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Anais da Academia Brasileira de Ciências

versão impressa ISSN 0001-3765versão On-line ISSN 1678-2690

An. Acad. Bras. Ciênc. vol.89 no.3 supl.0 Rio de Janeiro  2017  Epub 20-Jul-2017

http://dx.doi.org/10.1590/0001-3765201720160883 

Biological Sciences

Gill parasites of fish from two estuaries in northeastern Brazil: new hosts and geographical records

JÉSSICA E.S.A. GOLZIO1  2 

JÚLIA M. FALKENBERG1 

RAYSSA C.G. PRAXEDES1 

ANDERSON S. COUTINHO1 

MYLENA K. LAURINDO1 

ANDRÉ PESSANHA3 

RUBENS R. MADI4 

JOANA PATRÍCIO5 

ANA L. VENDEL6 

GEZA T.R. SOUZA4 

CLÁUDIA M. MELO4 

ANA CAROLINA F. LACERDA1  2 

1Universidade Federal da Paraíba, Laboratório de Hidrologia, Microbiologia e Parasitologia, Cidade Universitária, s/n, Castelo Branco, 58051-900 João Pessoa, PB, Brazil

2 Programa de Pós-Graduação em Zoologia (Ciências Biológicas), Universidade Federal da Paraíba, Cidade Universitária, s/n, Castelo Branco, 58051-900 João Pessoa, PB, Brazil

3 Programa de Pós-Graduação em Ecologia e Conservação, Universidade Estadual da Paraíba, Rua Baraúnas, 351, 58429-500 Campina Grande, PB, Brazil

4 Programa de Pós-Graduação em Saúde e Ambiente, Universidade Tiradentes, Av. Murilo Dantas, 300, Farolândia, 49032-490 Aracaju, SE, Brazil

5MARE-Marine and Environmental Sciences Centre, Faculty of Sciences and Technology, University of Coimbra, Coimbra, Portugal

6Universidade Estadual da Paraíba, Campus V, Rua Horacio Trajano, s/n, Cristo Redentor, 58070-450 João Pessoa, PB, Brazil

ABSTRACT

Parasites are important components of communities and constitute great part of the biological diversity found in ecosystems, providing valuable information about their hosts and the environment in which they live. However, despite its importance, parasitic diversity is still not well known in some regions of Brazil, especially with respect to fish parasites in the Northeast Region. The present study aims to perform the survey of gill parasites of fish from two tropical estuaries located in northeastern Brazil: Paraíba and Mamanguape rivers. Two collections were made in each estuary, one during the dry period (November / 2013) and the other during the rainy season (July / 2014). The fish were caught using a beach seine net, dragged along the main channel margin. After the identification, biometry and necropsy of the fish, their parasites were collected, stored and identified. For each species of parasite, the values ​​of prevalence, mean intensity and mean abundance were calculated. Of the 882 examined fish, belonging to four species, 145 were parasitized by at least one species of parasite. In total, 18 taxa of parasites of the groups Monogenea, Digenea, Nematoda, Copepoda and Isopoda were recorded, being the copepod Acusicola brasiliensis the most abundant species of parasite.

Key words: fish parasites; parasite diversity; ectoparasites; tropical estuaries

INTRODUCTION

Considering the importance of parasites in terms of biomass (Kuris et al. 2008) and also as determinants of the structure of the animal communities (Minchella and Scott 1991), the identification of these organisms can serve as the basis for a series of investigations, such as parasite-induced pathology (Pavanelli et al. 2002), the use of parasites as bioindicators of water quality (Lafferty 1997), ecological and economic impacts caused by invasive species and their parasites (Torchin et al. 2003), and studies on food webs (Lafferty et al. 2008) among others. Thus, it is necessary to study the parasites of hosts and areas that were not investigated previously.

