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8. Evolution of densoviruses

Author

Tijssen, P, primary, Bando, H, additional, Li, Y, additional, Jousset, F, additional, Zádori, Z, additional, Fédière, G, additional, El-far, M, additional, Szelei, J, additional, and Bergoin, M, additional

Published
2005
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17. Comprehensive annotation of Glossina pallidipes salivary gland hypertrophy virus from Ethiopian tsetse flies: a proteogenomics approach

Author

Abd-Alla, Adly M.M., Kariithi, Henry, Cousserans, F., Parker, N.J., Ince, Ikbal Agah, Scully, Erin D., Boeren, J.A., Geib, Scott M., Mekonnen, Solomon, Vlak, J.M., Parker, A.G., Vreysen, M.J.B., Bergoin, M., Abd-Alla, Adly M.M., Kariithi, Henry, Cousserans, F., Parker, N.J., Ince, Ikbal Agah, Scully, Erin D., Boeren, J.A., Geib, Scott M., Mekonnen, Solomon, Vlak, J.M., Parker, A.G., Vreysen, M.J.B., and Bergoin, M.

Abstract

Glossina pallidipes salivary gland hypertrophy virus (GpSGHV; family Hytrosaviridae) can establish asymptomatic and symptomatic infection in its tsetse fly host. Here, we present a comprehensive annotation of the genome of an Ethiopian GpSGHV isolate (GpSGHV-Eth) compared with the reference Ugandan GpSGHV isolate (GpSGHV-Uga; GenBank accession number EF568108). GpSGHV-Eth has higher salivary gland hypertrophy syndrome prevalence than GpSGHV-Uga.We show that the GpSGHV-Eth genome has 190 291 nt, a low G+C content (27.9 %) and encodes 174 putative ORFs. Using proteogenomic andtranscriptome mapping, 141 and 86 ORFs were mapped by transcripts and peptides, respectively. Furthermore, of the 174 ORFs, 132 had putative transcriptional signals [TATA-like box and poly(A) signals]. Sixty ORFs hadboth TATA-like box promoter and poly(A) signals, and mapped by both transcripts and peptides, implying that these ORFs encode functional proteins. Of the 60 ORFs, 10 ORFs are homologues to baculovirus and nudivirus core genes, including three per os infectivity factors and four RNA polymerase subunits (LEF4, 5, 8 and 9). Whereas GpSGHV-Eth and GpSGHV-Uga are 98.1 % similar at the nucleotide level, 37 ORFs in the GpSGHV-Eth genome had nucleotide insertions (n517) and deletions (n520) compared with their homologues in GpSGHV-Uga. Furthermore, compared with the GpSGHV-Uga genome, 11 and 24 GpSGHV ORFs were deleted and novel, respectively. Further, 13 GpSGHV-Eth ORFs were non-canonical; they had either CTG or TTG start codons instead of ATG. Taken together, these data suggest that GpSGHV-Eth and GpSGHV-Uga represent two different lineages of the same virus. Genetic differences combined with host and environmental factors possibly explain the differential GpSGHV pathogenesis observed in different G. pallidipes colonies.

Published
2016

34. Proteomic analysis of Glossina pallidipes salivary gland hypertrophy virus virions for immune intervention in tsetse fly colonies

Author

Kariithi, H.M., Ince, I.A., Boeren, S., Vervoort, J.J.M., Bergoin, M., van Oers, M.M., Abd-Alla, A.M.M., Vlak, J.M., Kariithi, H.M., Ince, I.A., Boeren, S., Vervoort, J.J.M., Bergoin, M., van Oers, M.M., Abd-Alla, A.M.M., and Vlak, J.M.

