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Cardiovascular flukes (Trematoda: Spirorchiidae) in Caretta caretta Linnaeus, 1758 from the Mediterranean Sea

Parasites & Vectors volume 10, Article number: 467 (2017) Cite this article

Abstract

Background

The northern Adriatic Sea represents one of the most important neritic foraging grounds for the loggerhead sea turtle Caretta caretta L. in the Mediterranean Sea. Four genera of blood flukes with variable prevalence and pathogenic impact have been reported worldwide in this species. Hapalotrema Looss, 1899 and Amphiorchis Price, 1934 are the only two genera reported in Mediterranean waters; however, updated data describing spirorchiidiasis in the central and eastern Mediterranean and infection prevalence are still lacking. This work aimed to investigate the presence and pathology of spirorchiidiasis in C. caretta in the Mediterranean Sea.

Methods

One hundred sixty-eight animals stranded along the northwestern Adriatic coast between 2009 and 2015 were submitted to necropsy and subsequent analyses for the detection of adult flukes, detection of eggs in the faeces and spleen and histopathology. Molecular analyses were carried out on hosts (mitochondrial D-loop) and parasites (28S gene and ITS2 spacer) to trace the turtle origins and identify the fluke phylogenetic relationships.

Results

Spirorchiidiasis was detected in 16.7% of the animals. Hapalotrema mistroides (Monticelli, 1899) and Neospirorchis sp. were found in twenty-six and ten cases, respectively. Adult flukes were found in six cases, while eggs were detectable through copromicroscopic examination for all infected turtles, and the results for the detection of eggs in the spleen agreed with the copromicroscopic analysis. Only mild lesions were observed. Eggs of types 1 and 3 were grossly visible in the gastrointestinal mucosa, vasculitis was rarely observed in the heart and great vessels, and multifocal granulomas were widespread in the tissues. Molecular identification unambiguously assigned the spirorchiid samples to H. mistroides and Neospirorchis sp. Genetic characterization of loggerhead mtDNA pointed to a Mediterranean origin of the turtle hosts.

Conclusion

This survey provides new data on the spread of spirorchiidiasis in the Mediterranean loggerhead sea turtle population and reports for the first time the presence of Neospirorchis spp. in this basin. The infections did not have a causal effect on the death nor a strong impact on the general health status of the animals.

Background

Infection by blood flukes of the family Spirorchiidae Stunkard, 1921 causes morbidity and mortality in marine turtle populations worldwide. The presence of adult flukes in the circulatory system of infected animals and the embolization of eggs through host vessels leads to lesions of varying severity, including arteritis, thrombosis, aneurysms of the great vessels and disseminated granulomas in all body districts [1,2,3].

Six genera of spirorchiids are currently recognized as parasites of marine turtles worldwide: Hapalotrema Looss, 1899; Neospirorchis Price, 1934; Carettacola Manter & Larson, 1950; Amphiorchis Price, 1934; Learedius Price, 1934; and Monticellius Mehra, 1939. Most of the reports of spirorchiidiasis in the marine environment concern the green turtle (Chelonia mydas Linnaeus, 1758); however, the infection is also well documented in the loggerhead sea turtle (Caretta caretta Linnaeus, 1758) in which species of the genera Hapalotrema, Neospirorchis, Carettacola and Amphiorchis have been reported.

Studies on the prevalence of infection in C. mydas report high percentages of positivity worldwide, ranging from 80 to 100% from Australia to Florida (USA) [3,4,5,6,7,8,9]. Similar surveys carried out on C. caretta from the north-western Atlantic region describe the prevalence as ranging between 33 and 96% [1, 4].

The genus Hapalotrema is globally distributed and is described in Florida and Australia [1, 4, 10,11,12,13]. Three species, i.e. H. synorchis Luhman, 1935, H. pambanensis Gupta & Mehrotra, 1981 and H. mistroides (Monticelli, 1989), have been reported in loggerhead sea turtles from both Florida and western Australia. Species of Neospirorchis have been isolated from C. caretta in the north-western Atlantic region [1, 11, 14, 15]. Neospirorchis pricei Manter & Larson, 1950 was morphologically identified by Manter & Larson [14] and by Stacy [11]; however, in the latter study molecular and phylogenetic analyses revealed the presence of other unidentified species among the collected specimens with different localization in the definitive hosts [11]. Species of the genus Carettacola have also been reported from the western Atlantic coast [4, 14], whereas there is only one report of Amphiorchis in C. caretta from the Mediterranean Sea [16].

