image/svg+xmlEste artículo es publicado por la revista Neotropical Helminthology de la Facultad de Ciencias Naturales y Matemática, Universidad Nacional Federico Villarreal, Lima, Perú auspiciado por la Asociación Peruana de Helmintología e Invertebrados Afines (APHIA). Este es un artículo de acceso abierto, distribuido bajo los términos de la licencia Creative Commons Atribución 4.0 Internacional (CC BY 4.0) [https:// creativecommons.org/licenses/by/4.0/deed.es] que permite el uso, distribución y reproducción en cualquier medio, siempre que la obra original sea debidamente citada de su fuente original.ISSN Versión impresa 2218-6425ISSN Versión Electrónica 1995-1043Neotropical Helminthology, 2022, 16(2), jul-dic:133-140.ORIGINAL ARTICLE / ARTÍCULO ORIGINAL1Universidade Federal do Pará. Brazil.2Instituto Nacional de Pesquisas da Amazônia. Brazil. Corresponding author* ajtineant@gmail.comAmanda Karen Silva Jtineant: https://orcid.org/0000-0001-7506-0794Jeannie Nascimento dos Santos: https://orcid.org/0000-0002-6612-6410Daniel Brito Porto: https://orcid.org/0000-0002-7640-7021José Celso de Oliveira Malta: https://orcid.org/0000-0003-1496-21901,2*1Amanda Karen Silva JtineantJeannie Nascimento dos Santos;; 22Daniel Brito Porto & José Celso de Oliveira MaltaABSTRACTSpecimens of Dekeiseria amazonica Rapp Py-Daniel, 1985 and Hypostomus oculeus(Fowler, 1943) captured from July 2015 to December 2016, in the Catalão Lake complex, Iranduba, Amazonas, were studied. The specimens of D. amazonicameasured 12 – 16.5 (13.70 ± 1.33) and weight (g) 29 – 59 (40.85 ± 9.78) and H. oculeus12 – 21 (15.80 ± 2.13) and weight (g) 75 - 125.40 (101.11 ± 14.28). Both species were parasitized by the acanthocephalan Gorytocephalus elongorchisThatcher, 1979 (Neoechinorhynchidae), parasitizing the intestine,with a prevalence of 55% and abundance of 18. The intensity ranged from 1 to 3 parasites and the average intensity was 1.63 parasites per fish for D. amazonica, and prevalence 59.25%, abundance 29. The intensity of 1 to 4, mean intensity 1.81 for H. oculeus. Two new hosts for G. elongorchisare recorded and their specificity for fish of the Loricariidae is highlighted. This is the first record of G. elongorchisparasitizing D. amazonicaand H. oculeus.Neotropical Helminthology133DOI: http://dx.doi.org/10.24039/rnh20221621483TWO NEW HOSTS FOR GORYTHOCEPHALUS ELONGORCHIS(ACANTHOCEPHALA: NEOECHINORHYNCHIDAE), IN DEKEISERIA AMAZONICAAND HYPOSTOMUS OCULEUS(SILURIFORMES: LORICARIIDAE) FROM THE BRAZILIAN AMAZONDOS NUEVOS HOSPEDEROS PARA GORYTHOCEPHALUS ELONGORCHIS(ACANTHOCEPHALA: NEOECHINORHYNCHIDAE), EN DEKEISERIA AMAZONICAE HYPOSTOMUS OCULEUS(SILURIFORMES: LORICARIIDAE) DE LA AMAZONÍA BRASILEÑADKeywords:Acanthocephala – Amazon – Loricariidae – Fish Parasite DDDart. 1=10-24art. 2=26-41Art 3 =42-51art. 4=52-59art. 5=60-65art 6=66-79art. 7=80-91art 8 =92-100art 9=102-111nota 1=112-116nota 2=118-123 rev =124-134
image/svg+xmlEjemplares de Dekeiseria amazonica Rapp Py-Daniel, 1985 e Hypostomus oculeus (Fowler, 1943) capturados entre julio de 2015 y diciembre de 2016 fueron analizados en el complejo lacustre de Catalão, Iranduba, Amazonas. Los ejemplares de D. amazonicamidieron 12 – 16,5 (13,70 ± 1,33) y peso (g) 29 – 59 (40,85 ± 9,78) y H. oculeus 12 – 21 (15,80 ± 2,13) y peso (g) 75 - 125,40 (101,11 ±14,28). Ambas especies fueron parasitadas por Acanthocephala Neoechinorhynchidae, Gorytocephalus elongorchisThatcher, 1979, parasitando el intestino, con una prevalencia de 55%, abundancia 18, intensidad varió de 1 a 3 parásitos por hospedero y la intensidad promedio fue de 1.63 parásitos por pez para D. amazonica, y prevalencia 59,25%, abundancia 29, intensidad de 1 a 4 parásitos, intensidad media de 1,81 para H. oculeus. Se registran dos nuevos huéspedes para G. elongorchisy se destaca su especificidad para los peces Loricariidae. Este es el primer registro de G. elongorchisparasitando