Caryologia. International Journal of Cytology, Cytosystematics and Cytogenetics 74(1): 127-133, 2021 Firenze University Press www.fupress.com/caryologia ISSN 0008-7114 (print) | ISSN 2165-5391 (online) | DOI: 10.36253/caryologia-1149 Caryologia International Journal of Cytology, Cytosystematics and Cytogenetics Citation: F. Dotti do Prado, A. Abri- gato de Freitas Mourão, F. Foresti, J. Augusto Senhorini, F. Porto-Foresti (2021) First cytogenetic characterization of the Amazon Catfish Leiarius marmoratus (Gill, 1870) and its hybrid with Pseu- doplatystoma reticulatum (Eigenmann & Eigenmann, 1889). Caryologia 74(1): 127-133. doi: 10.36253/caryologia-1149 Received: December 03, 2020 Accepted: April 26, 2021 Published: July 20, 2021 Copyright: © 2021 F. Dotti do Prado, A. Abrigato de Freitas Mourão, F. Foresti, J. Augusto Senhorini, F. Porto-Foresti. This is an open access, peer-reviewed article published by Firenze University Press (http://www.fupress.com/caryo- logia) and distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Data Availability Statement: All rel- evant data are within the paper and its Supporting Information files. Competing Interests: The Author(s) declare(s) no conflict of interest. ORCID FDP: 0000-0002-4189-0375 FF: 0000-0002-0862-0445 FPF: 0000-0001-8845-3845 First cytogenetic characterization of the Amazon Catfish Leiarius marmoratus (Gill, 1870) and its hybrid with Pseudoplatystoma reticulatum (Eigenmann & Eigenmann, 1889) Fernanda Dotti do Prado1, Andrea Abrigato de Freitas Mourão2, Fausto Foresti3, José Augusto Senhorini4, Fábio Porto-Foresti1,* 1 Faculdade de Ciências, Universidade Estadual Paulista Júlio de Mesquita Filho, Av. Eng. Luiz Edmundo Carrijo Coube, 17033-360, Bauru, São Paulo, Brazil 2 Universidade Paulista – UNIP, R. Luís Levorato, 140, 17048-290, Bauru, São Paulo, Brazil 3 Instituto de Biociências, Universidade Estadual Paulista Júlio de Mesquita Filho, Distrito de Rubião Júnior, 18618-970, Botucatu, São Paulo, Brazil 4 Centro nacional de pesquisa e conservação da biodiversidade aquática continental – CEPTA, Rodovia SP-2, 01 (Pref. Euberto Nemésio Pereira de Godoy), 13.630-970, Piras- sununga, São Paulo, Brazil *Corresponding author. Email: fp.foresti@unesp.br Abstract. This study reports the first cytogenetic characterization of the Amazonian catfish Leiarius marmoratus (“jandiá”) and its F1 (first generation) hybrid “cachandiá” with Pseudoplatystoma reticulatum (“cachara”). A diploid number of 56 chromosomes and a single argyrophilic nucleolus organizer region (Ag-NOR) in the short arm of two sub-telocentric chromosomes were observed for both L. marmoratus and P. reticula- tum, but with differences in the karyotype formula and the size of the chromosome pair with NORs. The hybrid showed 2n = 56 chromosomes with an intermediate kary- otype when compared to the parental species. A single Ag-NOR was maintained in the hybrid but located in two chromosomes with marked differences in size and presenting intraindividual variation in NOR activity (nucleolar dominance). For L. marmoratus and the hybrid, heterochromatic bands were predominately distributed in the termi- nal, centromeric, and sub-centromeric regions of some chromosomes and 5S rDNA sites located in two distinct sub-telocentric chromosomes, similar to the previously described for P. reticulatum. The data suggested that the hybrid karyotype might be insufficient for a precise discrimination of hybrids, however, Ag-NOR can be used as a chromosome marker to differentiate “cachandiá” from L. marmoratus and P. reticula- tum. The current study also provides insights into the chromosomal features of L. mar- moratus and contributes with novel cytogenetic information of this native Amazonian catfish included in the Pimelodidae family. Keywords: Pimelodidae, Hybrid karyotype, Cachandiá, Pintado da Amazônia, Yaque, Ag-NOR. 128 Fernanda Dotti do Prado et al. INTRODUCTION The long-whiskered catfish Leiarius