The early lymphocyte proliferation response in sheep exposed to Mycobacterium avium subsp. paratuberculosis compared to infection status

Immunobiology ◽  
2010 ◽  
Vol 215 (1) ◽  
pp. 12-25 ◽  
Author(s):  
Kumudika de Silva ◽  
Douglas Begg ◽  
Nicole Carter ◽  
Deborah Taylor ◽  
Lyrissa Di Fiore ◽  
...  
2017 ◽  
Vol 15 (1) ◽  
pp. e0502
Author(s):  
Ivan Mato ◽  
Natividad Pesqueira ◽  
Camino Factor ◽  
Fernando Camino ◽  
María L Sanjuán ◽  
...  

The paper was designed to assess the influence of Mycobacterium avium subsp. paratuberculosis (MAP) infection status of cows at culling (antibody positive vs negative) on carcass traits: weight and conformation and fat cover scores. A generalized least squares linear model was used to assess the influence of MAP on weight. Subsequently, a random effects logistic regression was completed in order to model the relation between MAP and conformation score (fair vs poor carcasses). A random effects ordered logistic model was used to estimate the influence on fat cover. The results indicated that seropositives had carcass weights 58.45 (34.65-83.35) kg lower than seronegatives. Regarding conformation score, the odds of having poor conformation instead of fair was 3.85 (1.35-11.85) times higher in seropositives. The odds of seropositives achieving a higher fat cover was approximately 5 (1.41-9.09) times lower than the odds for seronegatives. The estimated effects could be useful when assessing the economic benefits of a paratuberculosis control program.


Animals ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 20
Author(s):  
Luigi De Grossi ◽  
Davide Santori ◽  
Antonino Barone ◽  
Silvia Abbruzzese ◽  
Matteo Ricchi ◽  
...  

Paratuberculosis is a chronic disease of ruminants caused by Mycobacterium avium subsp. Paratuberculosis (MAP). Since isolation of MAP type I (S) is rarely reported in Italy, our research was aimed at isolating, by an inexpensive liquid culture manual method, this type of MAP isolates. At first, we used an ELISA to point out to serologically positive samples from five flocks. Secondly, we used a fecal direct IS900-qPCR on the ELISA positive samples, in order to detect shedder animals. Feces from IS900-qPCR positive samples were inoculated in solid and liquid culture media. IS900-qPCR was further used to test the growth of MAP isolates in liquid medium, which were further confirmed by f57-qPCR and submitted to typing by specific PCR in order to identify the MAP type. Twenty-eight samples (24 fecal and four tissutal samples) were processed by culture methods, resulting in the isolation of six type I MAP field isolates. Notably, no isolates were recovered by solid media, underlining the utility of this liquid method. Few data about this type of MAP are currently available in Italy, and further analyses should be carried out in order to study the origin and epidemiology of type I strains circulating in Italy.


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