Antichlamydial sterol from the red sea sponge callyspongia aff implexa

Planta Medica

Volumn 81, Issue 5, 2015, Pages 382-387

  Abdelmohsen, Usama Ramadan ^a,e   Cheng, Cheng ^a   Reimer, Anastasija ^b   Kozjak Pavlovic, Vera ^b   Ibrahim, Amany K ^c   Rudel, Thomas ^b   Hentschel, Ute ^a   Edrada Ebel, Ruangelie ^d   Ahmed, Safwat A ^c  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b UNIVERSITY OF WÜRZBURG   (Germany)

^c Suez Canal University   (Egypt)

^d UNIVERSITY OF STRATHCLYDE   (United Kingdom)

^e Minia University   (Egypt)

Author keywords

Callyspongia aff. implexa; Callyspongiidae; Chlamydia trachomatis; polyacetylene; Red Sea; sponges; sterol

Indexed keywords

ANTIINFECTIVE AGENT; BIOLOGICAL PRODUCT; CALLIMPLEXEN A; GAMMA-SITOSTEROL; GELLIUSTEROL E; POLYACETYLENE DERIVATIVE; SITOSTEROL DERIVATIVE; STEROL;

ANIMAL; CALLYSPONGIA; CHEMICAL STRUCTURE; CHEMISTRY; CHLAMYDIA TRACHOMATIS; DRUG EFFECTS; GROWTH, DEVELOPMENT AND AGING; ISOLATION AND PURIFICATION; SPONGE (PORIFERA);

ANIMALS; ANTI-BACTERIAL AGENTS; BIOLOGICAL PRODUCTS; CALLYSPONGIA; CHLAMYDIA TRACHOMATIS; MOLECULAR STRUCTURE; POLYACETYLENES; PORIFERA; SITOSTEROLS; STEROLS;

EID: 84939977682     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0035-1545721     Document Type: Article

References (31)

