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Page 38

ISSN:2171-6625

http://www.jneuro.com

September 18-19, 2017 | Dallas, USA

4

th

International Conference on

NEUROLOGY AND NEUROIMMUNOLOGY

Background:

Astrocytes have long been established as

sentinels for infection. Glial activation has downstream

effects on the blood-brain barrier and neurons. However,

for many years, astrocyte activation following host infection

was essentially limited to “astrogliosis”, with the occasional

addition of hypertrophy or atrophy. More recently, it has

become possible to quantify the degree to which astrocytes

are activated, and to discern which parameters are important

for astrocyte function.

Methods:

To determine how infectious agents alter

astrocyte activation, we “mined” the archives at Tulane

National Primate Research Center to find matched tissues

from macaques infected with SIV (the parental virus of HIV),

Chikungunya, Dengue and

Brucella.

Paraffin embedded

cortical tissues were cut at 6 µm thickness and stained for

GFAP and Toll-like receptor 2 for morphometric analyses

and innate immune activation, respectively. Morphometric

analyses were performed using Neurolucida software.

Routine measures included cell body area, total arbor, arbor

volume, number of dendrites, bifurcations, process endings

and modified Sholl analyses.

Results:

Bacterial infection (with

Brucella melitensis

)

induced increases in all the parameters indicated above.

In contrast, lentiviral infection induced decreases in the

measured parameters, with the exception of cell body area

in white matter, although that only occurred in animals with

active encephalitis. Two closely associated flavi viruses,

Chikungunya and Dengue, produced very different effects on

the astrocytes. Whereas Dengue infection induced increases

in all the parameters in white matter, Chikungunya induced

decreases in bifurcations and tips, with increases in process

volume in grey matter. Only cell body area was increased in

white matter.

Discussion:

Astrocytes respond rapidly to host infection.

While it is not hugely surprising that glia respond differently

to bacteria and viruses, what was surprising was that even

very closely associated viruses induce different responses

in astrocytes. We are currently generating software to

differentiate astrocytes based on morphometric data.

e:

amaclean@tulane.edu

Who will guard; the guards themselves?

Andrew G MacLean, Joseph Ramsey, Olivia Purcell, Kim M Lee and Kevin B Chiu

Tulane University, USA

J Neurol Neurosci, 8:5

DOI: 10.21767/2171-6625-C1-003