Endoparasites of the fish Pellona harroweri (Clupeiformes: Pristigasteridae) from the coast of Paraíba State, northeastern Brazil

Milla Silveira Pinto Brandão1

Gabriel Ponciano de Miranda2

Ana Carolina Figueiredo Lacerda3

Abstract

Despite the vast literature on fish parasites in Brazil, there are few studies about parasites in Northeast and, even more, on the coast of Paraíba. Among the fishes found on the region, Pellona harroweri stands out, found in high abundance and in great distribution throughout the Brazilian coast. The objectives of this study are to identify the parasites present in P. harroweri and to correlate the levels of parasitism with its length and relative condition factor. The specimens were collected by nets in October of 2015 in Praia da Penha – Paraíba and then they were identified and necropsied. For data analysis, the prevalence, mean intensity and average abundance values were used to measure parasite infection, the correlation between length and weight with parasite abundance and the relative condition factor (Kn). Among the 36 specimens of P. harroweri, 19 were parasitized, with a total of 59 parasites and two species: Parahemiurus anchoviae (Digenea: Hemiuridae) and Contracaecum sp. (larva) (Nematoda: Anisakidae). The length of the hosts presented no significant correlation with the abundance of P. anchoviae (rs= -0.220; p= 0.203) or Contracaecum sp. (rs= -0.156, p= 0.368) and no correlation with host Kn with the abundance of parasites (P. anchoviae: rs = -0.312, p = 0.068; Contracaecum sp.: rs = -0.019, p = 0.917) as well. This study shows the first record of a digenetic parasite and nematode Contracaecum sp. for P. harroweri.

Keywords: Ichthyoparasitology; Parahemiurus anchoviae; Contracaecum sp.; Relative factor condition.

Resumo

Apesar de haver vasta literatura sobre parasitos de peixes no Brasil, há poucos desses estudos no Nordeste e, menos ainda, na costa da Paraíba. Dentre os peixes encontrados na região, destaca-se a espécie Pellona harroweri, encontrada em toda a costa brasileira. Os objetivos dos autores com o presente trabalho foram identificar os parasitos presentes em P. harroweri e verificar se os índices parasitários estariam relacionados ao tamanho e grau de higidez dos hospedeiros. Os peixes foram coletados em outubro de 2015 na Praia da Penha, em João Pessoa, Paraíba, e posteriormente identificados e necropsiados. Dentre os 36 espécimes coletados de P. harroweri, 19 estavam parasitados, encontrando no total 59 parasitos, pertencentes a duas espécies: Parahemiurus anchoviae (Digenea: Hemiuridae) e Contracaecum sp. (larva) (Nematoda: Anisakidae). A abundância dos parasitos não apresentou correlação significativa com o comprimento padrão (P. anchoviae: rs= -0,220 e p= 0,203; Contracaecum sp.: rs= -0,156 e p= 0,368), nem com o fator de condição relativo dos hospedeiros (P. anchoviae: rs= -0,312 e p= 0,068; Contracaecum sp.: rs= -0,019 e p= 0,917). Este é o primeiro registro de parasitos dos grupos Digenea e Nematoda parasitando Pellona harroweri.

Palavras-chave: Ictioparasitologia; Parahemiurus anchoviae; Contracaecum sp.; Fator de condição relativo.

