Detection of Lawsonia intracellularis by one tube nested-PCR

Citation
Z. Pejsak et al., Detection of Lawsonia intracellularis by one tube nested-PCR, MED WETER, 57(10), 2001, pp. 723-726
Citations number
35
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
MEDYCYNA WETERYNARYJNA
ISSN journal
00258628 → ACNP
Volume
57
Issue
10
Year of publication
2001
Pages
723 - 726
Database
ISI
SICI code
0025-8628(200110)57:10<723:DOLIBO>2.0.ZU;2-0
Abstract
Swine proliferative enteropathy (PE) is caused by an obligate intracellular bacterium Lawsonia intracellularis (L. intracellularis) PE is a serious en teric disease of weaned pigs resulting in growth rate losses, increasing nu mber of death cases and costs of veterinary treatment. The aim of this stud y was, to develop and evaluate one tube nested - PCR technique for simple a nd fast L. intracellularis DNA detection in feces. Total DNA was extracted from feces which were taken directly from rectum of weaned piglets and fatteners with diarrhea using the Genomic DNA Prep Plus (R) kit (Helicionus, A&A Biotechnology). Five micro liters of DNA were ampl ified by two methods (standard and modified in closed one tube). For each m ethod were used two sets of PCR primers, which consisted of 20 - base pair (bp) oligonucleotides corresponding to 319 bp and 570 bp regions of p78 L. intracellularis sequence. The standard method consisting of 2 steps was performed in two separate rea ction tubes: first step PCR and second step nested - PCR. In single - tube method both steps were done in one closed tube. In this method all used rea gents for first step PCR were deposited in tube bottom, while reagents for nested - PCR were immobilized in a tube cap by carbohydrate trehalose. Afte r first step PCR was completed the tube was vortexed, centrifuged and the n ested - PCR was performed. This procedure was evaluated for examination 491 positive and negative feca l samples taken from different pig farms. Both techniques gave the same res ults wit positive and negative samples. It was concluded that the closed, o ne tube nested - PCR method was ver sensitive and less prone to give false positive results, compared to standard nested - PCR, carried out in separat e reaction tubes. The investigation showed that modified closed one tube nested - PCR method is a useful tool for rapid diagnosis of PE in pig population and could be p erformed for monitoring of L. intracellularis infections.