TY - JOUR
T1 - Correlation between Targeted qPCR Assays and Untargeted DNA Shotgun Metagenomic Sequencing for Assessing the Fecal Microbiota in Dogs
AU - Sung, Chi-Hsuan
AU - Pilla, Rachel
AU - Chen, Chih-Chun
AU - Ishii, Patricia Eri
AU - Toresson, Linda
AU - Allenspach-Jorn, Karin
AU - Jergens, Albert E.
AU - Summers, Stacie
AU - Swanson, Kelly S.
AU - Volk, Holger
AU - Schmidt, Teresa
AU - Stuebing, Helene
AU - Rieder, Johanna
AU - Busch, Kathrin
AU - Werner, Melanie
AU - Lisjak, Anja
AU - Gaschen, Frederic P.
AU - Belchik, Sara E.
AU - Tolbert, M. Katherine
AU - Lidbury, Jonathan A.
AU - Steiner, Joerg M.
AU - Suchodolski, Jan S.
PY - 2023/8
Y1 - 2023/8
N2 - 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 < 0 with any targeted taxa outside the reference interval, RI), mild-moderate changes (R = 0.24, 0 < DI < 2), and significant dysbiosis (R = 0.54, 0.73, and 0.91 for 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.
AB - 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 < 0 with any targeted taxa outside the reference interval, RI), mild-moderate changes (R = 0.24, 0 < DI < 2), and significant dysbiosis (R = 0.54, 0.73, and 0.91 for 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.
KW - Canine dysbiosis index
KW - Chronic enteropathy
KW - Microbiota
KW - quantitative PCR
KW - Shotgun metagenomic sequencing
KW - 413 Veterinary science
U2 - 10.3390/ani13162597
DO - 10.3390/ani13162597
M3 - Article
C2 - 37627387
SN - 2076-2615
VL - 13
JO - Animals
JF - Animals
IS - 16
M1 - 2597
ER -