Morphological characterization of pirarucu Arapaima gigas (Schinz, 1822) gonadal differentiation.

Szczegóły
Abstrakt

Tytuł:: Morphological characterization of pirarucu Arapaima gigas (Schinz, 1822) gonadal differentiation.
Autorzy:: da Costa Amaral A; Programa de Pós-graduação em Ciências Pesqueiras nos Trópicos, Universidade Federal do Amazonas, Manaus, Brazil.
Lima AF; Embrapa Pesca e Aquicultura, Palmas, Brazil.
Ganeco-Kirschnik LN; Embrapa Pesca e Aquicultura, Palmas, Brazil.
de Almeida FL; Embrapa Amazônia Ocidental, Manaus, Brazil.
Źródło:: Journal of morphology [J Morphol] 2020 Apr; Vol. 281 (4-5), pp. 491-499. Date of Electronic Publication: 2020 Mar 21.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
Język:: English
Imprint Name(s):: Publication: <2005- > : Hoboken, N.J. : Wiley
Original Publication: 1931- : Philadelphia, Pa. : Wistar Institute of Anatomy and Biology
MeSH Terms:: Sex Differentiation*
Fishes/*anatomy & histology
Gonads/*anatomy & histology
Animals ; Cell Differentiation ; Female ; Fishes/growth & development ; Fishes/physiology ; Male ; Ovary/anatomy & histology ; Ovary/cytology ; Testis/anatomy & histology ; Testis/growth & development ; Vitellogenesis
References:: Almeida, I., Ianella, P., Faria, M., Paiva, S., & Caetano, A. (2013). Bulked segregant analysis of the pirarucu (Arapaima gigas) genome for identification of sex-specific molecular markers. Genetics and Molecular Research, 12, 6299-6308.
Bruslé, J., & Bruslé, S. (1983). La gonadogenèse des Poissons. Reproduction Nutrition Development, 23, 453-491.
Cesar, M. P., Murgas, L. D. S., Araújo, R. V., & Drummond, C. D. (2005). Métodos para obtenção de população monossexo na piscicultura. Boletin Agropecuaria Universidade Federal de Lavras-MG, 69, 1-27.
Chen, W., & Ge, W. (2013). Gonad differentiation and puberty onset in the zebrafish: Evidence for the dependence of puberty onset on body growth but not age in females. Molecular Reproduction and Development, 80, 384-392.
Colombo, G., Grandi, G., & Rossi, R. (1984). Gonad differentiation and body growth in Anguilla anguilla L. Journal of Fish Biology, 24, 215-228.
Devlin, R. H., & Nagahama, Y. (2002). Sex determination and sex differentiation in fish: An overview of genetic, physiological, and environmental influences. Aquaculture, 208, 191-364.
Du, K., Wuertz, S., Adolfi, M., Kneitz, S., Stöck, M., Oliveira, M., … Schartl, M. (2019). The genome of the arapaima (Arapaima gigas) provides insights into gigantism, fast growth and chromosomal sex determination system. Scientific Reports, 28, 5293.
Fontenele, O. (1948). Contribuição para o conhecimento da biologia do pirarucu Arapaima gigas (Schinz, 1822) em cativeiro (Actinopterigii, Osteoglossidae). Revista Brasileira de Biologia, 8, 445-459.
Froese R, Pauly D. (2018) FishBase. Retrieved from http://www.fishbase.org/.
Godinho, H. P., Santos, J. E., Formagio, P. S., & Guimarães-Cruz, R. J. (2005). Gonadal morphology and reproductive traits of the Amazonian fish Arapaima gigas (Schinz, 1822). Acta Zoologica (Stockholm), 86, 289-294.
Grier, H. J., Uribe, M. C., & Parenti, L. R. (2007). Germinal epithelium, folliculogenesis, and postovulatory follicles in ovaries of rainbow trout, Oncorhynchus mykiss (Walbaum,1792) (Teleostei, Protacanthopterygii, Salmoniformes). Journal of Morphology, 268, 293-310.
Haugen, T., Almeida, F. F., Andersson, E., Bogerd, J., Male, R., Skaar, K. S., & Taranger, G. L. (2012). Sex differentiation in Atlantic cod (Gadus morhua L.): Morphological and gene expression studies. Reproductive Biology and Endocrinology, 10, 1-47.
Helfman, G. S., Collete, B. B., & Facey, D. (2000). Teleosts at last I: Bony-tongues through anglerfishes. In The diversity of fishes (pp. 221-243). Massachusetts: Blackwell.
Imbiriba, E. P. (2001). Potencial da criação de pirarucu, Arapaima gigas, em cativeiro. Acta Amazônica, 31, 229-316.
Le Menn, F., Cerdà, J., & Babin, P. J. (2007). Ultrastructural aspects of the ontogeny and differentiation of ray-finned fish ovarian follicles. In J. P. C. Babin & E. Lubzens (Eds.), The fish oocyte: From basic studies to biotechnological applications (pp. 1-37). Dordrecht, The Netherlands: Springer.
Lewis, Z. R., McClellan, M. C., Postlethwait, J. H., Cresko, W. A., & Kaplan, R. H. (2008). Female-specific increase in primordial germ cells marks sex differentiation in three-spine stickleback (Gasterosteus aculeatus). Journal of Morphology, 269, 909-921.
Lima, A. F., Varela, E. S., Maciel, P. O., Alves, A. L., Rodrigues, A. P. O., Torati, L. S., … Bezerra, T. A. (2015). Manejo de plantel de reprodutores de pirarucu. Palmas, Brasília: Embrapa.
Maack, G., & Segner, H. (2003). Morphological development of the gonads in zebrafish. Journal of Fish Biology, 62, 895-906.
Mazzoni, T., Lo Nostro, F., Antoneli, F., & Quagio-Grassiotto, I. (2018). Action of the metalloproteinases in gonadal remodeling during sex reversal in the sequential hermaphroditism of the teleostei fish Synbranchus marmoratus (Synbranchiformes: Synbranchidae). Cell, 7, 34.