In estuarine environments, marine water is diluted by freshwater from continental drainage, and these systems may have a free connection to the open ocean (Cameron and Pritchard 1963). The estuarine fish community is represented by resident and migrant, marine and freshwater species, many of which present feeding and / or economic value to fishermen living near the estuary. Fishes use these environments during some stage of the life cycle, such as feeding and breeding areas of larvae and young (Blaber 2000) or even during the whole life cycle, in the case of resident species.

In Brazil, the first study on parasitic fish fauna was conducted by the researcher Lauro Travassos at the Oswaldo Cruz Institute, in 1913; since then, the number of studies involving parasite taxonomy and distribution has increased in Brazil (Karling et al. 2014). Although several studies have already been carried out on the biota of the estuaries of Mamanguape and Paraíba rivers, Northeast Region of Brazil (Leonel et al. 2002, Xavier et al. 2012, Alves et al. 2016, Nóbrega-Silva et al. 2016, Medeiros et al. 2016, Dolbeth et al. 2016), none of them have considered a ubiquitous component of these communities: fish parasites.

The objective of this work was to identify the gill parasites of fish from the estuaries of the Mamanguape and Paraíba do Norte rivers, making new records of localities and hosts for the parasite species.

MATERIALS AND METHODS

STUDY AREAS

Two estuaries were considered in the present study: Paraíba do Norte (PN) (6°54’14” - 7°07’36”S; 34°58’16” - 34°49’31”W) and Mamanguape (MM) (6°43’02” - 6°51’54”S; 35°67’46” - 34°54’04”W) (Figure 1). The regional climate is hot and humid, with air temperature ranging from 25 to 30°C. The rainy season occurs from February to July and the dry season from October to December. Annual rainfall varies between 1750 and 2000 mm annually and the average water temperature ranges from 24 to 26°C (AESA 2010).

Figure 1 Estuaries of the river Paraíba do Norte (PN) (a) and Mamanguape (MM) (b), State of Paraíba, Brazil. Collection points and land use cover.  

The distance between the two estuaries is approximately 22 km. The MM is inserted within an Environmental Protection Area. On the other hand, the PN is located near the city of Cabedelo, where there the Cabedelo Port is responsible for a large flow of vessels, and is also close to the city of João Pessoa, capital of the state of Paraíba, whose metropolitan region aggregates five cities and approximately 1,100,000 inhabitants. In this way, the PN suffers more anthropogenic pressures of urban origin, with possible consequences for the aquatic biota.

SAMPLING

In both estuaries, the collections were carried out in November of 2013 (dry season) and in July 2014 (rainy season), locallities indicated in Figure 1. Sampling sites were defined along the estuaries (15 in the PN, 12 in the MM), aiming to capture fish species with different tolerance to salinity, migrants and residents. Fish were collected using three manual trawls (ICMBio License 31000-1) and transported to the laboratory immersed in ice inside thermal boxes. The weight and total length of the fish were recorded and then the individuals were fixed in 10% formalin. Posteriorly, fish were necropsied and their gills were removed and observed under stereomicroscope. The collected parasites were conserved in 70% ethanol. For identification of monegeneans, specimens were stained with Gomori´s trichrome and mounted in slides with Canada balsam, or directly mounted in Hoyer`s medium. Digeneans were stained in acetic carmine and nematodes were clarified in Amman`s Lactophenol, and mounted in permanent slides with Canada balsam. Copepods were mounted in slides with Hoyer’s medium and isopods were observed immersed in 70% ethanol in Petri dishes under the stereomicroscope. Permanent slides were mounted in Canada balsam. Identification was performed according to Travassos et al. (1967), Amado and Rocha (1996), Moravec (1998), Gibson et al. (2002) and Thatcher (2006). The values ​​of prevalence, mean intensity and mean abundance were expressed according to Bush et al. (1997). Differences on prevalence, mean intensities and mean abundances of parasites between estuaries and seasons were calculated by the Fisher`s exact test (for prevalence) and the Bootstrap test with 1000 replications (for intensity and abundance), using the Quantitative Parasitology web 1.0 software (Rózsa et al. 2000), considering α=0.05. The parasites identified to species level were deposited in the Paulo Young Invertebrate Collection (CIPY), Federal University of Paraíba.

