New occurrence of Kudoa orbicularis parasitizing the freshwater catfish Trachelyopterus galeatus (Siluriformes: Auchenipteridae) in the Brazlian Amazon regionAbstract
The aim of this was describe an infection by Kudoa orbicularis in freshwater catfish Trachelyopterus galeatus. A sample of 80 specimens of T. galeatus was collected in the municipality of Cachoeira do Arari, Marajó Island, in the state of Pará, Brazil. Pseudocysts were found in the muscle fibers of the epaxial and hypaxial regions of 85.0% of the specimens analyzed, reflecting a high infection rate. The pseudocysts contained spores that were pseudo-square in shape, with a mean length of 4.65 µm (range: 4.04–5.54) and mean width of 1.53 µm (1.56–1.74). Analyses on the morphology of the spores and a partial 934-bp sequence of the SSU rDNA gene confirmed that the microparasite was Kudoa orbicularis. This is the second record of this microparasite in a siluriform host in the Brazilian Amazon region.
Keywords: Freshwater fish; infection; molecular biology; Myxozoa; microparasite
Resumo
O objetivo deste estudo foi descrever a infecção por Kudoa orbicularis em Trachelyopterus galeatus. Foram analisados 80 espécimes de T. galeatus capturados no município de Cachoeira do Arari, ilha de Marajó, estado do Pará, Brasil. A presença de pseudocistos nas fibras musculares das regiões epiaxial e hipoaxial em 85,0% dos exemplares analisados, mostra alto grau de infecção. Os pseudocistos continham esporos de formato pseudoquadrado, medindo 4,65 (4,04-5,54) µm de comprimento e 5,25 (4,78-5,98) µm de largura, com quatro cápsulas polares de tamanho iguais medindo 2,22 (2,05-2,32) µm de comprimento e 1,53 (1,56-1,74) µm de largura. Através das análises morfológicas dos esporos e molecular de uma sequência parcial de 934bps do gene SSU rDNA, confirma que o microparasito é Kudoa orbicularis, sendo este o segundo registro desse microparasito em hospedeiro da ordem Siluriformes da Amazônia brasileira.
Palavras-chave: Peixe de água doce; biologia molecular; infecção; Myxozoa; microparasito
Introduction
The microscopic cnidarians of the subphylum Myxozoa are an important group of parasites of aquatic organisms that infect marine and freshwater vertebrates and invertebrates. They include the majority of the microorganisms that cause diseases in fish (KENT et al., 2001; LOM & DYKOVÁ, 2006).
The myxozoans of the genus Kudoa are typically star-shaped, square, pseudo-square or rounded in apical view, with four or more valves and polar capsules. They are found primarily in the muscle tissue of the host, and can cause postmortem myoliquefaction. These parasites may also infect other types of tissue, such as the brain, integument, kidney, fins, peritoneum, and mesentery (MORAN et al., 1999; SWEARER & ROBERTSON, 1999; WHIPPS et al., 2004; LOM & DYKOVÁ, 2006; CASAL, 2009; KRISTMUNDSSON & FREEMAN, 2014).
The morphological and morphometric analyses that are traditionally used to identify most myxozoan species may not be sufficient to confirm all taxa reliably. This highlights the need for complementary techniques: in particular, molecular biology, which has been widely used to identify fish parasites at species level (CLARK, 2006; MENEZES et al., 2010).
The fisheries of the Amazon region of Brazil are distinct from those of other regions of the country, in terms of the diversity of species harvested, the volume of the catches and the dependence of the local populations on this economic activity (BARTHEM & FABRÉ, 2004). One of the target species in the Amazon basin is the anujá catfish, Trachelyopterus galeatus Linnaeus, 1766, which is found in swamps and under rafts of floating vegetation. This economically valuable siluriform species, also known as the cangati or “cachorrinho de padre”, is an omnivorous fish found throughout South America, where it is an important source of food and income for many riverine communities (BORGES et al., 1999; COSTA-NETO, 2000; SANTOS et al., 2004; FERRARIS JR, 2003; SANTIM et al., 2015; SOUSA et al., 2016).
Trachelyopterus galeatus may be a host for an enormous diversity of pathogens. Parasites are relatively common in freshwater fish, and many cause tissue lesions that not only may be fatal to the fish, but also may reduce the quality and value of the fishery product, as well as being a potential risk to human health (FERRE, 2001; EIRAS et al., 2004; WOO, 2006).
The present report confirms the occurrence of infection by Kudoa orbicularis in T. galeatus from the in the Marajó Island, northern Brazil,. This parasite was found infecting the musculature of the fish, and was identified through a combination of morphological and molecular analyses.
