Wednesday, November 2, 2011

Making germs glow: New test helps save lives and cuts costs

 Replacing conventional laboratory tests with a new DNA sequence-based technology to identify pathogens causing bloodstream infections dramatically lowered mortality and health-care costs, a clinical study conducted by an interdisciplinary UA research team found.


Unlike conventional , a called PNA-FISH is designed to rapidly identify bloodstream pathogens by their . Results are available within hours instead of days providing pharmacists and physicians with information they can use to rapidly customize antimicrobial treatment for patients with infections.


PNA-FISH is an abbreviation for “peptide nucleic acid fluorescence in situ hybridization.” Rapid reporting of PNA FISH results to pharmacists and physicians cut the mortality of ICU patients with enterococcus or streptococcus bloodstream infections by almost half and slashed mortality from yeast infections by 86 percent. In addition, the intervention resulted in healthcare cost reduction of almost $5 million per year.


The interdisciplinary research team recently presented its results at the 51st Interscience Conference on Antimicrobial Agents and Chemotherapy in Chicago.


"Our goal was to decrease for patients with bloodstream infections, and we achieved that goal through a strong collaboration among research scientists at the UA's BIO5 Institute, clinical microbiology laboratory scientists at University of Arizona Medical Center, and an interdepartmental collaboration among the clinical laboratory, infectious disease pharmacy and physicians," said Donna Wolk, an associate professor at the UA's College of Medicine, who led the study. Wolk is division chief of clinical and molecular microbiology in the department of pathology at the UA.


Every year, more than 875,000 patients are diagnosed with bloodstream infections in the U.S., resulting in more than 90,000 deaths and significant costs to the health-care system.


According to Wolk, bloodstream infections can be difficult to treat because conventional diagnostic laboratory methods often require days to identify slow-growing bacteria and confirm which antimicrobials will work best. That lag-time forces physicians to prescribe broad-spectrum antibiotics until laboratory results can confirm the pathogen identity and antibiotic effectiveness patterns.


Overuse of antibiotics can lead to toxic side effects and disruption of the body's normal flora or beneficial bacteria, which can also lead to other infections.


The study assessed patients with positive blood cultures admitted to UA Medical Center-University Campus between August 2007 and March 2011. Outcomes and costs for 722 patients were analyzed, of which, 344 had PNA FISH performed. Board certified clinical microbiologists tested blood cultures and reported PNA FISH results to infectious disease pharmacists and physicians.


In conventional tests for , clinical microbiologists typically take a blood sample from the patient, mix it with a liquid growth medium and incubate it to stimulate microbial growth.


Once the microbes present in the sample have multiplied to large numbers, some of the liquid is transferred to a petri dish filled with solid agar growth medium and placed into an incubator to allow the growth of distinct and recognizable microbe colonies.


"It's a bit like a gardener waiting to pick the flowers," Wolk explained.


"It takes about a day to cultivate the fluid and at least another day to see the individual bacteria colonies on the agar. Once we see them growing, we can pick one to perform a biochemical profile, which identifies the pathogen and the best antibiotics to use, but that process wastes precious time."


PNA-FISH, on the other hand, bypasses this process. It uses fluorescent molecules tagged to genetic sequences that match those in the microbe. When added to a dried drop of blood culture containing pathogens, sequences that find their match inside the microbe stick, while those that don't are washed away. The process is not unlike placing a key into a lock – only the right key will fit.


Once the tagged genetic sequences link up, a clinical scientist views the slide under a special microscope that makes the fluorescent tags visible. The microbes' identity is confirmed by the color of their fluorescence.


"The tagged pathogens will glow, different colors for different microbes – it's like fireworks under our microscope," Wolk said, "and we feel a Fourth of July excitement because we know our laboratory is helping to save the lives of people in our community."


Wolk recognizes the importance of a university-based bench to bedside translational research approach to diagnosis of infections. With a vision that began in late 2006, she directs the BIO5's Infectious Disease Research Core Laboratory, or IDRC, where research scientists participate in clinical trials to verify the accuracy of new technology.


The IDRC works with bioindustry sponsors like AdvanDX, the manufacturer of PNA FISH, to obtain approval from the U.S. Food and Drug Administration to use the technology for patient care. Since its inception, IDRC has participated in more than 16 clinical trials in which research staff focus on developing faster and more precise diagnostic tests aimed at detecting and preventing infectious diseases and public health threats.


