Dhar P, Dhar DG, Rawat AKS, Srivastava S. Medicinal chemistry and biological potential of Cyperus rotundus Linn.: an overview to discover elite chemotype(s) for industrial use. Ind Crops Prod. 2017;108:232–47.
Kamala A, Middha SK, Gopinath C, Sindhura HS, Karigar CS. In vitro antioxidant potentials of Cyperus rotundus L. rhizome extracts and their phytochemical analysis. Pharmacogn Mag. 2018;14:261.
Kamala A, Middha SK, Karigar CS. Plants in traditional medicine with special reference to Cyperus rotundus L.: a review. Biotech. 2018;8:1–11.
Agarwal H, Nakara A, Shanmugam VK. Anti-inflammatory mechanism of various metal and metal oxide nanoparticles synthesized using plant extracts: a review. Biomed Pharmacother. 2019;109:2561–72.
Kumar SB, Krishna S, Pradeep S, Mathews DE, Ramya P, Murahari M, Murthy TK. Screening of natural compounds from Cyperus rotundus Linn against SARS-CoV-2 main protease (Mpro): an integrated computational approach. Comput Biol Med. 2021;134:104524–32.
Bezerra JJL, Pinheiro AAV. Traditional uses, phytochemistry, and anticancer potential of Cyperus rotundus L.(Cyperaceae): a systematic review. S Afr J Bot. 2022;144:175–86.
Kumar M, Rani M, Meher B. Review on pharmacology and phytochemistry of Cyperus rotundus L. Curr Res Pharm Sci. 2017;8:11–5.
Ryu B, Kim HM, Lee JS, Cho YJ, Oh MS, Choi JH, Jang DS. Sesquiterpenes from rhizomes of Cyperus rotundus with cytotoxic activities on human cancer cells in vitro. Helv Chim Acta. 2015;98:1372–80.
Nam JH, Nam DY, Lee DU. Valencene from the rhizomes of Cyperus rotundus inhibits skin photoaging-related ion channels and UV-induced melanogenesis in B16F10 melanoma cells. J Nat Prod. 2016;79:1091–6.
MacLachlan NJ, Dubovi EJ, Barthold SW, Swayne DF, Winton JR. Herpesvirales. In: Maclachlan NJ, Edward JD, editors. Fenner’s veterinary virology. Cambridge: Academic Press; 2017. p. 190–216.
Tran TT, Nazir S, Yegoraw AA, Assen AM, Walkden-Brown SW, Gerber PF. Detection of infectious laryngotracheitis virus (ILTV) in tissues and blood fractions from experimentally infected chickens using PCR and immunostaining analyses. Res Vet Sci. 2021;134:64–8.
Chen H, Muhammad I, Zhang Y, Ren Y, Zhang R, Huang X, Diao L, Liu H, Li X, Sun X, Abbas G. Antiviral activity against infectious bronchitis virus and bioactive components of Hypericum perforatum L. Front Pharmacol. 2019;10:1272.
García M, SpatzS GJS. Infectious laryngotracheitis. In: McMullin PF, Swayne DE, Boulianne M, Logue CM, McDougald LR, Nair V, Suarez DL, de Wit S, Grimes T, Johnson D, Kromm M, Prajitno TY, Rubinoff I, Zavala G, editors. Diseases of Poultry. Hoboken: Wiley; 2020. p. 161–79.
Jackwood M, De Wit S. Infectious Bronchitis. In: Mc Mullin PF, Swayne DE, Boulianne M, Logue CM, McDougald LR, Nair V, Suarez DL, de Wit S, Grimes T, Johnson D, Kromm M, Prajitno TY, Rubinoff I, Zavala G, editors. Diseases of poultry. Wiley: Hoboken; 2020. p. 167–88.
McKinley ET, Hilt DA, Jackwood MW. Avian coronavirus infectious bronchitis attenuated live vaccines undergo selection of subpopulations and mutations following vaccination. Vaccine. 2008;26:1274–84.