Materials and Methods
A total of 80 specimens of Trachelyopterus galeatus were collected in the region of Cachoeira do Arari, in the Marajó archipelago, state of Pará, northern Brazil (01°00’ S, 48°57’ W) between January 2016 and December 2017. These specimens had a mean total length of 13.00 ± 2.01 cm (range: 10.5–16.5 cm) and mean weight of 50.24 ± 15.64 g (27.97–80.3 g). Specimen collection had previously been authorized by the Brazilian Institute for the Environment and Renewable Natural Resources (IBAMA; through SISBIO, license number 27119-1) and by the Committee for the Ethical Use of Animals in Research of the Federal Rural University of Amazonia (under the number CEUA 013/2014).
After capture, the specimens were transported alive in aerated water from their natural habitat to the Carlos Azevedo Research Laboratory (LPCA) at UFRA, in Belém, state of Pará. In the laboratory, the specimens were maintained in aquaria, in water at a temperature of 28–30 °C. Before necropsy, they were anesthetized using tricaine methanesulfonate (MS-222) diluted in water at a concentration of 50 mg/L.
Following euthanasia, the specimens were first examined under a stereomicroscope to verify the presence of cysts, which were then observed by means of light microscopy. Once the parasitism had been confirmed, small (0.5 cm) samples of muscle tissue were obtained from infected epaxial and hypaxial tissue for common light microscopy and processing for molecular analyses.
For common light microscopy, the parasitized samples were fixed in 95% Davidson solution (ethanol, formaldehyde, acetic acid and distilled water) for 24 hours, embedded in paraffin, and stained with hematoxylin-eosin (HE) and Ziehl-Neelsen (LUNA, 1968). The stained slides and fresh spores were then photographed using a Zeiss Primo Star microscope with an attached Zeiss AxioCam ERc 5s camera, and the AxioVision 5.1 software. Some tissue samples containing cysts were analyzed by means of the differential interference contrast (DIC) technique, using a Zeiss AxioScope A1 microscope with a Zeiss AxioCam 512 color camera.
The fresh spores were measured in micrometers (µm), and the measurements were presented as means with minimum and maximum values between parentheses (LOM & DYKOVÁ, 1992). The prevalence of infection was determined as described by Bush et al. (1997).
For the molecular analysis, the myxozoan spores were collected and fixed in 80% ethanol. The DNA of the spores was extracted using the PureLink® Genomic DNA mini kit (Invitrogen, USA), following the protocol for extraction of “mammalian tissue and mouse/rat tail lysate” provided by the manufacturer. The DNA samples were quantified in a Biodrop Duo spectrophotometer (Biodrop).
Polymerase chain reactions (PCRs) were run to obtain small subunit ribosomal DNA (SSU rDNA), initially using the universal eukaryotic forward primer 18E (HILLIS & DIXON, 1991) and the reverse primer 18R (WHIPPS et al., 2003b). The PCR was run in a final volume of 25 µl, containing 1 x ReddyMix PCR master mix (Thermo Scientific, USA), 75 mM of Tris-HCl (pH 8.8), 20 mM of KCl, 0.1 (v/v) of Nonidet P40, 1.5 mM of MgCl2, 0.2 mM of each nucleotide triphosphate (Thermo Scientific, USA), 10 pmol of each primer, 1.25 U of Taq DNA polymerase (Thermo Scientific, USA) and the DNA template (10-50 ng/µl). The reaction protocol for the primers 18E and 18R consisted of 95 °C for 5 minutes, followed by 35 cycles of 95 °C for 60 seconds, 48 °C (annealing temperature) for 60 seconds and 72 °C for 120 seconds, with a final extension of 72 °C for 10 min.
Subsequently, 3 µl of the PCR mix was subjected to electrophoresis on 1% agarose gel with 1X tris-borate-EDTA (TBE), stained with SYBR® Safe (Invitrogen, USA). The result was viewed under blue light. The PCR products were purified using GFX™ PCR DNA and a gel band purification kit (GE Healthcare, UK), in accordance with the manufacturer’s instructions. The sequencing reactions were conducted using the Big Dye Terminator v3.1 cycle sequencing kit (Applied Biosystems, USA), following the manufacturer’s instructions, in an ABI 3100 genetic analyzer (Applied Biosystems, USA).
The sequences obtained through this procedure were aligned in the BioEdit software (HALL, 1999) and ambiguous bases were clarified using the respective chromatograms. Sequences of the SSU rDNA gene from the myxozoan species deposited in GenBank were aligned in Clustal X 1.8 (THOMPSON et al., 1997), at the default setting, to determine their phylogenetic relationships with the new species described here. High similarity scores in the basic local alignment search tool (BLAST) were used as the criterion for selecting the GenBank sequences for inclusion in the analysis. The jModelTest 0.1.1 software (GUINDON & GASCUEL, 2003; POSADA, 2008) was used to identify the optimal nucleotide substitution model for the dataset.
