New research identifies possible new treatment for gonorrhea

SAN FRANCISCO — New research led by the Oregon State University (OSU) has identified a possible new treatment for gonorrhea, a sexually transmitted disease whose numbers grow by 78 million new cases worldwide each year.

Gonorrhea can lead to endometritis, pelvic inflammatory disease, ectopic pregnancy, epididymitis and infertility. If untreated or improperly treated, it is highly damaging to reproductive and neonatal health. And babies born to infected mothers are at increased risk of blindness.

“The infections very often are silent,” said Aleksandra Sikora, an associate professor in the OSU College of Pharmacy. “Up to 50 percent of infected women don’t have symptoms, but those asymptomatic cases can still lead to some very severe consequences for the patient’s reproductive health, miscarriage or premature delivery.”

The need for better antibiotic therapy and a vaccine is pressing, especially for Neisseria gonorrhoeae, which is considered a “superbug” due to its resistance to all classes of antibiotics available for treating infections. N. gonorrhoeae strains resistant to the last effective treatment options have emerged, and failures in treatment are occurring.

Led by Sikora, researchers have identified a new therapy target, an enzyme known as AniA. The bacteria need the surface-exposed enzyme to respirate without oxygen, or anaerobically, which is their preferred method of respiration in the biofilms of the genitourinary tract. A biofilm is a group of one or more types of microorganisms that grow on a wet surface, such as dental plaque on teeth.

The team reported in Antimicrobial Agents and Chemotherapy that they identified a peptide, or multiple amino acids linked in a chain, that inhibits the AniA enzyme’s nitrite reductase activity, which in turn damages the bacteria’s ability to grow in the oxygen-poor biofilm environment.

“Bacteria in biofilms display increased resistance to antimicrobials,” Sikora explained. “The enzyme is only necessary for cell viability when these bacteria grow under anaerobic conditions, including when they grow in the biofilm. Most antibiotics target essential cell functions; this one doesn’t. It’s only at a certain stage of growth that the bacteria are affected, which means the development of resistance won’t be as fast.”

Through a technique known as biopanning, OSU researchers and their collaborators at the University of Kentucky found 29 unique peptides that bound with the targeted enzyme. One of them, known as C7-3, was identified as most promising for inhibiting the protein’s interaction with nitrite, necessary for anaerobic respiration.

“Imagine this research approach as having a pond with a lot of fish, and you’re using the protein as the bait,” Sikora, who has applied for a provisional patent, was quoted as explaining in a news release from OSU on Monday. “The peptides bind with the protein, and you go through multiple rounds to identify the peptides that have the strongest binding ability. You start with a billion peptides and end up with one that strongly inhibits the enzyme and ultimately kills the bacteria.”