全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Electron Micrographic Representations of Mechanisms of Action of Murine Norovirus on ATCC TIB-71 Cells and Level of Gene Expression

DOI: 10.4236/aim.2023.131003, PP. 32-47

Keywords: Norovirus, Plant Extracts, Transmission Electron Microscope, Prevention/Control

Full-Text   Cite this paper   Add to My Lib

Abstract:

Human noroviruses (HuNoV) are the number one cause of viral gastroenteritis worldwide resulting in a significant cause of morbidity and mortality in all age groups. However, despite the medical relevance of HuNoV, effective treatment against norovirus infection is yet to be developed. In this study, we investigated the anti-Noroviral activity of Hibiscus sabdariffa (HS) calyces and Zanthoxylum armatum (ZA) seeds using murine norovirus, a surrogate of human norovirus. The antiviral mechanisms of action were also examined using a gene expression studies and transmission electron microscopy. Our results showed that virus-infected cells were left potentially void of all the cell machineries whereas uninfected cells represent healthy normal and dividing cells. The infected treated cells with extracts showed restoration of the dense cytoplasm, cytoplasmic membrane, and the nucleus. These cells were also associated with the expression of ORF genes. This study demonstrates the antiviral properties of Hibiscus sabdariffa (HS) calyces and Zanthoxylum armatum (ZA) and thus indicates their potential as natural remedies to treat noroviruses.

References

[1]  Niendorf, S., Jacobsen, S., Faber, M., Eis-Hübinger, A.M., Hofmann, J. and Bock, C.T. (2016) Steep Rise in Norovirus Cases and Emergence of a New Recombinant Strain GII.P16-GII.2, Germany, Winter 2016. Eurosurveillance, 22, 30447.
https://doi.org/10.2807/1560-7917.ES.2017.22.4.30447
[2]  Cannon, J.L., Barclay, L., Collins, N.R., Wikswo, M.E., Castro, C.J., Magaña, L.C. and Vinjé, J. (2017) Genetic and Epidemiologic Trends of Norovirus Outbreaks in the United States from 2013 to 2016 Demonstrated Emergence of Novel GII.4 Recombinant Viruses. Journal of Clinical Microbiology, 55, 2208-2221.
https://doi.org/10.1128/JCM.00455-17
[3]  Fu, J.-G., Shi, C., Xu, C., Lin, Q., Zhang, J., Yi, Q. and Xing, Z. (2017) Outbreaks of Acute Gastroenteritis Associated with a Re-Emerging GII.P16-GII.2 Norovirus in the Spring of 2017 in Jiangsu, China Public Library of Science. PLOS ONE, 12, e0186090.
https://doi.org/10.1371/journal.pone.0186090
[4]  Iaconelli, M., Muscillo, M., Della Libera, S., Fratini, M., Meucci, L., De Ceglia, M. and La Rosa, G. (2017) One-Year Surveillance of Human Enteric Viruses in Raw and Treated Wastewaters, Downstream River Waters, and Drinking Waters. Food and Environmental Virology, 9, 79-88.
https://doi.org/10.1007/s12560-016-9263-3
[5]  Iloghalu, U. and Khatiwada, P. (2015) Phytochemicals: Natural Remedies for Emerging Viral Infection. Medicinal & Aromatic Plants, 4, Article 213.
[6]  Moore, M.D., Goulter, R.M. and Jaykus, L. (2015) Human Norovirus as a Foodborne Pathogen: Challenges and Developments. Annual Review of Food Science and Technology, 6, 411-433.
https://doi.org/10.1146/annurev-food-022814-015643
[7]  Saxena, K., Blutt, S.E., Ettayebi, K., Zeng, X., Broughman, J.R., Crawford, S.E. and Estes, M.K. (2016) Human Intestinal Enteroids: A New Model to Study Human Rotavirus Infection, Host Restriction, and Pathophysiology. Journal of Virology, 90, 43-56.
