{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,24]],"date-time":"2026-10-24T02:14:43Z","timestamp":1792808083189,"version":"4.5.0"},"reference-count":65,"publisher":"American Society for Microbiology","issue":"10","license":[{"start":{"date-parts":[[2025,10,7]],"date-time":"2025-10-07T00:00:00Z","timestamp":1759795200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,10,7]],"date-time":"2025-10-07T00:00:00Z","timestamp":1759795200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Microbiol Spectr"],"published-print":{"date-parts":[[2025,10,7]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      Liver abscesses (LA) in cattle are a polymicrobial infection, and the major bacterial pathogens associated are as follows:\n                      <jats:italic toggle=\"yes\">Fusobacterium necrophorum<\/jats:italic>\n                      subsp.\n                      <jats:italic toggle=\"yes\">necrophorum<\/jats:italic>\n                      (FNN),\n                      <jats:italic toggle=\"yes\">F. necrophorum<\/jats:italic>\n                      subsp.\n                      <jats:italic toggle=\"yes\">funduliforme<\/jats:italic>\n                      (FNF),\n                      <jats:italic toggle=\"yes\">Trueperella pyogenes<\/jats:italic>\n                      (TP), and\n                      <jats:italic toggle=\"yes\">Salmonella enterica<\/jats:italic>\n                      (SE). In polymicrobial infections, the contributions of individual species are difficult to assess. We hypothesized that species abundance in abscesses may be indicative of their contributions. Therefore, the objective was to develop a 4-plex quantitative PCR (qPCR) assay to determine prevalence and concentrations of the pathogens in LA (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      = 384) and matched ruminal (RT;\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      = 374) and colonic epithelial (CT;\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      = 256) tissues.\n                      <jats:italic toggle=\"yes\">Fusobacterium necrophorum<\/jats:italic>\n                      , either FNN or FNF, was detected in 85.9% of LA by qPCR, which was slightly lower than the culture-based prevalence (89.1%). Only 16.9% of LA were positive for FNF with no FNN. The concentrations of FNN or FNF were 7 to 7.5 log\n                      <jats:sub>10<\/jats:sub>\n                      CFU\/g. The qPCR assay identified more (\n                      <jats:italic toggle=\"yes\">P &lt;<\/jats:italic>\n                      0.01) samples (29.2%) as positive for TP than the culture method (16.7%). The mean concentration of TP was 5.9 log\n                      <jats:sub>10<\/jats:sub>\n                      CFU\/g. None of the LA was positive for SE by the qPCR assay. The prevalence of FN was greater (\n                      <jats:italic toggle=\"yes\">P &lt;<\/jats:italic>\n                      0.01) in RT than CT (73.2% vs. 16%). The concentrations were in the 4 to 5 log\n                      <jats:sub>10<\/jats:sub>\n                      CFU\/g. The low concentrations of TP suggest that it is unlikely to be the primary etiologic agent. Although SE was detected by culture method, it was not quantifiable, which suggests that the species does not contribute to the development of LA.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        Liver abscesses (LA) in cattle are a polymicrobial infection, and four bacterial pathogens are implicated:\n                        <jats:italic toggle=\"yes\">Fusobacterium necrophorum<\/jats:italic>\n                        subsp.\n                        <jats:italic toggle=\"yes\">necrophorum<\/jats:italic>\n                        (FNN) and subsp.\n                        <jats:italic toggle=\"yes\">funduliforme<\/jats:italic>\n                        (FNF),\n                        <jats:italic toggle=\"yes\">Trueperella pyogenes<\/jats:italic>\n                        (TP), and\n                        <jats:italic toggle=\"yes\">Salmonella enterica<\/jats:italic>\n                        (SE). In mixed infections, the species abundance may be indicative of their contributions. Our objective was to develop a quantitative PCR assay to determine prevalence and concentrations of the pathogens in LA (\n                        <jats:italic toggle=\"yes\">n<\/jats:italic>\n                        = 384) and matched ruminal (RT;\n                        <jats:italic toggle=\"yes\">n<\/jats:italic>\n                        = 374) and colonic tissues (CT;\n                        <jats:italic toggle=\"yes\">n<\/jats:italic>\n                        = 256). The dominant species in LA was FNN with a mean concentration of 7.0 log\n                        <jats:sub>10<\/jats:sub>\n                        CFU\/g. The subsp. FNF without FNN was prevalent in a small number of LA, with a mean concentration of 7.0 log\n                        <jats:sub>10<\/jats:sub>\n                        CFU. The concentration of TP was 5.0 log\u2081\u2080 CFU, which suggests that it is unlikely to be the primary etiologic agent. Although\n                        <jats:italic toggle=\"yes\">S. enterica<\/jats:italic>\n                        was prevalent in LA, none was quantifiable, which suggests that it is not contributing to LA.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.01888-25","type":"journal-article","created":{"date-parts":[[2025,9,8]],"date-time":"2025-09-08T12:00:21Z","timestamp":1757332821000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":2,"title":["Quantification of major bacterial pathogens in liver abscesses and matched ruminal and colonic epithelial tissues of feedlot 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