Few descriptions of spirorchiids in loggerhead sea turtles and green turtles exist for the Mediterranean area, and information on infection prevalence is not available. In the late nineteenth century, Monticelli described the blood fluke Mesogonimus constrictus (Leared, 1862) (syn. Hapalotrema mistroides) in a specimen of C. caretta (syn. Thalassochelys caretta Bonaparte, 1838) from the Gulf of Naples, off Italy [17], and the same species was reported by other authors in both loggerhead and green turtles from the Egyptian coast a few years later [18,19,20,21]. Recently, Santoro et al. [22] described severe lesions due to H. mistroides infection in a loggerhead sea turtle stranded along the Italian Tyrrhenian coastline. Amphiorchis spp. associated with severe disease were recently reported by Cribb et al. [16] in neonate loggerhead sea turtles kept in a facility in Valencia, Spain. No reports of the genera Neospirorchis and Carettacola are available for the Mediterranean Basin.

Methods for postmortem diagnosis include gross and microscopic observations of adult flukes, egg masses, and related lesions in the organs, tissues and vessels [2]. Other laborious techniques can be used to detect adult flukes in blood and organs [23] and to search for spirorchiid eggs in the spleen [7]; copromicroscopic examination has also been used to detect the presence of eggs in faecal material [1].

Parasite identification is achieved through observations of morphological features. However, intact adult parasites are often difficult to obtain from stranded animals, and success also depends on the preservation status of the carcasses [4]. The eggs represent the most resistant stage and have been classified into three types [1]: eggs with bipolar filaments (type 1) are attributed to different genera, i.e. Hapalotrema, Learedius, Monticellius and Amphiorchis; eggs with monopolar filament (type 2) are described for Carettacola; and round eggs (type 3) are attributed to Neospirorchis [1, 24]. Thus, egg morphology alone is a helpful but limited tool for parasite identification [4]. Molecular approaches are therefore important for overcoming the limits of morphological identification and are the basis for analyses of phylogenetic relationships within the family Spirorchiidae [11, 16, 25, 26]. Considering these factors, the aims of this work were to (i) obtain prevalence data on spirorchiidiasis in the central Mediterranean population of C. caretta using different diagnostic approaches; (ii) evaluate their pathogenic impacts on the host; and (iii) increase our knowledge for the identification of blood flukes by morphological and molecular methods.

Methods

Between June 2009 and November 2015, 168 loggerhead sea turtles were found stranded and dead along the north-western Adriatic coast of Italy from Grado (Udine Province; 45°41′N, 13°24′E) to Riccione (Rimini Province; 44°00′N, 12°39′E). Necropsy and parasitological examination were performed on the carcasses at the Department of Comparative Biomedicine and Food Sciences and the Department of Animal Medicine, Productions and Health of Padova University (Italy), respectively. Permission for the execution of necropsies on stranded sea turtles was endorsed by the local health authority to the University of Padova.

Anatomopathological analyses

Necropsies were performed following guidelines given by Flint et al. [2] and Poppi et al. [27]. Before starting the dissections, morphometric data were collected that included SCL (straight carapace length) measurements. A body condition score (BCS) was assigned to the carcasses after evaluation of the adipose tissue covering the ventral muscles. In animals that were freshly dead (n = 11) or in moderate decomposition (n = 99), all organs (adrenal gland, gastrointestinal tract, heart and major vessels, kidney, liver, lung, gonads, pancreas, salt gland, spleen, thyroid, thymus and urinary bladder) were separately observed to locate macroscopic vascular lesions or egg masses. The skull was opened for the examination of the brain only in fresh carcasses. In poorly preserved carcasses (n = 58), whenever possible, the heart, major vessels, gastrointestinal tract, and spleen were considered for gross examination.

