MIMUBLKO

Molecular and Immune Mechanisms Underlying Bovine Lameness

 Coordinatore TEAGASC - AGRICULTURE AND FOOD DEVELOPMENT AUTHORITY 

 Organization address address: Oak Park
city: CARLOW

contact info
Titolo: Ms.
Nome: Mary
Cognome: O'brien
Email: send email
Telefono: 3532542320
Fax: 3532542340

 Nazionalità Coordinatore Ireland [IE]
 Totale costo 177˙374 €
 EC contributo 177˙374 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2009-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-10-18   -   2012-10-17

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    TEAGASC - AGRICULTURE AND FOOD DEVELOPMENT AUTHORITY

 Organization address address: Oak Park
city: CARLOW

contact info
Titolo: Ms.
Nome: Mary
Cognome: O'brien
Email: send email
Telefono: 3532542320
Fax: 3532542340

IE (CARLOW) coordinator 177˙374.20

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

claw    health    cows    disorders    scoring    profiles    usefulness    welfare    disorder    biomarkers    did    stress    detection    hoof    expression    horn    physiological    neutrophils    gene    lameness    immune    gait   

 Obiettivo del progetto (Objective)

'Lameness is one of the most serious health and welfare disorders in the dairy industry. Research into the detection of, causes of, and treatments for lameness have focused on gait scoring and environmental effects on hoof disorders. However these methods have limited usefulness when it comes to early lameness detection. Gait scoring methodologies are subjective and have low repeatability, and hoof injuries only become visible 2 to 3 months after the initial insult to the hoof. Early and accurate lameness detection means overall prognosis and the welfare of cows is improved. Previous studies that have used a molecular approach to identifying biomarkers of lameness were confounded because the researchers did not differentiate between different types of hoof disorder, which have various aetiologies. Moreover, the studies did not attempt to determine whether any potential biomarkers would be useful for early identification of cows at risk of lameness. The degree to which lameness affects animal health may be influenced to a large part by leukocytes of the immune system. Neutrophils are phagocytic granulocytes of the innate immune system, are plentiful in bovine blood, and provide a crucial first-line defense against invading pathogens. Gene expression profiles in these cells are affected by stress (e.g. transportation stress). Cows display a physiological stress and sickness response to lameness, and thus investigation into the usefulness of changes in neutrophil gene expression as objective measures of lameness onset is warranted. Initially we will investigate changes in the physiological stress response and gene expression profiles in neutrophils of cows that have lameness caused by claw horn disorders. We will then investigate levels of expression of identified biomarkers in cows with various lameness severity. Finally we aim to investigate whether identified biomarkers could be used as early indicators of claw horn disorder development.'

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