Kw. Hasson et al., Role of lymphoid organ spheroids in chronic Taura syndrome virus (TSV) infections in Penaeus vannamei, DIS AQU ORG, 38(2), 1999, pp. 93-105
Lesion development was documented in Penaeus vannamei juveniles with experi
mentally induced, chronic phase Taura syndrome virus (TSV) infections, by b
oth routine histology and in situ hybridization, during a 48 wk time course
study. Histologically, the defining characteristics of TSV chronicity in P
. vannamei Include the absence of acute phase histological lesions, a low p
revalence of ectopic spheroid development, and rapid successive lymphoid or
gan spheroid (LOS) formation and morphogenesis. Three distinct LOS morphoty
pes (Types A, B, and C) were identified by light microscopy. The earliest d
etectable LOS, Type A, appeared to evolve from activated LO tubule phagocyt
es that had sequestered TSV. The succeeding LOS, Type B, contained necrotic
cells that were consistently TSV-positive by in situ hybridization for up
to 32 wk following an acute phase infection. These persistent, long-term in
fections suggested that TSV replication occurred within Type B LOS, and thi
s satisfied the definition of a chronic infection. The terminal Type C LOS
were consistently found to be TSV-negative and characterized by cells with
condensed basophilic nuclei, a reduction in overall cell size, and progress
ive atrophy leading to degradation without an inflammatory response. These
cellular changes are characteristic of apoptotic cells, suggesting that TSV
-infected LOS cells self-destruct, resulting in TSV elimination. TSV infect
ions appear to have 3 potential outcomes: (1) the virus may continue to rep
licate within LOS cells unchecked, (2) it may be eliminated by LOS cells, o
r (3) viral replication and elimination may occur concurrently, resulting i
n persistent infections. Ectopic spheroids were TSV-induced and observed in
sites normally occupied by tegmental glands within appendages, suggesting
that they developed from either hemolymph-borne phagocytes or fixed phagocy
tes associated with the gland. We suggest that these cellular masses arise
from migrating and/or resident phagocytes transformed in response to chroni
c viral infections or non-self substances too small for hemocyte encapsulat
ion. The possibility that spheroid development represents an unexplored and
significant branch of the cell-mediated immune response of penaeid shrimp
is discussed.