Inhibitory effect of silver nanomaterials on transmissible virus-induced host cell infections

Biomaterials

Volumn 35, Issue 13, 2014, Pages 4195-4203

  Lv, Xiaonan ^a,b   Wang, Peng ^b   Bai, Ru ^b   Cong, Yingying ^a   Suo, Siqingaowa ^a   Ren, Xiaofeng ^a   Chen, Chunying ^b  

^a NORTHEAST AGRICULTURAL UNIVERSITY   (China)

^b NATIONAL CENTER FOR NANOSCIENCE AND TECHNOLOGY   (China)

Author keywords

Antiviral treatment; P38 MAPK signaling pathway; Silver nanomaterials; Transmissible gastroenteritis virus

Indexed keywords

ANTIVIRAL AGENTS; CELL DEATH; CELL SIGNALING; COLLOIDS; ELECTRIC RESISTANCE MEASUREMENT; MAMMALS; MITOCHONDRIA; NANOSTRUCTURED MATERIALS; POLYMERASE CHAIN REACTION; SCANNING ELECTRON MICROSCOPY; SILVER NANOPARTICLES; SILVER NANOWIRES; TRANSMISSION ELECTRON MICROSCOPY; VIRUSES;

ANTIVIRAL TREATMENTS; ENVIRONMENTAL SCANNING ELECTRON MICROSCOPES; GASTROINTESTINAL TRACT; IMMUNOFLUORESCENCE ASSAY; MITOCHONDRIAL MEMBRANE POTENTIAL; P38 MAPK; SIGNALING PATHWAYS; TRANSMISSIBLE GASTROENTERITIS VIRUS;

SILVER METALLOGRAPHY;

ANTIVIRUS AGENT; CASPASE 3; MITOGEN ACTIVATED PROTEIN KINASE P38; NANOWIRE; NM 300; PROTEIN BAX; PROTEIN BCL 2; PROTEIN P53; SILVER; SILVER NANOPARTICLE; SILVER NANOWIRE; UNCLASSIFIED DRUG; XFJ 011; XFJ 04; METAL NANOPARTICLE; NANOMATERIAL;

ANIMAL CELL; ANIMAL TISSUE; ANTIVIRAL ACTIVITY; APOPTOSIS; ARTICLE; CELL MEMBRANE DEPOLARIZATION; CELL PROTECTION; CONCENTRATION RESPONSE; CONTROLLED STUDY; CORONAVIRUS INFECTION; DOWN REGULATION; DRUG CYTOTOXICITY; FLOW CYTOMETRY; HOST CELL; IMMUNOFLUORESCENCE TEST; IN VITRO STUDY; MALE; MITOCHONDRIAL MEMBRANE POTENTIAL; NONHUMAN; PARTICLE SIZE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REAL TIME POLYMERASE CHAIN REACTION; SCANNING ELECTRON MICROSCOPY; SIGNAL TRANSDUCTION; SWINE; TRANSMISSIBLE GASTROENTERITIS VIRUS; TRANSMISSION ELECTRON MICROSCOPY; VIRUS INHIBITION; WESTERN BLOTTING; ANIMAL; CELL LINE; CELL SURVIVAL; CHEMISTRY; DRUG EFFECTS; FLUORESCENT ANTIBODY TECHNIQUE; METABOLISM; PATHOGENICITY;

CORONAVIRIDAE; CORONAVIRUS; SUIDAE; TRANSMISSIBLE GASTROENTERITIS VIRUS;

ANIMALS; ANTIVIRAL AGENTS; CELL LINE; CELL SURVIVAL; FLOW CYTOMETRY; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; METAL NANOPARTICLES; NANOSTRUCTURES; P38 MITOGEN-ACTIVATED PROTEIN KINASES; SILVER; SWINE; TRANSMISSIBLE GASTROENTERITIS VIRUS;

EID: 84896721264     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2014.01.054     Document Type: Article

References (47)

