Project Start: New Active Substance Targeting Dreaded Hospital Germs

May 29, 2015 / B3C newswire / -- In the German Center for Infection Research (DZIF), scientists from the universities of Tübingen, Münster and Munich join forces and prepare together with the company Hyglos clinical studies on an active substance against the dreaded hospital pathogen Staphylococcus aureus: A highly effective protein from bacteria-specific viruses, so-called bacteriophages, shall rapidly kill the bacteria, which frequently occur in the nose. Due to the specific action, the natural microflora is maintained. Such prophylactic treatment of nasal colonization could counteract the spread of especially methicillin-resistant staphylococcus aureus (MRSA) in hospitals and thereby prevent infections in patients.

Every third person, according to expert estimates, carries the bacterium Staphylococcus aureus in their nose - which is not dangerous in the case of healthy individuals, however quickly becomes a problem if the carrier is admitted to a hospital. This since the pathogen can enter for example into wounds in connection with surgery and potentially cause dangerous infections. In addition there is a large risk of spread of the pathogen as a hospital bug. Especially feared are methicillin-resistant Staphylococcus aureus isolates, abbreviated MRSA, because of their resistance to many of the commonly used antibiotics.

“A rapid detection and effective elimination of MRSA colonization in the nose prior to a hospital stay is a crucial step in combating these hospital germs", so the conviction of Prof. Dr. Karsten Becker at the University Hospital Münster. The bacteria in the nose are increasingly resistant to the currently used antibiotic mupirocin and the duration of the decolonization and follow-up control is around one week. Under such circumstances, no effective MRSA prevention is possible for patients immediately in need of surgery.

Together with the Hyglos GmbH in Bernried and with support from the BMBF, scientists at the University Hospital Münster have developed a specific active substance in recent years and studied its effect: A phage lytic enzyme that is a protein from viruses that infect bacteria, specifically attacks Staphylococcus aureus cells and dissolve them. The protein was synthetically produced and optimized as a "designer protein" with the working name HY-133. "We do like to describe it as a MRSA-killing protein, even if it sounds somewhat sensational," explains Dr. Wolfgang Mutter from Hyglos GmbH. In fact, all Staphylococcus aureus cells, whether resistant or not resistant, will be killed by this new active substance within a very short time. And this without the natural microflora in the nose being destroyed nor does resistance develop.

In cooperation with the microbiologist Prof. Dr. Andreas Peschel, who coordinates the DZIF research on "Healthcare-associated and antibiotic-resistant infections", the active substance will now be prepared for clinical testing.

More than 1.5 million euros will be provided for HY-133 development within the DZIF: The substance will first be manufactured under GMP guidelines (manufacturing practice according to pharmaceutical standards) and subsequently be tested for preclinical toxicology. The pharmacist Prof. Dr. Gerhard Winter at the LMU Munich will develop a stable formulation, so that the substance may be conveniently and safely administered as a gel or in any other form to the patient.

The project will be conducted in view of subsequent clinical trials, in which the rapid decolonization of Staphylococcus aureus strains will be studied in the nasal flora of volunteers. "In addition to new antibiotics and vaccines we urgently need specific agents for decolonization of problematic germs. The HY-133 protein is a highly innovative active substance for this purpose, which could lead to many similar development programs", Prof. Dr. Andreas Peschel adds.