After a clinical trial, the next step in the translational pipeline is to assess which technology is most likely to benefit critically ill patients and move that technology from the research to the highly standardized and regulated hospital setting at UAMC. There, medically board-certified clinical laboratory scientists perform testing to quickly identify pathogens and relay information to pharmacists and physicians.


"The collaboration between the UA's pathology department and UA's BIO5 Institute was essential for us to establish a national model of bench-to-bedside laboratory practices," Wolk added. "Our collective translational capabilities are very unique and provide a long-awaited missing link for translating molecular microbiology methods into clinical microbiology laboratories for improving patient care."


"At the IDRC, our motto is simple," she said: "'Advancing diagnostics, saving lives.' We are very proud of the contribution our team makes, helping to improve the quality and efficiency of health care in our community and across the globe."


Provided by University of Arizona (news : web)

Researchers discover material with graphene-like properties

 After the Nobel Prize in Physics was awarded to two scientists in 2010 who had studied the material graphene, this substance has received a lot of attention. Together with colleagues from Korea, Dr. Frederik Wolff-Fabris from the Helmholtz-Zentrum Dresden-Rossendorf (HZDR) has now developed and analyzed a material which possesses physical properties similar to graphene. Its structure also resembles iron pnictides, i.e. high temperature superconductors, and it definitely has a promising future: Due to the position of the individual components in the Periodic Table of Elements, some of the atoms can simply be replaced by foreign atoms.


This creates new materials which can be superconductive, magnetic, or behave like topological insulators.


Earlier this year, Dr. Jun Sung Kim came from South Korea to use HZDR's Dresden High Magnetic Field Laboratory to analyze a number of material samples in high magnetic fields. For the first time ever, he and his colleague from Dresden, Dr. Frederik Wolff-Fabris, studied the metal SrMnBi2 and observed something amazing: The material consisting of the three elements strontium, manganese, and bismuth behaves physically similar to the "magical material" graphene.


Due to its composition and the position of its elements in the Periodic Table, SrMnBi2 permits simple and uncomplicated doping with foreign atoms. Inserting small amounts of foreign atoms alters the physical properties of a material. This might result in the creation of new magnets or superconductors.


SrMnBi2 is currently also in the focus of other research groups; but only the use of ultra-high magnetic fields, such as those generated in the Dresden High Magnetic Field Laboratory, permitted these precise results and, thus, a publication in the scientific journal Physical Review Letters. Later this year, Dr. Jun Sung Kim will return to Dresden to conduct additional experiments on SrMnBi2 with Dr. Wolff-Fabris.


Story Source:


The above story is reprinted (with editorial adaptations ) from materials provided by Helmholtz Association of German Research Centres.

Journal Reference:

Joonbum Park, G. Lee, F. Wolff-Fabris, Y. Koh, M. Eom, Y. Kim, M. Farhan, Y. Jo, C. Kim, J. Shim, J. Kim. Anisotropic Dirac Fermions in a Bi Square Net of SrMnBi2. Physical Review Letters, 2011; 107 (12) DOI: 10.1103/PhysRevLett.107.126402

New equation predicts molecular forces in hydrophobic interactions

The physical model to describe the hydrophobic interactions of molecules has been a mystery that has challenged scientists and engineers since the 19th century. Hydrophobic interactions are central to explaining why oil and water don't mix, how proteins are structured, and what holds biological membranes together. Chemical engineering researchers at UC Santa Barbara have developed a novel method to study these forces at the atomic level, and have for the first time defined a mathematical equation to measure a substance's hydrophobic character.


"This discovery represents a breakthrough that is a culmination of decades of research," says Professor Jacob Israelachvili. "The equation is intended to be a tool for scientists to begin quantifying and predicting molecular and surface forces between organic substances in water."


Using a light-responsive surfactant – a soap-like molecule related to fats and lipids – the researchers developed an innovative technique to measure or change the forces between layers of the molecule in water by using beams of UV or visible light. The result is a general equation that applies to even more complicated systems, such as cellular membranes or proteins.


"We were fortunate to find the right combination of experimental methods and theory," said Brad Chmelka, UCSB Chemical Engineering professor and co-author of the study. "The keys to our research were using a light-responsive surfactant molecule, a means of measuring these delicate surface forces, and applying knowledge of what to look for."


The highly-sensitive instrument they used to sense these molecular-level hydrophobic forces, called a surface forces apparatus, is a now-standard technique that was originally pioneered by Israelachili and colleagues in the 1970s.


New equation predicts molecular forces in hydrophobic interactions
Enlarge

This is Israelachvili?s equation. Credit: UCSB

"In basic chemistry, students learn about van der Waal forces – the weak forces that act between all . That theory was developed more than 100 years ago," explains Professor Israelachvili.

