TY - JOUR
T1 - Atomic resolution structures of human bufaviruses determined by cryo-electron microscopy
AU - Ilyas, Maria
AU - Mietzsch, Mario
AU - Kailasan, Shweta
AU - Väisänen, Elina
AU - Luo, Mengxiao
AU - Chipman, Paul
AU - Smith, J. Kennon
AU - Kurian, Justin
AU - Sousa, Duncan
AU - McKenna, Robert
AU - Söderlund-Venermo, Maria
AU - Agbandje-McKenna, Mavis
N1 - Funding Information:
The authors thank Joshua Hull for excellent technical support. We also thank the Electron microscopy core of the University of Florida (UF) Interdisciplinary Center for Biotechnology Research (ICBR) for access to electron microscopes utilized for negative stain electron microscopy and cryo-EM data collection. The Spirit and TF20 cryo-electron microscopes were provided by the UF College of Medicine (COM) and Division of Sponsored Programs (DSP). We thank Hong Zhou (University of California Los Angeles) and the NIH “West/Midwest Consortium for High-Resolution Cryo Electron Microscopy” project for access to the Electron Imaging Center for Nanomachines’s Titan Krios and K2 DED utilized for high-resolution data collection (MPI, HZ, MAM, and others). Data collection at Florida State University was made possible by NIH grants S10 OD018142-01Purchase of a direct electron camera for the Titan-Krios at FSU (PI Taylor), S10 RR025080-01 Purchase of a FEI Titan Krios for 3-D EM (PI Taylor), and U24 GM116788 The Southeastern Consortium for Microscopy of MacroMolecular Machines (PI Taylor). The University of Florida COM and NIH GM082946 (to MAM and RM) provided funds for the research efforts at the University of Florida. The Sigrid Jusélius Foundation and the Life and Health Medical Grant Association provided funds for the research efforts at the University of Helsinki, Finland (to MS-V).
Funding Information:
Acknowledgments: The authors thank Joshua Hull for excellent technical support. We also thank the Electron microscopy core of the University of Florida (UF) Interdisciplinary Center for Biotechnology Research (ICBR) for access to electron microscopes utilized for negative stain electron microscopy and cryo-EM data collection. The Spirit and TF20 cryo-electron microscopes were provided by the UF College of Medicine (COM) and Division of Sponsored Programs (DSP). We thank Hong Zhou (University of California Los Angeles) and the NIH “West/Midwest Consortium for High-Resolution Cryo Electron Microscopy” project for access to the Electron Imaging Center for Nanomachines’s Titan Krios and K2 DED utilized for high-resolution data collection (MPI, HZ, MAM, and others). Data collection at Florida State University was made possible by NIH grants S10 OD018142-01Purchase of a direct electron camera for the Titan-Krios at FSU (PI Taylor), S10 RR025080-01 Purchase of a FEI Titan Krios for 3-D EM (PI Taylor), and U24 GM116788 The Southeastern Consortium for Microscopy of MacroMolecular Machines (PI Taylor). The University of Florida COM and NIH GM082946 (to MAM and RM) provided funds for the research efforts at the University of Florida. The Sigrid Jusélius Foundation and the Life and Health Medical Grant Association provided funds for the research efforts at the University of Helsinki, Finland (to MS-V).
Publisher Copyright:
© 2018 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2018/1
Y1 - 2018/1
N2 - Bufavirus strain 1 (BuV1), a member of the Protoparvovirus genus of the Parvoviridae, was first isolated from fecal samples of children with acute diarrhea in Burkina Faso. Since this initial discovery, BuVs have been isolated in several countries, including Finland, the Netherlands, and Bhutan, in pediatric patients exhibiting similar symptoms. Towards their characterization, the structures of virus-like particles of BuV1, BuV2, and BuV3, the current known genotypes, have been determined by cryo-electron microscopy and image reconstruction to 2.84, 3.79, and 3.25 Å, respectively. The BuVs, 65–73% identical in amino acid sequence, conserve the major viral protein, VP2, structure and general capsid surface features of parvoviruses. These include a core β-barrel (βB-βI), α-helix A, and large surface loops inserted between these elements in VP2. The capsid contains depressions at the icosahedral 2-fold and around the 5-fold axes, and has three separated protrusions surrounding the 3-fold axes. Structure comparison among the BuVs and to available parvovirus structures revealed capsid surface variations and capsid 3-fold protrusions that depart from the single pinwheel arrangement of the animal protoparvoviruses. These structures provide a platform to begin the molecular characterization of these potentially pathogenic viruses.
AB - Bufavirus strain 1 (BuV1), a member of the Protoparvovirus genus of the Parvoviridae, was first isolated from fecal samples of children with acute diarrhea in Burkina Faso. Since this initial discovery, BuVs have been isolated in several countries, including Finland, the Netherlands, and Bhutan, in pediatric patients exhibiting similar symptoms. Towards their characterization, the structures of virus-like particles of BuV1, BuV2, and BuV3, the current known genotypes, have been determined by cryo-electron microscopy and image reconstruction to 2.84, 3.79, and 3.25 Å, respectively. The BuVs, 65–73% identical in amino acid sequence, conserve the major viral protein, VP2, structure and general capsid surface features of parvoviruses. These include a core β-barrel (βB-βI), α-helix A, and large surface loops inserted between these elements in VP2. The capsid contains depressions at the icosahedral 2-fold and around the 5-fold axes, and has three separated protrusions surrounding the 3-fold axes. Structure comparison among the BuVs and to available parvovirus structures revealed capsid surface variations and capsid 3-fold protrusions that depart from the single pinwheel arrangement of the animal protoparvoviruses. These structures provide a platform to begin the molecular characterization of these potentially pathogenic viruses.
KW - Bufavirus
KW - Cryo-EM and image reconstruction
KW - Parvoviruses
KW - Single-stranded DNA virus
UR - http://www.scopus.com/inward/record.url?scp=85040243012&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85040243012&partnerID=8YFLogxK
U2 - 10.3390/v10010022
DO - 10.3390/v10010022
M3 - Article
C2 - 29300333
AN - SCOPUS:85040243012
SN - 1999-4915
VL - 10
JO - Viruses
JF - Viruses
IS - 1
M1 - 22
ER -