Viral entry mechanisms: cellular and viral mediators of herpes simplex virus entry
Open accessAbstract
Herpes simplex virus type‐1 and type‐2 are highly prevalent human pathogens causing life‐long infections. The process of infection begins when the virions bind heparan sulfate moieties present on host cell surfaces. This initial attachment then triggers a cascade of molecular interactions involving multiple viral and host cell proteins and receptors, leading to penetration of the viral nucleocapsid and tegument proteins into the cytoplasm. The nucleocapsid is then transported to the nuclear membrane and the viral DNA is released for replication in the nucleus. Recent studies have revealed that herpes simplex virus entry or penetration into cells may be a highly complex process and the mechanism of entry may demonstrate unique cell‐type specificities. Although specificities clearly exist, past and ongoing studies demonstrate that herpes simplex virus may share certain common receptors and pathways that are also used by many other human viruses. This minireview helps to shed light on recent revelations on the herpes simplex virus entry process.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Herpes simplex virus infections
Whitley, R. J., & Roizman, B. (2001) · The Lancet · doi:10.1016/s0140-6736(00)04638-9 · Cited by 1,365 · see citing works
A Novel Role for 3-O-Sulfated Heparan Sulfate in Herpes Simplex Virus 1 Entry
Shukla, D., Liu, J., Blaiklock, P., Shworak, N. W., Bai, X., Esko, J. D., Cohen, G. H., Eisenberg, R. J., ROSENBERG, R. D., & Spear, P. G. (1999) · Cell · doi:10.1016/s0092-8674(00)80058-6 · Cited by 1,053 · see citing works
Self-citationRegulated Diversity of Heparan Sulfate*
Lindahl, U., Kusche-Gullberg, M., & Kjellén, L. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.39.24979 · Cited by 688 · see citing works
Microtubule-mediated transport of incoming herpes simplex virus 1 capsids to the nucleus
Sodeik, B., Ebersold, M. W., & Helenius, A. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.136.5.1007 · Cited by 687 · see citing works
Herpes simplex virus: receptors and ligands for cell entry
Spear, P. G. (2004) · Cellular Microbiology · doi:10.1111/j.1462-5822.2004.00389.x · Cited by 582 · see citing works
Crystal Structure of Glycoprotein B from Herpes Simplex Virus 1
Heldwein, E. E. Z., Lou, H., Bender, F. C., Cohen, G. H., Eisenberg, R. J., & Harrison, S. C. (2006) · Science · doi:10.1126/science.1126548 · Cited by 563 · see citing works
Herpesviruses and heparan sulfate: an intimate relationship in aid of viral entry
Shukla, D., & Spear, P. G. (2001) · Journal of Clinical Investigation · doi:10.1172/jci13799 · Cited by 497 · see citing works
Self-citationActin- and myosin-driven movement of viruses along filopodia precedes their entry into cells
Lehmann, M. J., Sherer, N. M., Marks, C. B., Pypaert, M., & Mothes, W. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200503059 · Cited by 403 · see citing works
Herpes Simplex Virus Glycoprotein D Bound to the Human Receptor HveA
Carfı́, A., Willis, S. H., Whitbeck, J. C., Krummenacher, C., Cohen, G. H., Eisenberg, R. J., & Wiley, D. C. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00298-2 · Cited by 391 · see citing works
Nimmerjahn, F., Milosevic, S., Behrends, U., Jaffee, E. M., Pardoll, D. M., Bornkamm, G. W., & Mautner, J. (2003) · European Journal of Immunology · doi:10.1002/eji.200323730 · Cited by 359 · see citing works
Nicola, A. V., McEvoy, A. M., & Straus, S. E. (2003) · Journal of Virology · doi:10.1128/jvi.77.9.5324-5332.2003 · Cited by 352 · see citing works
PILRα Is a Herpes Simplex Virus-1 Entry Coreceptor That Associates with Glycoprotein B
Satoh, T., Arii, J., Suenaga, T., Wang, J., Kogure, A., Uehori, J., Arase, N., Shiratori, I., Tanaka, S., Kawaguchi, Y., et al. (2008) · Cell · doi:10.1016/j.cell.2008.01.043 · Cited by 299 · see citing works
Pertel, P. E., Fridberg, A., Parish, M. L., & Spear, P. G. (2001) · Virology · doi:10.1006/viro.2000.0713 · Cited by 285 · see citing works
A novel role for phagocytosis-like uptake in herpes simplex virus entry
Clément, C., Tiwari, V., Scanlan, P. M., Vályi-Nagy, T., Yue, B. Y. J. T., & Shukla, D. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200509155 · Cited by 252 · see citing works