Bayesian inference was implemented through MrBayes, version 3.1.2 (RONQUIST & HUELSENBECK, 2003) using Markov chain Monte Carlo searches in two simultaneous runs of four chains of 5,000,000 generations, from which every 500th tree was sampled. The first thousand trees were discarded as burn-in, and the posterior probability of each node was calculated from the remaining trees, examined initially in TreeView X (PAGE, 1996). Genetic distances were computed in PAUP* 4.0b1 (SWOFFORD, 2003), using the default p parameter for the SSU rDNA gene.
Results
Morphological description
Common light microscopy revealed the presence of pseudocysts in the skeletal muscle fiber of the epaxial and hypaxial regions of the host specimens analyzed (Figure 1a). The pseudocysts, formed by agglomerations of Kudoa spores, were pseudo-square in shape with rounded edges in the apical view, and had four piriform polar capsules of equal size (Figures 1bc), although it was not possible to confirm the number of coils in the polar filament. The spores were 4.65 µm in length (range: 4.04–5.54) and 5.25 µm in width (4.78–5.98), with polar capsules 2.22 µm long (2.05–2.32) and 1.53 µm wide (1.56–1.74) (Table 1). Overall, 68 (85.0%) of the 80 T. galeatus specimens examined were infected by Kudoa orbicularis.
Photomicrographs of Kudoa orbicularis in Trachelyopterus galeatus: a) Pseudocyst (arrowhead) in the striated skeletal muscle fiber seen using DIC. Scale bar: 100 µm; b) Fresh spores (arrowhead). Scale bar: 5 µm; c) Detail of the spore (apical view) showing the four polar capsules (PC) seen using DIC. Scale bar: 5 µm.
Comparative descriptive measurements (means in μm, and ranges in parentheses) of Kudoa orbicularis and other species that parasitize the musculature of their fish hosts.
Histology
The histological analysis indicated that the pseudocysts had developed in the intracellular region of the muscle fibers. They had replaced the sarcoplasm of the fiber segments completely with Kudoa orbicularis spores, thus causing deformation of these structures, as well as some adjacent muscle fibers (Figures 2c). The spores were enveloped in a fine layer of sarcolemma (Figure 2c). The pseudocysts were located in the cytoplasm of the host fibers (Figure 2a), although no inflammatory response to the infection was observed in the host. Nor were any clinical symptoms confirmed, including myoliquefaction.
Photomicrographs of Kudoa orbicularis infecting Trachelyopterus galeatus: a) Pseudocysts (*) located in the cytoplasm (arrowheads) of the muscle fibers stained with HE. Scale bar: 20 µm; b) Histological section of the pseudocysts stained with HE (*). Scale bar: 20 µm; c) Pseudocyst (*) deforming the neighboring fibers (nf) and pseudocyst enveloped by a fine layer of sarcolemma (arrows) stained with Ziehl Neelsen. Scale bar: 20 µm.
Taxonomic Summary
Phylum Cnidaria Hatschek, 1888
Class Myxosporea Bütschli, 1881
Order Multivalvulida Shulman, 1959
Family Kudoidae Meglitsch, 1960
Genus Kudoa Meglitsch, 1947
Species: Kudoa orbicularis Azevedo et al., 2016
Type host: Trachelyopterus galeatus Linnaeus, 1766
Infection site: Striated skeletal musculature.
Type locality: Brazil, state of Pará, municipality of Cachoeira do Arari, Marajó Island (01°00’ S, 48°57’ W).
Prevalence: 85.0% (68/80) of the hosts examined were infected.
Phylogenetic analysis
A partial, 934 base-pair sequence of the SSU rDNA gene was obtained from the K. orbicularis spores found in the musculature of T. galeatus. This sequence was deposited in GenBank under accession number MK204656. Two clades, named A and B, were identified in the phylogenetic analysis (Figure 2). Clade A was divided into two subclades formed exclusively by marine Kudoa species, with the exception of K. orbicularis (AZEVEDO et al., 2016) and Kudoa amazonica (VELASCO et al., 2019), which clustered together with the other Kudoa species analyzed, with high nodal (posterior probability) support. In the phylogenetic analyzes Kudoa amazonica was a sister taxon of K.orbicularis.
The Kudoa species of clade A are found almost exclusively in the muscle tissues of their hosts, which are predominantly fish of the order Cichliformes, with tissue tropism in the musculature. However, some Kudoa species parasitize other types of tissue, such as the organs of the digestive system (esophagus and intestine), which is parasitized by Kudoa dianae (AF414692) and Kudoa cookii (JX090294); and the central nervous system (neurons and brain), which is infected by Kudoa neurophila (AY172511), Kudoa chaetodoni (DQ519387), Kudoa prunusi (AB573715), Kudoa lemniscati (JQ026222), and Kudoa lethrini (DQ519388). The Kudoa species that infect the digestive system were allocated to subclade A1 in the present analysis, together with the Kudoa species that infect the muscle tissue of host species belonging to a variety of fish orders. The Kudoa species that parasitize the nervous system present tropism that is characteristic of this type of tissue, and cluster in subclade A2, together with Kudoa igami (AB844444) and Kudoa thalassomi (AB844443), which infect the musculature. All the species in this subclade parasitize fish of the Cichliformes, and thus appear to have specialized in hosts of this order.