Resumen

A pesar de la literatura sobre parásitos de peces en Brasil ser amplia, hay pocos estudios sobre el tema en el Nordeste y, más aún, en la costa de Paraíba. Entre los peces encontrados en la región, se destaca la especie Pellona harroweri, encontrada en alta abundancia y en gran distribución por toda la costa brasileña. Los objetivos de este trabajo fueron identificar los parásitos presentes en P. harroweri y correlacionar los niveles de parasitismo a la longitud y factor de condición relativo de P. harroweri. Se realizó una recolección de arrastre en Octubre de 2015 en Praia da Penha - Paraíba, donde los especímenes fueron recolectados y posteriormente identificados y necropsiados. Sus parásitos fueron recolectados y fijados a etanol 70% para posterior identificación. Para el análisis de los datos, se utilizaron los valores de prevalencia, intensidad media y abundancia media para medir la infección por el parásito, además de la correlación entre la longitud y el peso con la abundancia de parásitos y el factor de condición relativo (Kn). Entre los 36 especímenes recogidos de P. harroweri, 19 peces estaban parasitados, encontrando un total de 59 parasitos, con dos especies distintas: Parahemiurus anchoviae (Digenea: Hemiuridae) y Contracaecum sp. (larva) (Nematoda: Anisakidae). La longitud no tuvo correlación con la abundancia de P. anchoviae (rs= -0,220, p= 0,203) o Contracaecum sp. (rs= -0,156, p= 0,368), así como tampoco tuvo correlación con el Kn de los huéspedes con la abundancia de parásitos (P. anchoviae: rs= -0,312 y p= 0,068; Contracaecum sp.: rs= -0,019 y p= 0,917). El trabajo muestra el primer registro de un parásito digenético y del nematodo Contracaecum sp. para Pellona harroweri.

Palabras-clave: Ictioparasitología; Parahemiurus anchoviae; Contracaecum sp.; Factor de condición relativo.

Introduction

Parasitism is a very common disharmonious interaction in species of fish (Luque et al. 2011). Parasites are a very important component of biodiversity and, despite the vast literature on fish parasites in Brazil (Pavanelli et al. 2013), there are few studies about parasites of marine fishes in northeastern Brazil and, even less, on the coast of Paraíba State. According to Jorge and Poulin (2018), this region belongs to areas where disproportionately few parasites have been discovered relative to local host richness.

The fish Pellona harroweri (Fowler, 1917) (Clupeiformes: Pristigasteridae), popularly known as “sardinha-manteiga”, is a commonly captured species in the coast of the city of João Pessoa. It is a small pelagic fish which occurs in shallow coastal waters in estuaries of tropical and subtropical regions (Muto et al. 2008), distributed along the Western Atlantic, from Panama, to southern Brazil (Froesy and Pauly, 2019). It feeds mostly on crustaceans, including copepods and luciferid shrimps (Criales-Hernández 2003). Pellona harroweri has no significant economic value, being more captured by trawling to serve as bait or subsistence fishing, and it represents an important food resource for organisms that occupy the next trophic level (Muto et al. 2008). Along its distribution range, it has been reported as a food item for mammals (Bordignon 2006), birds (Serrano and Azevedo-Junior 2005) and other species of fish such as Trichiurus lepturus (Duarte et al. 1999). Although its wide distribution range, there is only one parasitological record for P. harroweri, which is an unindentified cymothoid near the city of Santos, São Paulo State, Brazil (Sartor 1986).

According to Cordeiro (2007), a positive correlation of the length of the host to its parasite’s abundance indicates the tendency to favor the concentration of parasites, referring to the cumulative process of parasitic infestation, where larger fish may have more endoparasites because of the ingestion of intermediate hosts. The relative condition factor (Kn) (Le Cren 1951) is a measure or a quantitative indicator of fish welfare (Vazzoler 1996). This parameter has been widely used in the last decades and can be an important tool for the study of parasite-host interactions (Lizama et al. 2006). In normal conditions, the theoretically expected value is Kn = 1 and any event that interferes with fish health or well being, such as parasitism, can produce variations in this value (Lucas et al. 2011).

This study aims to identify the endoparasites of the fish P. harroweri from the coast of the Paraíba State, as well as to investigate possible correlations between parasitism indices and the length and the relative condition factor of the hosts.

