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NIH Director Zerhouni Provides Congressional Testimony
Fiscal Year 2007 Budget Request, House Subcommittee on Labor-HHS Appropriations
Dr. Elias A. Zerhouni, Director, April 6, 2006:
Mr. Chairman and distinguished members of the subcommittee, it is an honor and a privilege to appear before you today to present the National Institutes
of Health (NIH) budget request for Fiscal Year 2007 and discuss the priorities of NIH for this year and beyond.
The request for NIH is $28.4 billion in FY 2007, the same as the FY 2006 level for the Agency. The budget request will support the research programs
managed by NIH's Institutes and Centers. At this budget level, NIH will increase the biodefense research program by $110 million for Advanced Development.
Support for the Pandemic Influenza Preparedness Plan will increase by $17 million. We have also chosen to carefully invest in several trans-NIH strategic
initiatives. The NIH Roadmap, an incubator for new ideas and initiatives that will accelerate the pace of discovery, increases by $113 million. We
allocated $40 million to the Institutes and Centers to launch the Genes, Environment and Health Initiative to accelerate discovery of the major genetic
and environmental factors for diseases that have a substantial public health impact. We have also directed $15 million to the new "Pathway to Independence"
program to increase our support of new investigators.
For the full testimony, visit: www.nih.gov/.../fy2007directorsbudgetrequest.htm
NIDCR Update
The National Institute of Dental and Craniofacial Research (NIDCR) invites input as it develops research initiatives for Fiscal Year 2008. Themes for
the research initiatives and instructions on how to provide input are available at: www.nidcr.nih.gov/.../RequestforPublicInputResearchInitiativesFY2008.htm.
Respondents can also access the initiatives page by clicking the green button titled "Submit Comments on FY 2008 Research Initiatives" on the NIDCR home
page at www.nidcr.nih.gov.
NIDCR Research News
www.nidcr.nih.gov/.../default
Oral Bacterium May Have Greater Role in Systemic Disease than Previously Thought
Researchers have known for years that the oral bacterium with the torturously long name of Actinobacillus actinomycetemcomitans can cause juvenile
periodontal disease. Less well established is the bacterium’s possible role in systemic disease. Part of this uncertainty hinges on a conflicting
data on the bacterium's ability to break open red blood cells, a virulence trait called hemolysis that clinical microbiologists frequently evaluate
to identify pathogens in diagnostic laboratories. Some previous studies have indicated that certain strains of A. actinomycetemcomitans are beta
hemolytic, meaning they completely lyse red blood cells, while several other studies have found just the opposite. In the April issue of the
journal Infection and Immunity, NIDCR grantees report that the answer might fall somewhere in between. The scientist found that the bacterium's
hemolytic ability varied with the choice of growth medium employed in the laboratory. Interestingly, when beta hemolysis was detected, it was
conferred by the bacterium's much studied leukotoxin, suggesting the protein kills white and red blood cells alike. According to the authors,
their findings could have "important diagnostic significance." They explain that because most diagnostic laboratories tend to use the same
standardized growth medium and because most microbiology manuals already list A. actinomycetemcomitans as lacking beta hemolytic ability, the
bacterium's role in systemic disease may go undetected and thus be under reported. Based on their findings, the scientists propose taking a
closer look at the bacterium's hemolytic ability, particularly the key role of its leukotoxin in the process. To read more about this study,
visit http://iai.asm.org/...issue=4&resourcetype=HWCIT.
Study Links Alcohol Consumption to Premalignant Oral Lesions
When discussing oral cancer, dentists always mention the consumption of alcohol and tobacco products as increasing one's chances of developing a
premalignant sore, or lesion, in the mouth. These words, however, are meant literally: Consuming alcohol and tobacco products in combination increase
one's risk of developing an abnormal lesion. Far less well established in the medical literature is whether alcohol alone is an independent risk
factor. In the April issue of the journal Cancer Epidemiology Biomarkers and Prevention, NIDCR grantees and colleagues report the most substantial
data yet that it is. After evaluating 41,458 participants in the Health Professionals Follow-up Study, a large, prospective cohort of American male
health professionals - 58 percent of which are dentists - the scientists determined that alcohol was consistently associated with greater risk of
premalignant oral lesions. They found the risk remained constant in their analyses, regardless of drinking frequency, proportion consumed with
meals, type of beverage, or tobacco use history. In fact, the scientists found the association was strongest in those who had never used tobacco
products, an indication that alcohol was an independent risk factor. To read more about this study, please visit cebp.aacrjournals.org/cgi/content/abstract/15/4/774.
