MALDI-TOF MS analysis for detection of bovine coronavirus with tryptic peptides from viral proteins.

Katsuhiko Hayashi, Kenji Ohya, Tomoya Yoshinari, Shouhei Hirose, Souta Shimizu, Yuji Morita, Takahiro Ohnishi, Maiko Watanabe, Satoshi Taharaguchi, Hirohisa Mekata, Takahide Taniguchi, Yukiko Hara-Kudo
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Abstract

Bovine coronavirus (BCoV), a significant cattle pathogen causing enteric and respiratory diseases, is primarily detected using reverse transcription-polymerase chain reaction. Our objective was to develop a novel detection method for BCoV by matrix-assisted laser desorption/ionization‒time-of-flight mass spectrometry (MALDI-TOF MS). Peptide mass fingerprint analysis revealed that nucleocapsid (N), membrane (M), and hemagglutinin-esterase (HE) were three main BCoV proteins. Their tryptic peptides were used as target molecules for BCoV detection. When the tryptic digest of 107.0 viral copies was analyzed by MALDI-TOF MS, five peptides with relatively strong peaks were detected. The detection limit was between 105.0 and 106.0 copies per test for BCoV alone. To detect BCoV in the swab eluate, ultrafiltration purification achieved a detection limit between 106.0 and 107.0 copies per test, sufficient to detect BCoV-infected calves. Our findings offer valuable insights for BCoV detection by MALDI-TOF MS.

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