RESULTS AND DISCUSSION

In total, 882 hosts were analyzed from both estuaries, belonging to three species: Anchoa januaria (Steindachner, 1879) (Clupeiformes: Engraulidae) (total=260, PN=111, MM=149), Atherinella brasiliensis (Quoy & Gaimard, 1825) (Atheriniformes: Atherinopsidae) (total=408, PN=224, MM=184) and Mugil curema Valenciennes, 1836 (Mugiliformes: Mugilidae) (total=214, PN=124, MM=90). Total length of examined fish (mean±standard deviation, minimum-maximum): Anchoa januaria (54.6±27.9, 62-88), Atherinella brasiliensis (52.8±28.9, 9-129) and Mugil curema (56.6±32.6, 17-292)

Gill parasites belonging to 18 species of the groups Monogenea, Digenea, Nematoda, Copepoda and Isopoda (Table I) were collected, a total of 1,738 adult specimens. Of the 882 examined fish, belonging to three species, 145 were parasitized by at least one parasite taxa; most of them were Copepoda (N = 1,523), highlighting Acusicola brasiliensis Amado & Rocha, 1996 (N = 929) found in the hosts Atherinella brasiliensis and Anchoa januaria. New geographical records consider the first time the parasite taxa were recorded in northeastern Brazil.

TABLE I Taxa and catalog numbers of voucher specimens of gill parasites of fish from the estuaries (E) of the rivers Paraíba do Norte (PN) and Mamanguape (MM), in the rainy and dry seasons (S) and respective values of prevalence (P%), mean abundance (MA) and mean intensity (MI) of infection. Letters and symbols indicate new host-parasite record ( nh ),new geographical record ( ng ), and significant differences between estuaries or seasons(*). 

