TRANSMISSION OF INFECTIOUS SALMON ANEMIA (ISA) THROUGH NATURAL SECRETIONS AND EXCRETIONS FROM INFECTED SMELTS OF ATLANTIC SALMON SALMO-SALAR DURING THEIR PRESYMPTOMATIC PHASE
Gk. Totland et al., TRANSMISSION OF INFECTIOUS SALMON ANEMIA (ISA) THROUGH NATURAL SECRETIONS AND EXCRETIONS FROM INFECTED SMELTS OF ATLANTIC SALMON SALMO-SALAR DURING THEIR PRESYMPTOMATIC PHASE, Diseases of aquatic organisms, 26(1), 1996, pp. 25-31
Short-term (48 h) exposure of healthy Atlantic salmon Salmo salar L. s
melts to infectious salmon anemia (ISA)-inoculated cohort smelts showe
d that the disease was transmitted with near 100% mortality from Day 7
post-inoculation and onwards. This is more than a week before the ino
culated fish show any clinical signs and long before the typical petec
hial bleedings occur. A bloodborne transmission of the disease is ther
efore unlikely. Skin mucus, faeces, urine and blood, isolated from ISA
-inoculated smelt, transmitted the disease to healthy cohort smelt wit
h variable efficiency depending on how the inoculum was administered.
All the sources were infectious and transmitted the disease with high
efficiency when injected intraperitoneally (i.p.) into cohort smelt. A
fter i.p. injection, skin mucus had somewhat lower infectivity than bl
ood homogenates. Furthermore, in some experiments application of skin
mucus to the gills was as efficient as i.p. injection for transmission
of the disease. When introduced into the stomach none of the inocula
caused ISA. Coprophagy thus seems to be ineffective in the transmissio
n of TSA under laboratory conditions. Skin mucus from non-inoculated c
ohabitants exposed to ISA-inoculated smelts for 2 d transmitted the di
sease with close to 100% efficiency to healthy cohort smelts when inje
cted i.p. This indicates that the infectious agent is waterborne and a
bsorbed by the skin mucus rather than being secreted with the skin muc
us. Since healthy smelts have an intact skin barrier, proximity to ino
culation directly to the vascular bed seems unlikely. An ultrastructur
al study of 10 different organs, all in close proximity to the secreti
ons/excretions, revealed that at early stages of the disease, the viru
s was exclusively found in the pillar cells and endocardial cells. Thi
s indicates that the gills are the most Likely port of entry of the vi
rus. It also supports a causal relation between the observed virus and
the disease.