Abstract

Many species of tsetse flies (Diptera: Glossinidae) can be infected by a virus that causes salivary gland hypertrophy (SGH). The viruses isolated from Glossina pallidipes (GpSGHV) and Musca somestica (MdSGHV) have recently been sequenced. Tsetse flies with SGH have a reduced fecundity and fertility which cause a serious problem for mass rearing in the frame of sterile insect technique (SIT) programs to control and eradicate tsetse populations in the wild. A potential intervention strategy to mitigate viral infections in fly colonies is neutralizing of the GpSGHV infection with specific antibodies against virion proteins. Two major GpSGHV virion proteins of about 130 kDa and 50 kDa, respectively, were identified by Western analysis using polyclonal rabbit antibody raised against whole GpSHGV virions. The proteome of GpSGHV, containing the antigens responsible for the immune-response, was investigated by liquid chromatography tandem mass spectrometry (LC-MS/MS) and 61 virion proteins were identified by comparison with the genome sequence. Specific antibodies were produced in rabbits against seven candidate proteins including the ORF10 / C-terminal fragment, ORF47 and ORF96 as well as proteins involved in peroral infectivity PIF-1 (ORF102), PIF-2 (ORF53), PIF-3 (ORF76) and P74 (ORF1). Antiserum against ORF10 specifically reacted to the 130 kDa protein in a Western blot analysis and to the envelope of GpSGHV using immunogold-EM. This result suggests that immune intervention of viral infections in colonies of G. pallidipes is a realistic option

Published
2010

35. Two viruses that cause salivary gland hypertrophy in Glossina pallidipes and Musca domestica are closely related and form a distinct phylogenetic clade

Author

Garcia-Maruniak, A., Abd-Alla, A.M.M., Salem, T.Z., Parker, A.G., Lietze, V.U., van Oers, M.M., Maruniak, J.E., Kim, W., Burand, J.P., Cousserans, F., Robinson, A.S., Vlak, J.M., Bergoin, M., Boucias, D.G., Garcia-Maruniak, A., Abd-Alla, A.M.M., Salem, T.Z., Parker, A.G., Lietze, V.U., van Oers, M.M., Maruniak, J.E., Kim, W., Burand, J.P., Cousserans, F., Robinson, A.S., Vlak, J.M., Bergoin, M., and Boucias, D.G.

Abstract

Glossina pallidipes and Musca domestica salivary gland hypertrophy viruses (GpSGHV and MdSGHV) replicate in the nucleus of salivary gland cells causing distinct tissue hypertrophy and reduction of host fertility. They share general characteristics with the non-occluded insect nudiviruses, such as being insect-pathogenic, having enveloped, rod-shaped virions, and large circular double-stranded DNA genomes. MdSGHV measures 65x550 nm and contains a 124 279 bp genome (44 mol% G+C content) that codes for 108 putative open reading frames (ORFs). GpSGHV, measuring 50x1000 nm, contains a 190 032 bp genome (28 mol% G+C content) with 160 putative ORFs. Comparative genomic analysis demonstrates that 37 MdSGHV ORFs have homology to 42 GpSGHV ORFs, as some MdSGHV ORFs have homology to two different GpSGHV ORFs. Nine genes with known functions (dnapol, ts, pif-1, pif-2, pif-3, mmp, p74, odv-e66 and helicase-2), a homologue of the conserved baculovirus gene Ac81 and at least 13 virion proteins are present in both SGHVs. The amino acid identity ranged from 19 to 39 % among ORFs. An (A/T/G)TAAG motif, similar to the baculovirus late promoter motif, was enriched 100 bp upstream of the ORF transcription initiation sites of both viruses. Six and seven putative microRNA sequences were found in MdSGHV and GpSGHV genomes, respectively. There was genome. Collinearity between the two SGHVs, but not between the SGHVs and the nudiviruses. Phylogenetic analysis of conserved genes clustered both SGHVs in a single clade separated from the nudiviruses and baculoviruses. Although MdSGHV and GpSGHV are different viruses, their pathology, host range and genome composition indicate that they are related

Published
2009

36. Genome analysis of a Glossina pallidipes salivary gland hypertrophy virus reveals a novel, large, double-stranded circular DNA virus

Author

Abd-Alla, A.M.M., Cousserans, F., Parker, A.G., Jehle, J.A., Parker, N.J., Vlak, J.M., Robinson, A.S., Bergoin, M., Abd-Alla, A.M.M., Cousserans, F., Parker, A.G., Jehle, J.A., Parker, N.J., Vlak, J.M., Robinson, A.S., and Bergoin, M.