Parasite Deposit number Host E/S P% MI MA
Monogenea
Ligophorus mugilinus UFPB.PLATY02 M. curema PN 13.7 12.8±32.9 1.75±12.7
MM 5.6 9.6±11.8 0.50±3.3
Rainy 10.9 5.3±8.9 0.58±3.3
Dry 9.1 26.4±49.4 2.4±15.8
Digenea
Parahemiurus merus nh, ng UFPB.PLATY01 A. januaria PN 5.4 1.2±0.4 0.06±0.3
MM 28.9* 0.12±1.8* 0.62±1.4*
Rainy 3.8 1.0 0.04±0.1
Dry 25.6* 2.1±1.7 0.54±1.2*
Rhipidocotyle sp.nh A. brasiliensis MM 1.7 19.0±1.0 0.36±2.5
Dry 0.8 19.0±1.4 0.16±1.7
Nematoda
Pharingodonidae gen. sp.1 nh A. brasiliensis PN 1.3 2.0 0.03±0.2
Dry 1.3 2.0 0.03±0.2
Pharingodonidae gen. sp. nh A. brasiliensis PN 1.8 1.2±0.5 0.02±0.2
Dry 1.8 1.2±0.5 0.02±0.2
Copepoda
Acusicola brasiliensis UFPB-7346, 7347, 7348, 7349 A. brasiliensis PN 21 11.9±10.7 2.50±6.9
MM 16.8 11.4±9.2 1.93±5.7
Rainy 43.4* 11.8±10.3 5.12±8.9*
Dry 2.5 10.7±8.3 0.26±2.1
A. januaria nh PN 6.3 2.8±2.0 0.20±0.8
MM 13.4 2.2±1.9 0.30±1.0
Rainy 2.5 2.0±1.4 0.05±0.3
Dry 13.9* 2.4±2.0 0.33±1.1*
Bomolochus xenomelanirisi UFPB-7341 A. brasiliensis PN 0.9 1.0 0.01±0.1
MM 2.2 1.5±0.6 0.03±0.2
Rainy 3.6 1.3±0.5 0.05±0.3
Bomolochus nitidus nh, ng UFPB-7375 M. curema PN 4 1.6±0.5 0.06±0.3
Rainy 2.9 1.5±0.6 0.04±0.2
Dry 1.3 2.0 0.02±0.2
Caligidae gen. sp. M. curema PN 0.8 2.0 0.02±0.2
Dry 1.3 2.0 0.02±0.2
Ergasilus sp. M. curema PN 21.8* 20.8±18.2 4.5±12.0
MM 6.7 33.0±17.3 2.20±9.2
Rainy 24.0 23.1±18.4 5.54±13.3
Ergasilus atafonensis UFPB-7373 M. curema PN 18.5* 19.9±26.4 3.70±13.6
MM 7.8 22.6±27.3 1.70±9.4
Rainy 10.2 2.9±2.3 0.29±1.1
Dry 20.8* 36.0±27.8* 7.48±19.2*
Ergasilus bahiensis UFPB-7372 M. curema PN 9.7 2.5±2.1 0.24±0.9
MM 4.4 2.7±1.3 0.12±0.6
Rainy 11.7 2.5±1.8 0.29±1.0
Ergasilus caraguatubensis UFPB-7374 M. curema PN 4.0 2.2±2.2 0.09±0.6
MM 2.2 2.5±0.7 0.05±0.4
Rainy 5.1 2.3±1.8 0.11±0.6
Isopoda
Artystone sp. nh, ng A. januaria MM 1.3 1.5±0.7 0.02±0.2
Dry 1.1 1.5±0.7 0.02±0.2
Lironeca sp.nh A. januaria PN 0.9 1.0 0.01±0.1
Rainy 1.2 1.0 0.01±0.1
Mothocya argenosa UFPB-7337 A. brasiliensis PN 0.9 1.0 0.01±0.1
MM 1.6 1.0 0.02±0.1
Rainy 3 1.0 0.03±0.2
Mothocya nana nh, ng UFPB-7337 A. brasiliensis PN 1.3 1.0 0.01±0.1
MM 0.5 1.0 0.01±0.7
Rainy 1.8 1.0 0.02±0.1
Dry 0.4 1.0 0.01±0.1
Mothocya omidaptria nh, ng UFPB-7336 A. brasiliensis MM 1.1 1.0 0.01±0.1
Dry 0.8 1.0 0.01±0.1

It is important to emphasize that most of the analyzed hosts were in the juvenile phase; thus, it is possible that the parasite community has been underestimated, since studies point to the positive correlation between the standard host length and the parasite richness, either due to the increase in the time of exposure of the host to infecting stages, or due to the greater availability of space in larger hosts to be colonized by parasites (Poulin and Morand 2004).

Monogeneans are ectoparasites that often present high host specificity (Goater et al. 2014). In the present study, these parasites were observed only in the host Mugil curema. Ligophorus mugilinus (= Pseudohaliotrema mugilinus) (Hargis, 1955) is a parasite restricted to hosts of the family Mugilidae and, according to Sarabeev et al. (2005), is the only species of Ligophorus that is distributed in European and American waters. There are records of this parasite for M. liza in Brazil (Abdallah et al. 2009), M. cephalus in Ukraine (Sarabeev et al. 2005) and M. curema in Venezuela (Fuentes and Nasir 1990) and in Caribbean seas-Puerto Rico (Garcia and Williams 1985). This is the first record of L. mugilinus parasitizing M. curema in Brazil.