Signaling Molecule May Help Fight Biofilm-Related Infections
Scientific discovery typically involves a timely convergence of information and, in the April issue of the journal Antimicrobial Agents and
Chemotherapy, a team of NIDCR grantees offer such an example in the battle against the bacterium Staphylococcus aureus. S. aureus is
a leading cause of hospital-acquired infections from bacteria laden catheters and often plays a role in causing endocarditis, osteomyelitis, toxic shock
syndrome, and some skin disorders. This bacterial species is particularly problematic because it embeds itself within biofilms, or microbial communities,
where it can avoid antimicrobial agents and/or develop resistance to them. A few years ago, basic scientists discovered that yeast can release a
biochemical cell-to-cell signaling molecule called farnesol to communicate within their fungal communities. Subsequent work indicated that this
fungal signaling molecule may naturally render certain bacteria less adept at forming mature biofilms. These results led the NIDCR grantees to
evaluate in laboratory studies the effect of farnesol on both methicillin resistant and susceptible strains of S. aureus. Their results showed
that farnesol inhibited biofilm formation and, when coupled with antimicrobial agents, demonstrated a synergy to reduce substantially the growth
of S. aureus in the laboratory, particularly when this bacterial species was in its biofilm mode of growth. The authors concluded, "This observed
sensitization of resistant strains to antimicrobials and the observed synergistic effect with gentamicin indicate a potential application for
farnesol as an adjuvant therapeutic agent for the prevention of biofilm-related infections and promotion of drug resistance reversal." To read more
about this study, visit www.ncbi.nlm.nih.gov/...itool=pubmed_docsum.
Interestingly, the researchers also were able to show, in an article soon to be published in the journal FEMS Yeast Research, that farnesol was able
to reverse fluconazole resistance in the fungal strains of Candida albicans and Candida dubliensis.
First "Smart" Antimicrobial Reported
One of the problems with current antibiotics is they kill indiscriminately, numbering among their victims benign and/or beneficial species of bacteria
that inhabit our mouths, gut, intestine, and other parts of the body where biofilms form. This less-than-optimal treatment outcome has led some
scientists to ask whether it might be possible to create a new generation of antibiotics that selectively kills the bad bugs but leaves the good ones
alone. In the April issue of the journal Antimicrobial Agents and Chemotherapy, a team of scientists supported by NIDCR and dental industry sponsors
report taking an important step forward in designing these so-called "smart" antimicrobials. The scientists successfully synthesized a chimeric,
36-amino-acid compound that specifically targets Pseudomonas species. It consists of a peptide that locks onto Pseudomonas species like a homing
device on a missile and a second peptide that, once delivered, kills the bacteria. According to the authors, this marks the first synthetic,
target-specific antimicrobial of its kind and lays the intellectual foundation for developing additional smart antimicriobials. To read more
about this work, visit www.ncbi.nlm.nih.gov/...itool=pubmed_docsum.
Early Oral Biofilm May Be More Variable Than Once Thought
Shortly after brushing our teeth, it starts again. Certain oral bacteria attach anew to the clean enamel and serve as the foundation upon which
other bacteria touch down and develop into a larger, ecologically diverse oral biofilm. This everyday fact of oral microbiology has led some
dental researchers to try and characterize these initial colonizers as potential therapeutic targets to control the formation of the oral biofilm
and prevent tooth decay. In the April issue of the journal Applied and Environmental Microbiology, NIDCR scientists suggest these first bacterial
responders may be more variable than previously thought. Using molecular techniques that cast a much wider investigative net than previous studies,
the scientists discovered most of the early colonizers varied strikingly from person to person. In fact, more than two thirds of the bacterial
species identified were unique to each of the three people in the study. However, the scientists found 10 bacterial species were common in all
three people, suggesting possible core strains that are highly adaptable and which are common members of early biofilms. The scientists also
noted shifts over four to eight hours in the proportion of bacterial species present in the early biofilm. These changes may indicate that in
some early biofilms, only a subset of the early colonizers predominate over time. To read more about this study, visit aem.asm.org/.../2837?view=long&pmid=16597990.