Clade B is formed by species of the genus Unicapsula Davis, 1924, a member of the order Multivalvulida Shulman, 1959. Most of these species infect the skeletal musculature of their hosts, except for Unicapsula fatimae (KT894108), which is a parasite of the esophagus. Once again, however, all the host species of this clade are fish of the order Cichliformes (Figure 3).
Phylogenetic tree generated through Bayesian inference (BI) performed on the partial sequences of the SSU rDNA gene of Kudoa orbicularis retrieved from Trachelyopterus galeatus in the present study and from other closely-related myxozoans. The GenBank accession numbers are shown next to the species names. The numbers at each node are the posterior probabilities calculated through BI. The species analyzed in the present study is highlighted in bold type. Abbreviations: Mcl = musculature; DS = digestive system; CNS = central nervous system; S = Siluriformes; P = Cichliformes; T = Tetraodontiformes; G = Gadiformes; Sa = Salmoniformes; Sc = Scorpaeniformes.
The sequences were realigned for pairwise comparison of a subset of the Kudoa species that parasitize the musculature of their hosts. The minimum p distance recorded in the present study (Table 2) was 3.5% between the K. orbicularis analyzed here and K. orbicularis (KM192365). All other distances were over 4.0%, reaching a maximum of 6.0%, in the case of Kudoa whippsi and Kudoa empressmichikoae.
Pairwise p distances among the Kudoa species that parasitize the muscle tissues of their hosts.
Discussion
Kudoa orbicularis was described from the musculature of specimens of the cichlid Chaetobranchopsis orbicularis, a Cichliformes collected from the Arari River, in Marajó Island, Brazil (AZEVEDO et al., 2016). This is same locality from which the T. galeatus specimens analyzed in the present study were collected. The morphological features of the K. orbicularis spores and polar capsules found in T. galeatus were closely similar to those described by Azevedo et al. (2016) and Sindeaux-Neto et al. (2017) in the K. orbicularis specimens obtained from the host fish C. orbicularis. Despite being the same species, minor morphological differences in the size of myxozoan spores are typically found in different hosts (KOVALEVA et al., 1979; YANAGIDA et al., 2004). The K. orbicularis spores are much smaller than those of K.amazonica, Kudoa islandica, Kudoa inornata and Kudoa ogawai, although the polar capsules are larger than those of K. islandica (Table 1).
The spores of Kudoa quadricornis, infecting Carangoides fulvoguttatus (WHIPPS et al., 2003b), and Kudoa minithyrsites in Pempheris ypsilychnus (WHIPPS et al., 2003a), were observed developing intracellularly in the microfibrils of the host, as observed with K. orbicularis in the present study. The histology of K. orbicularis in the present study was similar to that of K. inornata observed in the skeletal musculature of Cynoscion nebulosus by Dyková et al. (2009), who also described a fine layer of sarcolemma enveloping the mature spores within the fibers. Similar configurations were described by Dyková et al. (2002) in the case of K. dianae infecting the esophageal musculature of Sphoeroides annulatus, and by Shirakashi et al. (2014) in Kudoa igami infecting the muscle tissue of Calotomus japonicus. In both cases, no evidence of inflammation or any other response to the presence of the parasite was observed in the host. However, Azevedo et al. (2016) and Sindeaux-Neto et al. (2017) did observe inflammation in the muscle tissue infected by K. orbicularis, as well as lethargic behavior in the host fish, including irregular tail movements and immobility, although these patterns were not observed in T. galeatus in the present study.
The similarities in the morphological characteristics of the K. orbicularis specimens observed in the present study, in comparison with the original description of this species (AZEVEDO et al., 2016), together with the muscle tissue tropism, the freshwater habit of the host and the geographical location of the two cases, all confirm the species identification. In addition to identification of Kudoa species based on morphological and morphometric parameters, a number of recent descriptions have also included molecular comparisons, which not only provide a more reliable diagnosis, but also enable analysis of phylogenetic patterns (EIRAS et al., 2014).
The phylogenetic tree derived from the molecular analyses that were applied in the present study (Figure 3) also confirmed the proximity of the K. orbicularis found in T. galeatus to the K. orbicularis sequence described by Azevedo et al. (2016), with maximum (100%) branch support and K. amazonica as a sister taxon, corroborated by the findings of Velasco et al. (2019). In addition to this significant genetic similarity, this is the only Kudoa species of clade A known to parasitize a freshwater host, in contrast with all the other Kudoa species included in this clade, which infect marine hosts. Hervio et al. (1997) observed that Kudoa species tend to group according to geographical location, rather than the morphological similarity of the spores, as confirmed in the present study.