Abstract

Several species of tsetse flies can be infected by the Glossina pallidipes salivary gland hypertrophy virus (GpSGHV). Infection causes salivary gland hypertrophy and also significantly reduces the fecundity of the infected flies. To better understand the molecular basis underlying the pathogenesis of this unusual virus, we sequenced and analyzed its genome. The GpSGHV genome is a double-stranded circular DNA molecule of 190,032 bp containing 160 nonoverlapping open reading frames (ORFs), which are distributed equally on both strands with a gene density of one per 1.2 kb. It has a high A+T content of 72%. About 3% of the GpSGHV genome is composed of 15 sequence repeats, distributed throughout the genome. Although sharing the same morphological features (enveloped rod-shaped nucleocapsid) as baculoviruses, nudiviruses, and nimaviruses, analysis of its genome revealed that GpSGHV differs significantly from these viruses at the level of its genes. Sequence comparisons indicated that only 23% of GpSGHV genes displayed moderate homologies to genes from other invertebrate viruses, principally baculoviruses and entomopoxviruses. Most strikingly, the GpSGHV genome encodes homologues to the four baculoviral per os infectivity factors (p74 [pif-0], pif-1, pif-2, and pif-3). The DNA polymerase encoded by GpSGHV is of type B and appears to be phylogenetically distant from all DNA polymerases encoded by large double-stranded DNA viruses. The majority of the remaining ORFs could not be assigned by sequence comparison. Furthermore, no homologues to DNA-dependent RNA polymerase subunits were detected. Taken together, these data indicate that GpSGHV is the prototype member of a novel group of insect viruses

Published
2008

37. Lutte biologique avec des virus entomopathogènes. Application aux ravageurs du palmier à huile et du cocotier

Author

Philippe, René, Veyrunes, J.C., Mariau, Dominique, and Bergoin, M.

Subjects
Élevage en masse, Limacodidae, H10 - Ravageurs des plantes, Virus des invertébrés, Lutte biologique, Coleoptera, Elaeis guineensis, Cocos nucifera, Insecte nuisible
Abstract

Les palmacées cultivées sont attaquées par de nombreuses espèces de chenilles défoliatrices, surtout de la famille des Limacodidae. Ces chenilles sont presque toujours infectées naturellement par des virus spécifiques. Des tests de diagnostic (ELISA, sonde nucléique), mis au point pour chaque virus intéressant, permettront l'analyse épidémiologique de ces maladies virales au champ et l'étude de la persistance des particules virales dans une population de chenilles. Ils faciliteront la décision d'une intervention par une détection rapide et sensible des virus dans une population de chenilles. Des succès ont été obtenus avec des préparations artisanales de virus de Sethothosea asigna et Setora nitens, en Indonésie et sur Sibine fusca en Colombie. Cette dernière a été éliminée par la pulvérisation aérienne d'une solution virale contenant l'équivalent de 10 chenilles mortes par hectare traité

Published
1997

38. Utilization of Nudaurelia-beta virus for biological control of the oil palm leaf-eating nettle caterpillar Setothosea asigna Van Eecke (Lepidoptera : Limacodidae) in Indonesia

Author

Prawirosukarto, Sudharto, Pardede, D., Veyrunes, J.C., Cousserans, François, Philippe, René, Desmier De Chenon, Roch, Mariau, Dominique, and Bergoin, M.

