Endophytic Fungi Penicillium species BCt Phytochemicals Inhibit Replication of Enzymes of Human Immuno-deficiency Virus 1 in in vitro and in silico Studies

DOI:

https://doi.org/10.37285/ijpsn.2021.14.5.6

Authors

  • Govindappa M Department of Studies in Botany, Davangere University, Shivagangotri, Davangere-577 007, Karnataka, India.
  • Channabasava 1Endophytic Natural Product Laboratory, Department of Biotechnology, Shridevi Institute of Engineering & Technology, Sira Road, Tumkur-572 106, Karnataka, India
  • Ritu Pawar Department of Studies in Botany, Davangere University, Shivagangotri, Davangere-577 007, Karnataka, India
  • Chandrasekhar Srinivasa Department of Studies in Biotechnology, Davangere University, Shivagangotri, Davangere-577 007, Karnataka, India;
  • Chandan Shivamallu Department of Biotechnology and Bioinformatics, School of Life Sciences, JSS Academy of Higher Education and Research, Mysore, India
  • Manoj-Kumar Arthikala Ciencias Agrogenómicas, Escuela Nacional de Estudios Superiores, Universidad Nacional Autónoma de México, León, C.P.37684, Mexico

Abstract



The present investigation was aimed to know the coumarins in the methanol extract of endophytic fungi, Penicillium species BCt isolated from Calophyllum tomentosum bark tissues using qualitative and GC-MS analysis. The endophytic extract was evaluated for anti-HIV activity on three replicating enzymes in vitro and in silico. The methanol extract of Penicillium species confirmed the presence of coumarins in four qualitative methods and yielded four different types of coumarins in GC-MS. In GC-MS analysis, totally seven different phytochemicals were identified based on retention time and compared with available library data. The four coumarins are coumarin (2H-1-benzopyran-2-one), coumaric acid (3-benzofuran-carboxylic acid), hynecromone (coumarin 4), 4-hydroxy-9-(3-methyl-2-butyl) furo (3,2-g) chloronen-7-one) and other three are common phytochemicals. The HIV-1 RT (98) was strongly inhibited by the endophytic fungal extract compared to integrase (118) and protease (158) in vitro analysis. Highest inhibition of integrase was observed with coumarilic acid (-17.62) when attached to Glu-35, Asn-38, Ser-39 amino acids. The protease was inhibited strongly by hymecromone (-16.39) when attached to amino acids of Val-77, Glu-34, Pro-79, Gly-78. The inhibition of RT was observed with coumarilic acid by attaching to Ala-445, Arg-567, Asp-456, Glu-478, Ser-499, Asn-474 (-23.54) significantly. Based on above results, the endophytic fungal coumarins have the ability to inhibit the three replicating enzymes of HIV-1 significantly. The in-silico results are evidence for how coumarins inhibiting the HIV replicating proteins by binding at specific amino acids. The results will help to understand how and where phytochemicals bind to target proteins to inhibit their action and it may help to identification of drugs to treat HIV. To validate our results, the in vivo research is needed.   

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Keywords:

Calophyllum tomentosusm, Penicillium species BCt, Phytochemicals, Enzyme inhibition, in silico assay

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Published

2021-09-01

How to Cite

1.
M G, Channabasava, Pawar R, Srinivasa C, Shivamallu C, Arthikala M-K. Endophytic Fungi Penicillium species BCt Phytochemicals Inhibit Replication of Enzymes of Human Immuno-deficiency Virus 1 in in vitro and in silico Studies . Scopus Indexed [Internet]. 2021 Sep. 1 [cited 2024 May 5];14(5):5624-33. Available from: https://ijpsnonline.com/index.php/ijpsn/article/view/2214

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Research Articles

References

Asif M (2015). Pharmacological activities and phytochemistry of various plant containing coumarin derivatives. Current Science Perspectives 1(3): 77-90.

Bhargava D, and Garg G (2011). Design, synthesis and in silico pharmacokinetic studies of some coumarin analogues. J Chem Pharm Res 3(2):50-57.

Brooijmans N (2009). Structural Bioinformatics, Second Edition Edited by Jenny Gu and Philip E. Bourne. John Wiley & Sons, Inc.

Cos P, Maes L, Berghe VD, Hermans N, Pieters L, and Vlietinck A (2004). Plant substances as anti-HIV agents selected according to their putative mechanism of action. J Nat Prod 67: 284–293.

de Clercq E (2000). Current lead natural products for the chemotherapy of human imunodeficiency virus (HIV) infection. Med Res Rev 20:323–349.

Dharmaratne HR, Tan GT, Marasinghe GP, and Pezzuto JM (2002). Inhibition of HIV-1 reverse transcriptase and HIV-1 replication by Calophyllum coumarins and xanthones. Planta Medica 68(1): 86-87.

Du L, Chen J, Yang LM, Zheng YT, Tang Y, Shen X, and Jiang HL (2008). D77, one benzoic acid derivative, functions as a novel anti-HIV-1 inhibitor targeting the interaction between integrase and cellular LEDGF/p75. Biochem Biophys Res Commun 375:139–144.

