United Press International - October 12, 2005
Steve Mitchell, Senior Medical Correspondent
The antibiotic, called plectasin, showed activity in lab tests against several species of bacteria, including strains of pneumonia-causing Streptococcus pneumoniae that are resistant to currently available antibiotics. Studies in mice indicated plectasin might be safe for use in humans and it protected the animals from bacterial infections that can be deadly.
The discovery opens up the door for identifying many new antibiotics, Dr. Michael Zasloff, co-author of the study and professor in the departments of surgery and pediatrics at Georgetown University Medical Center, told United Press International.
"This discovery will open up an almost inexhaustible supply of antibiotics," Zasloff said. "I do not believe that we will find ourselves in a position in which a microbe will appear for which we will not have an antibiotic to fight it," including strains that are resistant to currently available antibiotics, he added.
The particular fungus this compound was detected in, Pseudoplectania nigrella, was in a sense randomly chosen. Novozymes, a biotech company based in Denmark that led the research, was actually looking for enzymes, not antibiotics.
"So there is no reason not to expect that we will not find many, many more antibiotics of this class as we start to screen the thousands of fungi that are known to exist," Zasloff said.
He said he also expects to find antibiotics that block viruses because fungi use these compounds to protect themselves from pathogens and presumably some must be active against certain viruses present in their environment.
Further work conducted since the discovery of plectasin has already identified other antibiotic compounds in other fungi, Zasloff said. In addition, they have determined that plectasin "works by a different mechanism than any of the known antibiotics," which will make the development of resistance unlikely, he said.
"This finding (plectasin), and the existence of about 200,000 additional species of fungi, opens up a vast universe to explore for novel peptide antibiotics," study co-author Dr. Robert Lehrer, a professor of medicine at UCLA's School of Medicine, said in a statement.
Lehrer said that if plectasin is shown to be safe and effective in further studies in humans, it could be on the market as soon as 2012.
Plectasin has all the characteristics required to turn it into a drug, in terms of cost and the capability to produce it in sufficient amounts, Zasloff said.
The discovery, reported in the Oct. 13 issue of Nature, was made possible by the technique used by Zasloff and colleagues. Instead of traditional techniques, they did a genetic analysis, which enabled them to identify plectasin as a peptide that was similar to other antibiotic compounds called defensins. Traditional techniques for detecting antibiotics failed to turn up any significant amounts in this fungus and thus without the genetic screening, plectasin might have gone undetected, Zasloff said.
Defensins are peptides, or small proteins, that a wide range of plants and animals, including humans, produce to protect themselves from pathogens. Zasloff said researchers have already identified defensins that are active against viruses, such as HIV, but the trick is finding ones that aren't toxic and can be produced as a drug.
In laboratory tests conducted by the Danish National Center for Antimicrobials and Infection Control, plectasin was highly effective against S. pneumoniae and Streptococcus pyogenes -- bacteria that cause meningitis, pneumonia, strep throat, sepsis and flesh-eating infections.
Animal studies also yielded promising results. Plectasin was as effective as another antibiotic, vancomycin, in protecting mice against peritonitis, an infection in the lining of the abdominal cavity. The compound also offered comparable protection to penicillin in defending mice from pneumonia caused by S. pneumoniae.
E-mail: sciencemail@upi.com
051012
UP051005
Copyright © 2005 - United Press International. All rights reserved. Reproduced with permission. Reproduction of this article (other than one copy for personal reference) must be cleared through United Press International, Permissions Desk, 1510 H St. N.W. Washington DC 2005. Main Phone Switchboard: 202-898-8000 FAX: 202-898-8057 or 202-898-8147 Email: info@upi.com.
AEGiS is a 501(c)3, not-for-profit, tax-exempt, educational corporation. AEGiS is made possible through unrestricted funding from Boehringer Ingelheim, Bridgestone/Firestone Charitable Trust, Elton John AIDS Foundation UK, the National Library of Medicine, AIDS Walk of Orange County, and donations from users like you.
Always watch for outdated information. This article first appeared in 2005. This material is designed to support, not replace, the relationship that exists between you and your doctor.
AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.
Copyright ©1980, 2005. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content. .