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. 2020 Dec 24;37(5):701–719. doi: 10.1007/s12264-020-00614-3

Table 7.

Currently-available anterograde trans-neuronal viral tracers

Anterograde tracers Virus Properties Limitations
Polysynaptic
H129-G4[16] HSV-1 (H129)

Brightest anterograde tracer so far

Compatible with fMOST

Alternative tracer with red fluorescence

Can be used in tree shrew and rat

Potential retrograde labeling caused by axonal terminal pickup

High toxicity

No starter cell-specificity

H129dTK-TT [15] HSV-1

The first H129-derived anterograde tracer with fluorescence labeling

Polysynaptic tracing from Cre+ neuron population

High toxicity

Relatively low labeling intensity

Cannot trace from naïve neuron population without Cre

H129-EGFP [8] HSV-1 (H129)

First H129-derived anterograde tracer with EGFP labeling

First H129-derived anterograde tracer initiating polysynaptic tracing from naïve neuron populations

High toxicity

Relatively low labeling intensity

Monosynaptic

AAV2/1 [35]

AAV2/9 [35]

AAV

Easy access

Very low toxicity

Compatible with functional assays

No starter cell specificity

Very low transneuronal transmission efficiency

Very low labeling intensity, requiring a reporter system

H129-dTK [16] HSV-1 (H129)

First anterograde monosynaptic viral tracer

Suitable for both starter neuron specific and nonspecific tracing

Having an alternative tracer with green fluorescence

Relatively low labeling intensity in post-synaptic neurons

Relatively high cytotoxicity in starter neurons