1. Nam J.M., Thaxton C.S., Mirkin C.A. Nanoparticle-based bio-bar codes for the ultrasensitive detection of proteins. Science 2003, 301:1884-1886.
2. Zhang Z., Wang J., Chen C. Near-infrared light-mediated nanoplatforms for cancer thermo-chemotherapy and optical imaging. Adv Mater 2013, 25:3869-3880.
3. Li Y.F., Chen C. Fate and toxicity of metallic and metal-containing nanoparticles for biomedical applications. Small 2011, 7:2965-2980.
4. Sondi I., Salopek-Sondi B. Silver nanoparticles as antimicrobial agent: a case study on E.coli as a model for Gram-negative bacteria. JColloid Interface Sci 2004, 275:177-182.
5. Wright J., Lam K., Hansen D., Burrell R. Efficacy of topical silver against fungal burn wound pathogens. Am J Infect Control 1999, 27:344-350.
6. Elechiguerra J.L., Burt J.L., Morones J.R., Camacho-Bragado A., Gao X., Lara H.H., et al. Interaction of silver nanoparticles with HIV-1. JNanobiotechnol 2005, 3:1-10.
7. Sun L., Singh A.K., Vig K., Pillai S.R., Singh S.R. Silver nanoparticles inhibit replication of respiratory syncytial virus. JBiomed Nanotechnol 2008, 4:149-158.
8. Xiang D.X., Chen Q., Pang L., Zheng C.L. Inhibitory effects of silver nanoparticles on H1N1 influenza A virus invitro. JVirol Methods 2011, 178:137-142.
9. Rogers J.V., Parkinson C.V., Choi Y.W., Speshock J.L., Hussain S.M. Apreliminary assessment of silver nanoparticle inhibition of monkeypox virus plaque formation. Nanoscale Res Lett 2008, 3:129-133.
10. Lu L., Sun R., Chen R., Hui C.K., Ho C.M., Luk J.M., et al. Silver nanoparticles inhibit hepatitis B virus replication. Antivir Ther 2008, 13:253-262.
11. Ren X., Glende J., Yin J., Schwegmann-Wessels C., Herrler G. Importance of cholesterol for infection of cells by transmissible gastroenteritis virus. Virus Res 2008, 137:220-224.
12. Zhao Q., Zhu J., Zhu W., Li X., Tao Y., Lv X., et al. Amonoclonal antibody against transmissible gastroenteritis virus generated via immunization of a DNA plasmid bearing TGEV S1 gene. Monoclon Antib Inimmunodiagn Immunother 2013, 32:50-54.
13. Ren X., Meng F., Yin J., Li G., Li X., Wang C., et al. Action mechanisms of lithium chloride on cell infection by transmissible gastroenteritis coronavirus. PloS One 2011, 10.1371/journal.pone.0018669.
14. Zou H., Zarlenga D.S., Sestak K., Suo S., Ren X. Transmissible gastroenteritis Virus; identification of M protein-binding peptide ligands with antiviral and diagnostic potential. Virus Res 2013, 99:383-390.
15. Baram-Pinto D., Shukla S., Perkas N., Gedanken A., Sarid R. Inhibition of herpes simplex virus type 1 infection by silver nanoparticles capped with mercaptoethane sulfonate. Bioconjug Chem 2009, 20:1497-1502.
16. Mehrbod P., Motamed N., Tabatabaian M., Estyar R.S., Amini E., Shahidi M., et al. Invitro antiviral effect of "nanosilver" on influenza virus. JPharm Sci 2009, 17:88-93.
17. Everett H., McFadden G. Apoptosis: an innate immune response to virus infection. Trends Microbiol 1999, 7:160-165.
18. Lee S.M., Kleiboeker S.B. Porcine reproductive and respiratory syndrome virus induces apoptosis through a mitochondria-mediated pathway. Virology 2007, 365:419-434.
19. Eleouet J.F., Chilmonczyk S., Besnardeau L., Laude H. Transmissible gastroenteritis coronavirus induces programmed cell death in infected cells through a caspase-dependent pathway. JVirol 1998, 72:4918-4924.
20. Eléouët J.-F., Slee E.A., Saurini F., Castagné N., Poncet D., Garrido C., et al. The viral nucleocapsid protein of transmissible gastroenteritis coronavirus (TGEV) is cleaved by caspase-6 and-7 during TGEV-induced apoptosis. JVirol 2000, 74:3975-3983.
21. Ding L., Xu X., Huang Y., Li Z., Zhang K., Chen G., et al. Transmissible gastroenteritis virus infection induces apoptosis through FasL-and mitochondria-mediated pathways. Vet Microbiol 2012, 158:12-22.
22. Denizot F., Lang R. Rapid colorimetric assay for cell growth and survival: modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. JImmunol Methods 1986, 89:271-277.
23. Sui X., Yin J., Ren X. Antiviral effect of diammonium glycyrrhizinate and lithium chloride on cell infection by pseudorabies herpesvirus. Antivir Res 2010, 85:346-353.
24. Baba C., Yanagida K., Kanzaki T., Baba M. Colorimetric lactate dehydrogenase (LDH) assay for evaluation of antiviral activity against bovine viral diarrhoea virus (BVDV) invitro. Antivir Chem Chemother 2005, 16:33-39.