Subjects
fungi, Limacodidae, H10 - Ravageurs des plantes, Virus des invertébrés, Lutte biologique, Diagnostic de laboratoire, Test ELISA, Agent de lutte biologique, Sonde nucléique, Elaeis guineensis, Insecte nuisible
Abstract

Among of the oil palm leaf-eating nettle caterpillars in Indonesia, Setothosea asigna Van Eecke is the most important species, attacking indifferently the young and the old plantations. We have recently isolated from infected-dead larvae of this defoliator collected in North Sumatra a small RNA virus that we characterized as belonging to the #Nudaurelia-beta# group. This virus proved to be highly pathogenic for #S. asigna# larvae in laboratory conditions. In order to develop a method for the biological control of this pest based on the spraying of this virus in the oil palm plantations in Indonesia, we have prepared appropriate diagnosis tools i.e. : polyclonal antibodies against purified virions for ELISA tests and a cDNA probe for dot-blot analysis. Both diagnostic methods proved to be efficient for detecting the presence of the virus in infected caterpillars. The sensitivity of larvae according to the instar and to virus concentration was determined in laboratory conditions. Field applications of viral preparations were performed and the comparative results of larval population dynamics in treated and untreated plots will be presented.

Published
1996

41. Scoliose congénitale : une évaluation dans le plan frontal de 251 patients opérés, âgés de 14 ans ou plus

Author

Louis, M.-L., primary, Gennari, J.-M., additional, Loundou, A.-D., additional, Bollini, G., additional, Bergoin, M., additional, Bernard, J.-C., additional, Biot, B., additional, Bonnard, C., additional, Clément, J.-L., additional, Garin, C., additional, Kamoun, K., additional, Kreichati, G., additional, Lascombes, P., additional, Mallet, J.-F., additional, Miladi, L., additional, Sales de Gauzy, J., additional, Topouchian, V., additional, and Vital, J.-M., additional

Published
2010
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43. Mise en évidence d'un baculovirus de polyédrose nucléaire chez Latoia viridissima lépidoptère Limacodidae ravageur du palmier à huile et du cocotier en Côte d'Ivoire

Author

Kouassi, N.K., Fédière, Gilles, Lery, X., Philippe, René, and Bergoin, M.

Subjects
Biochimie, H10 - Ravageurs des plantes, Virus des invertébrés, Vecteur de maladie, Ultrastructure, Elaeis guineensis, Baculoviridae, Cocos nucifera, Insecte nuisible
Abstract

Parmi les défoliateurs du palmier à huile, le Lépidoptère Limacodidae Latoia viridissima est un des plus fréquemment observé en Côte d'Ivoire. Pendant les pullulations de cette espèce, des épizooties naturelles ont permis de mettre en évidence un baculovirus de polyédrose nucléaire. Ce dernier infecte cette espèce en association avec un picornavirus précédemment signalé. Les polyèdres, de forme globuleuse, sont localisés dans le noyau des cellules intestinales, ils renferment des virions pris dans une trame polypeptidique constituée principalement de polyédrine. Le génome du baculovirus est un ADN bicaténaire. L'infection de cultures primaires d'hémocytes de Latoia viridissima à partir de virus extrait par dissolution des polyèdres, a été réussie au laboratoire

Published
1991

44. Mise en évidence d'un baculovirus de polyedrose nucléaire chez Latoia viridissima Lépidoptère Limacodidae ravageur du palmier à huile et du cocotier en Côte d'Ivoire = detection of a nuclear polyhedrosis baculoviruses in Latoia viridissima, Limacodid Lepidoptera, a oil palm and coconut pest in Côte d'Ivoire

Author

Kouassi, N.K., Fédière, Gilles, Léry, Xavier, Philippe, R., and Bergoin, M.

