Identifying Pathogen and Allele Type Simultaneously in a Single Well Using Droplet Digital PCR

• Published in: mSphere Vol. 8; no. 1; p. e0049322
• Main Authors: Notsu, Kosuke, El Daous, Hala, Mitoma, Shuya, Wu, Xinyue, Norimine, Junzo, Sekiguchi, Satoshi
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 21-02-2023
• Subjects: Alleles; Animals; Antigens; Biomarkers; bovine leukemia virus; Bovine leukosis; Cattle; Chronic infection; Clinical Microbiology; Communicable Diseases - diagnosis; Communicable Diseases - genetics; diagnostic; digital PCR; Disease Susceptibility; enzootic bovine leukosis; Enzootic Bovine Leukosis - diagnosis; Enzootic Bovine Leukosis - genetics; Genes; Genetic Markers; Haplotypes; Histocompatibility Antigens Class II - genetics; Infections; Infectious diseases; Leukemia Virus, Bovine - genetics; Livestock; Major histocompatibility complex; Pathogens; Pol gene; Polymerase Chain Reaction - methods; Population genetics; Research Article; Viral infections; viral load quantification; digital PCR; enzootic bovine leukosis; viral load quantification; elite controller; diagnostic; major histocompatibility complex; bovine leukemia virus; BoLA-DRB3009:02; BoLA-DRB3016:01; allele-specific PCR; superspreader
• ISSN: 2379-5042; 2379-5042
• DOI: 10.1128/msphere.00493-22

In the transmission control of chronic and untreatable livestock diseases such as bovine leukemia virus (BLV) infection, the removal of viral superspreaders is a fundamental approach. On the other hand, selective breeding of cattle with BLV-resistant capacity is also critical for reducing the viral damage to productivity by keeping infected cattle. To provide a way of measuring BLV proviral load (PVL) and identifying susceptible/resistant cattle simply and rapidly, we developed a fourplex droplet digital PCR method targeting the BLV
gene, BLV-susceptible bovine major histocompatibility complex (
)-
allele, resistant
allele, and housekeeping RPP30 gene (IPATS-BLV). IPATS-BLV successfully measured the percentage of BLV-infected cells and determined allele types precisely. Furthermore, it discriminated homozygous from heterozygous carriers. Using this method to determine the impact of carrying these alleles on the BLV PVL, we found
-carrying cattle could suppress the PVL to a low or undetectable level, even with the presence of a susceptible heterozygous allele. Although the population of
-carrying cattle showed significantly higher PVLs compared with cattle carrying other alleles, their individual PVLs were highly variable. Because of the simplicity and speed of this single-well assay, our method has the potential of being a suitable platform for the combined diagnosis of pathogen level and host biomarkers in other infectious diseases satisfying the two following characteristics of disease outcomes: (i) pathogen level acts as a critical maker of disease progression; and (ii) impactful disease-related host genetic biomarkers are already identified.
While pathogen-level quantification is an important diagnostic of disease severity and transmissibility, disease-related host biomarkers are also useful in predicting outcomes in infectious diseases. In this study, we demonstrate that combined proviral load (PVL) and host biomarker diagnostics can be used to detect bovine leukemia virus (BLV) infection, which has a negative economic impact on the cattle industry. We developed a fourplex droplet digital PCR assay for PVL of BLV and susceptible and resistant host genes named IPATS-BLV. IPATS-BLV has inherent merits in measuring PVL and identifying susceptible and resistant cattle with superior simplicity and speed because of a single-well assay. Our new laboratory technique contributes to strengthening risk-based herd management used to control within-herd BLV transmission. Furthermore, this assay design potentially improves the diagnostics of other infectious diseases by combining the pathogen level and disease-related host genetic biomarker to predict disease outcomes.