Descrição cariotípica de peixes dos gêneros Baryancistrus, Parancistrus, Peckoltia e Ancistrus (Ancistrinae, Loricariidae) da Bacia Amazônica

The subfamily Ancistrinae is one of the most diversified among Loricariidae fish, including approximately 200 species, distributed in 26 genera. These fish are easily recognized by the presence of bony plates arranged in series along the body, and by the antero-ventral position of the mouth. Their common names are acaris, bodós, cascudos and sucker-mouth. Species of the subfamily Ancistrinae comprise an important social-economic resource, constituting one of the most important commercial activities in Altamira-PA. In this study, the karyotype of nine species of fish belonging to four different genera (Baryancystrus, Parancistrus, Peckoltia and Ancistru,$) of the subfamily Ancistrinae were analyzed through conventional (Giemsa, C-band and Ag-NORs) and fluorochrome (Chromomycin A3) techniques. The species of the genus Baryancistrus showed a diploid number 2n= 52, and FN=104. NORs were found in an interstitial position of the short arm of a biarmed chromosome. The species B. aff niveatus had large blocks of constitutive heterochromatin, rich in G-C. This character was considered apomorphic. Hence, the karyotype of this species was considered the most derived among the species of this genus. Genus Parancistrus includes species with a karyotypic structure very similar to the one found in Baryancistrus, and the position of NORs could be considered as a possible apomorphy shared by these two genera. The species of the genus Peckoltia showed a diploid number with 52 chromosomes, and FN=102, with large heterochromatic blocks in ali the species. These blocks comprised almost ali the long arras of some submetacentric and subtelocentric chromosome pairs, which could be considered as a possible apomorphy shared by the species of this group. NORs were found in the long arm of a submetacentric pair in P. vittata, and in the maximum of three chromosomes in Peckoltia spl and Peckoltia sp2. Ancistrus ranunculus showed the most derived karyotype among all the species analyzed in this study. This karyotype had 48 chromosomes and FN=80. Cytogenetic analyses so far suggest that inversions were the most important rearrangement that occurred during the chromosomal diversification of Ancistrinae, except in Ancistrus ranunculus, in which Robertsonian rearrangements were also observed.A subfamília Ancistrinae é uma das mais diversificadas entre os Loricariidae, incluindo cerca de 200 espécies distribuídas em 26 gêneros. Esses peixes são facilmente reconhecidos pela presença de placas ósseas dispostas em séries ao longo do corpo e pela presença de boca em posição ventral anterior. São vulgarmente conhecidos por acaris, bodós, cascudos. As espécies da subfamília Ancistrinae representam um importante recurso sócio-econômico, constituindo uma das mais importantes atividades comerciais no município de Altamira-PA. Foram analisadas, através das técnicas convencionais (Giemsa, bandeamento C e Ag-NORs) e técnica de fluorocromo (Cromomicina A3), dez espécies de peixes da subfamília Ancistrinae pertencentes a quatro gêneros (Baryancistrus, Parancistrus, Peckoltia e Ancistrus). As espécies do gênero Baryancistrus revelaram um número diplóide 2n= 52 e NF=104. A NOR foi encontrada em posição intersticial no braço curto de um par cromossômico do tipo meta/submetacêntrico. A espécie B. aff. niveatus apresentou grandes blocos heterocromáticos ricos em pares de bases G-C como apomorfia, sendo esta espécie considerada como mais derivada cariotipicamente entre os Baryancistrus. As espécies do gênero Parancistrus apresentaram uma estrutura cariotípica muito similar àquela encontrada em Baryancistrus, apresentando as Regiões Organizadoras de Nucléolos como uma provável sinapomorfia entre os dois gêneros. Os representantes do gênero Peckoltia possuem número diplóide 2n=52 e NF=102. Todas as espécies analisadas apresentaram grandes blocos heterocromáticos, envolvendo quase todos os braços longos de alguns pares cromossomos do tipo submetacêntricos e subtelocêntricos, sendo esta característica uma provável sinapornorfia para este grupo. A NOR foi localizada no braço longo de um par de cromossomos submetacêntricos em P. vittata e em no máximo três cromossomos nas espécies Peckoltia sp.1 e Peckoltia sp.2. A espécie Ancistrus ranunculus foi a que apresentou o cariótipo mais derivado entre as espécies estudadas, com o número dipló ide igual a 48 cromossomos e NF 80. As análises citogenéticas feitas até agora sugerem que os principais eventos de diversificação cariotípica para os Ancistrinae foram às inversões, a exceção de Ancistrus ranunculus que apresentou também rearranjos Robertsonianos

Differences In Karyotype Between Two Sympatric Species Of Gymnotus (Gymnotiformes: Gymnotidae) From The Eastern Amazon Of Brazil