25. Müller V., Chávez J.H., Reginatto F.H., Zucolotto S.M., Niero R., Navarro D., et al. Evaluation of antiviral activity of South American plant extracts against herpes simplex virus type 1 and rabies virus. Phytother Res 2007, 21:970-974.
26. Li Y., Liu Y., Fu Y., Wei T., Le Guyader L., Gao G., et al. The triggering of apoptosis in macrophages by pristine graphene through the MAPK and TGF-beta signaling pathways. Biomaterials 2012, 33:402-411.
27. Liu Y., Li W., Lao F., Liu Y., Wang L., Bai R., et al. Intracellular dynamics of cationic and anionic polystyrene nanoparticles without direct interaction with mitotic spindle and chromosomes. Biomaterials 2011, 32:8291-8303.
28. van Engeland M., Ramaekers F.C., Schutte B., Reutelingsperger C.P. Anovel assay to measure loss of plasma membrane asymmetry during apoptosis of adherent cells in culture. Cytometry 1996, 24:131-139.
29. Lee W.K., Spielmann M., Bork U., Thévenod F. Cd2+-induced swelling-contraction dynamics in isolated kidney cortex mitochondria: role of Ca2+ uniporter, K+ cycling, and protonmotive force. Am J Physiol Cell Physiol 2005, 289:C656-C664.
30. Filipe V., Hawe A., Jiskoot W. Critical evaluation of nanoparticle tracking analysis (NTA) by nanosight for the measurement of nanoparticles and protein aggregates. Pharm Res 2010, 27:796-810.
31. Burda C., Chen X., Narayanan R., El-Sayed M.A. Chemistry and properties of nanocrystals of different shapes. Chem Rev 2005, 105:1025-1102.
32. Qu Y., Li W., Zhou Y.L., Liu X.F., Zhang L.L., Wang L.M., et al. Full assessment of fate and physiological behavior of quantum dots utilizing caenorhabditis elegans as a model organism. Nano Lett 2011, 11:3174-3183.
33. Wang P., Nie X., Wang Y., Li Y., Ge C., Zhang L., et al. Multiwall carbon nanotubes mediate macrophage activation and promote pulmonary fibrosis through TGF-β/Smad signaling pathway. Small 2013, 9:1799-1811.
34. Penzes Z., González J.M., Calvo E., Izeta A., Smerdou C., Méndez A., et al. Complete genome sequence of transmissible gastroenteritis coronavirus PUR46-MAD clone and evolution of the Purdue virus cluster. Virus Genes 2001, 23:105-118.
35. Jiang X., Foldbjerg R., Miclaus T., Wang L., Singh R., Hayashi Y., et al. Multi-platform genotoxicity analysis of silver nanoparticles in the model cell line CHO-K1. Toxicol Lett 2013, 222(1):55-63.
36. Vaux D.L., Strasser A. The molecular biology of apoptosis. Proc Natl Acad Sci U S A 1996, 93:2239-2244.
37. Green D.R., Kroemer G. The pathophysiology of mitochondrial cell death. Science 2004, 305:626-629.
38. Shimizu S., Narita M., Tsujimoto Y. Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC. Nature 1999, 399:483-487.
39. Miyashita T., Krajewski S., Krajewska M., Wang H.G., Lin H., Liebermann D.A., et al. Tumor suppressor p53 is a regulator of bcl-2 and bax gene expression invitro and invivo. Oncogene 1994, 9:1799-1805.
40. Huang Y., Ding L., Li Z., Dai M., Zhao X., Li W., et al. Transmissible gastroenteritis virus infection induces cell apoptosis via activation of p53 signaling. JGen Virol 2013, 94:1807-1817.
41. Clerk A., Sugden P.H. The p38-MAPK inhibitor, SB203580, inhibits cardiac stress-activated protein kinases/c-Jun N-terminal kinases (SAPKs/JNKs). FEBS Lett 1998, 426:93-96.
42. Lakhani S.A., Masud A., Kuida K., Porter G.A., Booth C.J., Mehal W.Z., et al. Caspases 3 and 7: key mediators of mitochondrial events of apoptosis. Science 2006, 311:847-851.
43. Enjuanes L., Suñé C., Gebauer F., Smerdou C., Camacho A., Antón I.M., et al. Antigen selection and presentation to protect against transmissible gastroenteritis coronavirus. Vet Microbiol 1992, 33:249-262.
44. Gebauer F., Posthumus W., Correa I., Sae C., Smerdou C., Sanchez C.M., et al. Residues involved in the antigenic sites of transmissible gastroenteritis coronavirus S glycoprotein. Virology 1991, 183:225-238.
45. Schwegmann-Wessels C., Zimmer G., Schröder B., Breves G., Herrler G. Binding of transmissible gastroenteritis coronavirus to brush border membrane sialoglycoproteins. JVirol 2003, 77:11846-11848.
46. Meng F., Ren Y., Suo S., Sun X., Li X., Li P., et al. Evaluation on the efficacy and immunogenicity of recombinant DNA plasmids expressing spike genes from porcine transmissible gastroenteritis virus and porcine epidemic diarrhea virus. PloS One 2013, 10.1371/journal.pone.0057468.
47. Delmas B., Gelfi J., L'Haridon R., Vogel L.K., Sjöström H., Norén O., et al. Aminopeptidase N is a major receptor for the enteropathogenic coronavirus TGEV. Nature 1992, 357:417-420.