a D. amazonicay H. oculeus.134Neotropical Helminthology, 2022, 16(2), jul-dicRESUMENPalabras clave: Acanthocephala – Amazonas – Loricariidae – Parásito de peces INTRODUCTIONAcanthocephala species parasitize adult vertebrates and larval invertebrates. In the Amazon they are well represented, parasitizing fish species from different families. They are well known for having as their main feature a reversible proboscis with few to numerous spines, ranging from a few millimetres to more than a meter (Thatcher, 2006; Aquino-Pereira, 2010; Souza & Malta, 2010; Souza et al., 2018).Acanthocephala species are highly specific to definitive hosts and very little specific to their intermediate and paratenic hosts. They are less specific than other helminth groups and have more intermediate and paratenic hosts than parasitic species of other phyla. The variety of hosts depends more on their ecological similarities than on their taxonomic proximity (Poulin & Mouillot, 2003; Poulin, 2005).The host species in this study belong to the Loricariidae family, represented by fish with mainly detritivorous and iliophagous feeding habits. They have a ventral mouth, in the form of a suction cup, adapted to scrape and suck surfaces in search of food. They are benthic, some with adaptations to anoxic environments, using accessory organs as an oxygen reservoir. Their body almost entirely covered by bone plates with most of them active after sunset (Eigenmann & Eigenmann 1890; Regan, 1904; Bowen, 1983; Araújo-Lima et al., 1986). The objective of this work is to record new hosts for Gorythocephalus elongorchisThatcher, 1979, Acanthocephala, Neoechinorhynchidae for the Brazilian Amazon.The fish were collected in the Catalão lake complex (3º10`04``S and 59º54`45``W), municipality of Iranduba, about 10 km from the city of Manaus, Amazonas (Figure 1). The hosts were captured with gill nets, with meshes of 20 to 160 mm between adjacent nodes, randomly arranged at the collection site, with fishing every two hours during the day and night. The captured fish were screened and identified in the field and transported to the “Laboratory of Fish Parasitology (LPP)” at the Instituto Nacional de Pesquisas do Amazonas (INPA) in Manaus, state of Amazonas.Taxonomic studies were carried out according to Amin (1987, 2002 and 2013); and Thatcher (1979). For morphological studies, acanthocephalans were stained with hydrochloric alcoholic carmine, diaphanized in beech creosote and mounted in Canada balm between a slide and a coverslip, adapted from Amato et al.(1991) and Eiras et al.(2006). For the identification of acanthocephalan species, the bibliographies were used; Thatcher (1979, 1998 and 2006). Taxonomic data considered for specimen identification were body size and shape, type and number of proboscis spines, lemniscus and proboscis pouch, male and female reproductive system and type egg.Ethic aspects: For the present research, material MATERIAL AND METHODSSilva Jtineant et al.art. 1=10-24art. 2=26-41Art 3 =42-51art. 4=52-59art. 5=60-65art 6=66-79art. 7=80-91art 8 =92-100art 9=102-111nota 1=112-116nota 2=118-123 rev =124-134
image/svg+xml135Neotropical Helminthology, 2022, 16(2), jul-dicfrom a sample bank collected from July 2015 to December 2016 was used, under the SISBIO 26612-1 collection license and license from the Animal Use Ethics Committee - CEUA nº 036/2016 – INPA.Two new hosts for Gorythocephalus elongorchisLago Catalão, collection areaAmazonas stateSouth AmericaBrasil in the spot lightFigure 1.Collection area, Catalão lake, Brasil. Images obtained through the landsat /Copernicus system.RESULTSTwenty specimens of D. amazonicaand 27 specimens of H. oculeuswere analyzed. The fish measured (cm) 12 – 16.5 (13.7 ± 1.33) in length and weighed (g) 29 – 59 (40.85 ± 9.78) and (cm) 12 – 21 (15.80 ± 2.13) in length and weighed (g) 75 – 125.40 (101.11 ± 14.28), respectively.Gorythocephalus elongorchiswas found parasitizing the intestine of D. amazonicaand H. oculeus. The parasitic indices are in table 1. The highest values of the parasitic indices were for H. art. 1=10-24art. 2=26-41Art 3 =42-51art. 4=52-59art. 5=60-65art 6=66-79art. 7=80-91art 8 =92-100art 9=102-111nota 1=112-116nota 2=118-123 rev =124-134