https://doi.org/10.1128/JVI.01930-15
[8]  Rajagopalan, S. and Yoshikawa, T.T. (2016) Norovirus Infections in Long-Term Care Facilities. Journal of the American Geriatrics Society (JAGS), 64, 1097-1103.
https://doi.org/10.1111/jgs.14085
[9]  Lucht, J.M. (2015) Public Acceptance of Plant Biotechnology and GM Crops. Viruses, 7, 4254-4281.
https://doi.org/10.3390/v7082819
[10]  Scarpellini, E., Ianiro, G., Attili, F., Bassanelli, C., De Santis, A. and Gasbarrini, A. (2015) The Human Gut Microbiota and Virome: Potential Therapeutic Implications. Digestive and Liver Disease, 47, 1007-1012.
https://doi.org/10.1016/j.dld.2015.07.008
[11]  Nisa, H., Kamili, A.N., Nawchoo, I.A., Shafi, S., Shameem, N. and Bandh, S.A. (2015) Fungal Endophytes as Prolific Source of Phytochemicals and Other Bioactive Natural Products: A Review. Microbial Pathogenesis, 82, 50-59.
https://doi.org/10.1016/j.micpath.2015.04.001
[12]  Shakeri, A., Zirak, M.R. and Sahebkar, A. (2018) Ellagic Acid: A Logical Lead for Drug Development? Current Pharmaceutical Design, 24, 106-122.
https://doi.org/10.2174/1381612823666171115094557
[13]  Mwitari, P.G., Ayeka, P.A., Ondicho, J., Matu, E.N. and Bii, C.C. (2013) Antimicrobial Activity and Probable Mechanisms of Action of Medicinal Plants of Kenya: Withania Somnifera, Warbugia Ugandensis, Prunus Africana and Plectrunthus Barbatus. PLOS ONE, 8, e65619.
https://doi.org/10.1371/journal.pone.0065619
[14]  Saritha, K., Rajesh, A., Manjulatha, K., Setty, O.H. and Yenugu, S. (2015) Mechanism of Antibacterial Action of the Alcoholic Extracts of Hemidesmus indicus (L.) R. Br. ex Schult, Leucas aspera (Wild.), Plumbago zeylanica L., and Tridax procumbens (L.) R. Br. ex Schult. Frontiers in Microbiology, 6, Article 577.
https://doi.org/10.3389/fmicb.2015.00577
[15]  Tran, T.T., Kim, M., Jang, Y., Lee, H., Nguyen, H., Nguyen, T., Park, H., Dang, Q. and Kim, J.-C. (2017) Characterization and Mechanisms of Anti-Influenza Virus Metabolites Isolated from the Vietnamese Medicinal Plant Polygonum chinense. BMC Complementary and Alternative Medicine, 17, Article No. 162.
https://doi.org/10.1186/s12906-017-1675-6
[16]  Raina, H., Soni, G., Jauhari, N., Sharma, N. and Bharadvaja, N. (2014) Phytochemical Importance of Medicinal Plants as Potential Sources of Anticancer Agents. Turkish Journal of Botany, 38, 1027-1035.
https://doi.org/10.3906/bot-1405-93
[17]  Domaszewska-Szostek, A., Puzianowska-Kuźnicka, M. and Kuryłowicz, A. (2021) Flavonoids in Skin Senescence Prevention and Treatment. International Journal of Molecular Sciences, 22, Article 6814.
https://doi.org/10.3390/ijms22136814
[18]  Iloghalu, U., Holmes, B., Khatiwada, J. and Williams, L.L. (2019) Selected Plant Extracts Show Antiviral Effects against Murine Norovirus Surrogate. Advances in Microbiology, 9, 372-384.
https://doi.org/10.4236/aim.2019.94022
[19]  Su, X. and D’Souza, D. (2013) Naturally Occurring Flavonoids against Human Norovirus Surrogates. Food and Environmental Virology, 5, 97-102.
https://doi.org/10.1007/s12560-013-9106-4
[20]  Laue, M. and Bannert, N. (2010) Detection Limit of Negative Staining Electron Microscopy for the Diagnosis of Bioterrorism-Related Micro-Organisms. Journal of Applied Microbiology, 109, 1159-1168.