In this paper we describe the karyotypes of two sympatric species of Gymnotus from Marajó Island, Pará, in the Eastern Amazon basin of Brazil. One of these species, G. mamiraua, has not previously been identified from this area. Karyotype studies demonstrate that G. cf. carapo Linnaeus, has 2n=42 (30M/SM+12ST/A) and G. mamiraua Albert & Crampton, 2n=54 (50M/SM+4ST). The Nucleolar Organizer Region (NOR) was found in the distal region of the short arm of pair 20 in G. cf. carapo and in the interstitial region of pair 1 of G. mamiraua. Both species have centromeric constitutive heterochromatin (CH) in all chromosomes and some in interstitial or distal regions. In both species, 4′6-Diamidino-2-phenylindole (DAPI) staining has shown banding concordant with C-banding, whereas the Chromomycin A3 (CMA3) staining in both species agrees with the NOR location. The new data and review of cytogenetic data in Gymnotus presented here is concordant with a hypothesis that G. carapo is either a complex of populations, or a complex of morphologically similar cryptic species with distinct karyotypes. These taxa may be reproductively isolated by prezygotic reproductive isolation barriers (such as the structure of the Electric Organ Discharge), or by post-zygotic barriers (such as karyotypic formula). The understanding of the cytogenetic structure of G. carapo, combined with associated studies of signal diversity, will yield insight into the mechanisms underlying the origins and maintenance of high species diversity in Gymnotus. Copyright © 2007 Magnolia Press

Karyotypic diversity within the genus Makalata (Echimyidae: Echimyinae) of Brazilian Amazon: Chromosomal evidence for multiple species.

The genus Makalata is a taxonomically complex group of rodents on which few cytogenetic studies have been performed. Most of the published karyotypes were described based only on conventional chromosome staining. Here, we studied the karyotypes of Makalata from two Brazilian Amazonian states, Amapá and Pará, by Giemsa-staining, G- and C-banding, AgNO3-staining and FISH with 18S rDNA and telomeric sequences probes. We observed 2n = 66/FN = 124 in the Pará state population in Makalata sp; and 2n = 72/FN = 128 in the Amapá state population in M. didelphoides. Multiple chromosome rearrangements may have given rise to these karyotypes, which differ significantly from each other and from those reported in the literature. The chromosomal differences among the described Makalata karyotypes can act as a barrier to gene flow; since they are also associated with geographic barriers (e.g., rivers) and numerous molecular differences, they could be seen as evidence for reproductive isolation of populations from genus Makalata. Our data suggest that the genus is chromosomally diverse and the karyotypes may belong to different species. These karyotypes may prove useful as taxonomic markers for these rodents

Differences in karyotype between two sympatric species of Gymnotus (Gymnotiformes: Gymnotidae) from the eastern amazon of Brazil

In this paper we describe the karyotypes of two sympatric species of Gymnotus from Marajó Island, Pará, in the Eastern Amazon basin of Brazil. One of these species, G. mamiraua, has not previously been identified from this area. Karyotype studies demonstrate that G. cf. carapo Linnaeus, has 2n=42 (30M/SM+12ST/A) and G. mamiraua Albert & Crampton, 2n=54 (50M/SM+4ST). The Nucleolar Organizer Region (NOR) was found in the distal region of the short arm of pair 20 in G. cf. carapo and in the interstitial region of pair 1 of G. mamiraua. Both species have centromeric constitutive heterochromatin (CH) in all chromosomes and some in interstitial or distal regions. In both species, 4′6-Diamidino-2-phenylindole (DAPI) staining has shown banding concordant with C-banding, whereas the Chromomycin A3 (CMA3) staining in both species agrees with the NOR location. The new data and review of cytogenetic data in Gymnotus presented here is concordant with a hypothesis that G. carapo is either a complex of populations, or a complex of morphologically similar cryptic species with distinct karyotypes. These taxa may be reproductively isolated by prezygotic reproductive isolation barriers (such as the structure of the Electric Organ Discharge), or by post-zygotic barriers (such as karyotypic formula). The understanding of the cytogenetic structure of G. carapo, combined with associated studies of signal diversity, will yield insight into the mechanisms underlying the origins and maintenance of high species diversity in Gymnotus. Copyright © 2007 Magnolia Press

Chromosomal Diversification in Pseudacanthicus Species (Loricariidae, Hypostominae) Revealed by Comparative Mapping of Repetitive Sequences