Self-citationNicola, A. V., Hou, J., Major, E. O., & Straus, S. E. (2005) · Journal of Virology · doi:10.1128/jvi.79.12.7609-7616.2005 · Cited by 247 · see citing works
Atanasiu, D., Whitbeck, J. C., Cairns, T. M., Reilly, B., Cohen, G. H., & Eisenberg, R. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707452104 · Cited by 183 · see citing works
Subramanian, R. P., & Geraghty, R. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608374104 · Cited by 179 · see citing works
Human Papillomavirus Type 16 Entry: Retrograde Cell Surface Transport along Actin-Rich Protrusions
Schelhaas, M., Ewers, H., Rajamäki, M., Day, P. M., Schiller, J. T., & Helenius, A. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.1000148 · Cited by 168 · see citing works
The multipartite system that mediates entry of herpes simplex virus into the cell
Campadelli‐Fiume, G., Amasio, M., Avitabile, E., Cerretani, A., Forghieri, C., Gianni, T., & Menotti, L. (2007) · Reviews in Medical Virology · doi:10.1002/rmv.546 · Cited by 152 · see citing works
Banfield, B. W., Leduc, Y., Esford, L. E., Schubert, K. M., & Tufaro, F. (1995) · Journal of Virology · doi:10.1128/jvi.69.6.3290-3298.1995 · Cited by 137 · see citing works
Bender, F. C., Whitbeck, J. C., Lou, H., Cohen, G. H., & Eisenberg, R. J. (2005) · Journal of Virology · doi:10.1128/jvi.79.18.11588-11597.2005 · Cited by 136 · see citing works
Alternative Entry Receptors for Herpes Simplex Virus and Their Roles in Disease
Taylor, J. M., Lin, E., Susmarski, N., Yoon, M., Zago, A., Ware, C. F., Pfeffer, K., Miyoshi, J., Takai, Y., & Spear, P. G. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.06.005 · Cited by 134 · see citing works
Tiwari, V., Clément, C., Xu, D., Vályi-Nagy, T., Yue, B. Y. J. T., Liu, J., & Shukla, D. (2006) · Journal of Virology · doi:10.1128/jvi.00296-06 · Cited by 131 · see citing works
Self-citationUsing a 3-O-Sulfated Heparin Octasaccharide To Inhibit the Entry of Herpes Simplex Virus Type 1
Copeland, R. J., Balasubramaniam, A., Tiwari, V., Zhang, F., Bridges, A. S., Linhardt, R. J., Shukla, D., & Liu, J. (2008) · Biochemistry · doi:10.1021/bi800205t · Cited by 126 · see citing works
Self-citationYoon, M., Zago, A., Shukla, D., & Spear, P. G. (2003) · Journal of Virology · doi:10.1128/jvi.77.17.9221-9231.2003 · Cited by 122 · see citing works
Self-citationXu, D., Tiwari, V., Xia, G., Clément, C., Shukla, D., & Liu, J. (2005) · Biochemical Journal · doi:10.1042/bj20040908 · Cited by 120 · see citing works
Self-citationHerold, B. C., Gerber, S. I., Belval, B. J., Siston, A. M., & Shulman, N. S. (1996) · Journal of Virology · doi:10.1128/jvi.70.6.3461-3469.1996 · Cited by 108 · see citing works
Herpes simplex virus type 1 glycoprotein H binds to αvβ3 integrins
Parry, C. M., Bell, S., Minson, T., & Browne, H. M. (2004) · Journal of General Virology · doi:10.1099/vir.0.80567-0 · Cited by 103 · see citing works
Farnsworth, A., & Johnson, D. C. (2006) · Journal of Virology · doi:10.1128/jvi.80.7.3167-3179.2006 · Cited by 101 · see citing works
Gianni, T., Campadelli‐Fiume, G., & Menotti, L. (2004) · Journal of Virology · doi:10.1128/jvi.78.22.12268-12276.2004 · Cited by 95 · see citing works
Gianni, T., Amasio, M., & Campadelli‐Fiume, G. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.005728 · Cited by 95 · see citing works
A role for 3-O-sulfated heparan sulfate in cell fusion induced by herpes simplex virus type 1
Tiwari, V., Clément, C., Duncan, M. B., Chen, J., Liu, J., & Shukla, D. (2004) · Journal of General Virology · doi:10.1099/vir.0.19641-0 · Cited by 88 · see citing works
Self-citationArii, J., Uema, M., Morimoto, T., Sagara, H., Akashi, H., Ono, E., Arase, H., & Kawaguchi, Y. (2009) · Journal of Virology · doi:10.1128/jvi.02601-08 · Cited by 85 · see citing works
Akhtar, J., Tiwari, V., Oh, M.-J., Kovacs, M., Jani, A., Kovács, S. K., Vályi-Nagy, T., & Shukla, D. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-1807 · Cited by 83 · see citing works
Self-citationO'Donnell, C. D., Tiwari, V., Oh, M.-J., & Shukla, D. (2005) · Virology · doi:10.1016/j.virol.2005.11.003 · Cited by 82 · see citing works
Self-citationDixit, R., Tiwari, V., & Shukla, D. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.05.031 · Cited by 63 · see citing works
