Development of a multiplex real-time PCR assay using two thermocycling platforms for detection of major bacterial pathogens associated with bovine respiratory disease complex from clinical samples

John D. Loy, Laura Leger, Aspen M. Workman, Michael L. Clawson, Ece Bulut, Bing Wang

Research output: Contribution to journalArticle

Abstract

Bovine respiratory disease complex (BRDC) is one of the most significant diseases of cattle. Bacterial pathogens involved in BRDC include Mannheimia haemolytica, Mycoplasma bovis, Histophilus somni, and Pasteurella multocida. We developed and evaluated a multiplexed real-time hydrolysis probe (rtPCR) assay using block-based Peltier and rotary-based thermocycling on lung tissue, nasal swabs, and deep nasopharyngeal swabs. The rtPCR results were compared to culture or a gel-based M. bovis PCR using statistical analysis to determine optimum quantification cycle (Cq) cutoffs to maximize agreement. The limits of detection were 1.2–12 CFU/reaction for each pathogen. M. haemolytica was the most prevalent organism detected by rtPCR, and was most frequently found with P. multocida. The rtPCR assay enabled enhanced levels of detection over culture for all pathogens on both thermocycling platforms. The rotary-based thermocycler had significantly lower Cq cutoffs (35.2 vs. 39.7), which maximized agreement with gold standard culture or gel-based PCR results following receiver operating characteristic analysis to maximize sensitivity (Se) and specificity (Sp). However, overall assay Se and Sp were similar on both platforms (80.5% Se, 88.8% Sp vs. 80.1% Se, 88.3% Sp). Implementation of these tests could enhance the detection of these pathogens, and with high-throughput workflows could reduce assay time and provide more rapid results. The assays may be especially valuable in identifying coinfections, given that many more antemortem samples tested in our study were positive for 2 or more pathogens by rtPCR (n = 125) than were detected using culture alone (n = 25).

Original languageEnglish (US)
Pages (from-to)837-847
Number of pages11
JournalJournal of Veterinary Diagnostic Investigation
Volume30
Issue number6
DOIs
StatePublished - Nov 1 2018

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Bovine Respiratory Disease Complex
bovine respiratory disease
Multiplex Polymerase Chain Reaction
Real-Time Polymerase Chain Reaction
quantitative polymerase chain reaction
Mycoplasma bovis
Mannheimia haemolytica
Pasteurella multocida
Sensitivity and Specificity
pathogens
assays
Pasteurellaceae
Gels
Cattle Diseases
sampling
Polymerase Chain Reaction
microbial detection
Workflow
gels
Coinfection

Keywords

  • Bacterial pathogens
  • bovine respiratory disease
  • clinical specimens
  • real-time PCR
  • receiver operating characteristic analysis

ASJC Scopus subject areas

  • veterinary(all)

Cite this

Development of a multiplex real-time PCR assay using two thermocycling platforms for detection of major bacterial pathogens associated with bovine respiratory disease complex from clinical samples. / Loy, John D.; Leger, Laura; Workman, Aspen M.; Clawson, Michael L.; Bulut, Ece; Wang, Bing.

In: Journal of Veterinary Diagnostic Investigation, Vol. 30, No. 6, 01.11.2018, p. 837-847.

Research output: Contribution to journalArticle

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