Tissue samples (adrenal gland, n = 16; gastrointestinal tract, n = 66; heart and major vessels, n = 37; kidney, n = 47; liver, n = 45; lung, n = 42; gonads, n = 18; pancreas, n = 15; salt gland, n = 3; spleen, n = 52; thyroid, n = 15; thymus, n = 44; urinary bladder, n = 8) were collected, stored in 10% neutral buffered formalin, embedded in paraffin and sectioned at 4 μm for histological observation. The sections were stained with haematoxylin and eosin (HE) and observed under light microscopy (Olympus BX40F-3, Tokyo, Japan).

Parasitological analyses

Stool samples (n = 168) and organs (gastrointestinal tract, n = 126, spleen, n = 64, heart and major vessels, n = 140) were collected according to carcass conditions and thoroughly analysed for the presence of blood flukes and their eggs.

Faecal samples were collected from the terminal portion of the intestine in all animals. An aliquot of each sample was stored at -20 °C for molecular analysis, while another aliquot (2–5 g) was submitted to qualitative copromicroscopic analysis to search for eggs. A common centrifugal sedimentation/flotation technique was applied using a high-density solution (sodium nitrate, sodium thiosulphate and sucrose/1.450).

The gastrointestinal tract and serosal vessels were longitudinally opened and examined both grossly and under a dissecting microscope to detect eggs, adult worms, and related lesions.

A pre-weighed portion (2 g) of splenic tissue was diced and homogenized by a blender in tap water. The obtained fluid was centrifuged in a tube at 2000× rpm for 5 min. After removal of the supernatant, a high-density solution (sodium nitrate, sodium thiosulphate and sucrose/1.450) was added and mixed with the sediment until the tube was filled; a coverslip was left over the tube for a few minutes and finally observed under a light microscope (10×) for the detection of spirorchiid eggs.

The heart chambers and major vessels (left and right aortas, brachiocephalic trunk and pulmonary arteries) were opened through longitudinal sectioning and rinsed with tap water. The washes were then submitted to sedimentation in conic flasks, and the sediment was observed under a stereomicroscope. Adult flukes were collected, counted and fixed in 70% ethanol for identification. The parasites were clarified in Amman’s lactophenol or stained with Semichon’s acid carmine and mounted in Canada balsam. The morphometric characteristics were studied under a light microscope by a calibrated eyepiece micrometre (Olympus, ACH 40X-2) and compared with descriptions in the literature [13, 24]. Spirorchiid eggs detected in faeces and spleen were measured under a light microscope and classified as type 1, 2 or 3 depending on the presence and number of lateral processes according to Wolke et al. [1].

The concordance between the different parasitological methods used to diagnose spirorchiid infection (i.e. qualitative copromicroscopic analysis, search for eggs in the spleen and observation of adult flukes in the cardiovascular system) was calculated as the number of samples with identical results divided by the total number of samples commonly examined (% concordance). The data were also evaluated using kappa-type statistics [28], which express the proportion of agreement beyond chance and provide a value (parameter k) ranging from 0 (no agreement) to 1 (perfect agreement).

Genetic analysis of Caretta caretta hosts

To test the origin of the infected animals, a small amount (5 mm) of muscle tissues was collected from positive specimens. DNA was extracted using a QIAamp® DNA Mini and Blood Mini Kit (Qiagen GmbH, Hilden, Germany). A fragment of 815 bp of the mtDNA encompassing the control region (D-loop) was amplified by PCR using the primers LCM15382/H950 [29]. PCR conditions included an initial denaturing step at 94 °C for 3 min, followed by 36 cycles of 94 °C for 30 s, 52 °C for 30 s and 72 °C for 30 s, with a final step at 94 °C for 5 min. Amplification products were purified using a QIAquick PCR Purification Kit (Qiagen). A BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, California) and the same primers as those used in the first PCR were used in the sequencing reactions. Purification was carried out with an Agencourt CleanSEQ Dye Terminator Removal Kit (Beckman Coulter, Cassina De’Pecchi, Italy) and loaded onto an ABI Prism™ 3130 Genetic Analyzer (Applied Biosystems). Sequences were analysed, and base called using DNA Sequencing Analysis Software version 5.1 (Applied Biosystems). The multiple alignment programs included in the package Vector NTI version 9.1 (Invitrogen, Carlsbad, California) was used to align the sequences. D-loop haplotypes were classified by comparison to the mtDNA sequences available in GenBank and deposited in the Archie Carr Center for Sea Turtle Research database (ACCSTR; http://accstr.ufl.edu/files/cclongmtdna.pdf).