The adult digenean Parahemiurus merus (Linton 1910) (Hemiuridae) was found on the gills of the host Anchoa januaria. According to Fernandes et al. (2009), this is cosmopolitan parasite species that was recorded parasitizing the digestive tract of 28 species of host (only in South America), including the hosts Anchoa tricolor and Genypterus brasiliensis from Rio de Janeiro, Southeastern Brazil. Another Digenea observed in the present study was Rhipidocotyle sp., parasitizing Atherinella brasiliensis. Parasites of the genus Rhipidocotyle Diesing, 1858 (Bucephalidae) have been recorded in Brazil, in the digestive tract of the hosts Scomber colias Gmelin, 1789, Euthynnus alletteratus (Rafinesque, 1810), Acestrorhynchus lacustris (Lütken, 1875), Scomberomorus maculatus (Mitchill, 1825), Galeocharax humeralis (Valenciennes, 1824), Salminus brasiliensis (Cuvier, 1816), Salminus hilarii Valenciennes, 1850, Auxis thazard (Lacepède, 1800) and Katsuwonus pelamis (Linnaeus, 1758) (Kohn et al. 2007).

The two morphotypes of nematodes parasitizing Atherinella brasiliensis were identified as members of family Pharyngodonidae, by having oral aperture surrounded by four large cephalic papillae and oesophagical bulb. Nematodes of this family parasitizes the posterior gut of mainly lower vertebrates, with few species in mammals (Anderson 2000). Both morphotypes showed very low infestation values, and for this reason, a more precise identification was not possible due to the lack of available specimens. The low number of adult digeneans and nematodes can be explained by the fact that most of them are not ectoparasites, they were recovered from the gills circumstantially, probably as a consequence of the manipulation of the hosts during fish catching.

Copepods are the most important parasitic crustaceans of fish in the world (Eiras et al. 2016). The copepod Acusicola brasiliensis Amado & Rocha, 1996 (Ergasilidae) has been recorded parasitizing the fish Atherinella brasiliensis, Lile piquitinga and Opisthonema oglinum in the following Brazilian states: Bahia, Espírito Santo, Pará, Paraná and Sergipe (Eiras et al. 2016). Bomolochus xenomelanirisi Carvalho, 1955 (Bomolochidae) was described parasitizing Atherinella brasiliensis in the State of São Paulo. Ergasilus atafonensis Amado & Rocha, 1997 (Ergasilidae) has been described as parasitizing species of the genus Mugil in several Brazilian States (Eiras et al. 2016). The copepods Acusicola brasiliensis and Bomolochus xenomelanirisi parasites of Atherinella brasiliensis and Ergasilus atafonensis, E. bahiensis and E. caragatubensis parasite of M. curema, present previous records from the northeast of Brazil (El-Rashidy and Boxshall 2001, Luque and Tavares 2007, Eiras et al. 2016). Bomolochus nitidus, observed in Mugil curema, had already been recorded in M. cephalus in Arica and Lima, and in M. planatus in Rio de Janeiro (Eiras et al. 2016).

The species diversity of crustaceans parasites of marine fish in South America is about 400 species and 26 families, distributed in a large number of hosts (Eiras et al. 2016). The isopods are the second group of crustaceans with more species of fish parasites (Eiras et al. 2016). They are ectoparasites found on the gills and tegument, being easily visible macroscopically. In the present study, Mothocya nana (Schioedte & Meinert, 1884), M. omidaptria Bruce, 1986 and M. argenosa (Cymothoidae) were observed in Atherinella brasiliensis. Mothocya argenosa has no record of occurrence in Brazil. According to Luque et al. (2013), Mothocya nana was already observed in the state of Rio de Janeiro, in an unidentified host, and M. omidaptria was already observed in the same State, parasitizing the host Hyporhamphus unifasciatus. Thus, this is the first record of Mothocya nana and M. omidaptria parasitizing Atherinella brasiliensis, as well as the first record of Mothocya argenosa in Brazil. The isopod found parasitizing Anchoa januaria was identified as Artystone sp. by having the prehensile pereopods 1-6 and 7 ambulatory, and differentiated pleon and pleotelson. Specimens of Artystonehave been recorded in freshwater fishes in Brazil. Lironeca sp. was also recorded in the host A. januaria, but in the PN. Isopods of the genus have been recorded parasitizing several species of marine fishes in Brazil, including the northeast region (Luque et al. 2013).