Mazzoni, T. S., Grier, H. J., & Quagio-Grassiotto, I. (2014a). Germline cysts and the formation of the germinal epithelium during the female gonadal morphogenesis in Cyprinus carpio (Teleostei: Ostariophysi: Cypriniformes). The Anatomical Record: Advances in Integrative Anatomy and Evoltionary Biol., 293, 1581-1606.
Mazzoni, T. S., Grier, H. J., & Quagio-Grassiotto, I. (2014b). Male gonadal differentiation and the paedomorphic evolution of the testis in Teleostei. The Anatomical Record, 297, 1137-1162.
Meijide, F. J., Lo Nostro, F., & Guerrero, G. A. (2005). Gonadal development and sex differentiation in the cichlid fish Cichlasoma dimerus (Teleostei, Perciformes): A Lightand electron-microscopic study. Journal of Morphology, 264, 191-210.
Moura Carvalho, L. O. D., & Nascimento, C. N. B. (1992). Engorda de pirarucus (Arapaima gigas) em associação com búfalos e suínos. Belém: EMBRAPA-CPATU. Circular Técnica, 65, 21.
Nakamura, M., Kobayashi, T., Chang, X. T., & Nagahama, Y. (1998). Gonadal sex differentiation in teleost fish. The Journal of Experimental Zoology, 281, 362-372.
Nakamura, M., & Takahashi, H. (1973). Gonadal sex differentiation in Tilapia mossambica, with special regard to the time of estrogen treatment males. Bulletin of the Faculty of Fisheries Hokkaido University, 24, 1-13.
Oliveira, E. G., Pinheiro, A. B., Oliveira, V. Q., Silva Júnior, A. R. M., Moraes, M. G., Rocha, Í. R. C. B., & Costa, F. H. F. (2012). Effects of stocking density on the performance of juvenile pirarucu (Arapaima gigas) in cages. Aquaculture, 370, 96-101.
Padoa, E. (1937). Differenziazione e inversione sessuale (femminilizzazione) dia notti di trota (Salmo irideus) tratta ticonormone follicolare. Monitore Zoologico Italiano, 48, 195-203.
Patiño, R., Davis, K. B., Schoore, J. E., Uguz, C., Strüssmann, C. A., Parker, N. C., … Goudie, C. A. (1996). Sex differentiation of channel catfish gonads: Normal development and effects of temperature. The Journal of Experimental Zoology, 276, 209-218.
Pereira, N. O. (1954). O pirarucu. Rio de Janeiro, Brazil: Ministério da Agricultura, Divisão de Caça e Pesca.
Prado-Lima, M., & Val, A. L. (2015). Differentially expressed genes in the pituitary of the Amazonian fish Arapaima gigas. International Journal of Fisheries and Aquaculture, 7, 132-141.
Rasmussen, T. H., Jesperesen, A., & Korsgaard, B. (2006). Gonadal morphogenesis and sex differentiation in intraovarian embryos of the viviparous fish Zoarces viviparous (Teleostei, Perciformes, Zoarcidae): A histological and ultrastructural study. Journal of Morphology, 267, 1032-1047.
Satoh, N., & Egami, N. (1972). Sex differentiation of germ cells in the teleost, Oryzias latipes, during normal embryonic development. Journal of Embryology and Experimental Morphology, 28, 385-395.
Strüssmann, C. A., Takashima, F., & Toda, K. (1996). Sex differentiation and hormonal feminization in pejerrey Odontesthes bonariensis. Aquaculture, 139, 31-45.
Strüssmann, C. A., & Nakamura, M. (2002). Morphology, endocrinology, and environmental modulation of gonadal sex differentiation in teleost fishes. Fish Physiology and Biochemistry, 26, 13-29.
Torati, L. S., Lima, A. F., Kirschnik, L. N. G., & Migaud, H. (2019). Endoscopy and cannulation as non-invasive tools to identify sex and monitor reproductive development in Arapaima gigas. Copeia, 107, 287-296.
Torati, L. S., Migaud, H., Doherty, M. K., Siwy, J., Mullen, W., Mesquita, P. E., & Albalat, A. (2017). Comparative proteome and peptidome analysis of the cephalic fluid secreted by Arapaima gigas (Teleostei: Osteoglossidae) during and outside parental care. PLoS One, 12, e0186692.
Vialle, R. A., Souza, J. E. S., Paiva, L. K., Teixeira, D. G., Azevedo, A. S. P., Santos, A. M. R., & Hamoy, I. G. (2018). Whole genome sequencing of the pirarucu (Arapaima gigas) supports independent emergence of major teleost clades. Genome Biology and Evolution, 10, 2366-2379.
Vizziano-Cantonnet, D., Di Landro, S., Lasalle, A., Martínez, A., Mazzoni, T. S., & Quagio-Grassiotto, I. (2016). Identification of the molecular sex-differentiation period in the siberian sturgeon. Molecular Reproduction and Development, 83, 19-36.
Watanabe, L., Gomes, F., Vianez, J., Nunes, M., Cardoso, J., Lima, C., … Sampaio, I. (2018). De novo transcriptome based on next-generation sequencing reveals candidate genes with sex-specific expression in Arapaima gigas (Schinz, 1822), an ancient Amazonian freshwater fish. PLoS One, 13, e0206379.
Yamamoto, T. (1969). Sex differentiation. In W. S. Hoar & D. J. Randall (Eds.), Fish physiology (Vol. 3, pp. 117-175). New York, NY: Academic Press.
Contributed Indexing:: Keywords: early development; fish reproduction; germ cells; ovary; testis
Entry Date(s):: Date Created: 20200322 Date Completed: 20201015 Latest Revision: 20201015
Update Code:: 20240105
DOI:: 10.1002/jmor.21116
PMID:: 32198946
: Czasopismo naukowe