Estari M, Venkanna L, Sripriya D, and Lalitha R (2012). Human Immunodeficiency Virus (HIV-1) reverse transcriptase inhibitory activity of Phyllanthus emblica plant extract. Biol Med 4:178-182.

Govindappa M, Anil Kumar NV, and Gustavo S (2011). Crotalaria pallida extracts as putative HIV-protease inhibitors. J Res Biol 3:285-291.

Govindappa M, Kavya C. Hemmanur, Nithin S, Gopalakrishna Bhat K, and Channabasava (2011). In vitro anti-HIV activity of partially purified coumarin(s) isolated from fungal endophyte, Alternaria species of Calophyllum inophyllum. Pharmacol Pharm 6:321-328.

Kazmierski WM, Furfine E, Gray-Nunez Y, Spaltenstein A, and Wright L (2004). Potent inhibitors of the HIV-1 protease incorporating cyclic urea P1–P2 scaffold. Bioorg Med Chem Let 14: 5685–5687.

Kostova I, Ravela S, Genova P, and Argirova R (2006). Structure-activity relationships of synthetic coumarins as HIV-1 Inhibitors. Bioinorg Chem Appl 2006: 68274.

Levin A, Armon-Omer A, Rosenbluh J, Melamed-Book N, Graessmann A, Waigmann E, and Loyter A (2009). Inhibition of HIV-1 integrase nuclear import and replication by a peptide bearing integrase putative nuclear localization signal. Retrovirology 6: 112.

Martinez JP, Sasse F, Bronstrup M, Diez J, and Meyerhans A (2015). Antiviral drug discovery: broad-spectrum drugs from nature. Nat Prod Rep 32:29–48

Rege AA, and Chowdhury AS (2014). Evaluation of Ocimum sanctum and Tinospora cordifolia as Probable HIV Protease Inhibitors. InterJ Pharm Sci Rev Re 25:315-318.

Tewtrakul S, Miyashiro H, Hattori M, Yoshinaga T, Fujiwara T, Tomimori T, Kizu H, and Miyaichi Y (2001). Inhibitory effects of flavonoids on human immunodeficiency virus type-1 integrase. J Trad Med 18(6): 229-238.

Narayan CL, and Rai RV (2011). A screening strategy for selection of anti-HIV Integrase and anti-HIV protease inhibitors from plant extracts of Indian medicinal plants. Inter J Phytomed 3:312-318.

Sheikh S, Pardeshi T, Mujawar S, Deshmukh K, Sood N, Sharma P, and Chaudhary S (2015). Study of interaction between wild type and Mutant HIV-1 protease and cyclic urea inhibitor using in silico techniques. Inter J Comp Bioinform In Silico Model 4(3): 659-666.

Umashankar T, Govindappa M, and Ramachandra YL (2012). In vitro antioxidant and anti-HIV activity of endophytic coumarin from Crotalaria pallida Aiton. Planta Medica 78:102.

Umashankar T, Govindappa M, Ramachandra YL, and Channabasava R (2015a). Isolation and purification of p-coumaric acid from endophytic fungi, Alternaria species of Crotalaria pallida and in vitro cytotoxicity. Inter J Bio Pharm Res 6(2):96-104.

Umashankar T, Govindappa M, Ramachandra YL, Chandrappa CP, Padmalatha Rai S, and Channabasava R (2015b). Isolation, purification and in vitro cytotoxicity activities of coumarin isolated from endophytic fungi, Alternaria species of Crotalaria pallida. Indo American J Pham Res 5(2): 926-936.

Umashankar T, Govindappa M, and Ramachandra YL (2012). In vitro antioxidant and anti-HIV activity of endophytic coumarin from Crotalaria pallida Aiton. Planta Medica 78:102.

U.S. Food and Drug Administration (FDA) (2015). Antiretroviral Drugs Used in the Treatment of HIV Infection; U.S. Department of Health and Human Services: Silver Spring, MD, USA.

Venugopala KN, Rashmi V, and Odhav B (2013). Review on natural coumarin lead compounds for their pharmacological activity. BioMed Research Inter Article ID 963248, 14 pages.

Wellensiek BP, Ramakrishnan R, Bashyal BP, Eason Y, Gunatilaka AAL, and Ahmad N (2013). Inhibition of HIV-1 replication by secondary metabolites from endophytic fungi of desert plants. The Open Virology J 7:72-80.

Wiwat C, and Kwantrairat S (2013). HIV- 1 Reverse Transcriptase Inhibitors from Thai Medicinal Plants and Elephantopus scaber Linn. Mahidol University J Pharm Sci 40(3):35-44.

http://www.who.int/mediacentre/factsheets/fs297/en/2012

Zhang X, Huang N, and Zheng YT (2010). Advances in the study of anti-HIV natural compounds derived from traditional Chinese medicines (in Chinese). Acta Pharm Sin 45:141–153.