Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Oct;129(4):832-847.
doi: 10.1111/jam.14685. Epub 2020 May 20.

Design of a multiplex quantitative reverse transcription-PCR system to simultaneously detect 16 pathogens associated with bovine respiratory and enteric diseases

Affiliations

Design of a multiplex quantitative reverse transcription-PCR system to simultaneously detect 16 pathogens associated with bovine respiratory and enteric diseases

Y Goto et al. J Appl Microbiol. 2020 Oct.

Abstract

Aim: Bovine respiratory disease (BRD) and bovine enteric disease (BED) are two major diseases in cattle, resulting in severe economic losses in the dairy and beef industries. The two major diseases are associated with several factors such as viruses, bacteria, the health condition of the host and environmental factors. We aimed to design a new efficient diagnostic method, which rapidly detect causative pathogens, minimizing economic loss due to BRD and BED.

Methods and results: We designed a multiplex quantitative reverse transcription-PCR (qRT-PCR) system for the simultaneous diagnosis of 16 pathogens, including 12 viruses and 4 bacteria related to BRD and BED, based on single qRT-PCR assays in previous studies. The designed multiplex qRT-PCR was highly sensitive and has minimal detection levels which will be no different from those of single qRT-PCR. Moreover, the multiplex qRT-PCR could more efficiently detect the causative pathogens than conventional RT-PCR in test using a part of BRD and BED clinical samples. Furthermore, our data revealed that the multiplex qRT-PCR had high performance in its specificity and reproducibility tests.

Conclusions: Our system can effectively detect multiple BRD or BED related pathogens from each animal while testing several clinical samples via the multiplex qRT-PCR. It is more time-, cost- and labour-efficient than other diagnostic methods.

Significance and impact of the study: Rapid detection of infected animals from the herd using our system will greatly contribute to infection control and prompt treatment in field.

Keywords: bovine enteric disease; bovine respiratory disease; multiplex quantitative reverse-transcription-PCR; pathogens; rapid detection.

PubMed Disclaimer

References

    1. Al-Yousif, Y., Anderson, J., Chard-Bergstrom, C. and Kapil, S. (2002) Development, evaluation, and application of lateral-flow immunoassay (immunochromatography) for detection of rotavirus in bovine fecal samples. Clin Diagn Lab Immunol 9, 723-724.
    1. Aita, T., Kuwabara, M., Murayama, K., Sasagawa, Y., Yabe, S., Higuchi, R., Tamura, T., Miyazaki, A.et al. (2012) Characterization of epidemic diarrhea outbreaks associated with bovine torovirus in adult cows. Arch Virol 157, 423-431.
    1. Blas-Machado, U., Saliki, J.T., Boileau, M.J., Goens, S.D., Caseltine, S.L., Duffy, J.C. and Welsh, R.D. (2007) Fatal ulcerative and hemorrhagic typhlocolitis in a pregnant heifer associated with natural bovine enterovirus type-1 infection. Vet Pathol 44, 110-115.
    1. Boxus, M., Letellier, C. and Kerkhofs, P. (2005) Real time RT-PCR for the detection and quantitation of bovine respiratory syncytial virus. J Virol Methods 125, 125-130.
    1. Chang, K.O., Parwani, A.V., Smith, D. and Saif, L.J. (1997) Detection of group B rotaviruses in fecal samples from diarrheic calves and adult cows and characterization of their VP7 genes. J Clin Microbiol 35, 2107-2110.

MeSH terms