Self-citationStiles, K. M., Milne, R. S. B., Cohen, G. H., Eisenberg, R. J., & Krummenacher, C. (2008) · Virology · doi:10.1016/j.virol.2007.11.012 · Cited by 63 · see citing works
Tiwari, V., Oh, M., Kovacs, M., Shukla, S. Y., Vályi-Nagy, T., & Shukla, D. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06655.x · Cited by 62 · see citing works
Self-citationFocal Adhesion Kinase Plays a Pivotal Role in Herpes Simplex Virus Entry
Cheshenko, N., Liu, W., Satlin, L. M., & Herold, B. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503518200 · Cited by 60 · see citing works
Tiwari, V., Clément, C., Scanlan, P. M., Kowlessur, D., Yue, B. Y. J. T., & Shukla, D. (2005) · Journal of Virology · doi:10.1128/jvi.79.20.13173-13179.2005 · Cited by 58 · see citing works
Self-citationDavid, A. T., Baghian, A., Foster, T. P., Chouljenko, V. N., & Kousoulas, K. G. (2008) · Current Eye Research · doi:10.1080/02713680802130362 · Cited by 57 · see citing works
Galdiero, S., Vitiello, M., D’Isanto, M., Falanga, A., Cantisani, M., Browne, H. M., Pedone, C., & Galdiero, M. (2008) · ChemBioChem · doi:10.1002/cbic.200700457 · Cited by 49 · see citing works
Role of Nectin-1, HVEM, and PILR-α in HSV-2 Entry into Human Retinal Pigment Epithelial Cells
Shukla, S. Y., Singh, Y. K., & Shukla, D. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-2981 · Cited by 36 · see citing works
Self-citationPérez, A., Li, Q.-X., Pérez‐Romero, P., DeLassus, G. S., Lopez, S. R., Sutter, S. B., McLaren, N. C., & Fuller, A. O. (2005) · Journal of Virology · doi:10.1128/jvi.79.12.7419-7430.2005 · Cited by 31 · see citing works
A Novel Function of Heparan Sulfate in the Regulation of Cell-Cell Fusion
O'Donnell, C. D., & Shukla, D. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.037960 · Cited by 28 · see citing works
Self-citationFan, Q., Lin, E., Satoh, T., Arase, H., & Spear, P. G. (2009) · Journal of Virology · doi:10.1128/jvi.00087-09 · Cited by 28 · see citing works
Role of 3‐O‐sulfated heparan sulfate in virus‐induced polykaryocyte formation
Tiwari, V., ten Dam, G. B., Yue, B. Y. J. T., Kuppevelt, T. H. V., & Shukla, D. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.08.029 · Cited by 27 · see citing works
Self-citationRole of AF6 protein in cell‐to‐cell spread of Herpes simplex virus 1
Keyser, J., Lorger, M., Pavlovic, J., Radziwill, G., & Moelling, K. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.10.030 · Cited by 9 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Inhibition of SARS Pseudovirus Cell Entry by Lactoferrin Binding to Heparan Sulfate Proteoglycans
Lang, J., Yang, N., Deng, J., Liu, K., Yang, P., Zhang, G., & Jiang, C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023710 · Cited by 428 · see citing works
Heparan Sulfate Proteoglycans and Viral Attachment: True Receptors or Adaptation Bias?
Cagno, V., Tseligka, E. D., Jones, S. T., & Tapparel, C. (2019) · Viruses · doi:10.3390/v11070596 · Cited by 385 · see citing works
Recognition of herpesviruses by the innate immune system
Paludan, S. R., Bowie, A., Horan, K., & Fitzgerald, K. A. (2011) · Nature reviews. Immunology · doi:10.1038/nri2937 · Cited by 353 · see citing works
Pharmacology of Heparin and Related Drugs
Mulloy, B., Hogwood, J., Gray, E., Lever, R., & Page, C. P. (2015) · Pharmacological Reviews · doi:10.1124/pr.115.011247 · Cited by 341 · see citing works
Herpes Virus Fusion and Entry: A Story with Many Characters
Eisenberg, R. J., Atanasiu, D., Cairns, T. M., Gallagher, J. R., Krummenacher, C., & Cohen, G. H. (2012) · Viruses · doi:10.3390/v4050800 · Cited by 318 · see citing works
Terminal N-Linked Galactose Is the Primary Receptor for Adeno-associated Virus 9
Shen, S., Bryant, K. D., Brown, S. M., Randell, S. H., & Asokan, A. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.210922 · Cited by 281 · see citing works
Role of Lipids in Virus ReplicationPreprint
Lorizate, M., & Kräusslich, H. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004820 · Cited by 280 · see citing works
Johnson, K. E., Chikoti, L., & Chandran, B. (2013) · Journal of Virology · doi:10.1128/jvi.00082-13 · Cited by 271 · see citing works
The signaling networks of the herpesvirus entry mediator (TNFRSF14) in immune regulation
Steinberg, M. W., Cheung, T. C., & Ware, C. F. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01064.x · Cited by 245 · see citing works