marmoratus belongs to the Pimelodidae family, (Teleostei: Silu- riformes) (Lundberg and Littmann 2003) and is an endemic species that naturally occurs along the Amazon and Orinoco River basins. This fish is commonly known as “ jandiá”, “ jundiá amazônico”, “peixe-onça” in Brazil (Porto-Foresti et al. 2013), and “yaque” in other Andine countries (Mateo et al. 2008). Widely used in aquariums and local fisheries, L. marmoratus is also cultivated in Brazilian aquaculture to produce interspecific hybrids with the “cachara” catfish (Campos 2010, Hashimoto et al. 2012; Hashimoto et al. 2016). The “cachara” cor- respond to other native South American Pimelodidae fish classified as Pseudoplatystoma fasciatum (sensu latu) in the Amazon area or P. reticulatum (sensu strictu) in southern regions of South America as the Paraguay and Parana River basins (Buitrago-Suarez and Burr 2007). The hybrids between L. marmoratus and P. reticu- latum are usually named as “cachandiá”, “cachadia” or “jundiara” (Kubitza et al. 2011, Porto-Foresti et al. 2013) and are commercialized in the Southern regions of Bra- zil as “pintado da Amazônia”, “pintado amazônico” or simply “pintado” (Kubitza et al. 2011). Morphological data indicated that, spite with intermediate character- istics, these hybrids can externally resemble more to P. reticulatum (Coelho et al. 2021). Although the hybridi- zation practice can provide economic advantages dur- ing the production as low cannibalism and fast growth rates, accidental escapes or intentional releases of hybrids in the wild environment represents a serious problem, since they can present partial or total fertility and cause genetic introgression with native populations (Yabu et al. 2018). Despite the large biodiversity of fish found in the tropics, information is still lacking for several spe- cies and there is no cytogenetic data for any species of Leiarius including L. marmoratus. In this study, we per- formed the first cytogenetic characterization of L. mar- moratus and its hybrid “cachandiá” with P. reticulatum, and thereby provide new biological information of this important group of fishes. MATERIAL AND METHODS Seven juveniles of L. marmoratus previously breeded in captivity in CEPTA (Centro Nacional de Pesquisa e Conservação de Peixes Continentais, Pirassununga, SP, Brazil) and eight juveniles of the“cachandiá”hybrid (♀ P. reticulatum × ♂ L. marmoratus) were cytogenetical- ly analyzed in this study. Hybrids were artificially pro- duced through hormonal induction of parental species with carp pituitary extract. Mitosis was stimulated as described by Oliveira et al. (1988), fishes were anesthe- tized with benzocaine and then euthanized and depos- ited in the fish collection at Laboratório de Genética de Peixes UNESP (Universidade Estadual Paulista Júlio de Mesquita Filho) (Bauru, SP, Brazil). Chromosome prepa- ration and cytogenetic analysis were performed based on kidney cell suspensions basically according to Foresti et al. (1993). All fishes were previously identified with nuclear and mitochondrial species-specific molecular markers (Porto-Foresti et al. 2013) confirming them as pure L. marmoratus and the hybrid “cachandiá”. Chro- mosomal preparations of P. reticulatum were obtained from Prado et al. (2012) and new metaphases were used for the study of the karyotype formulae and Argyroph- ilic nucleolus organizer regions (Ag-NORs) Silver staining of the NOR was obtained follow- ing the technique of Howell and Black (1980). C-band- ing technique was applied according to Sumner (1972). Fluorescent in situ hybridization (FISH) was performed using 5S rDNA probes based on genomic DNA of another Pimelodidae species, Pseudoplatystoma corrus- cans. The probe was obtained by PCR using the primers 5SA (5´-TCAACCAACCACAAAGACATTGGCAC-́ 3) and 5SB (5´-TAGACTTCTGGGTGGCCAAAGGAAT- CA-́ 3) (Pendás et al. 1994). The PCR was performed in a total volume of 25 µL and contained 150 µM of dTTP, dGTP, and