Molecular characterization of the parasites

Parasite DNA was extracted using a NucleoSpin® Tissue Kit (Macherey-Nagel, Duren, Germany) for adult flukes and using a PSP® Spin Stool DNA Kit (Invitek GmbH, Berlin, Germany) for stool samples that were positive in the copromicroscopic analysis.

The internal transcribed spacer 2 (ITS2) region of the rDNA was amplified using the primers described by Stacy et al. [30]. Amplification was performed by a standard PCR followed by a semi-nested PCR. The forward primer SPIR1 (5′-GAG GGT CGG CTT ATT ATC TAT CA-3′) and the reverse primer SPIR2 (5′-TCA CAT CTG ATC CGA GGT CA-3′) were used in the standard PCR. The forward primer SPIR1 and the reverse primer HLC4 (5′-TCA CAT CTG ATC CGA GGT CA-3′) were used in the semi-nested PCR. The PCR reactions were performed with a 30 μl reaction volume composed of 1–3 μl DNA, 2 mM MgCl2, 0.2 mM dNTPs (MBI Fermentas, Darmstadt, Germany), 1× PCR buffer, 0.5 μM each of the forward and reverse primer, and 1 U Platinum Taq DNA Polymerase (Invitrogen), with the remainder of the volume composed of sterile water. Cycling conditions included an initial activation step at 95 °C for 5 min., followed by 35 cycles of 94 °C for 30 s, 56 °C for 30 s, and 72 °C for 30 s, with a final extension step of 72 °C for 10 min.

The 28S region of the rDNA was amplified using the primers described by Olson et al. [31]: LSU-5 (5′-TAG GTC GAC CCG CTG AAY TTA AGCA-3′) and 1500R (5′-GCT ATC CTG AGG GAA ACT TCG-3′). The PCR reactions were performed in a 30 μl reaction volume composed of 3–5 μl DNA, 2.5 mM MgCl2, 0.2 mM dNTPs (MBI Fermentas, Germany), 1× PCR buffer, 0.8 μM each of forward and reverse primer, 1 M Betaine solution, and 1.5 U Platinum Taq DNA Polymerase (Invitrogen), with the remainder of the volume composed of sterile water. Cycling conditions included an initial activation step at 95 °C for 4 min, followed by 35 cycles of 94 °C for 60 s, 56 °C for 60 s, and 72 °C for 120 s, with a final extension step at 72 °C for 4 min.

All positive samples from PCR were sequenced by the Macrogen company (Macrogen Europe, Amsterdam, the Netherlands). Single electropherograms were analysed with the software ChromasPro version 2.4.3 (Technelysium Pty Ltd., South Brisbane, Australia).

The consensus sequences were assembled with the SeqMan program (DNASTAR package, Lasergene). The new nucleotide sequence data reported in this paper are available in the GenBank, EMBL and DDBJ databases (accession numbers: LT617052, H. mistroides ITS2 and LT882715, H. mistroides 28S; LT617053, Neospirorchis sp. ITS2 and LT882716 Neospirorchis sp. 28S; see Additional file 1: Table S1).

Phylogenetic analysis

The nature of the newly generated sequences was confirmed by a BLAST search [32], performed against the non-redundant nucleotide database in GenBank. This search also allowed us to identify the orthologous sequences obtained for spirorchiids and species of closely related fluke families [31] (Additional file 1: Table S1).

The family Spirorchiidae is a paraphyletic group with respect to the Schistosomatidae [33]. Thus, we created two data sets containing all available ITS2 and 28S sequences of the family Spirorchiidae (Additional file 1: Table S1). We also included sequences of members of the family Schistosomatidae and species belonging to the family Aporocotylidae. These latter species were used as outgroups in the phylogenetic analyses.

After downloading the sequences listed in Additional file 1: Table S1, they were aligned and successively trimmed while considering the coverage of different portions of the evaluated markers. The trimming served to minimize the amount of missing data. The ITS2 and 28S datasets were aligned with the MAFFT program [34], which is available at the EBI website [35]. The multiple alignments were then imported into the MEGA 6 program [36] for analyses. The ITS2 alignment was 451 nt positions long, while the 28S alignment encompassed 700 nt positions.

