Researchers at the University of California, San Diego School of Medicine and Children’s Hospital and Health Center, San Diego have discovered that "Staph" bacteria use a protective golden armor to ward off the immune system, a finding with the potential to lead to new treatments for serious infections now increasingly resistant to standard antibiotics.
The research, featured on the cover of the July 18, 2005 issue of The Journal of Experimental Medicine, focused on the major human pathogen Staphylococcus aureus and the characteristic yellow-orange color for which it is named (“aureus” is Latin for “golden”).
Among the deadliest of all disease-causing organisms, “Staph” is the leading cause of human infections in the skin and soft tissues, bones and joints, abscesses and normal heart valves. Staph especially flourishes in the hospital setting, producing bloodstream and surgical wound infections. The spread of antibiotic resistant strains of Staph, referred to as methicillin-resistant Staphylococcus aureus or MRSA, has reached epidemic proportions and poses a major threat to the public health.
The UCSD team proved for the first time that the golden pigment that coats the surface of Staph is not just for decoration; rather, the molecules that give the bacteria its golden hue also help it resist killing by neutrophils, white blood cells with a front line role in immune defense against invading microbes.
Staph’s coloration reflects the production of molecules called carotenoids, similar to those present in carrots and other colorful vegetables and fruits. Dietary carotenoids have long been touted for their antioxidant properties with hope that they could slow aging or fight off cancer. The scientists found that pathogenic Staph took advantage of the antioxidant effects of its carotenoid pigment to extend its own life, by inactivating chemicals deployed by neutrophils that are lethal to most bacteria.
The UCSD team used a molecular genetic approach for their studies, knocking out the genes for carotenoid synthesis to generate a mutant strain of Staph that appeared white in color instead of the normal gold.
“We found that the nonpigmented Staph mutant became much more susceptible to oxidants such as hydrogen peroxide and singlet oxygen produced by neutrophils,” said George Liu, M.D., Ph.D., a research fellow in the UCSD department of pediatrics who spearheaded the studies. “Without its golden pigment, the Staph lost its ability to survive in human neutrophils or blood, and could no longer form an abscess when injected into the skin of experimental mice.”
The investigators proved that the antioxidant effects of the Staph pigment were the key factor in virulence by repeating experiments in blood from a human patient with chronic granulomatous disease (CGD), an inherited disorder in which neutrophils cannot produce oxidants and infections are common, as well as in mice engineered to possess the same genetic mutation. Without the oxidant assault, the ability of the nonpigmented strain to resist neutrophil killing and produce disease was equal to the golden Staph.