Children with Oral Clefts Show Pro-social Behavior with Peers
[Social Acceptance and Facial Behavior in Children with Oral Clefts; The Cleft Palate--Craniofacial Journal] 2006; Vol. 43(2): 58-68
Newswise -- Expecting downcast eyes and a general passive demeanor, researchers in a new study found instead that children with oral clefts
made more eye contact and initiated more conversations than their peers without clefts. This pro-social behavior may represent a compensatory effect
learned during early social interactions with peers, said the researchers. The study is published in the latest issue of The Cleft
Palate-Craniofacial Journal.
The findings were not consistent with previous research conducted on this topic regarding children with oral clefts. Previous studies concluded that
children with oral clefts tend to engage in more passive social behaviors. This change could be attributed to the studies’ different test locations.
Another factor could be that less timid children with oral clefts willingly accepted the invitation to the study.
In testing, the only system available to distinguish facial expressions is based on studies of adults. To aid further studies, the researchers
encourage the creation of a children’s developmental system, so that children’s facial expressions are more apparent and accurately measured.
To read the entire study, click here: www.allenpress.com/pdf/cpcj_43_309_226_236.pdf
The Cleft Palate-Craniofacial Journal is the bimonthly journal of the American Cleft Palate-Craniofacial Association. For more information, visit www.cpcjournal.org.
Funding Opportunities
Effects of Long Term Use of Antiretroviral Therapy on the Oral Mucosa (R21)
(RFA-DE-07-001)
National Institute of Dental and Craniofacial Research
Application Receipt Date(s): August 11, 2006
grants.nih.gov/grants/guide/rfa-files/RFA-DE-07-001.html
Pilot Studies: Oral Complications of Cancer Therapies (R21)
(PA-06-212)
National Institute of Dental and Craniofacial Research
Application Receipt/Submission Date(s): Multiple dates, see announcement.
grants.nih.gov/grants/guide/pa-files/PA-06-212.html
Pharmacogenetics of Fluoride (R01)
(PAR-06-214)
National Institute of Dental and Craniofacial Research
Application Receipt/Submission Date(s): May 15, 2006, 2007, 2008; September 15, 2006, 2007, 2008; January 15, 2007, 2008, 2009
grants.nih.gov/grants/guide/pa-files/PAR-06-214.html
Neurobiology Of Persistent Pain Mediated By The Trigeminal Nerve (R21)
(PAS-06-199)
National Institute of Dental and Craniofacial Research
Application Receipt/Submission Date(s): Multiple dates, see announcement.
grants.nih.gov/grants/guide/pa-files/PAS-06-199.html
Ontogeny Of Host Innate Immune Recognition Of And Response To Oral Microbes (R01)
(RFA-DE-07-004)
National Institute of Dental and Craniofacial Research
Application Receipt Date(s): August 14, 2006
grants.nih.gov/grants/guide/rfa-files/RFA-DE-07-004.html
NIDCR Exploratory and Developmental Grants in Clinical Research (R21)
(PAR-06-246)
National Institute of Dental and Craniofacial Research
Application Receipt/Submission Date(s): Multiple dates, see announcement.
grants.nih.gov/grants/guide/pa-files/PAR-06-246.html
Temporomandibular Joint and Muscle Disorders: Pathophysiological Mechanisms Linking Comorbid Conditions (R21)
(PA-06-268)
National Institute of Dental and Craniofacial Research
Application Receipt/Submission Date(s): Multiple dates, see announcement
grants.nih.gov/grants/guide/pa-files/PA-06-268.html |