image/svg+xml136oculeus. Both hosts serve as the final host for G. elongorchis. This species has a specificity for the Loricariidae family. This is the first record of this parasite for these two fish species.There was no correlation between host length and parasite abundance; the community status of G. elongorchiswas the same for both hosts (table 1).Table 1. Parasitic indices of Gorytocephalus elongorchisparasitizing Dekeiseria amazonicaand Hypostomus oculeusin the Catalão lake. P-prevalence; IR- Intensity range and MI- mean intensity; S- status comunity secondary.HostP (%)IRMIprD. amazonica55s1-31,60.940.01H. oculeus59.25s1-41,80.72-0.07Eight adults, one male and seven females (Fig. 2) in mm were measured: females length 18.5 ± 5.6 (11.8 – 29.4); width 1.6 ± 1.2 (0.8 - 4.5); crest width 0.08 (0.05 - 0.1); length of lemniscus major 1.8 ± 1.7 (2.6 – 3.8), lemniscus minor 1.4 ± 1.3 (2.3 – 2.7) wide; reproductive area 0.3±0.06 (0.3 – 0.5). Male length 11.5; width 1.2; crest width 0.05; greater lemniscus length 2.8; lemniscus minor 1.8 wide; anterior testis 1.6 x 0.3 and posterior 0.9 x 0.2. Reproductive area 0.4.Figure 2.Parte anterior fêmea adulta de Gorytocephalus elongorchis Escala = 1mm. Seta- crista.DISCUSSIONFew studies on the fish parasite fauna that occur in the Loricariidae family have been carried out for the Amazon region. Among them we can highlight: Hypostomus carinatus(Thatcher, 1979), and, Pterygoplichthhys pardalis(Castelnau, 1875) (Porto, 2009; Porto et al., 2012; Cardoso et al., 2017). Studies of fish fauna show us that there is limited understanding of the ecosystem as a whole (Bellay et al., 2013), and record of parasite species for D. amazonicaand H. oculeusis scarce or non-existent.For Antoniutti et al. (1985), among the Siluriformes, some species of Loricariidae are considered fish of great commercial value, being widely exploited in the rivers of the state of São Paulo. In the Amazon region, the Loricariidae P. pardalisis of great commercial value (Santos et al., 2006). There is no record of local consumption of the species in this study, D. amazonicaand H. oculeus, however, they are important species for the niche to which they are inserted and are of ornamental interest.For the Loricariidae, with more than 960 known species (Eschmeyer & Fong, 2017), four species Neotropical Helminthology, 2022, 16(2), jul-dicSilva Jtineant et al.art. 1=10-24art. 2=26-41Art 3 =42-51art. 4=52-59art. 5=60-65art 6=66-79art. 7=80-91art 8 =92-100art 9=102-111nota 1=112-116nota 2=118-123 rev =124-134
image/svg+xml137have record of parasitism by G. elongorchis. They are: P. pardalis(Porto et al., 2012), Hypostomus carinatus(Steindachner, 1881) (Thatcher, 1979, 2006), Hypostomus ventromaculatusBoeseman, 1968 (Borges et al., 2018) Peckoltia braueri (Eigenmann, 1912) (Cardoso et al., 2017). This work presents two new records of hosts for G. elongorchis, in fish of the Loricariidae family.In general, the parasitic fauna of fish is formed by a mixture of adult individuals and larval forms (Poulin & Leung, 2011). In this work, all specimens of G. elongorchiswere found in the adult form in both host species. In this case, we can say that D. amazonicaand H. oculeusare definitive hosts of G. elongorchis.Gorytocephalus elongorchisit was cited as parasitizing the intestine of Hypostomus carinatus(Thatcher, 1979, 2006); P. pardalis(Porto, 2009; Porto et al., 2012; Cardoso et al., 2017). The preference of G. elongorchisfor species of the Loricariidae family must be associated with the feeding habit and the niche explored by these