Material and methods

The fish were caught using nets at the Penha Beach (7º09’51.84”S 34º47’44.92”O), city of João Pessoa, State of Paraíba, in October 2015. In the laboratory, the fishes were identified, numbered, weighed, measured and necropsied. Organs were observed under stereomicroscope, and parasites were conserved in 70% ethanol. For identification, the specimens were clarified in Hoyer’s medium (Digenea) and Lactophenol of Amman (Nematoda), and stained with acetic carmine (Digenea) (Eiras et al. 2006). Permanent slides were mounted in Canada balsam. The identification of parasites was according to Thatcher (2006), Moravec (1998), Bray (1990). The prevalence (percentage of infected hosts in the sample), mean intensity (total number of parasites divided by the number of infected hosts), mean abundance (total number of parasites divided by the number of hosts analyzed) and the ecological terminology were used according to Bush et al. (1997). The data analysis used the correlation coefficient by Spearman “rs” to verify possible correlations between the standard length of the hosts and its condition factor and the abundance of parasites, considering α=0.05.

Results and Discussion

In total, 36 specimens of Pellona harroweri were collected. Nineteen hosts were parasitized by at least one parasite species. Fifty-nine parasites were collected, being identified as Parahemiurus anchoviae Pereira & Vaz 1930 (30 specimens) and larvae of Contracaecum sp. (29 specimens). Parasitological indexes are in Tab. 1.



Table 1. Endoparasites of 36 specimens of Pellona harroweri collected from the coast of João Pessoa, Paraíba State, and their parasitological indexes (P = prevalence, MI = mean intensity, MA = mean abundance, Min-Max = mínimo e máximo por hospedeiro, SD = standard deviation).

Parasite

P (%)

MI ± SD

MA ± SD

Min-Max

Parahemiurus anchoviae

25.7

3.33 ± 2.87

0.86 ± 2.03

1-8

Contracaecum sp.

45.7

1.81 ± 1.17

0.82 ± 1.20

1-3




The parasites from subclass Digenea, family Hemiuridae, were identified as Parahemiurus anchoviae based on a comparative study of Bray (1990) (Tab. 2). The parasite found has a subglobular oral sucker, pre-pharynx absent and subglobular pharynx. It presents a short esophagus, direction of ceca going from the anterior region to the ecsome, which is well developed and has a terminal pore. Nearly symmetrical testicles and oval or rounded seminal vesicle, located in the anterior half of the body. A post-testicular, oval or subglobular ovary. Uterus posterior to vitellaria, occasionally reaching the ecsome. Small and numerous eggs and two ovarian or irregular post-ovarian masses, representing the vitellaria. Distinct caeca only in the posterior region, reaching the ecsome.



Table 2. Size of body structures in micrometers (μm) comparing Parahemiurus anchoviae found in present study with Parahemiurus anchoviae (Bray 1990).

Structure

P. anchoviae (present study)

P. anchoviae (Overstreet 1969)

Body length and width

1510x230

505x158

Oral sucker

50x60

31x32

Pharynx

30x30

23x29

Acetabulum

12x160

70x75

Seminal vesicle

150x60

62x38

Testicle 1

110x70

54x35

Testicle 2

120x60

60x34

Ovary

70x80

38x48

Vitellaria

60x50

38-41x38-38

Eggs

20x10

21-13x9x12



The parasite Parahemiurus anchoviae was identified for having many similarities with the collected digenean parasites. Individuals from the family Hemiuridae have as main characteristic the ability to retract the final part of the posterior region of the body, known as ecsome (Coutinho 2016). Although the measures of P. anchoviae found to be almost twice the size of Parahemiurus anchoviae in Overstreet (1969) study, they present the same proportion of suckers (1>2.1). Also, the uterus going from the posterior region to the vitellaria, reaching the ecsome and going towards the anterior part, reaching the acetabulum and by the equal size of eggs. Still according to Bray (1990), the record of P. anchoviae in his article was recorded in Brazil.

Bray (1990) indicates that although individuals of the genus Parahemiurus show folds throughout their body, these folds are only considered good parameters for the identification of the individual when it is well fixed, since a material that was not properly fixed, that mainly belongs to hosts that have been frozen, the folds are not a good feature for the identification in question and may have been lost or distorted. Other parameters such as size ratio of the suckers and the size of the eggs might best help indicate the species.