Subjects
VIRUS ENTOMOPATHOGENE, METHODE D'ANALYSE, COCOTIER, ADN, INSECTE NUISIBLE, PALMIER A HUILE, BIOLOGIE MOLECULAIRE, LUTTE BIOLOGIQUE
Published
1991

47. Etude du ribovirus de Latoia viridissima Holland, ravageur de Palmacae en Afrique de l'Ouest : caractérisation, diagnostic sérologique, suivi épidémiologique = study of the ribovirus of Latoia viridissima Holland, a palm pest in West Africa : characterization diagnosis, serology and epidemiological monitoring

Author

Zeddam, Jean-Louis, Philippe, R., Veyrunes, J.C., Fédière, Gilles, Mariau, D., and Bergoin, M.

Subjects
VIRUS ENTOMOPATHOGENE, ARN, EPIDEMIOLOGIE, TEST ELISA, INSECTE NUISIBLE, BIOLOGIE MOLECULAIRE, LUTTE BIOLOGIQUE
Published
1990

48. Etude du Ribovirus de Latoia viridissima Holland ravageur de palmacées en Afrique de l'Ouest. Caractérisation - Diagnostic sérologique - Suivi épidémiologique

Author

Zeddam, Jean-Louis, Philippe, René, Veyrunes, J.C., Fédière, Gilles, Mariau, Dominique, and Bergoin, M.

Subjects
H10 - Ravageurs des plantes, Virus des invertébrés, Lutte biologique, Clonage moléculaire, Technique immunoenzymatique, Diagnostic, Elaeis guineensis, Insecte nuisible
Abstract

Une revue des entomopathogènes locaux régulant les populations naturelles de Latoia viridissima a montré que l'agent de contrôle le plus efficace était un virus. Afin de détecter rapidement et à faible coût ce ribovirus, appelé LvV, dans les échantillons biologiques, un test immunoenzymatique (ELISA) a été mis au point. A l'aide de cet outil, on a pu étudier l'aspect épidémiologique de la maladie dans les plantations de palmiers à huile. Le suivi mené sur le terrain durant trois mois au cours de deux pullulations successives de L. viridissima a précisé l'incidence de la virose à l'émergence des jeunes chenilles, son évolution au cours des différents stades larvaires et son impact sur la démographie du ravageur. Par ailleurs, le clonage moléculaire du génome viral a été entrepris

Published
1990

50. Impact of punctual mutations in the cap gene of Junonia coenia densovirus (JcDNV) on virus assembly and infectivity to Ld 652 cells and Spodoptera littoralis larvae