https://doi.org/10.1111/j.1365-2672.2010.04737.x
[21]  Garcia, A., Pratap, P.R., Lüpfert, C., Cornelius, F., Jacquemin, D., Lev, B., Allen, T. and Clarke, R.J. (2017) The Voltage-Sensitive Dye RH421 Detects a Na+, K+-ATPase Conformational Change at the Membrane Surface. Bochimica et Biophysica Acta-Biomembranes, 1859, 813-823.
https://doi.org/10.1016/j.bbamem.2017.01.022
[22]  Carmona-Rivera, C. and Kaplan, M.J. (2016) Induction and Quantification of NETosis. Current Protocols in Immunology, 115, 14.41.1-14.41.14.
https://doi.org/10.1002/cpim.16
[23]  Miller, S.E. (2010) Electron Microscopy of Viral Infections. In: Jerome, K.R., Ed., Lennette’s Laboratory Diagnosis of Viral Infections, CRC Press, Boca Raton, 173-196.
https://doi.org/10.3109/9781420084962.011
[24]  He, S.L. and Green, R. (2013) Northern Blotting. In: Colowick, S.P. and Kaplan, N.O., Eds., Methods in Enzymology, Elsevier Science & Technology, United States, 75-87.
https://doi.org/10.1016/B978-0-12-420037-1.00003-8
[25]  Vashist, S., Urena, L. and Goodfellow, I. (2012) Development of a Strand Specific Real-Time RT-qPCR Assay for the Detection and Quantitation of Murine Norovirus RNA. Journal of Virological Methods, 184, 69-76.
https://doi.org/10.1016/j.jviromet.2012.05.012
[26]  Soliman, S., Mohammad, M.G., El-Keblawy, A.A., Omar, H., Abouleish, M., Madkour, M. and Hosni, R.M. (2018) Mechanical and Phytochemical Protection Mechanisms of Calligonum Comosum in Arid Deserts Public Library of Science. PLOS ONE, 13, e0192576.
https://doi.org/10.1371/journal.pone.0192576
[27]  Nunes, M.A., Rodrigues, F., Alves, R.C. and Oliveira, M.B.P.P. (2017) Herbal Products Containing Hibiscus sabdariffa L., Crataegus spp., and Panax spp.: Labeling and Safety Concerns. Food Research International, 100, 529-540.
https://doi.org/10.1016/j.foodres.2017.07.031
[28]  Ashafa, A.O.T. and Alayande, K.A. (2017) Evaluation of Cytotoxic Effects and Antimicrobial Activities of Lecaniodiscus cupanioides (Planch.) Leaf Extract. Transactions of the Royal Society of South Africa, 72, 33-38.
https://doi.org/10.1080/0035919X.2016.1214851
[29]  Šmejkal, K., Malaník, M., Zhaparkulova, K., Sakipova, Z., Ibragimova, L., Ibadullaeva, G. and Žemlička, M. (2016) Kazakh Ziziphora Species as Sources of Bioactive Substances. Molecules (Basel, Switzerland), 21, Article 826.
https://doi.org/10.3390/molecules21070826
[30]  Raafat, K.M. and Samy, W. (2018) Phytochemical and Biological Evaluation of Ultrasound-Assisted Spray Dried Lonicera Etrusca for Potential Management of Diabetes. Records of Natural Products, 12, 367-379.
https://doi.org/10.25135/rnp.40.17.10.171
[31]  Anand, S., Mandal, S., Patil, P. and Tomar, S.K. (2016) Pathogen-Induced Secretory Diarrhea and Its Prevention. European Journal of Clinical Microbiology & Infectious Diseases, 35, 1721-1739.
https://doi.org/10.1007/s10096-016-2726-5
[32]  Zhang, T., Wen, F., Wu, Y., Goh, G.S.H., Ge, Z., Tan, L.P. and Yang, Z. (2015) Cross-Talk between TGF-Beta/SMAD and Integrin Signaling Pathways in Regulating Hypertrophy of Mesenchymal Stem Cell Chondrogenesis under Deferral Dynamic Compression. Biomaterials, 38, 72-85.
