Background
Leishmania
RNA virus-1 (LRV1) is a double-stranded RNA virus identified in 20–25% of
Viannia
—species endemic to Latin America, and is believed to accelerate cutaneous to mucosal leishmaniasis over time. Our objective was to quantify known virulence factor (VF) RNA transcript expression according to LRV1 status, causative species, and isolate source.
Methods
Eight cultured isolates of
Leishmania
were used, four of which were LRV1-positive (
Leishmania Viannia braziliensis
[
n
= 1],
L
. (
V
.)
guyanensis
[
n
= 1],
L
. (
V
.)
panamensis
[
n
= 2]), and four were LRV1-negative (
L
. (
V
.)
panamensis
[
n
= 3],
L
. (
V
.)
braziliensis
[
n
= 1]). Promastigotes were inoculated into macrophage cultures, and harvested at 24 and 48 h. RNA transcript expression of
hsp23
,
hsp70
,
hsp90
,
hsp100
,
mpi
,
cpb
, and
gp63
were quantified by qPCR.
Results
RNA transcript expression of
hsp100
(
p
= 0.012),
cpb
(
p
= 0.016), and
mpi
(
p
= 0.022) showed significant increases from baseline pure culture expression to 24- and 48-h post-macrophage infection, whereas
hsp70
(
p
= 0.004) was significantly decreased. A trend toward increased transcript expression of
hsp100
at baseline in isolates of
L
. (
V
.)
panamensis
was noted. Pooled VF RNA transcript expression by
L
. (
V
.)
panamensis
isolates was lower than that of
L
. (
V
.)
braziliensis
and
L
. (
V
.)
guyananesis
at 24 h (
p
= 0.03). VF RNA transcript expression did not differ by LRV1 status, or source of cultured isolate at baseline, 24, or 48 h; however, a trend toward increased VF RNA transcript expression of 2.71- and 1.93-fold change of
mpi
(
...