A Comparative Study of M. tuberculosis and M. bovis BCG of T cell responses
Project Number3F31AI094957-03S1
Former Number5F31AI094957-03
Contact PI/Project LeaderGRACE, PATRICIA
Awardee OrganizationNEW YORK UNIVERSITY SCHOOL OF MEDICINE
Description
Abstract Text
On October 29, 2012, the NYU Langone Medical Center was hit by the Superstorm Sandy, which caused
significant damages to the facilities used to conduct my research. Hurricane Sandy caused storm surges that
exceeded what our facilities could withstand, leading to significant flooding. The repercussions of this flooding
led to mechanical, electrical, and plumbing damages in many of the research buildings at NYU. These
damages led to immediate loss of experiments and reagents but have also long-term delays in the completion
of this project.
In the wake of Hurricane Sandy, access to all research buildings was limited due to health and safety issues.
Smilow Research Building, our main laboratory location, had no power for a week post-Sandy, which meant
that freezers and refrigerators containing reagents we use routinely for experimentation were lost. Full-power
and unrestricted access to the Smilow Research Building was not restored until one month post-Sandy. After
the re-opening of Smilow, an additional 2 months of our time was dedicated to cataloging research losses and
purchasing new reagents for experimentation.
The Berg Building, which houses our Biosafety Level 3 (ABSL3) facility, remains without power. This facility
housed animals infected with M. tuberculosis (M.tb) and is where we processed all infected samples prior to
the storm. All infectious samples from on-going experiments were stored in refrigerators and freezers within the
ABSL3 facility. We were able to save bacterial strains stored within our -80C freezer by supplying it with dry
ice, however many other samples from on-going experiments could not be saved. The loss of these
experimental samples is equal to a loss of three 6-week experiments. Work with the infected animals of the
ongoing experiments at that time was significantly delayed in the absence of a proper ABSL3 facility and
prevented the analysis of samples at key time points during infection. The ABSL3 located in Berg remains
without power, ventilation, running water, or elevator access; the reopening of this facility is projected to be in
September of this year, which will make it nearly a year post-Sandy, that this facility has been shut down.
In the meantime we have made use of a second BSL3 facility within the Smilow Research Building, which is
now operational on a limited basis to resume M. tuberculosis experiments. This facility was suited for in vitro
work, with one Tissue Culture (TC) hood available for TB work, which was a huge bottleneck for progress,
since amongst the TB labs at NYU we went from 4 available TC hoods to 1 available hood for experimentation.
With the exception of Aim 1 of this project, all other proposed experiments for this award require mouse
infections with M. tuberculosis. In April 2013, 6 months post-Sandy, we were able to expand to 2 TC hoods
(shared by 15 people), it was also at this time that we were able to relocate the aerosol unit from our ABSL3 in
the Berg Building to this Smilow BSL3. A satellite mouse housing facility has been built to accommodate our
need for infected animal housing post-Sandy. To-date, we are ~20% operational post-Sandy.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AddressAerosolsAnimal HousingAnimalsAntigen PresentationAntigen-Presenting CellsAntigensAwardBacteriaBehaviorBiologyCD4 Positive T LymphocytesCD8B1 geneCatalogingCatalogsCell CommunicationCellsCharacteristicsClinicalComparative StudyCultured CellsDataDendritic CellsDevelopmentDiseaseDry IceElevatorEnvironmental air flowFloodsFrequenciesGoalsHIVHealthHistocompatibility Antigens Class IIHouse miceHousingHumanHurricaneImageImmuneImmune responseImmunityImmunocompetentImmunologyIn VitroInfectionInferiorLaboratoriesLifeLocationLungMechanicsMedical centerMethodsMusMycobacterium tuberculosisPharmaceutical PreparationsPlumbingProcessPublic HealthPublicationsReagentRecording of previous eventsReportingResearchRunningSafetySamplingSiteSterilityT cell responseT-LymphocyteTechniquesTestingTimeTrainingTuberculosisTuberculosis VaccinesUpdateVirulentWaterWorkadaptive immunitybasebiomedical scientistbiosafety level 3 facilitycareerin vivoindexinginnovationmacrophagepreventpublic health researchresearch studyresidencetissue culturetuberculosis immunity
National Institute of Allergy and Infectious Diseases
CFDA Code
095
DUNS Number
121911077
UEI
M5SZJ6VHUHN8
Project Start Date
01-March-2014
Project End Date
28-February-2016
Budget Start Date
01-March-2014
Budget End Date
28-February-2016
Project Funding Information for 2014
Total Funding
$42,676
Direct Costs
$42,676
Indirect Costs
Year
Funding IC
FY Total Cost by IC
2014
NIH Office of the Director
$42,676
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 3F31AI094957-03S1
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Outcomes
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Clinical Studies
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