scholarly journals Bayesian validation of a serum and milk ELISA for antibodies against Mycobacterium avium subspecies paratuberculosis in Greek dairy goats across lactation

2014 ◽  
Vol 97 (2) ◽  
pp. 819-828 ◽  
Author(s):  
E. Angelidou ◽  
P. Kostoulas ◽  
L. Leontides
Keyword(s):  
Mycobacterium Avium ◽  
Mycobacterium Avium Subspecies Paratuberculosis ◽  
Dairy Goats ◽  
Milk Elisa

scholarly journals Mycobacterium avium Subspecies paratuberculosis DNA and Antibodies in Dairy Goat Colostrum and Milk

2019 ◽  
Vol 6 (4) ◽  
pp. 96 ◽  
Author(s):  
Karianne Lievaart-Peterson ◽  
Saskia Luttikholt ◽  
Maaike Gonggrijp ◽  
Robin Ruuls ◽  
Lars Ravesloot ◽  
...  
Keyword(s):  
Mycobacterium Avium ◽  
Mycobacterium Avium Subspecies Paratuberculosis ◽  
Clinical Signs ◽  
Dairy Goat ◽  
Economic Losses ◽  
Dairy Goats ◽  
Convenience Sample ◽  
Milk Samples ◽  
Zoonotic Risk ◽  
Goat Population

Mycobacterium avium subspecies paratuberculosis (MAP) is endemic in the Dutch dairy goat population causing economic loss, and negatively influencing welfare. Moreover, there are concerns about a potential zoonotic risk. Therefore the industry’s objectives are to decrease MAP prevalence, limit economic losses as well as reduce the concentration of MAP in (bulk) milk. To diminish within-farm spread of infection, vaccination, age dependent group housing with separation of newborns from adults, as well as rearing on artificial or treated colostrum and milk replacers are implemented. However, the importance of MAP contaminated colostrum and milk as a route of infection in dairy goat herds is unknown. Therefore the aim of this study was to detect the presence of MAP DNA in colostrum and milk from dairy goats in infected herds. A convenience sample of 120 colostrum samples and 202 milk samples from MAP infected dairy goat herds were tested by IS900 real-time Polymerase Chain Reaction (PCR) for MAP DNA. Furthermore, 22 colostrum samples and 27 post mortem milk samples of goats with clinical signs consistent with paratuberculosis from known infected herds were tested. The majority of samples were from goats vaccinated against MAP. Positive or doubtful PCR results were obtained in none of the 120 and two of the 22 colostrum samples, and in eight of the 202 and four of the 27 milk samples Negative PCR results were obtained in the remaining 140 (99%) colostrum samples and 217 (95%) milk samples.

Estimated prevalence of Mycobacterium avium subspecies paratuberculosis infection in herds of dairy goats in France

2010 ◽  
Vol 167 (11) ◽  
pp. 412-415 ◽  
Author(s):  
P. Mercier ◽  
C. Baudry ◽  
F. Beaudeau ◽  
H. Seegers ◽  
X. Malher
Keyword(s):  
Mycobacterium Avium ◽  
Mycobacterium Avium Subspecies Paratuberculosis ◽  
Dairy Goats

scholarly journals The Occurrence of Mycobacterium avium Subspecies paratuberculosis Positive Milk Antibody ELISA Results in Dairy Cattle under Varying Time Periods after Skin Testing for Bovine Tuberculosis

Animals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1224
Author(s):  
Nicole Bridges ◽  
Steven van Winden
Keyword(s):  
Mycobacterium Avium ◽  
Bovine Tuberculosis ◽  
Management Practices ◽  
Mycobacterium Avium Subspecies Paratuberculosis ◽  
Skin Testing ◽  
Apparent Prevalence ◽  
Elisa Testing ◽  
History Of ◽  
Antibody Elisa ◽  
Milk Elisa

Enzyme-linked immunosorbent assays (ELISA) are used to screen cows for Mycobacterium avium subspecies paratuberculosis (MAP) infections, informing Johne’s disease (JD) management practices in dairy herds. The causative agent of bovine tuberculosis (bTB), Mycobacterium bovis, and MAP share multiple antigens. Moreover, Mycobacterium avium subspecies avium is used in the single intradermal cervical comparative tests (SICCT) that are routinely used in early detection of cows infected with bTB. Although these are different types of immune responses, potentially the SICCT may interfere with the levels of MAP antibodies. This study aimed to clarify the relationship between the SICCT-MAP milk ELISA testing interval and apparent prevalence of JD risk statuses. Data from 51 herds were used, totalling 46,738 cow observations. The Poisson models showed that MAP milk ELISA testing at 14 day intervals post-SICCT statistically significantly increased the odds of detecting JD-positive cows compared to JD testing 85+ days post-SICCT. The odds ratio (OR) started at 2.5 in the first 14 day interval post-SICCT, increasing each two-week period to an OR of 4.0 at 57–70 days, to subsequently drop. Additionally, a herd history of bTB increased the odds of detecting JD-positive cows (OR = 1.2); this was relatively limited compared to the magnitude of the post-SICCT effect.

scholarly journals Detection of Mycobacterium avium Subspecies Paratuberculosis in Pooled Fecal Samples by Fecal Culture and Real-Time PCR in Relation to Bacterial Density

Animals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1605
Author(s):  
Annika Wichert ◽  
Esra Einax ◽  
Natalie Hahn ◽  
Anne Klassen ◽  
Karsten Donat
Keyword(s):  
Real Time ◽  
Mycobacterium Avium ◽  
Detection Probability ◽  
Mycobacterium Avium Subspecies Paratuberculosis ◽  
Positive Association ◽  
Significant Loss ◽  
Positive Sample ◽  
Bacterial Density ◽  
Fecal Samples ◽  
Real Time Quantitative Pcr

Within paratuberculosis control programs Mycobacterium avium subsp. paratuberculosis (MAP)-infected herds have to be detected with minimum effort but with sufficient reliability. We aimed to evaluate a combination of random sampling (RS) and pooling for the detection of MAP-infected herds, simulating repeated RS in imitated dairy herds (within-herd prevalence 1.0%, 2.0%, 4.3%). Each RS consisted of taking 80 out of 300 pretested fecal samples, and five or ten samples were repeatedly and randomly pooled. All pools containing at least one MAP-positive sample were analyzed by culture and real-time quantitative PCR (qPCR). The pool detection probability was 47.0% or 45.9% for pools of size 5 or 10 applying qPCR and slightly lower using culture. Combining these methods increased the pool detection probability. A positive association between bacterial density in pools and pool detection probability was identified by logistic regression. The herd-level detection probability ranged from 67.3% to 84.8% for pools of size 10 analyzed by both qPCR and culture. Pools of size 10 can be used without significant loss of sensitivity compared with pools of size 5. Analyzing randomly sampled and pooled fecal samples allows the detection of MAP-infected herds, but is not recommended for one-time testing in low prevalence herds.

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