https://doi.org/10.1016/j.biomaterials.2014.10.010
[33]  Varela-López, A., Bullón, P., Giampieri, F. and Quiles, J.L. (2015) Non-Nutrient, Naturally Occurring Phenolic Compounds with Antioxidant Activity for the Prevention and Treatment of Periodontal Diseases. Antioxidants, 4, 447-481.
https://doi.org/10.3390/antiox4030447
[34]  Zheng, D., Zou, Y., Cobbina, S.J., Wang, W., Li, Q., Chen, Y. and Wu, X. (2016) Purification, Characterization and Immunoregulatory Activity of a Polysaccharide Isolated from Hibiscus sabdariffa L. Journal of the Science of Food and Agriculture, 97, 1599-1606.
https://doi.org/10.1002/jsfa.7908
[35]  Rajab, N.F., Musa, S.M., Munawar, M.A., Mun, L.L., Yen, H.K., Ibrahim, F.W. and Meng, C.K. (2016) Anti-Neuroinflammatory Effects of Hibiscus Sabdariffa Linn. (Roselle) on Lipopolysaccharides-Induced Microglia and Neuroblastoma Cells. Kesan Anti-Neuroinflammatori Hibiscus sabdariffa Linn. (Roselle) Pada Aruhan Lipopolisakarida Sel Mikroglia dan Neuroblastoma. Jurnal Sains Kesihatan Malaysia, 14, 111-117.
https://doi.org/10.17576/jskm-2016-1402-13
[36]  Riaz, G. and Chopra, R. (2018) A Review on Phytochemistry and Therapeutic Uses of Hibiscus sabdariffa L. Biomedicine & Pharmacotherapy, 102, 575-586.
https://doi.org/10.1016/j.biopha.2018.03.023
[37]  Hajifaraji, M., Matlabi, M., Ahmadzadeh-Sani, F., Mehrabi, Y., Rezaee, M.S., Hajimehdipour, H. and Roghani, K. (2018) Effects of Aqueous Extracts of Dried Calyx of Sour Tea (Hibiscus sabdariffa L.) on Polygenic Dyslipidemia: A Randomized Clinical Trial. Avicenna Journal of Phytomedicine, 8, 24-32.
[38]  Purohit, S., Jugran, A.K., Bhatt, I.D., Palni, L.M.S., Bhatt, A. and Nandi, S.K. (2017) In Vitro Approaches for Conservation and Reducing Juvenility of Zanthoxylum armatum Dc: An Endangered Medicinal Plant of Himalayan Region. Trees: Structure & Function, 31, 1101-1108.
https://doi.org/10.1007/s00468-016-1494-2
[39]  Negi, J.S., Bisht, V.K., Bhandari, A.K., Bisht, R. and Negi, S.K. (2012) Major Constituents, Antioxidant and Antibacterial Activities of Zanthoxylum armatum DC. Essential Oil. Iranian Journal of Pharmacology & Therapeutics, 11, 68-72.
[40]  Roingeard, P. (2008) Viral Detection by Electron Microscopy: Past, Present and Future. Biology of the Cell, 100, 491-501.
https://doi.org/10.1042/BC20070173
[41]  Goldsmith, C.S. and Miller, S.E. (2009) Modern Uses of Electron Microscopy for Detection of Viruses. Clinical Microbiology Reviews, 22, 552-563.
https://doi.org/10.1128/CMR.00027-09
[42]  Madani, T.A., El-Tayb, M.E.A., et al. (2017) Electron Microscopy of Alkhumra Hemorrhagic Fever Virus. Mary Ann Liebert, 17, 195-199.
https://doi.org/10.1089/vbz.2016.2064
[43]  Monninger, M.K., Nguessan, C.A., Blancett, C.D., Kuehl, K.A., Rossi, C.A., Olschner, S.P., et al. (2016) Preparation of Viral Samples within Biocontainment for Ultrastructural Analysis: Utilization of an Innovative Processing Capsule for Negative Staining. Journal of Virological Methods, 238, 70-76.