dCTP; 100 µM of dATP; 1.5 mM MgCl2; 1x Taq buffer (20 mM Tris-HCl, pH 8.4 and 50 mM KCl); 0.5 unit (U) of Taq Polymerase (Invitrogen); 0.2 µM of each primer; and 10–50 ng of genomic DNA. Meta- phases were hybridized as described by Pinkel et al. (1986). The probe was digoxigenin-11-dUTP labelled and hybridization signals were developed using anti- digoxigenin-rhodamine. Cells in metaphase were pos- teriorly stained with 4’,6-diamidino-2-phenylindole (DAPI). Karyotype images were captured digitally with a fluorescence microscope (Olympus BX50) and pro- cessed for contrast and luminosity using Adobe Photo- shop CS5 software. Chromosomal morphology was determined based on arm ratio, according to Levan et al. (1964), chromo- somes were classified as metacentric (m), sub-metacen- tric (sm), sub-telocentric (st) and acrocentric (a), and arranged in decreasing size order for the karyotype organization. For the hybrid, chromosomes were not organized by pairs, but named with individual numbers (from 1 to 56) according to the morphology and also arranged in decreasing size order. 129First Cytogenetic Characterization of the Amazon Catfish and Its Hybrid RESULTS L. marmoratus showed a diploid number of 56 chro- mosomes organized as 20 m + 12 sm + 10 st + 14 a (fun- damental number = 98) (Fig. 1A). Ag-NORs were located in the terminal region of the short arm of the sub-telo- centric chromosome pair number 20 (Fig. 1A). P. reticu- latum presented 2n= 56 chromosomes distributed in a karyotype of 20 m + 12 sm + 12 st + 12 a (fundamental number = 112) (Fig. 1C) and a single Ag-NOR stained in the short arm of the sub-telocentric pair number 18 (Fig. 1C). For both species, the Ag-NOR region was heteromorphic (Fig. 1A, 1C) and corresponding with a conspicuous secondary constriction when stained with Giemsa (Fig. 1A, 1C). The hybrid presented a diploid number of 56 chro- mosomes, organized in a karyotype formula intermedi- ate to the parental species, with 20 m + 12 sm + 11 st + 13 a (NF = 99) (Fig. 1B). Two non-homologous sub- telocentric chromosomes (39 and 42) of different sizes possessed Ag-NOR signals in the terminal region of the short arm (Fig. 1B). Nucleolar dominance was verified for all hybrid individuals (Table 1), counting a total of 154 metaphases presenting one active NOR (Fig. 2B) in contrast with 39 metaphases presenting Ag-NOR signals in two chromosomes (Fig. 2A). Results of nucleus analy- sis (Table 1) also showed a majority of cells presenting only one active Ag-NOR (115) (Fig. 3B) versus 37 nuclei Figure 1. Karyotype of Leiarius marmoratus (A), the hybrid “cachandiá” (B) and Pseudoplatystoma reticulatum (C) after Giemsa staining. In the box, the NOR-bearing chromosomes. Figure 2. Metaphases of the hybrid “cachandiá” after Ag-NOR staining. In (A), a metaphase presenting two chromosomes of dif- ferent sizes with Ag-NORs and (B) a metaphase with nucleolar dominance and only one Ag-NOR. Arrows indicates the NOR- bearing chromosomes. Figure 3. Nucleous of the hybrid “cachandiá” after Ag-NOR stain- ing. In (A), nucleous presenting two Ag-NORs and (B) nucleous with only one Ag-NOR. 130 Fernanda Dotti do Prado et al. with two marks (Fig. 3A). Nucleolar dominance varied intraindividually, i.e., each individual presented both metaphases or nucleous with one or two active NORs. Heterochromatic bands of L. marmoratus were located in the pericentromeric and terminal areas of some chromosomes and the Ag-NOR sites (Fig. 4A). For this species, 5S rDNA sites were located at the pericen- tromeric region of the short arm of two sub-telocentric chromosomes, distinct from the Ag-NOR chromosome pairs that were identified by a secondary constriction (Fig. 5A). For the hybrid, C-bands marked the termi- nal and pericentromeric areas of some chromosomes as well as the NOR sites (Fig. 4B) and 5S rDNA hybridiza- tion signals were located in the terminal regions of two sub-telocentric chromosomes and were distinct from