1. Thomas T. RA, Kavlekar D. P., LokaBharathi P. A. Marine drugs from sponge-microbe association - a review. Mar Drugs: 2010; 8 1417 1468
2. Hentschel U., Usher K. M., Taylor M. W. Marine sponges as microbial fermenters. FEMS Microbiol Ecol: 2006; 55 167 177
3. Hertiani T., Edrada-Ebel R., Ortlepp S., van Soest R. W., de Voogd N. J., Wray V., Hentschel U., Kozytska S., Müller W. E., Proksch P. From anti-fouling to biofilm inhibition: new cytotoxic secondary metabolites from two Indonesian Agelas sponges. Bioorg Med Chem: 2010; 18 1297 1311
4. Mol V. PL, Raveendran T. V., Parameswaran P. S. Antifouling activity exhibited by secondary metabolites of the marine sponge, Haliclona exigua (Kirkpatrick). Int Biodeter Biodegr: 2009; 63 67 72
5. Faulkner D. J. Marine natural products. Nat Prod Rep: 2002; 19 1 48
6. Blunt J. W., Copp B. R., Munro M. H., Northcote P. T., Prinsep M. R. Marine natural products. Nat Prod Rep: 2005; 22 15 61
7. Proksch P., Putz A., Ortlepp S., Kjer J., Bayer M. Bioactive natural products from marine sponges and fungal endophytes. Phytochem Rev: 2010; 9 475 489
8. Laport M. S., Santos O. CS, Muricy G. Marine sponges: potential sources of new antimicrobial drugs. Curr Pharm Biotechnol: 2009; 10 86 105
9. Tsukamoto S., Kato H., Hirota H., Fusetani N. Seven new polyacetylene derivatives, showing both potent metamorphosis-inducing activity in ascidian larvae and antifouling activity against barnacle larvae, from the marine sponge Callyspongia truncate. J Nat Prod: 1997; 60 126 130
10. Youssef D., van Soest R., Fusetani N. New polyacetylenic alcohols with cytotoxic activity from the Red Sea sponge Callyspongia sp. J Nat Prod: 2003; 66 679 687
11. Uno M., Ohta S., Ohta E., Ikegami S. Callyspongins A and B: novel polyacetylene sulfates from the marine Callyspongia truncate. J Nat Prod: 1996; 59 1146 1148
12. Sera Y., Adachi K., Shizuri Y. A new epidioxy sterol as an antifouling substance from a Palauan marine sponge, Lendenfeldia chondrodes. J Nat Prod: 1999; 62 152 154
13. Youssef D. T., Ibrahim A. K., Khalifa S. I., Mesbah M. K., Mayer A. M., van Soest R. W. New anti-inflammatory sterols from the two Red Sea sponges Scalarispongia species and Callyspongia siphonella. Nat Prod Commun: 2009; 5 27 31
14. Somani J., Bhullar V. B., Workowski K. A., Farshy C. E., Black C. M. Multiple drug-resistant Chlamydia trachomatis associated with clinical treatment failure. J Infect Dis: 2000; 181 1421 1427
15. Stephens R. S. The cellular paradigm of chlamydial pathogenesis. Trends Microbiol: 2003; 11 44 51
16. Ray K. J., Zhou Z. X., Cevallos V., Chin S., Enanoria W., Lui F., Lietman T. M., Porco T. C. Estimating community prevalence of ocular Chlamydia trachomatis infection using pooled polymerase chain reaction testing. Ophthal Epidemiol: 2014; 21 86 91
17. Fan H. Blindness-causing trachomatous trichiasis biomarkers sighted. Invest Ophthalmol Vis Sci: 2012; 53 2560
18. Ratnam S., Jang D., Gilchrist J., Smieja M., Poirier A., Hatchette T., Flandin J. F., Chernesky M. Workflow and maintenance characteristics of five automated laboratory instruments for the diagnosis of sexually transmitted infections. J Clin Microbiol: 2014; 52 2299 2304
19. Sandoz K. M., Rockey D. D. Antibiotic resistance in Chlamydiae. Future Microbiol: 2010; 5 1427 1442
20. Sharma M., Rudel T. Apoptosis resistance in Chlamydia -infected cells: a fate worse than death? FEMS Immunol Med Microbiol: 2009; 55 154 161
21. Beatty W. L., Morrison R. P., Byrne G. I. Persistent chlamydiae: from cell culture to a paradigm for chlamydial pathogenesis. Microbiol Rev: 1994; 58 686 699
22. Hogan R. J., Mathews S. A., Mukhopadhyay S., Summersgill J. T., Timms P. Chlamydial persistence: beyond the biphasic paradigm. Infect Immun: 2004; 72 1843 1855
23. Salin O., Alakurtti S., Pohjala L., Siiskonen A., Maass V., Maass M., Yli-Kauhaluoma J., Vuorela P. Inhibitory effect of the natural product betulin and its derivatives against the intracellular bacterium Chlamydia pneumoniae. Biochem Pharmacol: 2010; 80 1141 1151
24. Horan A. C., Shearer M. C., Hedge V., Beyazova M. L., Brodsky B. C., King A., Berrie R., Cardaci K., Nimeck M. A family of novel macrocyclic lactones, the saccharocarcins produced by Saccharothrix aerocolonigenes subsp. antibiotica. I. Taxonomy, fermentation, isolation and biological properties. J Antibiot (Tokyo): 1997; 50 119 125
25. Gallimore W. A., Kelly M., Scheuer P. J. Gelliusterols A-D, new acetylenic sterols from a sponge, Gellius species. J Nat Prod: 2001; 64 741 744
26. Hesse M., Meier H., Zeeh B. Spektroskopische Methoden in der organischen Chemie. 3rd ed. Stuttgart Thieme Verlag: 1987; 36
27. Umeyama A., Nagano C., Arihara S. Three novel C-21 polyacetylenes from the marine sponge Callyspongia sp. J Nat Prod: 1997; 60 131 133
28. Carballeira N. M., Shalabi F. Novel brominated phospholipid fatty acids from the Caribbean sponge Petrosia sp. J Nat Prod: 1993; 56 739 746
29. Wylie J. L., Hatch G. M., McClarty G. Host cell phospholipids are trafficked to and then modified by Chlamydia trachomatis. J Bacteriol: 1997; 179 7233 7242
30. Gilk S. D., Cockrell D. C., Luterbach C., Hansen B., Knodler L. A., Ibarra J. A., Steele-Mortimer O., Heinzen R. A. Bacterial colonization of host cells in the absence of cholesterol. PLoS Pathog: 2013; 9 e1003107
31. Wang Y., Kahane S., Cutcliffe L. T., Skilton R. J., Lambden P. R., Clarke I. N. Development of a transformation system for Chlamydia trachomatis: restoration of glycogen biosynthesis by acquisition of a plasmid shuttle vector. PLoS Pathog: 2011; 7 e1002258