hosts, which facilitates contact with the intermediate host. The feeding habit of the host is a characteristic to be considered, as it has a strong relationship with the incidence of endoparasites (Dogiel, 1961). Another factor is the richness of the fauna of aquatic arthropods in the Amazon, insects and crustaceans that serve as intermediate hosts for several groups of parasites (Junk & Robertson, 1993).Gorytocephalus elongorchiswas described from the intestine of Hypostomus carinatus(Steindachner, 1881) captured in Lake Janauacá, Solimões River, in the state of Amazonas (Thatcher, 1979, 2006). Gorytocephalus elongorchisdoes not have attachment structures that could cause great pathogenicity in its hosts. It has a very small proboscis and low infestation intensity. A maximum of ten individuals were found in the intestine of H. carinatus.Hypostomus carinatusis detritivorous, has a long and delicate intestine with a slow movement. G. elongorchisdoes not need a strong fixation organ. These characteristics of its host made it possible for it to be present in the intestine, with minimal tissue damage and without its elimination (Thatcher, 1981). The host specimens studied in this work, D. amazonicaand H. oculeus, showed low intensity of G. elongorchis1 – 3 in D. amazonicaand 1 – 4 in H. oculeus, and were not attached to the wall. intestines of their hosts.Gorytocephalus elongorchiswas the only species of Acanthocephala found parasitizing P. pardalisin the floodplain lakes of the Solimões River in the state of Amazonas (Porto, 2017). Pterygoplichthys pardaliscaptured in the Fortaleza stream, in the state of Amapá, were also parasitized by G. elongorchisand parasitized the abdominal cavity (Cardoso et al., 2017). In this work, all specimens of G. elongorchiswere found parasitizing the intestine of H. oculeus (MI 1.8) and D. amazonica (MI 1.6).Gorytocephalus elongorchisis specific to fish of the Loricariidae family that are its definitive hosts (Porto et al., 2012). In this work, two new hosts for G. elongorchisare known and the first record of parasites for these hosts.The prevalence of parasitism by G. elongorchiswas recorded in P. pardalisby Porto (2017) and varied between 3.9% and 36.3% in different lakes in the stretch between the cities of Coari and Manaus. Cardoso et al.(2017) found a prevalence of 45.5%. In this study, the recorded prevalence was 55% for D. amazonicaand 59.25% for H. oculeus.Porto (2017), studying the P. pardalisparasite fauna in different lakes, recorded the community status among populations of G. elongorchis, based on prevalence, as satellite and secondary species. Analyzing the prevalence found by Cardoso et al. (2017), the prevalence of the population of G. elongorchis(45%) is classified as a secondary species. In this work, G. elongorchisis a secondary species, with prevalence for D. amazonicaand for H. oculeusbetween 33 and 66%.Communities made up of secondary species are an indication that the parasite community is in balance, they parasitize similar organs and the parasite rates do not show significant differences (Hanski, 1982; Bush & Holmes, 1986; Price, 1987). In the works by Porto (2009), Porto et al.(2012) and Porto (2017), G. elongorchiswas found parasitizing the intestine. Cardoso et al.(2017) recorded the parasitism of G. elongorchisin the Neotropical Helminthology, 2022, 16(2), jul-dicTwo new hosts for Gorythocephalus elongorchisart. 1=10-24art. 2=26-41Art 3 =42-51art. 4=52-59art. 5=60-65art 6=66-79art. 7=80-91art 8 =92-100art 9=102-111nota 1=112-116nota 2=118-123 rev =124-134