Bray (1990) cites that P. anchoviae was found parasitizing the hosts Pomatomus saltator in Santa Catarina and Anchoa lyolepis in Florida, United States (Overstreet 1969). Also, P. anchoviae was recorded in Lycengraulis grossidens and Mugil planatus in Rio de Janeiro, Santos and São Paulo (Kohn and Fernandes 2016). The present work indicates that this is the first record of P. anchoviae for Pellona harroweri and for the Northeast region of Brazil.

The nematode Contracaecum sp. larva belongs to family Anisakidae and has a long body of 4950 μm with maximum width 200 μm. The larva has a round head with a small ventral tooth followed by excretory pore and poorly developed lips. Muscular esophagus with 625 μm followed by a glandular esophagus of 275 μm. Nervous ring not observed. Glandular esophagus overlapping the intestine, which extends towards the muscular esophagus. It has a conical and striated end. The nematode Contracaecum sp. (larva) was identified according to Moravec (1988) because it has a small ventral tooth next to lips and the intestine extending towards the muscular esophagus in anterior region.

According to Madi and Silva (2005) and Santos et al. (2016) the genus Contracaecum sp. was recorded in Argentina, Venezuela, Chile, Mexico, Uruguay, Peru and Colombia. This genus has more than 40 records in Brazil, including Aluterus monoceros, Centropomus undecimalis, Diapterus rhombeus, Epinephelus masrginatus, Heptranchias perlo, Lophius gastrophysus, Menthicirrhus americanos, Mustelus canis, Oligoplites saurus, Paralonchurus brasiliensis, Scomberomorus brasiliensis, Trichiurus lepturus e Urophycis brasiliensis, besides Cichla ocellaris and Hoplias malabaricus in Paraná, and Scomberomorus cavalla and S. maculatus in Ceará (Martins et al. 2003; Santos et al. 2016; Klein 1973).

The length of the hosts varied between 5.0 and 8.6 cm (6.9±0.8) and their weight between 2.9 and 13.6 g (7.7±2.4). The correlation between host length and parasite abundance was calculated for each parasite species. There was no correlation between host length and abundance of P. anchoviae (rs=-0.220, p=0.203) or Contracaecum sp. (rs=-0.156, p=0.368), indicating that as the amount of parasites was relatively low, and the abundance of parasites found did not relate to the length of the hosts. This was also observed in studies by Paraguassú and Luque (2007) and by Azevedo et al. (2007) that, since host body length can be an indicator of their age, suggest that food items in different age groups should be similar and that there should be no variation in habitat use in this species, relative to endoparasites.

The condition factor is a measure or quantitative indicator of fish welfare (Vazzoler 1996). In normal conditions, the expected value is Kn=1 and any event that interferes with fish health, such as parasitism can produce variations in this value (Lucas et al. 2011). The Kn of the hosts varied between 0.92 and 1.10 and there was no significant correlation between the Kn and the abundance of the parasites P. anchoviae (rs = -0.312, p = 0.068) or Contracaecum sp. (rs = -0.019, p = 0.917), indicating that the amount of parasite did not correlate with the condition of the hosts. Studies by Lemos et al. (2007) and Santos et al. (2013) presented similar results, where Kn was not significantly correlated with the abundance of parasites. Relative condition factor`s variations can occur due to diverse environmental conditions and behavioral aspects of the species and by factor such as age, sex or fish maturity (Vazzoler 1996; Le Cren 1951).

Conclusions

This is the first record of endoparasites in P. harroweri, as well as the first record of P. anchoviae in northeastern Brazil. The abundances of the recorded parasites, Parahemiurus anchoviae and Contracaecum sp., were not correlated with the host’s length or relative condition factor.

References

Azevedo RK, Abdallah VD, Luque JL (2007). Ecologia da comunidade de metazoários parasitos do Apaiarí Astronotus ocellatus (Cope, 1872) (Perciformes: Cichlidae) do Rio Guandu, Estado do Rio de Janeiro, Brasil. Revista Brasileira de Parasitologia Veterinária, 16(1):15-20.

