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. 2019 Oct 7;101(6):1312–1321. doi: 10.4269/ajtmh.18-0959

Table 1.

Overview of histopathological findings of mice subcutaneously infected with autoluminescent Mycobacterium ulcerans into the tail

Clinical picture Identifier Bioluminescence (in photons/s) area under the curve Acid-fast bacilli Inflammation Tissue damage Vascular involvement Inflammatory cell type Degree of inflammation
Severe pathology (sacrificed at week 8) 84 1.36E+08 ++ +++ +++ n/a PC, MΦ, and LYM Severe, multifocal, and chronic
85 1.35E+08 +++ +++ +++ n/a PC, MΦ, LYM, and EOS Severe, multifocal, and chronic
88 1.72E+07 ++ +++ +++ ++ PC, MΦ, and LYM Severe, multifocal, and chronic
Moderate pathology 86 1.97E+06 + + + MΦ and LYM Mild to moderate, chronic, and multifocal
89 3.69E+06 + +/++ ++ ++ PC and MΦ Mild, diffuse, and chronic
No macropathology 81 2.15E+06 + + MΦ and LYM Moderate, chronic, and focal
82 692641 None
83 872438 + + + MΦ and LYM Moderate, chronic, and multifocal
87 7.24E+06 ++ +++ +++ ++ PC, MΦ, and LYM Locally severe and chronic
90 0 + + + PC, MΦ, EOS, and NEU Mild, chronic, and multifocal

EOS = eosinophil; LYM = lymphocyte; MΦ = macrophage; NEU = neutrophil; PC = plasma cell; not applicable. Animals were divided by clinical pathology in severe pathology, moderate pathology, and no marcopathology. Photons per second analyzed by IVIS imaging are shown in comparison with histological results. The amount of photos/second as a proxy for bacterial quantity correlated with pathology, except in mouse 87, where no clinical pathology was seen.