The phylogenetic analyses were performed according to the maximum likelihood (ML) and Bayesian inference (BI) methods [37]. The IqTree program (version 1.5.4) was used for ML analyses [38]. One hundred independent tree searches were performed to avoid entrapment in local optimal trees. The molecular evolution models selected by the IqTree program [39] were as follows: TVM + I + G4 for the 28S dataset and GTR + I + G4 for the ITS2 dataset. The statistical support for tree topologies was computed by performing 10,000 ultrafast bootstrap replicates [40]. The program MrBayes (version 3.2.6) was used for BI analyses [41]. Two simultaneous runs, each of four chains, were performed in all analyses. Each run consisted of 1,000,000 generations, and trees were sampled every 100 generations (trees generated = 2 × 104). Stationarity was considered reached when the average standard deviation of split frequencies was less than 0.005. ‘Burn-in’ was very stringent, and only the last 2000 generated trees were used to compute the majority-rule posterior consensus trees. The evolutionary model applied in Bayesian analyses was the GTR + I + G [37]. Pairwise distances among sequences were calculated with the MEGA 6 program [36].

Results

Parasitological analyses

Spirorchiidiasis was observed in 28 of the 168 examined animals (16.7%). The results of the analyses used to detect and identify adult flukes and spirorchiid eggs in the cardiovascular district, stool samples and spleen are reported in Table 1.

Table 1 Biometric data and results of analyses for Caretta caretta positive for spirorchiid infection
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Adult flukes were found inside the heart and at the beginning of the major vessels in six animals. Because of the poor conditions of the specimens, the morphological approaches only permitted identification of the parasites as members of Hapalotrema based on the presence of multiple testes anterior and posterior to the ovary and terminal genitalia.

Copromicroscopic examination proved positive results for spirorchiid eggs in 28 cases; type 1 and 3 eggs were found in 26 and 10 animals, respectively (15.5 and 6.0%), and there were 8 cases of mixed infection. The analyses carried out on spleen samples revealed the presence of spirorchiid eggs in 17 cases; type 1 and 3 eggs were observed in 16 and one sample(s), respectively. Of 28 animals found positive in the copromicroscopic exam, 14 specimens had eggs (i.e. type 1, type 3 or both) that were detected on the gastrointestinal walls. All animals with eggs in the spleen and adults in the cardiovascular system were also positive in the copromicroscopic analysis. Table 2 shows the comparisons among the performed techniques regarding the percentage of concordance and level of agreement (parameter k). The copromicroscopic analysis was in excellent agreement with the evaluation of eggs in the spleen (n = 64), whereas the correspondence with the evaluation of adults in cardiovascular system was only fair (n = 140).

Table 2 Comparison between copromicroscopic examination and evaluation of spirorchiids in the spleen and cardiovascular system
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Genetic analyses of Caretta caretta hosts

Twenty-one of 28 positive C. caretta were genetically analysed. Sequences of the same length (815 bp) were obtained for all the samples (Table 1). The comparison of these sequences with those registered in the databases for C. caretta led to the identification of three already known D-loop haplotypes. CC-A2.1 (GenBank: EU179445) was the most frequent haplotype and was detected in 19 host specimens (91%). One individual (4.5%) collected in 2013 exhibited the haplotype CC-A2.8 (FM200217), while the haplotype CC-A32.1 (JF837822) was recorded for one turtle (4.5%) collected in 2014.

Anatomopathological findings

Body condition score of the positive animals is shown in Table 1.

Spirorchiid eggs were detected in the intestinal mucosa and submucosa only in animals found to be positive by copromicroscopic exam. The distribution pattern of the eggs on the intestinal walls was macroscopically different for the two types. Type 1 eggs were arranged in small clusters or disseminated as single elements in the mucosal layer. Type 3 eggs were arranged in highly visible, serpiginous masses included in the mucosal layer or, less frequently, as large clusters with a cyst-like appearance and black (Fig. 1).