the NOR pair (Fig. 5B). DISCUSSION Conventional cytogenetics remains a powerful tool to characterize ichthyofauna biodiversity and to eluci- date features of populations and species at the chromo- somal level (Cioffi et al. 2018). The Neotropical region presents one of the most diverse ichthyofauna in the world (Reis et al. 2016), and the Amazonian Basin in special, harbors a rich variety of endemic fishes. In this region, Pimelodidae catfishes are very diverse, with spe- cies presenting the most diverse variations on body size, colours and ecological roles in the aquatic environment (Lundberg and Littmann, 2003). Despite that, a great amount of fish species has never been biologically or genetically studied. Recent findings showed efforts to cytogenetically characterize Pimelodidae species in the Amazonian region, providing important data for this group of fishes, as the described for Pimelodus (Fonseca et al 2018) and the giant catfishes Phractocephalus hemi- oliopterus (Swarça et al. 2017) and Brachyplatystoma fila- mentosum (Gonçalvez et al. 2014). The present study describes the first cytogenetic description of L. marmoratus and contributes to charac- terize the rich biodiversity of Amazonian fishes. L. mar- moratus shared cytogenetic characteristics commonly observed in Pimelodidae fishes as a diploid number of 56 chromosomes, a global pattern of heterochromatic bands distributed in terminal, peri and centromeric areas of the chromosomes, single Ag-NOR and 5S rDNA sites (Swarça et al. 2007, Nirchio et al. 2013; Swarça et al. 2017, Girardi et al. 2018). P. reticulatum presented the same chromosomal characteristics than previously described by Prado et al. (2012) and similar to other Pseudo- platystoma species as P. corruscans (Prado et al. 2012), P.metaense and P. orinocoense (Nirchio et al. 2013). The same conserved pattern of 2n=56 chromosomes, single Ag-NOR and 5S rDNA sites was verified, supporting the close relationships within this group of fishes. Pimelodidae family is characterized by a majority of species with conservative karyotypes which can be explained by the hypothesis that more dispersive and migratory species usually presents more stable karyo- types (Bertollo et al. 2017). This information corrobo- rates the observed in this study for L. marmoratus and P. reticulatum, two large size catfishes presenting long distance reproductive migratory habits. Table 1. Number of metaphases and nucleus presenting one or two Ag-NORs for the hybrid “cachandiá”. Ag-NORs Number Metaphases 1 2 154 39 Nucleus 1 2 115 37 Figure 4. Metaphases of Leiarius marmoratus (A) and the hybrid “cachandiá” (B) after C-banding. Arrows indicate the putative NOR- bearing chromosomes. Figure 5 Metaphases of Leiarius marmoratus (A) and the hybrid “cachandiá” (B) after hybridization in situ with 5S rDNA. Arrows indicates the 5S rDNA sites (red). 131First Cytogenetic Characterization of the Amazon Catfish and Its Hybrid Despite the conserved chromosomal characteristics, L. marmoratus and P. reticulatum showed variation in the karyotypic formula, with differences in the number of sub-telocentric and acrocentric chromosomes and the NOR-bearing chromosomes with a remarkable differ- ence in size between the species. Variability in the kary- otype formula without changes on the diploid number is a common feature in the Pimelodidae family, also veri- fied for other Pseudoplatystoma species (Porto-Foresti et al. 2000; Nirchio et al. 2003) and among the Pimelodi- dae family (Swarça et al 2000), which can be explained by structural chromosomal rearrangements as pericen- tric inversions during their evolution and speciation events (Swarça et al. 2000; 2000) A polymorphism of Ag-NOR marks between the homologous chromosomes were detected for L. marmo- ratus and P. reticulatum in this study (Fig. 1A, 1C - box- es), which is a relatively common feature observed for several groups of fishes including Characiformes (Vicari et