In the other subclades, some Kudoa species were grouped according to host specificity, tissue tropism and/or geographical region. The second cluster of subclade A1, for example, groups 07 Kudoa species that parasitize the muscle tissue of perciform fish, but are from distinct localities. The third cluster is formed by two species (K. quadricornis and K. paraquadricornis) that parasitize the muscle tissue of perciform fish: in this case, from the same locality, Heron Island in Australia. The first of these clusters had 92% branch support, and the second had 100% support.
The findings from the present study thus support the hypothesis that the tissue tropism found in some Kudoa species has a genetic component, although there are also significant deviations (BURGER et al., 2007). In the fourth cluster, for example, which includes the Kudoa species not grouped through any of these factors, the parasites infect different types of tissue, and are found in a broad diversity of fish orders and geographical localities, with branch support of only 90%. However, what these species do have in common is the marine habitat of their hosts. Subclade A2, which has branch support of 64%, includes Kudoa species that infect different types of tissue, but is supported by the specificity of its hosts, such that all these parasites are found in perciform fish.
The present study confirmed that K. orbicularis may infect fish hosts belonging to different orders, which indicates that this microparasite is not host-specific. Although many Kudoa species are host-specific, a number of species are known to infect different types of host. These species include Kudoa hypoepicardialis, which has been found infecting seven different host species belonging to seven different genera and families (BLAYLOCK et al., 2004), while Kudoa thyrsites is known to infect fish of different families and is thought to have cosmopolitan distribution (WHIPPS & KENT, 2006; JONES et al., 2016).
The relationships among Kudoa species, based on their morphology, tissue tropism, habitat (freshwater vs. saltwater) and geographical region, and the results from the phylogenetic analysis of the present study conclusively support the conclusion that T. galeatus was infected by K. orbicularis, a species described previously in C. orbicularis (AZEVEDO et al., 2016). This is the second record of the occurrence of a Kudoa parasite in a (Siluriformes host in the Brazilian Amazon region.
References
-
Azevedo C, Rocha S, Matos E, Oliveira E, Matos P, Al-Quraishy S, et al. Ultrastructural and phylogenetic description of Kudoa orbicularis n. sp. (Myxosporea: Multivalvulida): a parasite infecting the muscle of the fish Chaetobranchopsis orbicularis (Teleostei: Cichlidae) in the Amazon Region. J Eukaryot Microbiol 2016; 63(1): 27-36. http://dx.doi.org/10.1111/jeu.12244 PMid:26095978.
» http://dx.doi.org/10.1111/jeu.12244 - Barthem RB Fabré NN. Biologia e diversidade dos recursos pesqueiros da Amazônia. In: Rufino ML, editor. A pesca e os recursos pesqueiros na Amazônia brasileira Manaus: Ibama/ProVárzea; 2004. p. 17-62.
-
Blaylock RB, Bullard SA, Whipps CM. Kudoa hypoepicardialis n. sp. (Myxozoa: Kudoidae) and associated lesions from the heart of seven perciform fishes in the northern Gulf of Mexico. J Parasitol 2004; 90(3): 584-593. http://dx.doi.org/10.1645/GE-161R PMid:15270103.
» http://dx.doi.org/10.1645/GE-161R - Borges SAGV Gurgel HCB Canan B. Estrutura populacional de Parauchenipterus galeatus Linnaeus 1766 (Siluriformes Auchenipteridae) da Lagoa do Jiqui Parnamirim Rio Grande do Norte. Rev Ceres 1999; 46(264): 209-218.
-
Burger MAA, Cribb TH, Adlard RD. Patterns of relatedness in the Kudoidae with descriptions of Kudoa chaetodoni n. sp. and K. lethrini n. sp. (Myxosporea: Multivalvulida). Parasitology 2007; 134(5): 669-681. http://dx.doi.org/10.1017/S0031182006001995 PMid:17234042.
» http://dx.doi.org/10.1017/S0031182006001995 -
Bush AO, Lafferty KD, Lotz JM, Shostak AW. Parasitology meets ecology on its own terms: Margolis et al. revisited. J Parasitol 1997; 83(4): 575-583. http://dx.doi.org/10.2307/3284227 PMid:9267395.
» http://dx.doi.org/10.2307/3284227 - Casal G. Microsporidioses e Mixosporidioses da ictiofauna portuguesa e brasileira: caracterização ultrastrutural e filogenética [Tese]. Portugal: Universidade do Porto; 2009.
- Casal G Matos E Matos P Azevedo C. Ultrastructural description of a new myxosporean parasite Kudoa aequidens sp. n. (Myxozoa Myxosporea) found in the sub-opercular musculature of Aequidens plagiozonatus (Teleostei) from the Amazon liver. Acta Protozool 2008; 47: 135-141.