The host species that presented the highest number of parasite taxa were Atherinella brasiliensis and Mugil curema, with seven parasite taxa each. Atherinella brasiliensis also presented the highest number of analyzed hosts. Atherinella brasiliensis is considered estuarine resident and habitually live at the mouth of the rivers (Pessanha et al. 2000, Fávaro et al. 2003). This characteristic, together with the great diversity of the estuarine ecosystem, possibly favors the acquisition of parasites by the hosts, which remain for longer in this environment rich in infecting stages. On the other hand, the species Mugil curema is distributed among estuaries and shallow coastal marine regions, being considered a catadrome species, as mature individuals migrate to spawn in the ocean (Ibáñez and Gutiérrez-Benítez 2004); In addition, this species exhibits schooling behavior (Carvalho et al. 2007). Considering all the parasites found in M. curema are monoxenic (they do not require intermediate hosts to complete their cycle), it is possible that the schooling behavior has favored the infestation of these hosts by the recorded parasites.

Regarding differences between the studied estuaries, ten taxa of parasites were recorded in both estuaries, five only in the PN and three only in the MM. Three out of the ten taxa recorded in both estuaries presented significant differences in parasitism indexes: P. merus showed higher values of prevalence, mean intensity and mean abundance in the MM; Ergasilus sp. and E. atafonensis showed higher values of prevalence in the PN. The digenean Parahemiurus merus is a typical gastrointestinal parasite, and its presence on the gills was considered accidental, as previously discussed; thus, its prevalence reported in the present study does not reflect its actual prevalence in the sample, since only the gills of the hosts were examined for parasites. The highest prevalence of Ergasilus sp. and Ergasilus atafonensis in the PN may be related to local features of the hosts and/or environmental factors; the PN is an estuary under strong anthropogenic pressure, while the MM is located inside a protected area. The increased prevalence of parasitic copepods on mugilid fishes from anthropogenically impacted coastal marine systems was reported by Dzikowski et al. (2003), and the authors stated that monoxenous parasites appear to be more adapted to survival in some polluted habitats, and the copepod populations may have been enhanced by possible immune suppression of the fish. All the species found in only one of the two studied estuaries presented low values of prevalence (≤4%) and mean abundance (<1); therefore, it is possible that they could be recorded in the other estuary using greater sampling effort.

Five parasite taxa were observed in the rainy and dry seasons, and three of them presented significant differences between seasons. Acusicola brasiliensis showed higher values of prevalence and mean abundance in the rainy season for the host Atherinella brasiliensis, and in the dry season for the host A. januaria. Parahemiurus merus also presented higher prevalence and abundance in the dry season. Six taxa were observed only in the dry season, and five only in the rainy season. Differences between seasons could be explained by fluctuations on the availability of suitable hosts during different seasons, considering that the abundance and the diversity of fishes are higher in the rainy season in the MM (Xavier et al. 2012).

In conclusion, the present study constitutes the first study on the parasites of fish in estuaries in the Paraíba State, showing new geographical records and hosts for these environments and the Northeast region. This is an important contribution to the knowledge of the local parasite diversity, serving as a basis for future studies that seek to correlate the parasites to the conditions of their hosts, as well as the environmental conditions in which they are inserted.

ACKNOWLEDGMENTS

The authors thank the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for the financing of the PVE/CAPES project (Process 173/2012): “What lessons can be learned from ecological functioning in the estuarine systems of the state of Paraiba? An analysis of the effect of natural and anthropogenic disturbances” and the Science without Borders Program (Special Visiting Researcher). CAPES also funded J. Golzio through a master scholarship. The Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) funded J. Falkenberg and A. Coutinho through an undergraduate scholarship (Scientific Initiation). Thanks also to Saulo Vital for the map.

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Received: December 16, 2016; Accepted: March 08, 2017

Correspondence to: Ana Carolina Figueiredo Lacerda E-mail: acflacerda@dse.ufpb.br

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