Cited by 172Seaweed-derived Bioactive CompoundsPolysaccharides Composition and ApplicationsPolysaccharides and Plant Cell Walls

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In vitro antiviral activities of sulfated polysaccharides from a marine microalga (Cochlodinium polykrikoides) against human immunodeficiency virus and other enveloped viruses

Hasui, Masahiko, Matsuda, Masahiro, Okutani, Koichi, Shigeta, Shiro·1995·International Journal of Biological Macromolecules

DOI 10.1016/0141-8130(95)98157-t

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Abstract

A marine microalga, Cochlodinium polykrikoides, produces extracellular sulfated polysaccharides. Isolation and purification of the polysaccharides were accomplished by precipitation with ethanol and Cetavlon, followed by DEAE-cellulose column chromatography (polysaccharides A1 and A2). These polysaccharides, which were homogeneous when analysed by both ultracentrifugal and electrophoretic methods, were composed of mannose, galactose, glucose and uronic acid, together with sulfate groups (S = 7-8% w/w). Both A1 and A2 inhibited the cytopathic effect of influenza virus types A and B in MDCK cells, that of respiratory syncytial virus types A and B in HEp-2 cells, that of human immunodeficiency virus type 1 in MT-4 cells; and, except A1 for herpes simplex virus type 1 and A2 for parainfluenza virus type 2 in HMV-2 cells, the cochlodinium polysaccharides showed no antiviral activity against parainfluenza virus types 2 and 3, measles virus, mumps virus or herpes simplex virus type 1 in HMV-2 cells. No cytotoxicity for host cells was observed with these polysaccharides at a concentration of 100 micrograms ml-1. Inhibitory effects on various viruses were achieved at concentrations that were not markedly inhibitory to the blood coagulation process.

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PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394
Colorimetric Method for Determination of Sugars and Related Substances
DuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956) · Analytical Chemistry · doi:10.1021/ac60111a017 · Cited by 52,269
A NEW SPECIFIC COLOR REACTION OF HEXURONIC ACIDS
Dische, Z. (1947) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)35155-4 · Cited by 2,128
Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds
Pauwels, R., Balzarini, J. M., Baba, M., Snoeck, R., Schols, D., Herdewijn, P. A., Desmyter, J., & Clercq, E. D. (1988) · Journal of Virological Methods · doi:10.1016/0166-0934(88)90134-6 · Cited by 1,646
Sulfated polysaccharides are potent and selective inhibitors of various enveloped viruses, including herpes simplex virus, cytomegalovirus, vesicular stomatitis virus, and human immunodeficiency virus
Baba, M., Snoeck, R., Pauwels, R., & Clercq, E. D. (1988) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.32.11.1742 · Cited by 545
Polysaccharides as antiviral agents: antiviral activity of carrageenan
González, M. E., Alarcón, B., & Carrasco, L. (1987) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.31.9.1388 · Cited by 187
Dextran Sulfate Is Poorly Absorbed after Oral Administration
Lorentsen, K. J., Hendrix, C. W., Collins, J. M., Kornhauser, D. M., Petty, B. G., Klecker, R. W., Flexner, C., Eckel, R. H., & Lietman, P. S. (1989) · Annals of Internal Medicine · doi:10.7326/0003-4819-111-7-561 · Cited by 132
Extracellular slime associated with Proteus mirabilis during swarming
Stahl, S. J., Stewart, K. R., & Williams, F. D. (1983) · Journal of Bacteriology · doi:10.1128/jb.154.2.930-937.1983 · Cited by 69
In vitro activity of mannan sulfate, a novel sulfated polysaccharide, against human immunodeficiency virus type 1 and other enveloped viruses
Ito, M., Baba, M., Hirabayashi, K., Matsumoto, T., Suzuki, M., Suzuki, S., Shigeta, S., & Clercq, E. D. (1989) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/bf01963907 · Cited by 48
Self-citation
Adsorption, Penetration and Uncoating of Herpes Simplex Virus
Hochberg, E., & Becker, Y. (1968) · Journal of General Virology · doi:10.1099/0022-1317-2-2-231 · Cited by 46

Show all 14 references

Research works printed but not linked: 4

Takemoto, 1966, Prog. Med. Virol., 8, 314
Baba, 1988, 85, 6132
Chang, 1988, 189, 304
Vermylen, 1960, Thromb. Diath. Haemorrh., 5, 267

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Authors: Hasui, M., Matsuda, M., Okutani, K., & Shigeta, S.
Affiliations: Kagawa University (JP)
Venue: International Journal of Biological Macromolecules
Publisher: Elsevier BV
Published: 1995-01
Volume: 17
Issue: 5
Pages: 293-297
ISSN: 0141-8130 (ISSN-L)
DOI: 10.1016/0141-8130(95)98157-t
OpenAlex: W2047601275
Cited by: 172
References: 14
Citations by year: 2026: 4 · 2025: 5 · 2024: 10 · 2023: 6 · 2022: 24 · 2021: 18 · 2020: 11 · 2019: 5 · 2018: 8 · 2017: 5 · 2016: 5 · 2015: 7 · 2014: 5 · 2013: 7 · 2012: 6
FWCI: 3.65
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: International Journal of Biological Macromolecules (publishedVersion)
PubMed (publishedVersion)
Funders: Japan Society for the Promotion of Science
Topics: Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Seaweed-derived Bioactive Compounds
Life Sciences › Agricultural and Biological Sciences › Food Science › Polysaccharides Composition and Applications
Life Sciences › Agricultural and Biological Sciences › Plant Science › Polysaccharides and Plant Cell Walls
Keywords: sulfated polysaccharides, Cochlodinium polykrikoides, marine microalgae, antiviral activity, HIV-1, enveloped viruses, influenza virus, respiratory syncytial virus, herpes simplex virus type 1, parainfluenza virus type 2, uronic acid, polysaccharide purification, cytopathic effect inhibition, marine natural products
MeSH terms: Animals, Antiviral Agents, Cell Division, Cell Line, Chromatography, Drug Evaluation, Preclinical, Humans, Kidney, Laryngeal Neoplasms, Influenza A virus, Polysaccharides, Respiratory Syncytial Viruses, Spectrophotometry, Infrared, Sulfates, Tumor Cells, Cultured, Virus Replication, HIV-1, Simplexvirus, Eukaryota

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In vitro antiviral activities of sulfated polysaccharides from a marine microalga (Cochlodinium polykrikoides) against human immunodeficiency virus and other enveloped viruses

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