Author

Iatrou, Kostas, Couble, Pierre, Abd-Alla, A., Jousset, F-X., Cousserans, F., Bergoin, M., Abe, H., Fujii, T., Mita, K., Ajimura, M., Shimada, T., Sahara, K., Tamura, T., Altstein, M., Hariton, A., Davidovitch, M., Ben-Aziz, O., Barat-Houari, M., Hilliou, F., Jousset, F.-X., Sofer, L., Deleury, E., Rocher, J., Ravallec, M., Galibert, L., Feyereisen, R., Fournier, P., Volkoff, A-N., Baxter, Simon W., Chamberlain, Nicola, Papa, Riccardo, Humphray, Sean J., ffrench-Constant, Richard H., McMillan, W. Owen, Jiggins, Chris D., Behere, G.T., Russell, D., Batterham, P., Tay, W. T., Beldade, P., Rudd, S., Gruber, J.D., Long, A.D., Breugelmans, B., Simonet, G., de Velde, S. Van, Soest, S. Van, Smagghe, G., Broeck, J. Vanden, Clark, R., Brown, S., Heckel, D., Jiggins, C. D., Collins, S., Vogler, A. P, Chamberlain, N., Baxter, S., Jiggins, C., ffrench-Constant, R.H., Chortyk, O., Friz, J., Thompson, C., Kumar, P., Tice, C., Vertin, B., Palli, R., Kumar, M., Meyer, A., Meteyer, T., Smith, H., Cress, D., Li, B., Hormann, R., Collinge, Derek, Gordon, Karl, Behm, Carolyn, Whyard, Steve, Alençon, d', Audant, E., Bernard-Samain, P., Bidegainberry, S., Brehélin, V., Brun-Barale, M., Cousserans, A., Duvic, C., Escoubas, B., Feyereisen, J-M., Fournier, R., Gagneur, Ph., Gordon, C., Gimenez, K., Heckel, S., Hotelier, D., Hilliou, Th., Mita, F., Negre, K., Sabourault, V., Suraporn, C., Volkoff, S., Weissenbach, N., Maria, De Simone Anna, Angela, Sorrentino, Francesca, Di Cara, Polito, Lino, Anna, Digilio F., Drezen, J-M, Bezier, A., Lesobre, J., Huguet, E., Dupuy, C., Eleftherianos, I., Millichap, P. J., Felföldi, G., Gökcen, F., Waterfield, N., Clarke, D. J., ffrench-Constant, R. H., Reynolds, S. E., Elias, M., Joron, M., Willmott, K., Kaiser, V., Silva-Brandão, K. L., Freitas, A.V.L., Arias Mejía, C., Gomez Pineres, L.M., Brower, A.V.Z., Escoubas, J.-M., Girard, P.-A., Volkoff, N., Boublik, Y., D'Alençon, E., Taillez, P., Brehélin, M., Venekei, I., Fischer, H. M., Wheat, C. W., Wittstock, U., Heckel, D. G., Vogel, H., Freitak, D., Katsuma, S., Futahashi, R., Fujiwara, H., Garel, Annie, Briolay, Jérôme, Brouilly, Patrick, Royer, Corinne, Sasanuma, Shun-ichi, Sasanuma, Motoe, Keime, Céline, Gandrillon, Olivier, Chavancy, Gérard, Mita, Kasuei, Geber, M., Faye, I., Terenius, O., Goldsmith, M., Proestou, D., Carter, D., Nicholson, E., Wu, C., Zhang, H., Gopinathan, K. P., Parthasarathy, R., Dhawan, S., Gordon, K., Colebatch, G., Campbell, P.M., Horne, I., East, P.D., Hughes, T.M., Marcus, J.M., Serbielle, C., Douris, V., Lalmanach, G., Iatrou, K., Iga, Masatoshi, Sekimoto, Takayuki, Elmogy, Mohamed, Iwami, Masafumi, Sakurai, Sho, Jacquin-Joly, E., Merlin, C., Malpel, S., Pelletier, J., Brigaud, I., François, M-C., Maïbèche, M., Jarvis, D.L., Aumiller, J.J., Geisler, C., Hensley, J., Hollister, J.R., Shi, X., Jiggins, Chris