• Something wrong with this record ?

An intra-laboratory cultural and real-time PCR method comparison and evaluation for the detection of subclinical paratuberculosis in dairy herds

A. Heuvelink, AA. Hassan, H. van Weering, E. van Engelen, M. Bülte, Ö. Akineden,

. 2017 ; 62 (3) : 197-205. [pub] 20161217

Language English Country United States

Document type Comparative Study, Evaluation Study, Journal Article

Mycobacterium avium subsp. paratuberculosis (MAP) is a vigorous microorganism which causes incurable chronic enteritis, Johne's disease (JD) in cattle. A target of control programmes for JD is to accurately detect MAP-infected cattle early to reduce disease transmission. The present study evaluated the efficacy of two different cultural procedures and a TaqMan real-time PCR assay for detection of subclinical paratuberculosis in dairy herds. Therefore, sixty-one faecal samples were collected from two Dutch dairy herds (n = 40 and n = 21, respectively) which were known to be MAP-ELISA positive. All individual samples were assessed using two different cultural protocols in two different laboratories. The first cultural protocol (first laboratory) included a decontamination step with 0.75% hexadecylpyridinium chloride (HPC) followed by inoculation on Herrold's egg yolk media (HEYM). The second protocol (second laboratory) comprised of a decontamination step using 4% NaOH and malachite green-oxalic acid followed by inoculation on two media, HEYM and in parallel on modified Löwenstein-Jensen media (mLJ). For the TaqMan real-time PCR assay, all faecal samples were tested in two different laboratories using TaqMan® MAP (Johne's) reagents (Life Technologies). The cultural procedures revealed positive reactions in 1.64% of the samples for cultivation protocol 1 and 6.56 and 8.20% of the samples for cultivation protocol 2, respectively. The results of the TaqMan real-time PCR performed in two different laboratories yielded 13.11 and 19.76% positive reaction. The kappa test showed proportional agreement 0.54 between the mLJ media (second laboratory) and TaqMan® real-time PCR method (second laboratory). In conclusion, the TaqMan real-time PCR could be a strongly useful and efficient assay for the detection of subclinical paratuberculosis in dairy cattle leading to an improvement in the efficiency of MAP control strategies.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17016923
003      
CZ-PrNML
005      
20170517121956.0
007      
ta
008      
170517s2017 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s12223-016-0488-1 $2 doi
035    __
$a (PubMed)27988836
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Heuvelink, Annet $u GD Animal Health Service, Amsbergstraat 7, Postbus 9, 7400 AA, Deventer, The Netherlands.
245    13
$a An intra-laboratory cultural and real-time PCR method comparison and evaluation for the detection of subclinical paratuberculosis in dairy herds / $c A. Heuvelink, AA. Hassan, H. van Weering, E. van Engelen, M. Bülte, Ö. Akineden,
520    9_
$a Mycobacterium avium subsp. paratuberculosis (MAP) is a vigorous microorganism which causes incurable chronic enteritis, Johne's disease (JD) in cattle. A target of control programmes for JD is to accurately detect MAP-infected cattle early to reduce disease transmission. The present study evaluated the efficacy of two different cultural procedures and a TaqMan real-time PCR assay for detection of subclinical paratuberculosis in dairy herds. Therefore, sixty-one faecal samples were collected from two Dutch dairy herds (n = 40 and n = 21, respectively) which were known to be MAP-ELISA positive. All individual samples were assessed using two different cultural protocols in two different laboratories. The first cultural protocol (first laboratory) included a decontamination step with 0.75% hexadecylpyridinium chloride (HPC) followed by inoculation on Herrold's egg yolk media (HEYM). The second protocol (second laboratory) comprised of a decontamination step using 4% NaOH and malachite green-oxalic acid followed by inoculation on two media, HEYM and in parallel on modified Löwenstein-Jensen media (mLJ). For the TaqMan real-time PCR assay, all faecal samples were tested in two different laboratories using TaqMan® MAP (Johne's) reagents (Life Technologies). The cultural procedures revealed positive reactions in 1.64% of the samples for cultivation protocol 1 and 6.56 and 8.20% of the samples for cultivation protocol 2, respectively. The results of the TaqMan real-time PCR performed in two different laboratories yielded 13.11 and 19.76% positive reaction. The kappa test showed proportional agreement 0.54 between the mLJ media (second laboratory) and TaqMan® real-time PCR method (second laboratory). In conclusion, the TaqMan real-time PCR could be a strongly useful and efficient assay for the detection of subclinical paratuberculosis in dairy cattle leading to an improvement in the efficiency of MAP control strategies.
650    _2
$a zvířata $7 D000818
650    12
$a asymptomatické infekce $7 D058345
650    _2
$a bakteriologické techniky $x metody $7 D001431
650    _2
$a skot $7 D002417
650    _2
$a nemoci skotu $x diagnóza $7 D002418
650    _2
$a feces $x mikrobiologie $7 D005243
650    _2
$a diagnostické techniky molekulární $x metody $7 D025202
650    _2
$a Mycobacterium avium subsp. paratuberculosis $x klasifikace $x genetika $x růst a vývoj $x izolace a purifikace $7 D016927
650    _2
$a Nizozemsko $7 D009426
650    _2
$a paratuberkulóza $x diagnóza $7 D010283
650    _2
$a kvantitativní polymerázová řetězová reakce $x metody $7 D060888
650    _2
$a senzitivita a specificita $7 D012680
650    _2
$a odběr biologického vzorku $x metody $7 D013048
655    _2
$a srovnávací studie $7 D003160
655    _2
$a hodnotící studie $7 D023362
655    _2
$a časopisecké články $7 D016428
700    1_
$a Hassan, Abdulwahed Ahmed $u Department of Veterinary Public Health, College of Veterinary Medicine, University of Mosul, Mosul, Iraq. Food Sciences, Institute of Veterinary Food Science, Justus Liebig University Giessen, Frankfurter Str. 92, 35392, Giessen, Germany.
700    1_
$a van Weering, Hilmar $u GD Animal Health Service, Amsbergstraat 7, Postbus 9, 7400 AA, Deventer, The Netherlands.
700    1_
$a van Engelen, Erik $u GD Animal Health Service, Amsbergstraat 7, Postbus 9, 7400 AA, Deventer, The Netherlands.
700    1_
$a Bülte, Michael $u Food Sciences, Institute of Veterinary Food Science, Justus Liebig University Giessen, Frankfurter Str. 92, 35392, Giessen, Germany.
700    1_
$a Akineden, Ömer $u Dairy Sciences, Institute of Veterinary Food Science, Justus Liebig University Giessen, Ludwigstr. 21, 35390, Giessen, Germany. oemer.akineden@vetmed.uni-giessen.de. $7 gn_A_00002953
773    0_
$w MED00011005 $t Folia microbiologica $x 1874-9356 $g Roč. 62, č. 3 (2017), s. 197-205
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27988836 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20170517 $b ABA008
991    __
$a 20170517122343 $b ABA008
999    __
$a ok $b bmc $g 1205445 $s 977732
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 62 $c 3 $d 197-205 $e 20161217 $i 1874-9356 $m Folia microbiologica $n Folia microbiol. (Prague) $x MED00011005
LZP    __
$a Pubmed-20170517

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...