https://doi.org/10.1016/j.jviromet.2016.10.005
[44]  Yu, Y., Tan, Q., Zhao, W., Zhang, X., Ma, J., Wu, Z., Zhu, Z. and Cui, Y. (2017) Characterization of an Orf Virus Isolated from an Outbreak in Heilongjiang Province, China. Archives of Virology, 162, 3134-3149.
https://doi.org/10.1007/s00705-017-3426-x
[45]  Carrasco, L. (2018) Mechanisms of Viral Toxicity in Animal Cells. CRC Press, Boca Raton.
https://doi.org/10.1201/9781351074353
[46]  Ailte, I., Lingelem, A.B.D., Kvalvaag, A.S., Kavaliauskiene, S., Brech, A., Koster, G. and Sandvig, K. (2017) Exogenous Lysophospholipids with Large Head Groups Perturb Clathrin-Mediated Endocytosis. Traffic, 18, 176-191.
https://doi.org/10.1111/tra.12468
[47]  Prosser, D.C. and Wendland, B. (2016) DePFth Perception in Clathrin-Mediated Endocytosis. Developmental Cell, 37, 387-388.
https://doi.org/10.1016/j.devcel.2016.05.017
[48]  Ruba, A. and Yang, W. (2016) O-GlcNAc-ylation in the Nuclear Pore Complex. Cellular and Molecular Bioengineering, 9, 227-233.
https://doi.org/10.1007/s12195-016-0440-0
[49]  Lin, D.H., Stuwe, T., Schilbach, S., Rundlet, E.J., Perriches, T., Mobbs, G. and Hoelz, A. (2016) Architecture of the Symmetric Core of the Nuclear Pore. Science (American Association for the Advancement of Science), 352, aaf1015.
https://doi.org/10.1126/science.aaf1015
[50]  Lieberman, P.M. (2008) Chromatin Organization and Virus Gene Expression. Journal of Cellular Physiology, 216, 295-302.
https://doi.org/10.1002/jcp.21421
[51]  Wang, X., Ma, Z., Kong, X. and Lv, Z. (2016) Effects of RNAs on Chromatin Accessibility and Gene Expression Suggest RNA-Mediated Activation. The International Journal of Biochemistry & Cell Biology, 79, 24-32.
https://doi.org/10.1016/j.biocel.2016.08.004
[52]  Schmidt, H.B. and Görlich, D. (2016) Transport Selectivity of Nuclear Pores, Phase Separation, and Membraneless Organelles. Trends in Biochemical Sciences, 41, 46-61.
https://doi.org/10.1016/j.tibs.2015.11.001
[53]  Wang, S.Z., Zheng, Y.L., Xiang, F., Li, S. and Yang, G.L. (2016) Antifungal Activity of Momordica charantia Seed Extracts toward the Pathogenic Fungus Fusarium solani L. Journal of Food and Drug Analysis, 24, 881-887.
https://doi.org/10.1016/j.jfda.2016.03.006
[54]  Kohn, L.K., Foglio, M.A., Rodrigues, R.A., Sousa, I.D.O., Martini, M.C., Padilla, M.A. and Arns, C.W. (2015) In-Vitro Antiviral Activities of Extracts Of plants of the Brazilian Cerrado against the Avian Metapneumovirus (aMPV). Revista Brasileira de Ciência Avícola, 17, 275-280.
https://doi.org/10.1590/1516-635X1703275-280
[55]  Latika, B., Aseesh, P. and Sushma, T. (2013) An Overview on Phytomedicinal Approaches of Zanthoxylum armatum DC. An Important Magical Medicinal Plant. Journal of Medicinal Plants Research, 7, 366-370.