"According to the van der Waals theory, however, oil and water shouldn't separate and surfactants shouldn't form membranes, but they do. There has been no proven theory to account for these special hydrophobic interactions. Such behaviors are crucial for life as we know it to exist."


Hydrophobic and hydrophilic interactions are central to the disciplines of chemistry, physics, and biology that have fueled modern developments in industries from detergents to pharmaceuticals and new biotechnologies. The new equation is expected to impact applications in water filtration, membrane separations, biomedical research, gene therapy methods, biofuel production, and food chemistry.


Virus and disease propagation in the human body are directly linked to hydrophobic properties on a cellular level. One of the problems related to chemotherapy treatments for cancer is being able to direct a drug specifically to cancer cells, instead of the entire body. Israelachvili and his colleagues foresee their discovery having an impact in biomedical research that attempts to understand and treat diseases.


"Cell membranes are complex and discriminating structures, allowing the transmission of various signals into cells and mediating specific interactions with bacteria and viruses," said Jean Chin, Ph.D., who oversees membrane structure grants at the National Institute of General Medical Sciences of the National Institutes of Health. "This study, by enhancing our understanding of the role played by hydrophobic forces in membrane dynamics, will expand what we know about membrane structure and function, as well as microbial infection pathways."


"Understanding how water and oil-like substances interact is enormously important for explaining the properties and functions of many biological and engineering materials," says Dr. Robert Wellek, Program Director in the Directorate for Engineering at the National Science Foundation. "The UCSB and USC teams have elegantly combined concepts from synthetic chemistry, photophysics, and chemical engineering to unravel and quantify the elusive hydrophobic interaction. NSF is very pleased that its grantees have been able to contribute important fundamental knowledge in this important area."


Details of the research were published this month in the Proceedings of the National Academy of Sciences. Their research was made possible by support from the National Science Foundation, the National Institutes of Health, and the Procter & Gamble Company.


"We've known for a long time what we were aiming for. It's a bit like climbing a mountain," said Professor Israelachvili. "The whole thing started at the very bottom. I've been searching for the keys to this interaction for thirty years. We are thrilled with the findings, but it took a lot of steps over carefully chosen paths to get there."


Provided by University of California - Santa Barbara (news : web)

Why oxygen becomes the undoing of proteins

 Scientists from the Faculty of Biology and Biotechnology at the RUB have published a report in the Journal of Biological Chemistry explaining why enzymes used for the production of hydrogen are so sensitive to oxygen. In collaboration with researchers from Berlin, they used spectroscopic methods to investigate the time course of the processes that lead to the inactivation of the enzyme's iron center.


"Such enzymes, the so-called hydrogenases, could be extremely significant for the production of hydrogen with the help of biological or chemical catalysts," explains Camilla Lambertz from the RUB study group for photobiotechnology. "Their extreme sensitivity to oxygen is however a major problem. In future, our results could help to develop enzymes that are more robust."


Oxygen as a friend and as an enemy


Oxygen is crucial for the survival of most animals and plants. It is however toxic for many living creatures if the concentration thereof is too high, and some organisms can even only exist entirely without oxygen. Sensitivity to oxygen is also present at the protein level. A large number of enzymes, for example, hydrogenases are known to be irreversibly destroyed by oxygen. Hydrogenases are biological catalysts that convert protons and electrons into technically usable hydrogen. The RUB team of Prof. Thomas Happe is doing research on so-called [FeFe]-hydrogenases which are capable of producing particularly large amounts of hydrogen. The generation of hydrogen takes place at the H-cluster, consisting of a di-iron and four-iron subcluster which, together with other ligands, form the reactive center.


Oxygen attacks the iron centers


The researchers, working in collaboration with Dr. Michael Haumann's team in Berlin, discovered that oxygen binds to the di-iron center of the hydrogenase, which initiates the inactivation of another part of the enzyme consisting of four further iron atoms. In this project, sponsored by the BMBF, it was possible to show the diverse phases of the inactivation process for the first time using the so-called X-ray absorption spectroscopy. The researchers used the synchroton radiation source Swiss Light Source in Switzerland for this specific type of measurement. It generates particularly strong rays, thus enabling the characterization of metal centers in proteins. Amongst other things, the scientists thus determined the chemical nature of the iron centers and the distance from the surrounding atoms using atomic resolution.