Orłowski, P., Tomaszewska, E., Gniadek, M., Bąska, P., Nowakowska, J., Sokołowska, J., Nowak, Z., Donten, M., Celichowski, G., Grobelny, J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104113 · Cited by 212 · see citing works
Virostatic potential of micro–nano filopodia-like ZnO structures against herpes simplex virus-1
Mishra, Y. K., Adelung, R., Röhl, C., Shukla, D., Spors, F., & Tiwari, V. (2011) · Antiviral Research · doi:10.1016/j.antiviral.2011.08.017 · Cited by 209 · see citing works
Self-citationBourgade, K., Garneau, H., Giroux, G., Le Page, A. Y., Bocti, C., Dupuis, G., Frost, E. H., & Fülöp, T. (2015) · Biogerontology · doi:10.1007/s10522-014-9538-8 · Cited by 208 · see citing works
Antoine, T. E., Mishra, Y. K., Trigilio, J., Tiwari, V., Adelung, R., & Shukla, D. (2012) · Antiviral Research · doi:10.1016/j.antiviral.2012.09.020 · Cited by 195 · see citing works
Self-citationHu, Y., Lin, S., Huang, C., Zulueta, M. M. L., Liu, J.-Y., Chang, W., & Hung, S. (2011) · Nature Chemistry · doi:10.1038/nchem.1073 · Cited by 192 · see citing works
Cell Entry Mechanisms of HSV: What we have Learned in Recent Years
Agelidis, A. M., & Shukla, D. (2015) · Future Virology · doi:10.2217/fvl.15.85 · Cited by 191 · see citing works
Self-citationHerpes Simplex Virus Cell Entry Mechanisms: An Update
Madavaraju, K., Koganti, R., Volety, I., Yadavalli, T., & Shukla, D. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.617578 · Cited by 194 · see citing works
Self-citationPhosphatidylserine receptors: Enhancers of enveloped virus entry and infection
Møller-Tank, S., & Maury, W. J. (2014) · Virology · doi:10.1016/j.virol.2014.09.009 · Cited by 186 · see citing works
Vaccinia virus strains use distinct forms of macropinocytosis for host-cell entry
Mercer, J., Knébel, S., Schmidt, F. I., Crouse, J., Tait‐Burkard, C., & Helenius, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004618107 · Cited by 171 · see citing works
Herpes simplex virus infects most cell types in vitro: clues to its success
Karasneh, G. A., & Shukla, D. (2011) · Virology Journal · doi:10.1186/1743-422x-8-481 · Cited by 165 · see citing works
Self-citationThe Interplay between Adeno-Associated Virus and Its Helper Viruses
Meier, A. F., Fraefel, C., & Seyffert, M. (2020) · Viruses · doi:10.3390/v12060662 · Cited by 160 · see citing works
Neonatal Herpes Simplex Virus Infection
James, S. H., & Kimberlin, D. W. (2014) · Clinics in Perinatology · doi:10.1016/j.clp.2014.10.005 · Cited by 158 · see citing works
The Synthetic Antiviral Drug Arbidol Inhibits Globally Prevalent Pathogenic Viruses
Pécheur, E., Borisevich, V., Halfmann, P., Morrey, J. D., Smee, D. F., Prichard, M. N., Mire, C. E., Kawaoka, Y., Geisbert, T. W., & Polyak, S. J. (2016) · Journal of Virology · doi:10.1128/jvi.02077-15 · Cited by 158 · see citing works
Auriti, C., Rose, D. U. D., Santisi, A., Martini, L., Piersigilli, F., Bersani, I., Ronchetti, M. P., & Caforio, L. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2021.166198 · Cited by 162 · see citing works
Nanostructures for the Inhibition of Viral Infections
Szunerits, S., Barras, A., Khanal, M., Pagneux, Q., & Boukherroub, R. (2015) · Molecules · doi:10.3390/molecules200814051 · Cited by 132 · see citing works
Nanomedicine as an emerging approach against intracellular pathogens
Li, B., & Armstead (2011) · International Journal of Nanomedicine · doi:10.2147/ijn.s27285 · Cited by 130 · see citing works
Tiwari, V., Darmani, N. A., Yue, B. Y. J. T., & Shukla, D. (2009) · Phytotherapy Research · doi:10.1002/ptr.3085 · Cited by 125 · see citing works
Self-citationGescher, K., Hensel, A., Hafezi, W., Derksen, A., & Kühn, J. (2010) · Antiviral Research · doi:10.1016/j.antiviral.2010.10.007 · Cited by 118 · see citing works
Neonatal Herpes Simplex Virus Infection
James, S. H., & Kimberlin, D. W. (2015) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2015.05.001 · Cited by 116 · see citing works
Nanoparticles in Antiviral Therapy
Milovanović, M., Arsenijević, A., Milovanović, J., Kanjevac, T., & Arsenijević, N. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-52733-0.00014-8 · Cited by 114 · see citing works
Anti-heparan Sulfate Peptides That Block Herpes Simplex Virus Infection in Vivo
