Transcriptome analysis of reproductive tract tissues of male river prawn Macrobrachium americanum.

BACKGROUND: The river prawn, Macrobrachium americanum (M. americanum), is one of the largest prawns of the genus in Latin America and is an amphidromous species distributed along the Pacific coast of America. This prawn has commercial value due to its size and taste, making it a good option for aquaculture production. Its culture has been attempted in ponds and concrete tanks, but no successful technique can still support commercial production. Understanding the mechanisms that regulate reproduction at the molecular level is very important. This knowledge can provide tools for manipulating transcripts, which could increase the number or size of animals in the culture. Our understanding of the mechanism that regulates the reproduction of M. americanum at the molecular level is limited. AIM: Perform and analyze the transcriptome assembly of the testes, vas deferens, and terminal ampulla of M. americanum. to provide new molecular information about its reproduction. METHODS AND RESULTS: The cDNA library was constructed and sequenced for each tissue to identify novel transcripts. A combined transcriptome with the three tissues was assembled using Trinity software. Unigenes were annotated using BLASTx and BLAST2GO. The transcriptome assembly generated 1,059,447 unigenes, of which 7222 genes had significant hits (e-value < 1 × 10-5) when compared against the Swiss-Prot database. Around 75 genes were related to sex determination, testis development, spermatogenesis, spermiogenesis, fertilization, maturation of testicular cells, neuropeptides, hormones, hormone receptors, and/or embryogenesis. CONCLUSIONS: These results provide new molecular information about M. americanum reproduction, representing a reference point for further genetic studies of this species.

Advancing the knowledge of the nematode Echinocephalus pseudouncinatus (Gnathostomatidae, Spirurida): Morphological and molecular identification, new host, and host specificity in two coexisting pen shells (Bivalvia: Pinnidae).

The life cycle of Echinocephalus pseudouncinatus has not been described in detail to date, as is also the case of other species in the genus. This study contributes to the information available about the life history of the genus, particularly E. pseudouncinatus, by (1) using molecular techniques (small subunit rRNA gene [SSU rRNA] sequences) to identify larvae of this species; (2) describing the most conspicuous morphological characteristics that distinguish the species by scanning electron microscopy; (3) describing histological characteristics of the internal anatomy of larvae and the lesions caused by them in the gonads of hosts; (4) reporting new host and reporting evidence of host specificity of E. pseudouncinatus between two species of edible pen shells coexisting in the northern Pacific of Mexico; and (5) analyzing the frequency of infested gonads by host sex, size, and gonadal development stage. The molecular analysis confirmed the morphological and histological diagnosis of E. pseudouncinatus larvae infesting gonads of Atrina maura and Pinna rugosa in Ojo de Liebre and San Ignacio lagoons. The morphological characterization of larvae provides internal details of the cephalic bulb (including rows of hooks and ballonets), neural chord, and cell types of the body wall. Histopathological findings such as degenerated and atretic gametes and the displacement of gonadal tissue in hosts infested with E. pseudouncinatus larvae are discussed in terms of temperature anomalies caused by the "Godzilla El Niño". The frequency of infestation increased with shell length and gonadal development in A. maura, with a higher infestation frequency in females versus males observed at both study sites. Our findings expand the list of hosts of E. pseudouncinatus, which was previously unknown as a parasite of P. rugosa. In P. rugosa, infestation frequencies are noticeably lower (<1 %) compared with those observed in A. maura (>30 %) at both study sites, suggesting host-specific requirements or preferences in E. pseudouncinatus larvae.

Transcriptome analysis of Catarina scallop (Argopecten ventricosus) juveniles treated with highly-diluted immunomodulatory compounds reveals activation of non-self-recognition system.

Marine bivalve hatchery productivity is continuously challenged by apparition and propagation of new diseases, mainly those related to vibriosis. Disinfectants and antibiotics are frequently overused to prevent pathogen presence, generating a potential negative impact on the environment. Recently, the use of highly diluted compounds with immunostimulant properties in marine organisms has been trailed successfully to activate the self-protection mechanisms of marine bivalves. Despite their potential as immunostimulants, little is known about their way of action. To understand their effect, a comparative transcriptomic analysis was performed with Argopecten ventricosus juveniles. The experimental design consisted of four treatments formulated from pathogenic Vibrio lysates at two dilutions: [(T1) Vibrio parahaemolyticus and Vibrio alginolyticus 1D; (T2) V. parahaemolyticus and V. alginolyticus 7C]; minerals [(T3) PhA+SiT 7C], scorpion venom [(T4) ViT 31C]; and one control (C1) hydro-alcoholic solution (ethanol 1%). The RNA sequencing (RNAseq) analysis showed a higher modulation of differentially expressed genes (DEG) in mantle tissue compared to gill tissue. The scallops that showed a higher number of DEG related to immune response in mantle tissue corresponded to T1 (V. parahaemolyticus and V. alginolyticus lysate) and T3 (Silicea terra® - Phosphoric acid®). The transcriptome analysis allowed understanding some interactions between A. ventricosus juveniles and highly-diluted treatments.