In a survey of 27 Penaeus monodon culture ponds stocked with postlarvae (si
milar to PL10) at medium density (similar to 40 shrimp m(-2)), single-step
nested white spot syndrome virus (WSSV) PCR was used to measure the WSSV in
fection rates in the shrimp populations within 1 mo after stocking. Seven p
onds were initially WSSV-free, and the shrimp in 5 of these were harvested
successfully. In the ponds (n = 6) where detection rates were higher than 5
0 %, mass mortality occurred during the growth period, and none of these po
nds was harvested successfully. In a subsequent study, P. monodon brooders
were classified into 3 groups according to their WSSV infection status befo
re and after spawning brooders that were WSSV-positive before spawning were
assigned to group A; spawners that became WSSV-positive only after spawnin
g were assigned to group B; and group C consisted of brooders that were sti
ll WSSV-negative after spawning. WSSV screening showed that 75, 44 and 14 %
, respectively, of group A, B and C brooders produced nauplii that were WSS
V-positive. Most (57 %; 16/28) of the brooders in group A produced nauplii
in which the WSSV prevalence was high (> 50 %). When a pond was stocked wit
h high-prevalence nauplii from 1 of these group A brooders, an outbreak of
white spot syndrome occurred within 3 wk and only similar to 20 % of the in
itial population survived through to harvest (after 174 d). By contrast, 2
other ponds stocked with low-prevalence and WSSV-negative nauplii (derived
respectively from 2 brooders in group B), both had much higher survival rat
es (70 to 80 %) and yielded much larger (similar to3 x by weight) total har
vests, We conclude that testing the nauplii is an effective and practical s
creening strategy for commercially cultured P. monodon.