Tiwari, V., Liu, J., Vályi-Nagy, T., & Shukla, D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.201103 · Cited by 108 · see citing works
Self-citationWatterson, D., Kobe, B., & Young, P. R. (2011) · Journal of General Virology · doi:10.1099/vir.0.037317-0 · Cited by 106 · see citing works
Exploitation of Cytoskeletal Networks during Early Viral Infection
Walsh, D., & Naghavi, M. H. (2018) · Trends in Microbiology · doi:10.1016/j.tim.2018.06.008 · Cited by 99 · see citing works
Glycosylation of viral proteins: Implication in virus–host interaction and virulence
Feng, T., Zhang, J., Chen, Z., Pan, W., Chen, Z., Yan, Y., & Dai, J. (2022) · Virulence · doi:10.1080/21505594.2022.2060464 · Cited by 101 · see citing works
Mother-to-Child Transmission of Herpes Simplex Virus
James, S. H., Sheffield, J. S., & Kimberlin, D. W. (2014) · Journal of the Pediatric Infectious Diseases Society · doi:10.1093/jpids/piu050 · Cited by 100 · see citing works
Ron‐Doitch, S., Sawodny, B., Kühbacher, A., David, M. M. N., Samanta, A., Phopase, J., Burger‐Kentischer, A., Griffith, M., Golomb, G., & Rupp, S. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.03.025 · Cited by 100 · see citing works
Melissa officinalis Extract Inhibits Attachment of Herpes Simplex Virus in vitro
Astani, A., Reichling, J., & Schnitzler, P. (2012) · Chemotherapy · doi:10.1159/000335590 · Cited by 98 · see citing works
Anti-Viral Properties of Amyloid-β Peptides
Bourgade, K., Dupuis, G., Frost, E. H., & Fülöp, T. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-160517 · Cited by 96 · see citing works
A New Class of Synthetic Peptide Inhibitors Blocks Attachment and Entry of Human Pathogenic Viruses
Krepstakies, M., Lucifora, J., Nagel, C., Zeisel, M. B., Holstermann, B., Hohenberg, H., Kowalski, I., Gutsmann, T., Baumert, T. F., Brandenburg, K., et al. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis273 · Cited by 92 · see citing works
Potential of carbohydrate‐binding agents as therapeutics against enveloped viruses
François, K. O., & Balzarini, J. M. (2010) · Medicinal Research Reviews · doi:10.1002/med.20216 · Cited by 90 · see citing works
Current and Emerging Therapies for Ocular Herpes Simplex Virus Type-1 Infections
Koganti, R., Yadavalli, T., & Shukla, D. (2019) · Microorganisms · doi:10.3390/microorganisms7100429 · Cited by 81 · see citing works
Self-citationHeparan Sulfate Proteoglycans in Viral Infection and Treatment: A Special Focus on SARS-CoV-2
Pasquale, V. D., Quiccione, M. S., Tafuri, S., Avallone, L., & Pavone, L. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126574 · Cited by 82 · see citing works
de Oliveira, A. P., Adams, S. D., Lee, L. H., Murray, S. R., Hsu, S., Hammond, J. R., Dickinson, D. P., Chen, P., & Chu, T.-C. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.11.006 · Cited by 80 · see citing works
Role of Microvesicles in the Spread of Herpes Simplex Virus 1 in Oligodendrocytic Cells
Bello-Morales, R., Praena, B., de la Nuez, C., Rejas, M. T., Guerra, M., Galán-Ganga, M., Izquierdo, M., Calvo, V., Krummenacher, C., & López‐Guerrero, J. A. (2018) · Journal of Virology · doi:10.1128/jvi.00088-18 · Cited by 76 · see citing works
Extracellular Vesicles in Viral Spread and Antiviral Response
Bello‐Morales, R., Ripa, I., & López‐Guerrero, J. A. (2020) · Viruses · doi:10.3390/v12060623 · Cited by 76 · see citing works
Entry of Herpesviruses into Cells: The Enigma Variations
Krummenacher, C., Carfı́, A., Eisenberg, R. J., & Cohen, G. H. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-7651-1_10 · Cited by 73 · see citing works
Imaging Lysosomal pH Alteration in Stressed Cells with a Sensitive Ratiometric Fluorescence Sensor
Xue, Z., Zhao, H., Liu, J., Han, J., & Han, S. (2017) · ACS Sensors · doi:10.1021/acssensors.7b00035 · Cited by 73 · see citing works
Membrane Protein of Human Coronavirus NL63 Is Responsible for Interaction with the Adhesion Receptor
Naskalska, A., Dąbrowska, A., Szczepański, A., Milewska, A., Jasik, K. P., & Pyrć, K. (2019) · Journal of Virology · doi:10.1128/jvi.00355-19 · Cited by 73 · see citing works
Biology and pathogenesis of cytomegalovirus in periodontal disease
Contreras, A., Botero, J. E., & Slots, J. (2013) · Periodontology 2000 · doi:10.1111/j.1600-0757.2012.00448.x · Cited by 71 · see citing works