D, Joron, Mathieu, Mallet, James, Jostova, P., Svatos, A., Pichova, Iva, Kadono-Okuda, K., Ito, K., Nohata, J., Yamamoto, K., Sasanuma, M., Sasanuma, S., Eguchi, R., Hara, W., Kiyokawa, I., Kobayashi, I., Uchino, K., Sezutsu, H., Kanda, T., Miura, T., Ohashi, T., Katayama, K., Kourti, A., Gkouvitsas, T., Kusakabe, T., Mon, H., Takahashi, M., Lee, J.M., Kawaguchi, Y., Labropoulou, V., Stefanou, D., Magkrioti, C., Andronopoulou, E., Swevers, L., Lapointe, R., Tanaka, K., Barney, W., Whitfield, J., Banks, J., Béliveau, C., Stoltz, D., Webb, B.A., Cusson, M., Lee, Siu Fai, Heckel, David G., Li, Yi, Guarino, Linda A., Li, Muwang, Li, Minhui, Guo, Qiuhong, Miao, Xuexia, Hou, Chengxiang, Lin, Hongxuan, Huang, Yongping, Li, Lan, Zheng, Sichun, Ladd, Tim, Zhang, Dayu, Buhlers, Deborah, Krell, Peter J., Arif, Basil M., Retnakaran, Arthur, Feng, Qili, Doucet, Daniel, Machado, Ednildo, Swevers, Luc, Makhijani, Kalpana, Bharathi, V, Kannan, Ramakrishnan, Shashidhara, L S, Mauchamp, Bernard, Jalabert, Audrey, Rocha, Martine Da, Grenier, Anne-Marie, Labas, Valérie, Vinh, Joëlle, Mita, Kazuei, Kadono-Okuda, Keiko, Miao, Yungen, Yue, Wanfu, Li, Xinghua, Wu, Xiaofeng, Miller, T.A., Park, Y., Ren, X., Kasahara, M., Sasaki, S., Nagayasu, Y., Yamada, T., Kanamori, H., Namiki, N., Kitagawa, M., Yamashita, H., Yasukochi, Y., Rvikumar, G., Shimomura, M., Nagamura, Y., Shin-I, T., Morishita, S., Sasaki, T., Sugahara, R., Monteiro, Antónia, Chen, Bin, Ramos, Diane, Kamal, Firdous, Glaser, Gary, Stockslager, Steven, Nieberding, C., Schneider, V., Vos, H. De, Lassance, J.M., Lofstedt, C., Brakefield, P.M., Nighorn, A., Papanicolaou, A., Blaxter, M.L., Jiggins, C.D., Papantonis, A., Sourmeli, S., Lecanidou, R., Rocha, M. Da, Royer, C., Pennacchio, F., Falabella, P., Varricchio, P., Malva, C., Pohl, Nelida, Sison-Mangus, Marilou, Briscoe, Adriana D., Saenko, S.V., Satish, V., Shukla, J.N., Nagaraju, J., Frank, Scholz, Tine, Lesch, Susann, Beez, Traute, Holthusen, Ines, Anderl, Geuenich, Silvia, Tina, Trenczek, Kojima, K., Niimi, T., Hatakeyama, M., Shiotsuki, Takahiro, Tan, An-Jiang, Tamura, Toshiki, Simpson, Robert, Newcomb, Richard, Beuning, Lesley, Yauk, Yah-Khing, Crowhurst, Ross, Gatehouse, Heather, Gatehouse, Laurence, Markwick, Ngaire, Chagne, Dave, Gleave, Andrew, Christeller, John, Strand, M. R., Soin, T., Loocke, K. Van, Wheelock, C., Harada, T., Akamatsu, M., Nakagawa, Y., Truman, JW, Hiruma, K, Allee, JP, MacWhinnie, SGB, Champlin, D, Riddiford, LM, Turnbull, M.W., Vitkova, M., Kubickova, S., Marec, F., Kroymann, J., Mithöfer, A., Boland, W., Vogt, R.G., Franco, M-d., Bohbot, J, Fernandez, K., Kobres, P., Hanna, J., Poppy, J., Webb, Bruce A., Gill, Torrence A., Fath-Goodin, Angelika, Kroemer, Jeremy, Wedde, M., Altincicek, B., Vilcinskas, A., Wee, Choon Wei, Robin, Charles, Heckel, David G, Wheat, Christopher W., Labandeira, Conrad, Andolfatto, P., Feng, Q., Simpson, R., Vogel, Heiko, Williams, A. K., Xia, Qingyou, Zhou, Zeyang, Lu, Cheng, Xiang, Zhonghuai, Zhang, Liang, Yamamoto, Kimiko, Narukawa, Junko, Nohata, Junko, Suetsugu, Yoshitaka, Minami, Hiroshi, Shimomura, Michihiko, Yukuhiro, K., Itoh, M., Banno, Y., Kômoto, N., Kosegawa, E., Hirokawa, M., Tatematsu, K., Nishimura, M., Maekawa, H., Kawanishi, Y., Nakajima, Y., and Krell, Peter J

Subjects
Article
Published
2007

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