Pseudacanthicus is a genus of Neotropical fish with eight valid species, in addition to numerous lineages not formally identified. It occurs along the Amazon and Tocantins River basins, in Suriname and in the Guiana shield. There are no karyotypic data in the literature for species of this genus. Here, the karyotypes of three Pseudacanthicus species (P. spinosus, P. leopardus and Pseudacanthicus sp.) were comparatively analyzed by classical cytogenetics and fluorescence in situ hybridization using 18S and 5S rDNA probes, U2 snDNA and telomeric sequences. The analyzed species presented 52 chromosomes and KF = 18 m + 34 sm. Constitutive heterochromatin occurred in blocks on a few chromosomes. The 18S rDNA occurred in a single pair; interestingly, P. leopardus presented only one locus of this sequence in its diploid genome. The 5S rDNA sequence occurred in only one pair in P. leopardus, and in multiple sites in Pseudacanthicus sp. and P. spinosus. The snDNA U2 occurred in only one pair in all analyzed species. Telomeric sequences did not show interstitial sites. Although Pseudacanthicus species share the same 2n and KF, repetitive sequence analysis revealed karyotypic diversity among these species. The occurrence of DNA double-strand breaks related to fragile sites, unequal crossing over and transpositions is proposed as the mechanism of karyotypic diversification, suggesting that the conservation of the karyotypic macrostructure is only apparent in this group of fish

Mechanisms of Karyotypic Diversification in <i>Ancistrus</i> (Siluriformes, Loricariidae): Inferences from Repetitive Sequence Analysis

Ancistrus is a highly diverse neotropical fish genus that exhibits extensive chromosomal variability, encompassing karyotypic morphology, diploid chromosome number (2n = 34–54), and the evolution of various types of sex chromosome systems. Robertsonian rearrangements related to unstable chromosomal sites are here described. Here, the karyotypes of two Ancistrus species were comparatively analyzed using classical cytogenetic techniques, in addition to isolation, cloning, sequencing, molecular characterization, and fluorescence in situ hybridization of repetitive sequences (i.e., 18S and 5S rDNA; U1, U2, and U5 snDNA; and telomere sequences). The species analyzed here have different karyotypes: Ancistrus sp. 1 (2n = 38, XX/XY) and Ancistrus cirrhosus (2n = 34, no heteromorphic sex chromosomes). Comparative mapping showed different organizations for the analyzed repetitive sequences: 18S and U1 sequences occurred in a single site in all populations of the analyzed species, while 5S and U2 sequences could occur in single or multiple sites. A sequencing analysis confirmed the identities of the U1, U2, and U5 snDNA sequences. Additionally, a syntenic condition for U2-U5 snDNA was found in Ancistrus. In a comparative analysis, the sequences of rDNA and U snDNA showed inter- and intraspecific chromosomal diversification. The occurrence of Robertsonian rearrangements and other dispersal mechanisms of repetitive sequences are discussed

Preparado cardiopulmonar Heart and lung experimental preservatnio

Trata-se de um método de preservação do conjunto coraçâo-pulmâo isolado em condições fisiológicas. Após abertura do tórax, é instituída a autoperfusâo ex-corpore que se obtém pela canulação do tronco braquicefálico e veia cava superior, conectando-se a um reservatório situado a 1 metro de altura, de tal maneira que, pela contração ventricular esquerda, o sangue é impulsionado ao reservatório, retorna ao coração direito e segue as vias normais, passando pelos pulmões, onde é oxigenado. A seguir, sem qualquer interrupção dos batimentos e da ventilação, o bloco é retirado do tórax e acondicionado no Recipiente para Conservação e Transporte do Conjunto Cardiopulmonar à temperatura normal. Foram empregados 28 cães, com peso entre 18 e 28 kg, tendo sido feito 8 preservações, para se testar o método, e 10 preservações, para transplante cardiopulmonar em 10 cães receptores. Foram monitorizados, continuamente, eletrocardiograma, pressão intraórtica, pressão ventricular esquerda, DP/DT, índice tempo-tensáo e trabalho cardíaco que mostraram valores estáveis e satisfatórios, tanto na fase de preservação, quanto após o transplante. Os gases sangüíneos guardaram relação com as diferentes misturas administradas à ventilação. A análise microscópica de fragmentos do músculo cardíaco e tecido pulmonar retirado ao final dos procedimentos não revelou alterações significativas decorrentes do método.<br>A simple method is presented which proved to be effective for maintaining the heart and lungs viable and functioning in good hemodynamic and metabolic conditions outside of the body, for a period of up to 7 hours. After this, the heart-lung preparation is transplanted to another animal which maintains good parameters also for 3 hours. The hemodynamic, biochemical and histological features of this preparation are presented. In conclusion, preservation of a heart-lung allograft in a dynamic state provides a means to transport donor organs over long distances, and appears to be suitable to serve as a graft for heart or heart-lung transplantation