-
Clark TG. Molecular approaches and techniques. In: Woo PTK, editor. Fish diseases and disorders: protozoan and metazoan infections 2nd ed. Oxfordshire: Cab International; 2006. p. 725-752. http://dx.doi.org/10.1079/9780851990156.0725
» http://dx.doi.org/10.1079/9780851990156.0725 - Costa-Neto EM. Conhecimento e usos tradicionais de recursos faunísticos por uma comunidade afro-brasileira. Resultados preliminares. Interciencia 2000; 25(9): 423-431.
-
Dyková I, Fajer Avila EJ, Fiala I. Kudoa dianae sp. n. (Myxosporea: Multivalvulida) a new parasite of bullseye puffer Sphoeroides annulatus (Tetraodontiformes: Tetraodontidae). Folia Parasitol (Praha) 2002; 49(1): 17-23. http://dx.doi.org/10.14411/fp.2002.006 PMid:11993546.
» http://dx.doi.org/10.14411/fp.2002.006 -
Dyková I, Buron I, Fiala I, Roumillat WA. Kudoa inornata sp. n. (Myxosporea: Multivalvulida) from the skeletal muscles of Cynoscion nebulosus (Teleostei: Sciaenidae). Folia Parasitol (Praha) 2009; 56(2): 91-98. http://dx.doi.org/10.14411/fp.2009.014 PMid:19606785.
» http://dx.doi.org/10.14411/fp.2009.014 - Eiras JC Pavanelli GC Takemoto RM. Henneguya paranaensis sp. n. (Myxozoa Myxobolidae) a parasite of the teleost fish Prochilodus lineatus (Characiformes Prochilodontidae) from the Paraná river Brazil. Bull Eur Assoc Fish Pathol 2004; 24(6): 308-311.
-
Eiras JC, Saraiva A, Cruz C. Synopsis of the species of Kudoa Meglitsch 1947 (Myxozoa: Myxosporea: Multivalvulida). Syst Parasitol 2014; 87(2): 153-180. http://dx.doi.org/10.1007/s11230-013-9461-4 PMid:24474038.
» http://dx.doi.org/10.1007/s11230-013-9461-4 - Ferraris CJ Jr. Family Auchenipteridae. In: Reis RE, Kullander SO, Ferraris CJ Jr, editors Check list of the freshwater fishes of South and Central America Porto Alegre: Edipucrs; 2003. p. 470-482.
- Ferre I. Anisakiosis y otras zoonosis parasitarias transmitidas por consume de pescado. AquaTIC (Zaragoza) 2001; 14(6): 1-21.
-
Guindon S, Gascuel O. A simple fast and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 2003; 52(5): 696-704. http://dx.doi.org/10.1080/10635150390235520 PMid:14530136.
» http://dx.doi.org/10.1080/10635150390235520 - Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT. Nucleic Acids Symp Ser 1999; 41: 95-98.
-
Hervio DML, Khattra J, Devlin RH, Kent ML, Sakanari J, Yokoyama H. Taxonomy of Kudoa species (Myxosporea) using a small-subunit ribosomal DNA sequence. Can J Zool 1997; 75(12): 2112-2119. http://dx.doi.org/10.1139/z97-846
» http://dx.doi.org/10.1139/z97-846 -
Hillis DM, Dixon MT. Ribosomal DNA: molecular evolution and phylogenetic inference. Q Rev Biol 1991; 66(4): 411-453. http://dx.doi.org/10.1086/417338 PMid:1784710.
» http://dx.doi.org/10.1086/417338 -
Jones SRM, Cho S, Nguyen J, Mahony A. Acquired resistance to Kudoa thyrsites in Atlantic salmon Salmo salar following recovery from a primary infection with the parasite. Aquaculture 2016; 451: 457-462. http://dx.doi.org/10.1016/j.aquaculture.2015.10.002
» http://dx.doi.org/10.1016/j.aquaculture.2015.10.002 -
Kasai A, Li Y, Mafie E, Sato H. Morphological and molecular genetic characterization of two Kudoa spp. K. musculoliquefaciens and K. pleurogrammi n. sp. (Myxosporea: Multivalvulida) causing myoliquefaction of commercial marine fish. Parasitol Res 2016; 115(5): 1883-1892. http://dx.doi.org/10.1007/s00436-016-4928-2 PMid:26822736.
» http://dx.doi.org/10.1007/s00436-016-4928-2 -
Kent ML, Andree KB, Bartholomew JL, El-Matbouli M, Desser SS, Devlin RH, et al. Recent Advances in Our Knowledge of the Myxozoa. J Eukaryot Microbiol 2001; 48(4): 395-413. http://dx.doi.org/10.1111/j.1550-7408.2001.tb00173.x PMid:11456316.