Lee SW, Markham PF, Coppo MJ, Legione AR, Markham JF, Noormohammadi AH, Browning GF, Ficorilli N, Hartley CA, Devlin JM. Attenuated vaccines can recombine to form virulent field viruses. Science. 2012;337:188.
Lee HJ, Youn HN, Kwon JS, Lee YJ, Kim JH, Lee JB, Park SY, Choi IS, Song CS. Characterization of a novel live attenuated infectious bronchitis virus vaccine candidate derived from a Korean nephropathogenic strain. Vaccine. 2010;28:2887–94.
Collisson EW, Pei J, Dzielawa J, Seo SH. Cytotoxic T lymphocytes are critical in the control of infectious bronchitis virus in poultry. Dev Comp Immunol. 2000;24:187–200.
Ladman BS, Pope CR, Ziegler AF, Swieczkowski T, Callahan JM, Davison S, Gelb J Jr. Protection of chickens after live and inactivated virus vaccination against challenge with nephropathogenic infectious bronchitis virus PA/Wolgemuth/98. Avian Dis. 2002;46:938–44.
Abdel-Sabour MA, Al-Ebshahy EM, Khaliel SA, Abdel-Wanis NA, Yanai T. Isolation and molecular characterization of novel infectious bronchitis virus variants from vaccinated broiler flocks in Egypt. Avian Dis. 2017;61:307–10.
Bayoumi M, El-Saied M, Amer H, Bastami M, Sakr EE, El-Mahdy M. Molecular characterization and genetic diversity of the infectious laryngotracheitis virus strains circulating in Egypt during the outbreaks of 2018 and 2019. Arch Virol. 2020;165:661–70.
Singh K, Mishra A, Sharma D, Singh K. Antiviral and antimicrobial potentiality of nano drugs. In: Mohapatra S, Ranjan S, Dasgupta N, Kumar R, Thomas S, editors. Applications of targeted nano drugs and delivery systems. Amsterdam: Elsevier; 2019. p. 343–56.
Rajeshkumar S, Bharath LV, Geetha R. Broad spectrum antibacterial silver nanoparticle green synthesis: characterization, and mechanism of action. In: Shukla AK, Iravani S, editors. Green synthesis, characterization and applications of nanoparticles. Amsterdam: Elsevier; 2019. p. 429–44.
Das M, Chatterjee S. Green synthesis of metal/metal oxide nanoparticles toward biomedical applications: boon or bane. In: Shukla AK, Iravani S, editors. Green synthesis, characterization and applications of nanoparticles. Amsterdam: Elsevier; 2019. p. 265–301.
Sasidharan S, Pottail L. Antimicrobial activity of metal and non-metallic nanoparticles from Cyperus rotundus root extract on infectious disease causing pathogens. J Plant Biochem Biotechnol. 2020;29:134–43.
Solaiman MA, Ali MA, Abdel-Moein NM, Mahmoud EA. Synthesis of Ag-NPs developed by green-chemically method and evaluation of antioxidant activities and anti-inflammatory of synthesized nanoparticles against LPS-induced NO in RAW 264.7 macrophages. Biocatal Agric Biotechnol. 2020;29:101832.
Naikoo GA, Mustaqeem M, Hassan IU, Awan T, Arshad F, Salim H, Qurashi A. Bioinspired and green synthesis of nanoparticles from plant extracts with antiviral and antimicrobial properties: a critical review. J Saudi Chem Soc. 2021;25: 101304.
Haslam E. Natural polyphenols (vegetable tannins) as drugs: possible modes of action. J Nat Prod. 1996;59:205–15.
Medini F, Megdiche W, Mshvildadze V, Pichette A, Legault J, St-Gelais A, Ksouri R. Antiviral-guided fractionation and isolation of phenolic compounds from Limonium densiflorum hydroalcoholic extract. C R Chim. 2016;19:726–32.
