Multiplex Immunochromatographic Assay for Serologic Diagnosis of Major Infectious Diseases in Laboratory Mice

Author:

Tosa Noriko1,Ishida Tomoko2,Yoshimatsu Kumiko3,Hayashimoto Nobuhito4,Shiokawa Kanae4,Takakura Akira2,Arikawa Jiro5

Affiliation:

1. Institute for Animal Experimentation, Department of Microbiology, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan

2. ICLAS Monitoring Center, Central Institute for Experimental Animals, Kawasaki, Japan

3. Department of Microbiology, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan;, Email: yosimatu@med.hokudai.ac.jp

4. Department of Microbiology, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan

5. Institute for Animal Experimentation, Department of Microbiology, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan; Department of Microbiology, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan

Abstract

Serologic monitoring of infectious diseases is important for microbial control in colonies of laboratory mice. Rapid and simple tests that do not require killing animals are valuable for this purpose. In this study, we developed a multiplex immunochromatographic assay (ICA) for detection of antibodies to mouse hepatitis virus (MHV), Sendai virus (also known as hemagglutinating virus of Japan [HVJ]), and Clostridium piliforme (The pathogen that causes Tyzzer disease), which are major infectious diseases in mice. For this assay, an ICA strip was put into a microtube containing 150 μL PBS and either 0.75 μL mouse serum or 1.5 μL whole blood. Binding antibodies were visualized by using protein A-conjugated colloidal gold. Under these conditions, multiplex ICA simultaneously and specifically detected antibodies to multiple antigens. To evaluate the sensitivity and specificity of multiplex ICA, positive serum samples for each infectious disease were used. Sensitivities of the multiplex ICA test for MHV, HVJ, and C. piliforme were 100%, 100%, and 90%, respectively. No nonspecific reaction was observed in any of the 30 positive sera. In addition, 10 samples of uninfected sera did not show any bands except for the control line. These observations indicate high specificity of the multiplex ICA test. Moreover, the multiplex ICA could be applied to diluted blood. These results indicate that the multiplex ICA is appropriate for rapid, simple, and safe serologic testing of laboratory mice.

Publisher

American Association for Laboratory Animal Science

Subject

Animal Science and Zoology

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