Bordignon MO. 2006. Diet of the fishing bat Noctilio leporinus (Linnaeus) (Mammalia, Chiroptera) in a mangrove area of southern Brazil. Revista Brasileira de Zoologia, 23(I):256-260. DOI: 10.1590/S0101-81752006000100019

Bray RA. 1990. A review of the genus Parahemiurus Vaz & Pereira, 1930 (Digenea: Hemiuridae). Systematic Parasitology, 15:1-21. DOI: 10.1007/BF00009914

Bush AO, Lafferty KD, Lotz JM, Shostak AW (1997). Parasitology meets ecology on its own terms: Margolis et al. revisited. Journal of Parasitology, 83(4):575-583. DOI: 10.7939/R3J38KV04.

Cordeiro AS. 2007. Composição e estrutura das comunidades de metazoários parasitos da corvina, Micropogonias furnieri (Perciformes: Sciaenidae) do litoral brasileiro. Programa de Pós-Graduação em Biologia Animal, Universidade Federal Rural do Rio de Janeiro, Rio de Janeiro.

Bouillon M, Beirne P. 2016. CorelDraw® Graphics Suite X8. Ottawa, Canadá.

Coutinho, AS. 2016. Ectoparasitos de Anchoa januaria (Clupeiformes: Engraulidae) em dois estuários da Paraíba. Tese de Monografia apresentada ao Curso de Ciências Biológicas da Universidade Federal da Paraíba, João Pessoa.

Criales-Hernández M. 2003. Composición de la dieta de Pellona harroweri (Fowler) (Picses: Pristigasteridae) en La Guarija, Caribe Colombiano. Boletín de Investigaciones Marinas y Costeras, (32):279-282.

Duarte LO, García CB, Moreno I, Melo G, Navajas P, Sandoval N, D. von Schiller D. 1999. Atlas demográfico de los peces demersales del Golfo de Salamanca, Caribe colombiano. Dinámica poblacional, Distribución, Alimentación y Reproducción. Libro digital (CDROM). Santa Marta, Colombia: Invemar, Colciencias, ISBN 95950-6-5

Eiras JC, Takemoto, RM, Pavanelli GC. 2006. Métodos de estudio y técnicas laboratoriales en parasitología de peces. Espanha: Editorial Acribia, 133p.

Froese R, Pauly D. Editors. 2019. FishBase. World Wide Web electronic publication. www.fishbase.org, version (02/2019).

Poulin R, Jorge F. 2018. The geography of parasite discovery across taxa and over time. Parasitology, 146(2): 168-175. doi.org/10.1017/S003118201800118X

Kohn A, Fernandes B. 2016. In: Capítulo VI: Trematoda. Eiras et al. Parasitos de peixes marinhos da América do Sul. Rio Grande: Editora da FURG.

Le Cren ED. 1951. The length-weight relationship and seasonal cycle in gonad weight and condition in the Perch (Perca fluviatilis). Journal of Animal Ecology, 20(2):201-219.

Lemos JG, Tavares-Dias M, Sales RSA, Nobre-Filho GR, Fim JDI. 2007. Parasitos nas brânquias de Brycon amazonicus (Characidae, Bryconinae) cultivados em canais de igarapé do Turumã-Mirim, estado do Amazonas, Brasil. Acta Scientiarum Biological Sciences, 29(2):217-222.

Lizama M, Takemoto, R, Pavanelli, G. 2006. Parasitism influence on the hepato, splenosomatic and weight/length relation and relative condition factor of Prochilodus lineatus (Valenciennes, 1836) (Prochilodontidae) of the upper Paraná River floodplain, Brasil. Revista Brasileira de Parasitologia Veterinária, 15(3):116-122.

Lucas APC, Fernandes ES, Tarifa DS, Lizama MAP, Takemoto RM. 2011. Relação entre fator de condição relativo (Kn) e abundância de endoparasitos de Trachydoras Paraguayensis (Eigenmann & Ward, 1907) (Osteichthyes: Doradidae) na planície de inundação do alto Rio Paraná, Paraná – Brasil. Maringá, Paraná: VII EPCC – Encontro Internacional de Produção Científica Cesumar.