» http://dx.doi.org/10.1111/j.1550-7408.2001.tb00173.x - Kovaleva AA Shulman SS Yakovlev VN. Myxosporidia of the genus Kudoa (Myxosporidia Multivalvulida) of the Atlantic Ocean basin. In: Trudy Zoologicheskogo Instituta – TZI. Systematics and ecology of sporozoans and cnidosporidians Vol. 87. Leningrado: TZI; 1979. p. 42-64.
-
Kristmundsson Á, Freeman MA. Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland. Int J Parasitol Parasites Wildl 2014; 3(2): 135-146. http://dx.doi.org/10.1016/j.ijppaw.2014.06.001 PMid:25161912.
» http://dx.doi.org/10.1016/j.ijppaw.2014.06.001 - Lom J Dyková I. Protozoan parasites of fishes Amsterdam: Elsevier; 1992. (Development in Aquaculture and Fisheries Science; Vol. 26).
-
Lom J, Dyková I. Myxozoan genera: Definition and notes on taxonomy life-cycle terminology and pathogenic species. Folia Parasitol (Praha) 2006; 53(1): 1-36. http://dx.doi.org/10.14411/fp.2006.001 PMid:16696428.
» http://dx.doi.org/10.14411/fp.2006.001 - Luna LG. Manual of histologic staining methods of the armed forces institute of pathology 3th ed. New York: McGraw-Hill; 1968.
-
Menezes PJ, Lupatini M, Antoniolli ZI, Blume E, Junges E, Manzoni CG. Variabilidade genética na região its do rDNA de isolados de Trichoderma spp. (Biocontrolador) e Fusarium oxysporum f. sp. Chrysanthemi. Cienc Agrotec 2010; 34(1): 132-139. http://dx.doi.org/10.1590/S1413-70542010000100017
» http://dx.doi.org/10.1590/S1413-70542010000100017 -
Moran JDW, Whitaker DJ, Kent ML. A review of the myxosporean genus Kudoa Meglitsch 1947 and its impact on the international aquaculture industry and commercial fisheries. Aquaculture 1999; 172(1-2): 163-196. http://dx.doi.org/10.1016/S0044-8486(98)00437-2
» http://dx.doi.org/10.1016/S0044-8486(98)00437-2 -
Page RDM. Tree view: an application to display phylogenetic trees on personal computers. Comput Appl Biosci 1996; 12(4): 357-358. http://dx.doi.org/10.1093/bioinformatics/12.4.357 PMid:8902363.
» http://dx.doi.org/10.1093/bioinformatics/12.4.357 -
Posada D. jModelTest: phylogenetic model averaging. Mol Biol Evol 2008; 25(7): 1253-1256. http://dx.doi.org/10.1093/molbev/msn083 PMid:18397919.
» http://dx.doi.org/10.1093/molbev/msn083 -
Ronquist F, Huelsenbeck JP. MrBayes 3: bayesian phylogenetic inference under mixed models. Bioinformatics 2003; 19(12): 1572-1574. http://dx.doi.org/10.1093/bioinformatics/btg180 PMid:12912839.
» http://dx.doi.org/10.1093/bioinformatics/btg180 - Santim M Lopes TM Baggio MM Agostinho AA Bialetzki A. Mudanças ontogênicas no trato digestório e na dieta de Trachelyopterus galeatus. Bol Inst Pesca 2015; 41(1): 57-68.
- Santos GM Merona B Juras AA Jégu M. Peixes do Baixo Rio Tocantins: 20 anos depois da Usina Hidrelétrica Tucuruí Brasília: Eletronorte; 2004. 216 p.
-
Shirakashi S, Yamane K, Ishitani H, Yanagida T, Yokoyama H. First report of Kudoa species in the somatic muscle of the Japanese parrotfish Calotomus japonicus (Scaridae) and a description of Kudoa igami n. sp. (Myxozoa: Multivalvulida). Parasitol Res 2014; 113(7): 2515-2524. http://dx.doi.org/10.1007/s00436-014-3901-1 PMid:24770717.
» http://dx.doi.org/10.1007/s00436-014-3901-1 -
Sindeaux-Neto JL, Velasco M, Santos P, Matos P, Matos E. Infecção por Kudoa orbicularis (Myxozoa: Multivalvulidae) na musculatura de Chaetobranchopsis orbicularis Steindachner 1875 oriundo da Ilha de Marajó na região Amazônica do Brasil. Arq Bras Med Vet Zootec 2017; 69(6): 1601-1606. http://dx.doi.org/10.1590/1678-4162-8989
» http://dx.doi.org/10.1590/1678-4162-8989 -
Sousa DG, Mendes NCB, Pereira LJG, Fernandes SCP, Bentes BS. Estrutura populacional e reprodução do Anujá Trachelyopterus galeatus (Linnaeus 1766) em uma área de uso sustentável da Zona Costeira Amazônica. Biota Amazôn 2016; 6(2): 41-49. http://dx.doi.org/10.18561/2179-5746/biotaamazonia.v6n2p41-49
» http://dx.doi.org/10.18561/2179-5746/biotaamazonia.v6n2p41-49 -
Swearer SE, Robertson DR. Life history pathology and description of Kudoa ovivora n. sp. (Myxozoa Myxosporea): an ovarian parasite of Caribbean labroid fishes. J Parasitol 1999; 85(2): 337-353. http://dx.doi.org/10.2307/3285645 PMid:10219318.
