Detection of individual microbial pathogens by proximity ligation

• BACKGROUND: Nucleic acid amplification allows the detection of single infectious agents. Protein-based assays, although they provide information on ongoing infections, have substantially less detection sensitivity.METHODS: We used proximity ligation reactions to detect proteins on bacteria and virus particles via nucleic acid amplification. Antibodies recognizing viral or bacterial surface proteins were equipped with DNA strands that could be joined by ligation when several antibodies were bound in proximity to surface proteins of individual infectious agents.RESULTS: Detection sensitivities similar to those of nucleic acid-based detection reactions were achieved directly in infected samples for a parvovirus and an intracellular bacterium.CONCLUSIONS: This method enables detection of ligated DNA strands with good sensitivity by real-time PCR and could be of value for early diagnosis of infectious disease and in biodefense.

Keyword

Animals

Antibodies; Monoclonal

Bacterial Proteins/analysis/genetics

Bacteriological Techniques

Biotinylation

Enzyme-Linked Immunosorbent Assay

Feces/microbiology

Female

Fetus/virology

Lawsonia Bacteria/*classification/genetics/immunology

Mice

Mice; Inbred BALB C

Nucleic Acid Amplification Techniques

Parvoviridae Infections/veterinary/virology

Parvovirus; Porcine/*classification/genetics/immunology

Pregnancy

Pregnancy Complications; Infectious/veterinary/virology

Sensitivity and Specificity

Swine

Swine Diseases/virology

Viral Proteins/analysis/genetics

Virion/classification/genetics

Virology/methods

Publication and Content Type

ref (subject category)

art (subject category)