Arleevskaya, M., Kravtsova, O., Lemerle, J., Renaudineau, Y., & Tsibulkin, A. P. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01296 · Cited by 66 · see citing works
Gescher, K., Kühn, J., Lorentzen, E. U., Hafezi, W., Derksen, A., Deters, A. M., & Hensel, A. (2011) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2010.12.038 · Cited by 68 · see citing works
Evasion of Early Antiviral Responses by Herpes Simplex Viruses
Suazo, P. A., Ibañez, F. J., Retamal-Díaz, A. R., Paz-Fiblas, M. V., Bueno, S. M., Kalergis, A. M., & González, P. A. (2015) · Mediators of Inflammation · doi:10.1155/2015/593757 · Cited by 67 · see citing works
Syndecan receptors: pericellular regulators in development and inflammatory disease
Gopal, S., Arokiasamy, S., Pataki, C. A., Whiteford, J. R., & Couchman, J. (2021) · Open Biology · doi:10.1098/rsob.200377 · Cited by 64 · see citing works
Cerqueira, C., Liu, Y., Kühling, L., Chai, W., Hafezi, W., Kuppevelt, T. H. V., Kühn, J., Feizi, T., & Schelhaas, M. (2013) · Cellular Microbiology · doi:10.1111/cmi.12150 · Cited by 64 · see citing works
Genital Herpes: Insights into Sexually Transmitted Infectious Disease
Jaishankar, D., & Shukla, D. (2016) · Microbial Cell · doi:10.15698/mic2016.09.528 · Cited by 64 · see citing works
Self-citationAggarwal, A., Saksena, M. M., Boadle, R. A., Kelly, B., Diefenbach, R. J., Alam, W., & Cunningham, A. L. (2012) · Journal of Virology · doi:10.1128/jvi.07016-11 · Cited by 63 · see citing works
Rajtar, B., Skalicka‐Woźniak, K., Świątek, Ł., Stec, A., Boguszewska, A., & Polz‐Dacewicz, M. (2017) · Food and Chemical Toxicology · doi:10.1016/j.fct.2017.05.011 · Cited by 63 · see citing works
Herpesviruses and MicroRNAs: New Pathogenesis Factors in Oral Infection and Disease?
Naqvi, A. R., Shango, J., Seal, A., Shukla, D., & Nares, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02099 · Cited by 62 · see citing works
Self-citationXu, X., Zhang, Y., & Li, Q. (2019) · Reviews in Medical Virology · doi:10.1002/rmv.2054 · Cited by 62 · see citing works
Cheng, A. Z., Moraes, S. N., Attarian, C., Yockteng-Melgar, J., Jarvis, M. C., Biolatti, M., Galitska, G., Dell’Oste, V., Frappier, L., Bierle, C. J., et al. (2019) · Journal of Virology · doi:10.1128/jvi.01539-19 · Cited by 63 · see citing works
Glycoprotein targeted therapeutics: a new era of anti‐herpes simplex virus‐1 therapeutics
Antoine, T. E., Park, P. J., & Shukla, D. (2013) · Reviews in Medical Virology · doi:10.1002/rmv.1740 · Cited by 60 · see citing works
Self-citationDrug-encapsulated carbon (DECON): A novel platform for enhanced drug delivery
Yadavalli, T., Ames, J. M., Agelidis, A. M., Suryawanshi, R. K., Jaishankar, D., Hopkins, J., Thakkar, N., Koujah, L., & Shukla, D. (2019) · Science Advances · doi:10.1126/sciadv.aax0780 · Cited by 60 · see citing works
Self-citationRevisiting Regulated Cell Death Responses in Viral Infections
Balaya, R. D. A., Prasad, T. S. K., & Kandasamy, R. K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137023 · Cited by 59 · see citing works
Tiwari, V., & Shukla, D. (2010) · Journal of General Virology · doi:10.1099/vir.0.024166-0 · Cited by 59 · see citing works
Self-citationRedwan, E. M. M. M., El‐Fakharany, E. M., Uversky, V. N., & Linjawi, M. H. (2014) · BMC Complementary and Alternative Medicine · doi:10.1186/1472-6882-14-219 · Cited by 59 · see citing works
HSV ‐1 Glycoproteins Are Delivered to Virus Assembly Sites Through Dynamin‐Dependent Endocytosis
Albecka, A., Laine, R. F., Janssen, A. F. J., Kaminski, C. F., & Crump, C. M. (2015) · Traffic · doi:10.1111/tra.12340 · Cited by 57 · see citing works
Defining nervous system susceptibility during acute and latent herpes simplex virus-1 infection
Menendez, C. M., & Carr, D. J. J. (2017) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2017.02.020 · Cited by 60 · see citing works
Extracellular matrix in plants and animals: hooks and locks for viruses
Stavolone, L., & Lionetti, V. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01760 · Cited by 59 · see citing works
Badr, G., Ramadan, N. K., Sayed, L. H., Badr, B. M., Omar, H. E.-D. M., & Selamoğlu, Z. (2017) · Europe PMC (PubMed Central) · doi:10.22038/ijbms.2017.8573 · Cited by 58 · see citing works
Herpes Simplex Virus Type-1: Replication, Latency, Reactivation and its Antiviral Targets
