This project will refine factors that define the protocol for mating compatible strains of Aspergillus fumigatus in order to decrease the time required to complete the meiotic cycle. A. fumigatus is an important mould pathogen of immunocompromised hosts. The frequency of infections is increasing and the morbidity and mortality attributable to invasive disease remains unacceptably high. Although molecular genetic techniques have enabled researchers to make good progress in investigating factors involved in the biology of the organism and the pathogenesis of disease, the addition of classical genetics to the armamentarium of the research community would markedly enhance our ability to study this organism. The primary barrier to the widespread use of classical genetics is the prolonged period required for completion of the mating cycle. The six month incubation renders this approach unfeasible for routine use. The hypothesis is that by methodically evaluating environmental conditions under which mating takes place, the current system can be optimized.
In Specific aim 1, the environmental conditions, including medium, water, temperature, atmosphere, and light, will be optimized to reduce the time required for mating between isolates of A. fumigatus. Our goal is to achieve a 4 - 6 week window for the completion of the cycle, and our preliminary data shows that the required time has already been reduced by 1/3 - 1/2. In the second specific aim, commonly used markers for the molecular manipulation of A. fumigatus will be evaluated for their effect upon mating. Drug markers, auxotrophic markers, and other factors, such as ablation of NHEJ, will be evaluated. Completion of these studies should provide the A. fumigatus research community with a powerful new tool to use in research on this important pathogen.

Public Health Relevance

Aspergillus fumigatus is an important pathogen of people who have compromised immune systems, such as patients undergoing organ transplantation or cancer chemotherapy. Invasive aspergillosis is very difficult to diagnose and treat, which results in high mortality among infected patients. One of the tools that can be used to study this organism is classical or Mendelian genetics, which can be used in conjunction with molecular techniques. At the present time, completion of the mating cycle requires six months, making it too slow to be of benefit to the research community. By varying the conditions, we have already reduced the time to 3 - 4 months. This projects aims to reduce the time further, so that the process will be complete within 4 - 6 weeks.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Research Grants (R03)
Project #
1R03AI096014-01
Application #
8176151
Study Section
Pathogenic Eukaryotes Study Section (PTHE)
Program Officer
Duncan, Rory A
Project Start
2011-07-15
Project End
2013-06-30
Budget Start
2011-07-15
Budget End
2012-06-30
Support Year
1
Fiscal Year
2011
Total Cost
$78,500
Indirect Cost
Name
University of Cincinnati
Department
Pathology
Type
Schools of Medicine
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221