Govea-Salas M, Rivas-Estilla AM, Rodríguez-Herrera R, Lozano-Sepúlveda SA, Aguilar-Gonzalez CN, Zugasti-Cruz A, Salas-Villalobos TB, Morlett-Chávez JA. Gallic acid decreases hepatitis C virus expression through its antioxidant capacity. Exp Ther Med. 2016;11:619–24.
Kane CJ, Menna JH, Sung CC, Yeh YC. Methyl gallate, methyl-3, 4, 5-trihydroxybenzoate, is a potent and highly specific inhibitor of herpes simplex virus in vitro. II. Antiviral activity of methyl gallate and its derivatives. Biosci Rep. 1988;8:95–102.
Savi LA, Leal PC, Vieira TO, Rosso R, Nunes RJ, Yunes RA, Creczynski-Pasa TB, Barardi CR, Simões CM. Evaluation of anti-herpetic and antioxidant activities, and cytotoxic and genotoxic effects of synthetic alkyl-esters of gallic acid. Drug Res. 2005;55:66–75.
Musarra-Pizzo M, Pennisi R, Ben-Amor I, Mandalari G, Sciortino MT. Antiviral activity exerted by natural products against human viruses. Viruses. 2021;13:828.
Treml J, Gazdová M, Šmejkal K, Šudomová M, Kubatka P, Hassan ST. Natural products-derived chemicals: breaking barriers to novel anti-HSV drug development. Viruses. 2020;12:154.
Xu CH, Chen YQ, Yin ZQ, Rui WA, Hu HY, Liang XX, He CL, Yin LZ, Gang Y, Zou YF, Li LX. Kaempferol inhibits Pseudorabies virus replication in vitro through regulation of MAPKs and NF-κB signaling pathways. J Integr Agric. 2021;20:2227–39.
Hung PY, Ho BC, Lee SY, Chang SY, Kao CL, Lee SS, Lee CN. Houttuynia cordata targets the beginning stage of herpes simplex virus infection. PLoS ONE. 2015;10: e0115475.
Benassi-Zanqueta É, Marques CF, Valone LM, Pellegrini BL, Bauermeister A, Ferreira IC, Lopes NP, Nakamura CV, Dias Filho BP, Natali MR, Ueda-Nakamura T. Evaluation of anti-HSV-1 activity and toxicity of hydroethanolic extract of Tanacetum parthenium (L.) Sch. Bip. (Asteraceae). Phytomedicine. 2019;1:249–54.
Yoon KN, Alam N, Lee KR, Shin PG, Cheong JC, Yoo YB, Lee TS. Antioxidant and antityrosinase activities of various extracts from the fruiting bodies of Lentinus lepideus. Molecules. 2011;16:2334–47.
Tutunchi H, Naeini F, Ostadrahimi A, Hosseinzadeh-Attar MJ. Naringenin, a flavanone with antiviral and anti-inflammatory effects: a promising treatment strategy against COVID-19. Phytother Res. 2020;34:3137–47.
Miao M, Xiang L. Pharmacological action and potential targets of chlorogenic acid. Adv Pharmacol. 2020;87:71–88.
Sathiya CK, Akilandeswari S. Fabrication and characterization of silver nanoparticles using Delonixelata leaf broth. Spectrochim Acta Part A Mol Biomol Spectrosc. 2014;128:337–41.
Gaikwad S, Ingle A, Gade A, Rai M, Falanga A, Incoronato N, Russo L, Galdiero S, Galdiero M. Antiviral activity of mycosynthesized silver nanoparticles against herpes simplex virus and human parainfluenza virus type 3. Int J Nanomed. 2013;8:4303.
Orlowski P, Tomaszewska E, Gniadek M, Baska P, Nowakowska J, Sokolowska J, Nowak Z, Donten M, Celichowski G, Grobelny J, Krzyzowska M. Tannic acid modified silver nanoparticles show antiviral activity in herpes simplex virus type 2 infection. PLoS ONE. 2014;9: e104113.
Vidhu VK, Aromal SA, Philip D. Green synthesis of silver nanoparticles using Macrotyloma uniflorum. Spectrochim Acta A Mol Biomol Spectrosc. 2011;83:392–7.