Inactivation in three phases


The team of researchers from Bochum and Berlin used a new experimental procedure. They initially brought the hydrogenase sample into contact with oxygen for a few seconds to minutes and finally for a couple of hours and then suppressed all proceeding reactions by deep-freezing it in liquid nitrogen. The subsequently gained spectroscopic data was used for the development of a model for a three-phase inactivation process. According to this model, an oxygen molecule initially binds to the di-iron center of the hydrogenase, which leads to the development of an aggressive oxygen species. In the subsequent phase, this attacks and modifies the four-iron center. During the final phase, further oxygen molecules bind and the entire complex disintegrates.


"The entire process thus consists of a number of consecutive reactions that are distinctly separated in time," says Lambertz. "The velocity of the entire process is possibly dependent on the phase during which the aggressive oxygen species moves from the di-iron to the four-iron center. We are currently elaborating further experiments to investigate this."


The above story is reprinted (with editorial adaptations ) from materials provided by Ruhr-Universitaet-Bochum, via AlphaGalileo.

Journal Reference:

C. Lambertz, N. Leidel, K. G. V. Havelius, J. Noth, P. Chernev, M. Winkler, T. Happe, M. Haumann. O2-reactions at the six-iron activesite (H-cluster) in [FeFe]-hydrogenase. Journal of Biological Chemistry, 2011; DOI: 10.1074/jbc.M111.283648

Oxygen inactivates the enzyme function in three phases: study

Scientists from the Faculty of Biology and Biotechnology at the RUB have published a report in the Journal of Biological Chemistry explaining why enzymes used for the production of hydrogen are so sensitive to oxygen. In collaboration with researchers from Berlin, they used spectroscopic methods to investigate the time course of the processes that lead to the inactivation of the enzyme's iron center.

"Such enzymes, the so-called hydrogenases, could be extremely significant for the production of hydrogen with the help of biological or ", explains Camilla Lambertz from the RUB study group for photobiotechnology. "Their extreme sensitivity to is however a major problem. In future, our results could help to develop enzymes that are more robust."

Oxygen as a friend and as an enemy

Oxygen is crucial for the survival of most animals and plants. It is however toxic for many living creatures if the concentration thereof is too high, and some organisms can even only exist entirely without oxygen. Sensitivity to oxygen is also present at the . A large number of enzymes, for example, hydrogenases are known to be irreversibly destroyed by oxygen. Hydrogenases are biological catalysts that convert protons and electrons into technically usable hydrogen. The RUB team of Prof. Thomas Happe is doing research on so-called [FeFe]-hydrogenases which are capable of producing particularly large amounts of hydrogen. The generation of hydrogen takes place at the H-cluster, consisting of a di-iron and four-iron subcluster which, together with other , form the reactive center.

Oxygen attacks the iron centers

The researchers, working in collaboration with Dr. Michael Haumann's team in Berlin, discovered that oxygen binds to the di-iron center of the hydrogenase, which initiates the inactivation of another part of the consisting of four further . In this project, sponsored by the BMBF, it was possible to show the diverse phases of the inactivation process for the first time using the so-called X-ray absorption spectroscopy. The researchers used the synchroton radiation source Swiss Light Source in Switzerland for this specific type of measurement. It generates particularly strong rays, thus enabling the characterization of metal centers in proteins. Amongst other things, the scientists thus determined the chemical nature of the iron centers and the distance from the surrounding atoms using atomic resolution.

Inactivation in three phases

The team of researchers from Bochum and Berlin used a new experimental procedure. They initially brought the hydrogenase sample into contact with oxygen for a few seconds to minutes and finally for a couple of hours and then suppressed all proceeding reactions by deep-freezing it in liquid nitrogen. The subsequently gained spectroscopic data was used for the development of a model for a three-phase inactivation process. According to this model, an oxygen molecule initially binds to the di-iron center of the hydrogenase, which leads to the development of an aggressive oxygen species. In the subsequent phase, this attacks and modifies the four-iron center. During the final phase, further oxygen molecules bind and the entire complex disintegrates. "The entire process thus consists of a number of consecutive reactions that are distinctly separated in time", says Lambertz. "The velocity of the entire process is possibly dependent on the phase during which the aggressive oxygen species moves from the di-iron to the four-iron center. We are currently elaborating further experiments to investigate this."

More information: C. Lambertz, N. Leidel, K.G.V. Havelius, J. Noth, P. Chernev, M. Winkler, T. Happe, M. Haumann (2011) O2-reactions at the six-iron active site (H-cluster) in [FeFe]-hydrogenase, Journal of Biological Chemistry, doi: 10.1074/jbc.M111.283648

Provided by Ruhr-University Bochum