[56]  Abu-Irmaileh, B.E. and Afifi, F.U. (2003) Herbal Medicine in Jordan with Special Emphasis on Commonly Used Herbs. Journal of Ethnopharmacology, 89, 193-197.
https://doi.org/10.1016/S0378-8741(03)00283-6
[57]  AbouZid, S.F. and Mohamed, A.A. (2011) Survey on Medicinal Plants and Spices Used in Beni-Sueif, Upper Egypt. Journal of Ethnobiology and Ethnomedicine, 7, Article No. 18.
https://doi.org/10.1186/1746-4269-7-18
[58]  Alzweiri, M., Al Sarhan, A., Mansi, K., Hudaib, M. and Aburjai, T. (2011) Ethnopharmacological Survey of Medicinal Herbs in Jordan, the Northern Badia Region. Journal of Ethnopharmacology, 137, 27-35.
https://doi.org/10.1016/j.jep.2011.02.007
[59]  Da-Costa-Rocha, I., Bonnlaender, B., Siever, H., Pischel, I. and Heinrich, M. (2014) Hibiscus sabdafiffa L.—A Phytochemical and Pharmacological Review. Food Chemistry, 165, 424-443.
https://doi.org/10.1016/j.foodchem.2014.05.002
[60]  Wagner, E.M. and Jones, J. (2013) Monitoring Gene Expression: Quantitative Real-Time RT-PCR. In: Freeman, L., Ed., Lipoproteins and Cardiovascular Disease. Methods in Molecular Biology, Humana Press, Totowa, NJ, 19-45.
https://doi.org/10.1007/978-1-60327-369-5_2
[61]  Nguyen, T.T.-T.N., Shynlova, O. and Lye, S.J. (2016) Matrix Metalloproteinase Expression in the Rat Myometrium during Pregnancy, Term Labor, and Postpartum. Biology of Reproduction, 95, 1-14.
https://doi.org/10.1095/biolreprod.115.138248
[62]  Farrar, J.S. and Wittwer, C.T. (2017) High-Resolution Melting Curve Analysis for Molecular Diagnostics. In: Patrinos, G.P., Ed., Molecular Diagnostics, Academic Press, Cambridge, MA, 79-102.
https://doi.org/10.1016/B978-0-12-802971-8.00006-7
[63]  Bull, R.A., Hansman, G.S., Clancy, L.E., Tanaka, M.M., Rawlinson, W.D. and White, P.A. (2005) Norovirus Recombination in ORF1/ORF2 Overlap. Emerging Infectious Diseases, 11, 1079-1085.
https://doi.org/10.3201/eid1107.041273
[64]  Fraisse, A., Coudray-Meunier, C., Martin-Latil, S., Hennechart-Collette, C., Delannoy, S., Fach, P. and Perelle, S. (2017) Digital RT-PCR Method for Hepatitis A Virus and Norovirus Quantification in Soft Berries. International Journal of Food Microbiology, 243, 36-45.
https://doi.org/10.1016/j.ijfoodmicro.2016.11.022
[65]  Drozd, E., Krzysztoń-Russjan, J. and Gruber, B. (2016) Doxorubicin Treatment of Cancer Cells Impairs Reverse Transcription and Affects the Interpretation of RT-qPCR Results. Cancer Genomics & Proteomics, 13, 161-170.
[66]  Sanchez, E.L. and Lagunoff, M. (2015) Viral Activation of Cellular Metabolism. Virology, 479-480, 609-618.
https://doi.org/10.1016/j.virol.2015.02.038
[67]  Herod, M.R., Salim, O., Skilton, R.J., Prince, C.A., Ward, V.K., Lambden, P.R. and Clarke, I.N. (2014) Expression of the Murine Norovirus (MNV) ORF1 Polyprotein is Sufficient to Induce Apoptosis in a Virus-Free Cell Model. PLOS ONE, 9, e90679.
https://doi.org/10.1371/journal.pone.0090679
[68]  de Graaf, M., van Beek, J. and Koopmans, M.P.G. (2016) Human Norovirus Transmission and Evolution in a Changing World. Nature Reviews Microbiology, 14, 421-433.
https://doi.org/10.1038/nrmicro.2016.48

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133