Luque JL, Aguiar JC, Vieira FM, Gibson DI, Santos CP. 2011. Checklist of Nematoda associated with the fishes of Brazil. Zootaxa, 3082(1). DOI: 10.11646/zootaxa.3082.1.1

Madi RR, Silva MSR. 2005. Contracaecum Railliet & Henry, 1912 (Nematoda, Anisakidae): o parasitismo relacionado à biologia de três espécies de peixes piscívoros no reservatório do Jaguari, SP. Revista Brasileira de Zoociências, 7(1):15-24.

Martins ML, Santos RS, Takahashi HK, Marengoni NG, Fujimoto RY. 2003. Infection and susceptibility of three fish species from the Paraná River, Presidente Epitácio, State of São Paulo, Brazil, to Contracaecum sp. larvae (Nematoda: Anisakidae). Acta Scientiarum. Animal Sciences Maringá, 25(1):73-78.

Moravec, F. 1998. Nematodes of freshwater fishes of the Neotropical Region. Praga: Academy of Sciences of the Czech Republic. 464 p.

Muto EY, Malfara DT, Coelho LI, Soares LSH. 2008. Alimentação das sardinhas Pellona harroweri (Fowler, 1919) e Chirocentrodon bleekerianus (Poey, 1867), na região costeira de Santos, estado de São Paulo. In: Braga ES (Org.). Oceanografia e mudanças globais. São Paulo: Instituto Oceanográfico, 287-302.

Overstreet RM. 1969. Digenetic trematodes of marine teleost fishes from Biscayne Bay, Florida. Tulane Studies in Zoology and Botany, (15):119-176.

Paraguassú AR, Luque JL. 2007. Metazoários parasitos de seis espécies de peixes do Reservatório de Lajes, Estado do Rio de Janeiro, Brasil. Revista Brasileira de Parasitologia Veterinária, 16(3):121-128.

Pavanelli G, Eiras JC, Yamaguchi MU, Takemoto RM. 2015. Zoonoses Humanas Transmissíveis por Peixes no Brasil. Maringá, Paraná: UniCesumar, 145 p.

Santos CP, Lopes KC, Gibson DI. 2016. In: Capítulo VIII: Nematoda. Eiras et al. Parasitos de peixes marinhos da América do Sul. Rio Grande: Editora da FURG.

Santos EF, Tavares-Dias M, Pinheiro DA, Neves LR, Marinho RGB, Dias MKR. 2013. Fauna parasitária de Tambaqui Colossoma macropomum (Characidae) cultivado em tanque-rede no estado do Amapá, Amazônia oriental. Acta Amazonica, 43:105 – 112. DOI: 10.2312/Actafish.2009.6.1.29-34

Sartor SM. 1986. Incidência de isópodes parasitas (Cymothoidae) em peixes da plataforma continental Brasileira. Boletin do Instituto Oceanográfico, 34(1): 1-12.

Serrano IL, Azevedo-Júnior SM. 2005. Dieta das aves marinhas do Parque Nacional dos Abrolhos, Bahia, Brasil. Ornithologia, 1(1): 75-92.

Statsoft. 2007. Análise e manipulação de dados inseridos usando algoritmos, funções e testes. Statistica, version 8.0. Available in www.statsoft.com

Thatcher VE. 2006. Amazon Fish Parasites. vol. 1. 2 ed. Bulgaria: Pensoft, 508 p.

Vazzoler A. 1996. Biologia da reprodução de peixes teleósteos: teoria e prática. Maringá, Paraná: Eduem.


1 Federal University of Paraíba (UFPB). E-mail: milla.silveira1@gmail.com

2 Federal University of Paraíba (UFPB). Postgraduate Course in Biological Sciences (Zoology) (PPGCB/UFPB). E-mail: gabrielpmjp@gmail.com

3 Federal University of Paraíba (UFPB). Postgraduate Course in Biological Sciences (Zoology) (PPGCB/UFPB). E-mail: acflacerda@dse.ufpb.br