» http://dx.doi.org/10.2307/3285645 - Swofford DL. PAUP*. Phylogenetic analysis using parsimony (*and other methods) v. 4.0 beta 10. Sunderland: Sinauer Associates; 2003.
-
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997; 25(24): 4876-4882. http://dx.doi.org/10.1093/nar/25.24.4876 PMid:9396791.
» http://dx.doi.org/10.1093/nar/25.24.4876 -
Velasco M, Sindeaux-Neto JL, Videira M, Nascimento LCS, Gonçalves EC, Matos E. Kudoa amazonica n. sp. (Myxozoa; Multivalvulida) a parasite of the esophageal musculature of the freshwater catfish Hypophthalmus marginatus (Siluriformes: Pimelodidae) from a river of the Amazon region. Microb Pathog 2019; 130: 247-252. http://dx.doi.org/10.1016/j.micpath.2019.03.017 PMid:30898656.
» http://dx.doi.org/10.1016/j.micpath.2019.03.017 -
Whipps CM, Adlard RD, Bryant MS, Kent ML. Two unusual myxozoans Kudoa quadricornis n. sp. (Multivalvulida) from the muscle of goldspotted trevally (Carangoides fulvoguttatus) and Kudoa permulticapsula n. sp. (Multivalvulida) from the muscle of spanish mackerel (Scomberomorus commerson) from the Great Barrier Reef Australia. J Parasitol 2003a; 89(1): 168-173. http://dx.doi.org/10.1645/0022-3395(2003)089[0168:TUMKQN]2.0.CO;2 PMid:12659322.
» http://dx.doi.org/10.1645/0022-3395(2003)089[0168:TUMKQN]2.0.CO;2 -
Whipps CM, Adlard RD, Bryant MS, Lester RJG, Findlav V, Kent ML. First report of three Kudoa species from eastern Australia: Kudoa thyrsites from mahi mahi (Coryphaena hippurus) Kudoa amamiensis and Kudoa minithyrsites n. sp from sweeper (Pempheris ypsilychnus). J Eukaryot Microbiol 2003b; 50(3): 215-219. http://dx.doi.org/10.1111/j.1550-7408.2003.tb00120.x PMid:12836879.
» http://dx.doi.org/10.1111/j.1550-7408.2003.tb00120.x -
Whipps CM, Grossel G, Adlard RD, Yokoyama H, Bryant MS, Munday BL, et al. Phylogeny of the Multivalvulidae (Myxozoa: Myxosporea) based on comparative ribosomal DNA sequence analysis. J Parasitol 2004; 90(3): 618-622. http://dx.doi.org/10.1645/GE-153R PMid:15270109.
» http://dx.doi.org/10.1645/GE-153R -
Whipps CM, Kent ML. Phylogeography of the cosmopolitan marine parasite Kudoa thyrsites (Myxozoa: Myxosporea). J Eukaryot Microbiol 2006; 53(5): 364-373. http://dx.doi.org/10.1111/j.1550-7408.2006.00114.x PMid:16968454.
» http://dx.doi.org/10.1111/j.1550-7408.2006.00114.x -
Woo PTK. Fish diseases and disorders protozoan and metazoan infections 2nd ed. UK: CAB International; 2006. http://dx.doi.org/10.1079/9780851990156.0000
» http://dx.doi.org/10.1079/9780851990156.0000 -
Yanagida T, Nomura Y, Kimura T, Fukuda Y, Yokoyama H, Ogawa K. Molecular and morphological redescriptions of enteric Myxozoans Enteromyxum leei (formerly Myxidium sp. TP) and Enteromyxum fugu comb. n. (syn. Myxidium fugu) from cultured tiger puffer. Fish Pathol 2004; 39(3): 137-143. http://dx.doi.org/10.3147/jsfp.39.137
» http://dx.doi.org/10.3147/jsfp.39.137 -
Yokoyama H, Yanagida T, Shirakashi S. Kudoa ogawai n. sp. (Myxozoa: Multivalvulida) from the trunk muscle of Pacific barrelfish Hyperoglyphe japonica (Teleostei: Centrolophidae) in Japan. Parasitol Res 2012; 110(6): 2247-2254. http://dx.doi.org/10.1007/s00436-011-2756-y PMid:22173453.
» http://dx.doi.org/10.1007/s00436-011-2756-y
Publication Dates
-
Publication in this collection
29 July 2019 -
Date of issue
Jul-Sep 2019
History
-
Received
12 Mar 2019 -
Accepted
22 May 2019