image/svg+xmlvisceral cavity. Thatcher (1979, 1991), recorded G. elongorchisparasitizing the intestine of H. carinatuscollected in Lake Janauacá, Amazonas. In this study, collected G. elongorchisspecimens were found parasitizing the intestine of D. amazonicaand H. oculeus.The parasite specificity depends, first, on the ecological conditions that allow the encounter between parasite and host, the ability to invade and evolve and the behavior of the host (Ferreira, 1973). Gorythocephalus elongorchisis specific for species of the Loricariidae family, species with similar behavior and feeding habits, which share the same ecological niche.This study discovers two new hosts for G. elongorchis, expanding the knowledge of the number of hosts for this parasite. It makes the first record of parasites for D. amazonicaand H. oculeus, and adds more knowledge about the parasite dynamics in fish from the Amazon.The authors thank the Cell Biology and Helminthology Laboratory of the Federal University of Pará, in Belém, Brazil, where the necropsies and taxonomic studies were performed for this work.138ACKNOWLEDGMENTSspecies in two subgenera.Systematic Parasitology, vol. 53, pp. 1-18.Amin, OM. 2013. Classification of the Acanthocephala.Folia Parasitologica, vol. 60, pp. 273-305.Aquino-Pereira, SL. 2010. Composição e estrutura das infracomunidades parasitárias de Brycon amazonicus (Spix & Agassiz, 1829) explotada nos rios Juruá e Purus, tributários do rio Solimões e desembarcada em Manaus no Estado do Amazonas, Brasil. [Tese de Doutorado, Instituto Nacional de Pesquisas da Amazônia. Manaus, Amazonas]. Antoniutti, DM, Ranzani-Paiva, MJT & Godinho, HM. 1985. Morfologiadas gônadas, escala de maturidade e fator de condição de Plecostomusalbopunctatus Regan, 1908 (Osteichthyes, Loricariidae) do Rio Jaguarí, São Paulo,Brasil.Boletim do Instituto de Pesca, vol.12, pp. 87-103.Araújo-Lima, CARM, Forsberg, RV & Martinelli, L. 1986. Energy sources fordetritívorous fishes in the Amazon.Science, vol. 234, pp. 1256-1258.Bellay, S, Oliveira, EF, Almeida-Neto, M, Lima-Junior, DP, Takemoto, RM & Luque, JL. 2013. Developmental stages of parasites influence the structure of fish-parasite networks.Plos One, vol. 8, pp. 1-6.Borges, WF, Oliveira, M, Santos, GG & Tavares-Dias, M. 2018. Parasites in Loricariidae from Brazil: checklist and new records for fish from the Brazilian Amazon.Acta Scientiarum. Biological Sciences, vol. 40, pp. 1-9. Bowen, SH. 1983. Detritivory in neotropical fish communities. Environmental Biologyof Fishes, vol. 9, pp. 137-144.Bush, AO & Holmes, JC. 1986. Intestinal helminthes of lesser scaup ducks: an interactive community. Canadian Journal of Zoology, vol. 64, pp. 142-154.Cardoso, ACF, Oliveira, MSB, Neves, LR & Tavares-Dias, M. 2017. Metazoan fauna parasitizing Peckoltia braueriand Pterygoplichthys pardalis(Loricariidae) catfishes from the northeastern Brazilian Amazon. Acta Amazonica, vol. 47, pp. 147-154.Dogiel, VA. 1961. Ecology of the parasites ofAmato, JFR, Boeger, WA & Amato, SB. 1991. Protocolos para laboratório: coleta e processamento de parasitos de pescado. Imprensa Universitária, Rio de Janeiro. Amin, OM. 1987. Key to families and subfamilies of Acanthocephala, with the erection of a new class (Polyacanthocephala) and new order (Polyacanthorhynchida). Journal of parasitology, vol. 73, pp. 1216-1219.Amin, OM. 2002. Revision of NeoechinorhynchusStiles et Hassall, 1905 (Acanthocephala: Neoechinorhynchidae) with Keys to 88 BIBLIOGRAPHIC REFERENCESNeotropical Helminthology, 2022, 16(2), jul-dicSilva Jtineant et al.art. 1=10-24art. 2=26-41Art 3 =42-51art. 4=52-59art. 5=60-65art 6=66-79art. 7=80-91art 8 =92-100art 9=102-111nota 1=112-116nota 2=118-123 rev =124-134
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image/svg+xml140Neotropical Helminthology, 2022, 16(2), jul-dicTwo new hosts for Gorythocephalus elongorchisRondônia state, Brazil. Amazoniana,vol. 15, pp. 51-55.Thatcher, VE. 2006.a Amazon fish parasites. 2Ed., Editora Aquatic Biodiversity in Latin America, Sofia, Moscow.Received June 28, 2022.Accepted September 6, 2022.art. 1=10-24art. 2=26-41Art 3 =42-51art. 4=52-59art. 5=60-65art 6=66-79art. 7=80-91art 8 =92-100art 9=102-111nota 1=112-116nota 2=118-123 rev =124-134