Withering syndrome in the abalone Haliotis diversicolor supertexta.

Abalone aquaculture is a small but growing industry in Thailand and is based on both the exotic Haliotis diversicolor supertexta and the native H. asinina. Withering syndrome (WS) in abalone is caused by an infection with the Rickettsia-like organism (RLO) 'Candidatus Xenohaliotis californiensis' and has been spread to many countries globally. The present study reports the first observation of the WS-RLO agent in the small abalone, H. diversicolor supertexta in Thailand, Taiwan (ROC) and the People's Republic of China (PRC). Under light microscopy, the RLO was observed as intracytoplasmic inclusions within epithelial cells lining the post-esophagus and, to a minor extent, the intestine of H. diversicolor. Under transmission electron microscopy, inclusions were characterized as colonies of rod-shaped bacteria, 200 x 1800 nm in size, within a vesicle in the cytoplasm of the infected cell. The RLO from the small abalone bound with WS-RLO-specific in situ hybridization probes and was amplified by polymerase chain reaction (PCR), using primers designed from the 16S rDNA sequence of the original WS-RLO from California, USA. The PCR product of RLO samples from both the PRC and Thailand showed extremely high identity with the California WS-RLO (100 and 99%, respectively). These data combined with the history of abalone movements for aquaculture purposes indicate that RLOs observed in Thailand, Taiwan and the PRC are the WS-RLO that originated from California.

Different responses to infectious hypodermal and hematopoietic necrosis virus (IHHNV) in Penaeus monodon and P. vannamei.

Infectious hypodermal and hematopoietic necrosis virus (IHHNV) is widespread in cultured Penaeus monodon and P. vannamei in Thailand. It causes runt-deformity syndrome that is characterized by physical abnormalities and stunted growth in P. vannamei, but causes no apparent disease in P. monodon. In both species, the virus may produce Cowdry Type A inclusions in tissues of ectodermal and mesodermal origin, but these are common in P. vannamei and rare in P. monodon. The virus can be more easily detected in both species by IHHNV-specific PCR primers. By in situ hybridization (ISH) using specific IHHNV probes, fixed phagocytes associated with myocardial cells tended to show strong positive reactions in both shrimp species. Ovarian and neural tissue (neurons in the nerve ganglia and glial cells in the nerve cord) were ISH positive for IHHNV only in P. vannamei. By transmission electron microscopy, necrotic cells were found in the gills of IHHNV-infected P. vannamei, while paracrystalline arrays of virions and apoptotic cells rather than necrotic cells were found in the lymphoid organ of IHHNV-infected P. monodon. Thus, it is possible that apoptosis in P. monodon contributes to the absence of clinical disease from IHHNV. These findings reveal different responses to IHHNV infection by the 2 shrimp species. A curious feature of IHHNV infection in P. monodon was inconsistency in the comparative viral load amongst tissues of different specimens, as detected by both ISH and real-time PCR. This inconsistency in apparent tissue preference and the reasons for different cellular responses between the 2 shrimp species remain unexplained.