Skip to main content
. Author manuscript; available in PMC: 2019 Nov 15.
Published in final edited form as: Prog Mol Biol Transl Sci. 2019 Jul 3;168:299–322. doi: 10.1016/bs.pmbts.2019.06.002

Table 1.

Functional contribution of infections to PD phenotypes in animal models.

Virus Animal Manipulation Outcome References
H5N1 C57BL/6J mice Intranasal inoculation Microglial activation, alpha-synuclein phosphorylation and aggregation. Nigral dopaminergic neuron loss Jang et al.63
H1N1 C57BL/6J mice Intranasal inoculation Microglial activation in the SNpc. Reduced levels of neurotrophic factors and increased neuroinflammation markers Sadasivan et al.64
H1N1 C57BL/6J mice+ MPTP Intranasal inoculation Increased loss of nigral dopaminergic neurons Sadasivan et al.65
Japanese encephalitis Fischer rats Intracerebral inoculation Nigral dopaminergic neuron loss and gliosis. L-DOPA-responsive bradykinesia Ogata et al.66
Bacteria Animal Manipulation Outcome References
Curli producing E. coli Aged Fischer 344 rats Oral administration Microglial and astroglial activation. Increased alpha-synuclein deposition Chen et al.67
Other Animal Manipulation Outcome References
PD patients microbiota Germ-free Th1-αSyn mice Oral administration Increased motor dysfunction Sampson et al.68