Haggag EG, Elshamy AM, Rabeh MA, Gabr NM, Salem M, Youssif KA, Youssif KA, Samir A, Muhsinah AB, Alsayari A, Abdelmohsen UR. Antiviral potential of green synthesized silver nanoparticles of Lampranthus coccineus and Malephora lutea. Int J Nanomed. 2019;14:6217.
Lotfy WA, Alkersh BM, Sabry SA, Ghozlan HA. Biosynthesis of silver nanoparticles by Aspergillus terreus: characterization, optimization, and biological activities. Front Bio eng Biotechnol. 2021;9:633468–633468.
Koduru JR, Kailasa SK, Bhamore JR, Kim KH, Dutta T, Vellingiri K. Phytochemical-assisted synthetic approaches for silver nanoparticles antimicrobial applications: a review. Adv Colloid Interface Sci. 2018;256:326–39.
Griffin AM. The nucleotide sequence of the glycoprotein gB gene of infectious laryngotracheitis virus: analysis and evolutionary relationship to the homologous gene from other herpesviruses. J Gen Virol. 1991;72:393–8.
Galdiero S, Falanga A, Vitiello M, Cantisani M, Marra V, Galdiero M. Silver nanoparticles as potential antiviral agents. Molecules. 2011;16:8894–918.
Moosa AA, Ridha AM, Al-Kaser M. Process parameters for green synthesis of silver nanoparticles using leaves extract of Aloe vera plant. Int J Multi Curr Res. 2015;3:966–75.
Barbir R, Goessler W, Ćurlin M, Micek V, Milić M, Vuković B, Milić M, Ljubojević M, DomazetJurašin D, VinkovićVrček I. Protein corona modulates distribution and toxicological effects of silver nanoparticles in vivo. Part Part Syst Charact. 2019;36:1900174.
DenrahS SM. Design of experiment for optimization of nitrophenol reduction by green synthesized silver nanocatalyst. Chem Eng Res Des. 2019;144:494–504.
Basavegowda N, Mishra K, Lee YR. Synthesis, characterization, and catalytic applications of hematite (α-Fe2O3) nanoparticles as reusable nanocatalyst. Adv Nat Sci Nanosci Nanotechnol. 2017;8: 025017.
Liaudanskas M, Zymonė K, Viškelis J, Klevinskas A, Janulis V. Determination of the phenolic composition and antioxidant activity of pear extracts. J Chem. 2017;12:1–9.
Callison SA, Hilt DA, Boynton TO, Sample BF, Robison R, Swayne DE, Jackwood MW. Development and evaluation of a real-time Taqman RT-PCR assay for the detection of infectious bronchitis virus from infected chickens. J Virol Methods. 2006;138:60–5.
Mahmoudian A, Kirkpatrick NC, Coppo M, Lee SW, Devlin JM, Markham PF, Browning GF, Noormohammadi AH. Development of a SYBR Green quantitative polymerase chain reaction assay for rapid detection and quantification of infectious laryngotracheitis virus. Avian Pathol. 2011;40:237–42.
Fatima M, Sadaf Zaidi NU, Amraiz D, Afzal F. In vitro antiviral activity of Cinnamomum cassia and its nanoparticles against H7N3 influenza a virus. J Microbiol Biotechnol. 2016;26:151–9.
Devanathan S, Dahl TA, Midden WR, Neckers DC. Readily available fluorescein isothiocyanate-conjugated antibodies can be easily converted into targeted phototoxic agents for antibacterial, antiviral, and anticancer therapy. Proc Natl Acad Sci USA. 1990;87:2980–4.
E Silva FDAS, de Azevedo CAV. A new version of the assistat-statistical assistance software. In: computers in agriculture and natural resources, proceedings of 4thWorld Congress Conference; July 23–25: Anais. Orlando, Florida USA: American Society of Agricultural and Biological Engineers; 2006. p. 393.
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