Full Text Finder

Arapaima gigas is a giant air-breathing and bony tongue fish from the Amazon basin and a promising species for aquaculture. A. gigas farming industry is still not established because of the lack of information on its reproductive physiology. Reproduction in captivity cannot be manipulated or stimulated, and the identification of males and females in a broodstock is not easy. We aimed to reveal the morphological sex differentiation of pirarucu as studies involving gonad development are essential to understanding the reproductive physiology of any species. We performed histological analysis on the whole body and extracted the gonads of 150 juveniles. The first sign of ovary differentiation is the sex-specific rearrangement of the germ cells. In 9 cm total length females, the germ cells group into nests and are restricted to the lateral face of the gonad, in close contact with the abdomen wall. With further development, this region invaginates and that later develops into ovigerous lamellae. Meiosis starts soon after ovary differentiation. In males, the germ cells are scattered along the elongated differentiating testis at first, and later become more restricted to the central region where the spermatogonial cysts start to develop. Somatic and germ cells are jointly involved in the cellular reorganization during gonadal differentiation, specifically when the germ cells begin to establish new associations during the development of both the germinal epithelium and stroma. RESEARCH HIGHLIGHTS: In Arapaima gigas, the ovary differentiation occurs in 9 cm TL females and it is marked by the rearrangement of germ and somatic cells; and the germ cells entering meiosis with no formation of ovarian cavity; testis differentiation occurs later and meiosis does not start in males smaller than 80 cm TL.
(© 2020 Wiley Periodicals, Inc.)

Informacja