Animals
(Aug 2023)
Correlation between Targeted qPCR Assays and Untargeted DNA Shotgun Metagenomic Sequencing for Assessing the Fecal Microbiota in Dogs
Chi-Hsuan Sung,
Rachel Pilla,
Chih-Chun Chen,
Patricia Eri Ishii,
Linda Toresson,
Karin Allenspach-Jorn,
Albert E. Jergens,
Stacie Summers,
Kelly S. Swanson,
Holger Volk,
Teresa Schmidt,
Helene Stuebing,
Johanna Rieder,
Kathrin Busch,
Melanie Werner,
Anja Lisjak,
Frederic P. Gaschen,
Sara E. Belchik,
M. Katherine Tolbert,
Jonathan A. Lidbury,
Joerg M. Steiner,
Jan S. Suchodolski
Affiliations
Chi-Hsuan Sung
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
Rachel Pilla
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
Chih-Chun Chen
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
Patricia Eri Ishii
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
Linda Toresson
Department of Equine and Small Animal Medicine, Faculty of Veterinary Medicine, Helsinki University, 00014 Helsinki, Finland
Karin Allenspach-Jorn
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA
Albert E. Jergens
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA
Stacie Summers
Carlson College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331, USA
Kelly S. Swanson
Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61820, USA
Holger Volk
Department of Small Animal Medicine and Surgery, University of Veterinary Medicine, 30545 Hannover, Germany
Teresa Schmidt
Department of Small Animal Medicine and Surgery, University of Veterinary Medicine, 30545 Hannover, Germany
Helene Stuebing
Clinic of Small Animal Medicine, Ludwig-Maximilians University, 80539 Munich, Germany
Johanna Rieder
Department of Small Animal Medicine and Surgery, University of Veterinary Medicine, 30545 Hannover, Germany
Kathrin Busch
Clinic of Small Animal Medicine, Ludwig-Maximilians University, 80539 Munich, Germany
Melanie Werner
Clinic for Small Animal Internal Medicine, Vetsuisse Faculty, 8057 Zurich, Switzerland
Anja Lisjak
Small Animal Clinic of Veterinary Faculty Ljubljana, University of Ljubljana, 1000 Ljubljana, Slovenia
Frederic P. Gaschen
Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA
Sara E. Belchik
Department of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61820, USA
M. Katherine Tolbert
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
Jonathan A. Lidbury
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
Joerg M. Steiner
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
Jan S. Suchodolski
Gastrointestinal Laboratory, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77840, USA
DOI
https://doi.org/10.3390/ani13162597
Journal volume & issue
Vol. 13,
no. 16
p.
2597
Abstract
Read online
DNA shotgun sequencing is an untargeted approach for identifying changes in relative abundances, while qPCR allows reproducible quantification of specific bacteria. The canine dysbiosis index (DI) assesses the canine fecal microbiota by using a mathematical algorithm based on qPCR results. We evaluated the correlation between qPCR and shotgun sequencing using fecal samples from 296 dogs with different clinical phenotypes. While significant correlations were found between qPCR and sequencing, certain taxa were only detectable by qPCR and not by sequencing. Based on sequencing, less than 2% of bacterial species (17/1190) were consistently present in all healthy dogs (n = 76). Dogs with an abnormal DI had lower alpha-diversity compared to dogs with normal DI. Increases in the DI correctly predicted the gradual shifts in microbiota observed by sequencing: minor changes (R = 0.19, DI 2, DI > 5, and DI > 8, respectively), compared to dogs with a normal DI (DI < 0, all targets within the RI), as higher R-values indicated larger dissimilarities. In conclusion, the qPCR-based DI is an effective indicator of overall microbiota shifts observed by shotgun sequencing in dogs.
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