de Mello, C. P. P., Bloom, D. C., & Paixão, I. C. N. D. P. (2015) · Antiviral Therapy · doi:10.3851/imp3018 · Cited by 56 · see citing works
Diversity of Heparan Sulfate and HSV Entry: Basic Understanding and Treatment Strategies
Tiwari, V., Tarbutton, M., & Shukla, D. (2015) · Molecules · doi:10.3390/molecules20022707 · Cited by 53 · see citing works
Self-citationEmerging Roles of Heparanase in Viral Pathogenesis
Thakkar, N., Yadavalli, T., Jaishankar, D., & Shukla, D. (2017) · Pathogens · doi:10.3390/pathogens6030043 · Cited by 53 · see citing works
Self-citationExtracellular Vesicles in Herpes Viral Spread and Immune Evasion
Bello‐Morales, R., & López‐Guerrero, J. A. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02572 · Cited by 53 · see citing works
Su, D., Li-ping, H., Shi, C., Li, Y., Qian, S., Feng, Z., & Yu, L. (2024) · Virulence · doi:10.1080/21505594.2024.2425744 · Cited by 54 · see citing works
Recent advances in vaccine development for herpes simplex virus types I and II
Coleman, J. L., & Shukla, D. (2013) · Human Vaccines & Immunotherapeutics · doi:10.4161/hv.23289 · Cited by 52 · see citing works
Self-citationMatos, P. M., Marin, M., Ahn, B., Lam, W. A., Santos, N. C., & Melikyan, G. B. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.462028 · Cited by 52 · see citing works
Neonatal herpes simplex virus infection: From the maternal infection to the child outcome
Rose, D. U. D., Bompard, S., Maddaloni, C., Bersani, I., Martini, L., Santisi, A., Longo, D., Ronchetti, M. P., Dotta, A., & Auriti, C. (2023) · Journal of Medical Virology · doi:10.1002/jmv.29024 · Cited by 51 · see citing works
Cytotoxic, Virucidal, and Antiviral Activity of South American Plant and Algae Extracts
Faral‐Tello, P., Mirazo, S., Dutra, C., Parada, A. P., Geis‐Asteggiante, L., Frabasile, S., Koncke, E., Davyt, D., Cavallaro, L. V., Heinzen, H., et al. (2012) · The Scientific World JOURNAL · doi:10.1100/2012/174837 · Cited by 51 · see citing works
Batista, F. M., López-Sanmartín, M., Grade, A., Morgado, I. M., Valente, M., Navas, J. I., Power, D. M., & Ruano, F. (2014) · Aquaculture · doi:10.1016/j.aquaculture.2014.09.016 · Cited by 48 · see citing works
Diverse Functions of Glycosaminoglycans in Infectious Diseases
Aquino, R. S., Lee, E. S., & Park, P. W. (2010) · Progress in molecular biology and translational science · doi:10.1016/s1877-1173(10)93016-0 · Cited by 47 · see citing works
Mediators and Mechanisms of Herpes Simplex Virus Entry into Ocular Cells
Farooq, A. V., Vályi-Nagy, T., & Shukla, D. (2010) · Current Eye Research · doi:10.3109/02713681003734841 · Cited by 47 · see citing works
Self-citationMuñoz‐Fernández, M. Á., Diez, R. C., Vacas‐Córdoba, E., García‐Broncano, P., de la Mata, F. J., Gómez, R., & Maly, M. (2016) · International Journal of Nanomedicine · doi:10.2147/ijn.s95301 · Cited by 47 · see citing works
Sharma, D., Sharma, S., Akojwar, N., Dondulkar, A., Yenorkar, N. Y., Pandita, D., Prasad, S. K., & Dhobi, M. (2023) · Vaccines · doi:10.3390/vaccines11020206 · Cited by 45 · see citing works
Contribution of N-linked glycans on HSV-2 gB to cell–cell fusion and viral entry
Luo, S., Hu, K., He, S., Wang, P., Zhang, M., Huang, X., Du, T., Zheng, C., Liu, Y., & Hu, Q. (2015) · Virology · doi:10.1016/j.virol.2015.04.005 · Cited by 45 · see citing works
Jaishankar, D., Buhrman, J. S., Vályi-Nagy, T., Gemeinhart, R. A., & Shukla, D. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-18365 · Cited by 45 · see citing works
Self-citationClinical Management of Herpes Simplex Virus Keratitis
Labib, B. A., & Chigbu, D. I. (2022) · Diagnostics · doi:10.3390/diagnostics12102368 · Cited by 44 · see citing works
Tannic acid modification of metal nanoparticles: possibility for new antiviral applications
Krzyżowska, M., Tomaszewska, E., Ranoszek‐Soliwoda, K., Bień, K., Orłowski, P., Celichowski, G., & Grobelny, J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-47720-8.00013-4 · Cited by 44 · see citing works
Zebrafish: Modeling for Herpes Simplex Virus Infections
Antoine, T. E., Jones, K. S., Dale, R. M., Shukla, D., & Tiwari, V. (2013) · Zebrafish · doi:10.1089/zeb.2013.0920 · Cited by 43 · see citing works
Self-citationBasal Autophagy Is Required for Herpes simplex Virus-2 Infection
