Bull World Health Organ 52, 523-534. [PubMed]
Watanabe, Y., Raghwani, J., Allen, J. D., Seabright, G. E., Li, S., Moser, F., Huiskonen, J. T., Strecker, T., Bowden, T. A. & Crispin, M. (2018). Structure of the Lassa virus glycan shield provides a model for immunological resistance. Proc Natl Acad Sci USA 115, 7320-7325. [PubMed]
Webb, P. A., Justines, G. & Johnson, K. M. (1975). Infection of wild and laboratory animals with Machupo and Latino viruses. Bull World Health Organ 52, 493-499. [PubMed]
West, B. R., Hastie, K. M. & Saphire, E. O. (2014). Structure of the LCMV nucleoprotein provides a template for understanding arenavirus replication and immunosuppression. Acta Crystallogr D Biol Crystallogr 70, 1764-1769. [PubMed]
Wildy, P. (1971). Classification and nomenclature of viruses - First Report of the International Committee on Nomenclature of Viruses. Basel, Switzerland: S. Karger.
Wilson, S. M. & Clegg, J. C. S. (1991). Sequence analysis of the S RNA of the African arenavirus Mopeia: an unusual secondary structure feature in the intergenic region. Virology 180, 543-552. [PubMed]
Windbichler, K., Michalopoulou, E., Palamides, P., Pesch, T., Jelinek, C., Vapalahti, O., Kipar, A., Hetzel, U. & Hepojoki, J. (2019). Antibody response in snakes with boid inclusion body disease. PLoS One 14, e0221863. [PubMed]
Wolff, H., Lange, J. V. & Webb, P. A. (1978). Interrelationships among arenaviruses measured by indirect immunofluorescence. Intervirology 9, 344-350. [PubMed]
Wu, Z., Du, J., Lu, L., Yang, L., Dong, J., Sun, L., Zhu, Y., Liu, Q. & Jin, Q. (2018). Detection of hantaviruses and arenaviruzses in three-toed jerboas from the Inner Mongolia Autonomous Region, China. Emerg Microbes Infect 7, 35. [PubMed]
York, J., Romanowski, V., Lu, M. & Nunberg, J. H. (2004). The signal peptide of the Junin arenavirus envelope glycoprotein is myristoylated and forms an essential subunit of the mature G1-G2 complex. J Virol 78, 10783-10792. [PubMed]
Young, P. R. & Howard, C. R. (1983). Fine structure analysis of Pichinde virus nucleocapsids. J Gen Virol 64 (Pt 4), 833-842. [PubMed]
Zhong, L., Xiao, T.-Y., Huang, J., Dai, L.-Y. & Liu, X.-Y. (2011). Histopathological examination of bivalve mussle Hyriopsis cumingii Lea artifically infected by virus. Acta Hydrobiol Sinica 34, 666-671.
Евсеев, А. А., Дворецкая, В. И., Богатиков, Г. В., Пшеничнов, В. А. & Мустафин, Р. М. (1991). Экспериментальная лихорадка Ласса у павианов гамадрилов" target="ictvref">PubMed]. Вопр Вирусол 36, 150-152. [PubMed]
Лукашевич, И. С., Орлова, С. В., Марьянкова, Р. Ф. & Баркар, Н. Д. (1985). Патогенность вируса Ласса для лабораторных мышей. Вопр Вирусол 30, 595-599. [PubMed]