Brain lesion and PrP<sup>res</sup> deposit distribution of the wild-type mice-passaged recombinant PMSA products after secondary transmission in wild-type mice.

Histopathological assessment of spongiform lesions and PrP<sup>res</sup> deposits of PMSA preparations stMI-03, btMI-05 and btMI-09 after secondary transmission into C57BL/6 mice(which was unsuccessful already at first passage for stMI-01) shows moderate to intense spongiform changes upon hematoxylin and eosin staining (H&E), as can be seen in the thalamic region of representative animals from each group. PrP<sup>res</sup> deposits, labeled with 6C2 mAb (1:1,000), were detectable but very faint, all showing punctate or granular deposits associated with glia or neurons and in the neuropil (see digitally enlarged images on the left). Spongiform lesion profiles and PrP<sup>res</sup> deposition profiles, shown on the right, represent the mean semi-quantitative scoring (0–4, vertical axis, ± standard error of the mean -error bars-) of the spongiform lesions (continuous line, black) and the immunohistochemical labelling of PrP<sup>res</sup> deposits (dashed line, black) against 14 brain regions. Although there are some differences, mostly in terms of spongiform lesion intensity, stMI-03, btMI-05, and btMI-09-inoculated animals show highly coincident lesions and PrP<sup>res</sup> staining, suggesting infection by the same strain or the convergence of the recombinant preparations <i>in vivo</i> to the same strain through selection or adaptation. H&E: Hematoxylin and eosin staining; IHC: Immunohistochemistry. (DOCX)

Publication Details

Journal
Figshare
Published
2025-01-22
DOI
https://doi.org/10.1371/journal.ppat.1012890.s007
Primary Topic
Immunotoxicology and immune responses
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article

Brain lesion and PrPres deposit distribution of the wild-type mice-passaged recombinant PMSA products after secondary transmission in wild-type mice.

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Immunotoxicology and immune responses
article

Brain lesion and PrPres deposit distribution of the wild-type mice-passaged recombinant PMSA products after secondary transmission in wild-type mice.

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Abstract

Histopathological assessment of spongiform lesions and PrP<sup>res</sup> deposits of PMSA preparations stMI-03, btMI-05 and btMI-09 after secondary transmission into C57BL/6 mice(which was unsuccessful already at first passage for stMI-01) shows moderate to intense spongiform changes upon hematoxylin and eosin staining (H&E), as can be seen in the thalamic region of representative animals from each group. PrP<sup>res</sup> deposits, labeled with 6C2 mAb (1:1,000), were detectable but very faint, all showing punctate or granular deposits associated with glia or neurons and in the neuropil (see digitally enlarged images on the left). Spongiform lesion profiles and PrP<sup>res</sup> deposition profiles, shown on the right, represent the mean semi-quantitative scoring (0–4, vertical axis, ± standard error of the mean -error bars-) of the spongiform lesions (continuous line, black) and the immunohistochemical labelling of PrP<sup>res</sup> deposits (dashed line, black) against 14 brain regions. Although there are some differences, mostly in terms of spongiform lesion intensity, stMI-03, btMI-05, and btMI-09-inoculated animals show highly coincident lesions and PrP<sup>res</sup> staining, suggesting infection by the same strain or the convergence of the recombinant preparations <i>in vivo</i> to the same strain through selection or adaptation. H&E: Hematoxylin and eosin staining; IHC: Immunohistochemistry. (DOCX)

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Immunotoxicology and immune responses
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