Yakoub, A. M., & Shukla, D. (2015) · Scientific Reports · doi:10.1038/srep12985 · Cited by 43 · see citing works
Self-citationVallbracht, M., Backović, M., Klupp, B. G., Rey, F. A., & Mettenleiter, T. C. (2019) · Advances in virus research · doi:10.1016/bs.aivir.2019.05.007 · Cited by 41 · see citing works
Heparanase-Regulated Syndecan-1 Shedding Facilitates Herpes Simplex Virus 1 Egress
Hadigal, S. R., Koganti, R., Yadavalli, T., Agelidis, A. M., Suryawanshi, R. K., & Shukla, D. (2019) · Journal of Virology · doi:10.1128/jvi.01672-19 · Cited by 42 · see citing works
Self-citationZhang, M., Liu, Y., Wang, P., Guan, X., He, S., Luo, S., Li, C., Hu, K., Jin, W., Du, T., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1401538 · Cited by 42 · see citing works
Wang, Z., Jia, J., Wang, L., Li, F., Wang, Y., Jiang, Y., Song, X., Qin, S., Zheng, K., Ye, J., et al. (2020) · Virology Journal · doi:10.1186/s12985-020-01315-z · Cited by 41 · see citing works
Oncolytic Herpes Simplex Viruses as a Paradigm for the Treatment of Cancer
Bommareddy, P. K., Peters, C. W., Saha, D., Rabkin, S. D., & Kaufman, H. L. (2017) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-030617-050254 · Cited by 41 · see citing works
Skin Viral Infections: Host Antiviral Innate Immunity and Viral Immune Evasion
Lei, V., Petty, A. J., Atwater, A. R., Wolfe, S. A., & MacLeod, A. S. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.593901 · Cited by 43 · see citing works
Kumar, B., Dutta, D., Iqbal, J., Ansari, M. A., Roy, A., Leela, C., Pisano, G. C., Veettil, M. V., & Chandran, B. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005960 · Cited by 40 · see citing works
Effect of black tea extract on herpes simplex virus-1 infection of cultured cells
Cantatore, A., Randall, S. D., Traum, D., & Adams, S. D. (2013) · BMC Complementary and Alternative Medicine · doi:10.1186/1472-6882-13-139 · Cited by 40 · see citing works
Natural bioactive compounds from marine fungi (2017–2020)
Wang, H., Sun, S., Liu, M., Yan, M., Liu, Y.-F., Zhu, Z., & Zhang, Z. (2021) · Journal of Asian Natural Products Research · doi:10.1080/10286020.2021.1947254 · Cited by 39 · see citing works
Role of L-Particles during Herpes Simplex Virus Infection
Heilingloh, C. S., & Krawczyk, A. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.02565 · Cited by 38 · see citing works
Initial Contact: The First Steps in Herpesvirus Entry
Azab, W., & Osterrieder, N. (2017) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-319-53168-7_1 · Cited by 36 · see citing works
Sharma, V., Mobeen, F., & Prakash, T. (2016) · International Journal of Genomics · doi:10.1155/2016/9543274 · Cited by 36 · see citing works
- Authors
- Akhtar, J., & Shukla, D.
- Affiliations
- University of Illinois Chicago (US)
- Corresponding author
- Shukla, Deepak
- ORCID
- Shukla, Deepak
- Venue
- The FEBS Journal
- Publisher
- Wiley
- Published
- 2009-11-27
- Volume
- 276
- Issue
- 24
- Pages
- 7228-7236
- ISSN
- 1742-464X (ISSN-L)
- 1742-4658
- PMC
- PMC2801626
- OpenAlex
- W1501808502
- Cited by
- 292
- References
- 48
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 17 · 2023: 15 · 2022: 17 · 2021: 18 · 2020: 19 · 2019: 14 · 2018: 18 · 2017: 23 · 2016: 23 · 2015: 21 · 2014: 20 · 2013: 17 · 2012: 20
- FWCI
- 2.23
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- FEBS Journal (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Research to Prevent Blindness
- National Institutes of Health
- National Eye Institute (EY 01792, P30EY001792)
- National Institute of Allergy and Infectious Diseases (R01AI057860)
- Topics
- Health Sciences › Medicine › Epidemiology › Herpesvirus Infections and Treatments
- Health Sciences › Medicine › Epidemiology › Cytomegalovirus and herpesvirus research
- Health Sciences › Medicine › Epidemiology › Virology and Viral Diseases
- Keywords
- herpes simplex virus type 1, herpes simplex virus type 2, viral entry, heparan sulfate, viral attachment, tegument proteins, viral DNA replication, cell type specificity, host-virus interaction
- MeSH terms
- Cell Communication, Humans, Membrane Fusion, Membrane Glycoproteins, Pseudopodia, Receptors, Immunologic, Viral Envelope Proteins, Herpesvirus 2, Human, Herpesvirus 1, Human, Heparan Sulfate Proteoglycans, Virus Internalization
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review