Observation on the morphological and gonadal aspects of Cladonema radiatum (Class: Hydrozoa) from Tuticorin Bay, Southeast coast of India.

Studies on the hydrozoan fauna (Phylum: Cnidaria; Class: Hydrozoa) of the Indian waters during the 20th century were few in number (Nagale and Apte, 2013a, b). They originated in the early 1900s (Annandale, 1907; Ritchie, 1910, Thornely, 1916, Gravely, 1927), focussing on the taxonomy of hydroids in the 1960s along the southern coast, including Lakshadweep and Andaman Islands (Mammen, 1963, 1965a, b) and in the 1980s along the northern coast (Venugopalan Wagh, 1986). Species of the hydrozoan family Cladonematidae (Anthoathecata; Capitata) include benthic, creeping and swimming hydroids comprising four genera viz., Cladonema, Eleutheria, Staurocladia and the nomen dubium Dendronema (Schuchert, 2021). Cladonema differs from other genera of Cladonematidae by the branched tentacles either with an adhesive structure or cnidocytes and having nematocysts in oral knobs (Ghory et al., 2020 Farias et al., 2020). The taxonomy of Cladonema is uncertain and species in the genus have undergone several rounds of grouping and splitting. Gershwin Zeidler (2008) gave a detailed account of 13 putative species of Cladonema. However, Schuchert (2021) considered six species to be valid viz., C. radiatum, C. californicum, C. myersi, C. novaezelandiae, C. pacificum and C. timmsii. Studies on the genus Cladonema from Indian waters are patchy, with a brief report of its occurrence among other hydroids (Sastry and Chandramohan, 1989; Santhakumari and Nair, 1999; Arun et al., 2018). Among these records from India, C. myersi was collected from an experimental aquarium with seawater from an unknown location (Prasad, 1961). The present study documents the occurrence and describes the morphology and gonadal features of Cladonema radiatum from Tuticorin Bay, Gulf of Mannar, Southeast coast of India.

Isolation and characterization of pathogenic Vibrio alginolyticus from sea cage cultured cobia (Rachycentron canadum (Linnaeus 1766)) in India.

Mass mortalities of cobia, Rachycentron canadum, sub-adults occurred during August 2013 in cage culture in the Gulf of Mannar, Mandapam Tamil Nadu, India. The epizootic of disease was started with typical classical clinical signs followed by acute mortality. Grossly, severe haemorrhage and congestion were observed in the gastric mucosa. The abdomen was distended with peritoneal fluid. The heart revealed haemopericardium and fibrinous pericardium. Histologically, the gastric mucosa showed severe erosion and necrosis. Haemorrhagic pericarditis and an increased size of the melano macrophage centre (MMC) in the tail kidney were other histopathological changes. Vibrio sp. was isolated from the gastric lesions and heart blood swab of moribund fishes and it was found to be virulent to the cobia fingerlings. After the challenge, the same bacterium could be re-isolated from moribund fingerlings. The 16S ribosomal RNA of the isolate was amplified and blast analysis of the sequence confirmed that the pathogen was Vibrio alginolyticus. The confirmation was also correlated with its cultural, biochemical and pathomorphological changes. This is the second report and the first incidence of epizootics with severe pathological lesions in cultured cobia in India. The study throws light on the pathology of vibriosis. By practising cage farm management measures, occurrences of infection may be prevented. SIGNIFICANCE AND IMPACT OF THE STUDY: The epizootics of vibriosis caused serious economic losses to farmers. Natural blooms of the pathogen can be prevented by sea cage management measures such as, changing the inner net of the cages, changing the location of the cages to relatively clean water (about 50 m apart) from the affected site and providing shade over the cages while the water temperature rises. Supplementation of the feed with immunostimulants and mineral mixture may be practised to improve the immune response against infection. Early diagnosis and sea cage management measures may prevent occurrences of the infection.

Time resolved collapse of a folding protein observed with small angle x-ray scattering.

High-intensity, "pink" beam from an undulator was used in conjunction with microfabricated rapid-fluid mixing devices to monitor the early events in protein folding with time resolved small angle x-ray scattering. This Letter describes recent work on the protein bovine beta-lactoglobulin where collapse from an expanded to a compact set of states was directly observed on the millisecond time scale. The role of chain collapse, one of the initial stages of protein folding, is not currently understood. The characterization of transient, compact states is vital in assessing the validity of theories and models of the folding process.

Characterization of glycosylated variants of beta-lactoglobulin expressed in Pichia pastoris.

Glycosylated variants of beta-lactoglobulin (BLG) were produced in the methylotrophic yeast Pichia pastoris to mimic the glycosylation pattern of glycodelin, a homologue of BLG found in humans. Glycodelin has three sites for glycosylation, corresponding to amino acids 63-65 (S1), 85-87 (S2) and 28-30 (S3) of BLG. These three sites were engineered into BLG to produce the variants S2, S12 and S123, which carried one, two and three glycosylation sites, respectively. The oligosaccharides on these BLG variants ranged from (mannose)(9)(N-acetylglucosamine)(2) (Man(9)GN(2)) to Man(15)GN(2) and were of the alpha-linked high mannose type. The variant S123 exhibited highest levels of glycosylation, with the range of glycans being Man(9-14)GN(2). Digestion of S123 with alpha-1,2 linkage specific mannosidase resulted in a single product corresponding to Man(6)GN(2). These results indicated a glycosylation pattern consisting of a Man(5)GN(2) structure extended by 4-9 mannose residues attached mainly by alpha-1,2 linkages. The results also indicated extension of the Man(5)GN(2) structure by a single alpha-1,6-linked mannose. The N-linked glycosylation pathway in P.pastoris is significantly different from that in Saccharomyces cerevisiae, with the addition of shorter outer chains to the core and no alpha-1,3 outer extensions.