al. 2006), Cypriniformes (Supiwong et al. 2012), Silu- riformes (Swarça et al. 2005; Prado et al. 2012) and oth- ers fishes (Kasiroek et al. 2017). Differences in NOR size have been attributed to structural events such as chro- mosomal breaks, duplications of the ribosomal DNA clusters or differences in NOR activity. Association of NORs with secondary constrictions in the same chro- mosome region is also a common feature in fishes (For- esti et al. 1981, Feldberg and Bertollo 2014), also detected in this work for L. marmoratus and P. reticulatum. Data for other Pimelodidae species also related NOR poly- morphisms as verified for P. metaense and P. orinocoense (Nirchio et al. 2013) with the NOR-bearing chromosome heteromorphic in size and correspondent with Ag-posi- tive signals on the short arms of the chromosomes. The “cachandiá” hybrid presented the same diploid number, similar 5S rDNA bands and similar patterns of heterochromatin than the verified for L. marmoratus and P. reticulatum. This chromosomal pattern followed the previously observed for the parental species, which were apparently maintained in the hybrid. However, different karyotype formulae and chromosomes with Ag-NOR were observed for the hybrid. Hybrid chromo- somes were organized in a karyotype intermediate to the parental species, formed by non-homologous chromo- somes. The lack of homology could be clearly visualized by the chromosome number 11 (sub-telocentric) and the chromosome number 13 (acrocentric) (Fig. 1B), without their respective homologous pair, and the presence of Ag-NORs in two non-homologous chromosomes with a marked difference in size (39 and 42). Cytogenetic is an important tool to discriminate hybrids from theirs parental species (Hashimoto et al. 2009) with applications for aquaculture and conser- vation. Chromosome morpholog y visualized by the karyoty pe, Ag-NORs, hibridization of rDNA genes or C-bands can be used as chromosome markers to identify species and hybrids and to elucidate chromo- somal heritage in hybrids (Hashimoto et al. 2009). In this study, the intermediate karyotype of the hybrid “cachandiá” is probable insufficient to establish a pre- cise chromosoma l diagnosis since the dif ferences between the chromosome types were very subtle and might vary in classifications according to chromosom- al condensation. Conventional cytogenetic techniques as chromosomal morphology were also not sufficient to differentiate hybrids of P. reticulatum and P. corrus- cans (Prado et al. 2012). Otherwise, Ag-NORs were very specific for the hybrid, located in two non-homologous chromosomes different in size, allowing an accurate diagnosis of the hybrid. The presence of NORs in chro- mosomes with distinct morphology have been previous- ly detected for hybrids of Pimelodus (Hashimoto et al. 2009) and a similar situation was observed for species of Cobitiis and their hybrids (Grabowska et al. 2019). A considerable number of metaphases or nucleolus with only one active NOR indicated dominant rDNA expres- sion of one parental species in the hybrid, fact already described for other hybrid of fishes (Hashimoto et al., 2012; Prado et al., 2012). Data obtained in this study may be valuable for hybrid identification in Brazilian aquaculture and sug- gested that Ag-NOR is a marker to identify the “cachan- diá” hybrid by a simple and low-cost cytogenetic tech- nique. Chromosomal data also contributes with novel information for the Amazonian catfish L. marmoratus to be future included in evolutionary and cytogenetic stud- ies of Pimelodidae fishes. ACKNOWLEDGMENTS This work was supported by the Fundação de Amp- aro à Pesquisa do Estado de São Paulo (FAPESP) and Conselho Nacional de Desenvolvimento Científico e Tec- nológico (CNPq). REFERENCES Bertollo LAC, Bello Cioffi M, Galetti Jr PM, Moreira Fil- ho O. 2017. Contributions to the cytogenetics of the Neotropical fish fauna. 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