Fig. 1
figure 1

Intestinal lesions in Caretta caretta associated with Hapalotrema mistroides and Neospirorchis sp. Different pattern of distribution on the intestinal district are easily visible for the two genera. Type 1 eggs are scattered on the intestinal wall, grossly looking as small brownish spots (a) composed of a low number of fusiform eggs as revealed by stereomicroscopy (b). Big masses of type 3 eggs are visible on the intestinal mucosa as elongated black serpiginous stripes (c), formed by thousands of elements (d). Different patterns of distribution are easily visible in this case of mixed infection, in which type 3 eggs appear like grouped in a cyst like structure (e). Multifocal granulomatous enteritis (f; HE) with multinucleated giant cells (black arrow) surrounding a core of eggs and necrotic debris is detectable in intestinal sections with minimal fibrotic reaction (inset). Abbreviation: HE, haematoxylin and eosin. Scale-bars: a, 0.5 cm; b, 1 mm; c, 0.37 cm; d, 560 μm; e, 350 μm; f, 150 μm (inset: 120 μm)

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Egg clusters were surrounded by mild granulomatous inflammation with multinucleated giant cells, rare mixed inflammatory cells, and a thin fibrous capsule. Single elements and small groups of eggs (n = 3–5) were not associated with any inflammatory reaction. Granulomas were seen in the spleen, lung, thymus, and pancreas surrounding small, multifocal groups of eggs. Isolated eggs were also observed in the gastric walls, liver, heart, kidney, adrenal gland, salt glands, and urinary bladder wall.

Mild to moderate arteritis was observed in four of six animals from which adult parasites were isolated. The beginning of the major vessels was the most affected section (Fig. 2). Small proliferative plaques were grossly visible on the intima with rough irregular surface. At histology, fibro-muscular proliferations were visible inside the intima of the inflamed vessels; isolated eggs were frequently seen more deeply in the vessel walls without any associated inflammatory processes. In one case, extensive sub-endothelial inflammatory infiltrate was observed in association with multiple degenerated eggs.

Fig. 2
figure 2

a Heart and great vessels. Small proliferative plaques are visible on the supravalvular region on the intima of a great vessel in a specimen of C. caretta infected with Hapalotrema mistroides. b Heart, atrium (HE). Raised irregular plaques of severe chronic endocarditis and extensive fibroplasia with multifocal areas of undetermined mesenchymal cells surrounding some eggs (inset). Abbreviation: HE, Haematoxylin and eosin. Scale-bars: a, 1 cm; b, 290 μm (inset: 135 μm)

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Molecular identification of parasites and phylogenetic analysis

The ITS2 sequences were obtained for twenty-three faecal samples positive for type 1 eggs and six adult flukes (one from each positive animal). All ITS2 sequences were identical. A BLAST search identified the ITS2 sequence from a specimen of H. mistroides (H. mistroides GU937893, Additional file 1: Table S1) as the closest relative to the ITS2 sequences in the current study. Pairwise comparisons among the new sequences and H. mistroides A ITS2 showed an identity of 99.63% (i.e. one base A vs G was different over 270 bases of the alignment). The different base is located near the 3′ end, a portion not included in the phylogenetic analysis. Thus, the newly generated sequences were assigned to H. mistroides (see below). The ITS2 sequences obtained from eight faecal samples positive for type 3 eggs were found to be identical. These sequences were compared with data available in GenBank and were found to be identical to those obtained from Neospirorchis sp. Neogen11 (KU601335) (Additional file 1: Table S1).

The 28S partial sequences obtained from four adults of H. mistroides were identical. Similarly, the 28S sequences obtained from five samples of Neospirorchis sp. eggs were identical. We obtained a single haplotype for both taxa.

The ML tree obtained from the ITS2 alignment is presented in Fig. 3. The BI consensus tree exhibited a topology that was mostly congruent except for the arrangement of the Neospirorchis clade (see below). The family Spirorchiidae was paraphyletic with respect to the Schistosomatidae. Two major clades occurred within Spirorchiidae. The first clade included exclusively taxa belonging to the genus Neospirorchis. The second clade contained the other analysed spirorchiid taxa and was a sister group of the Schistosomatidae. The Neospirorchis clade received strong bootstrap and BI posterior probability support. Neospirorchis sp. Italy (LT617053) was placed within the Neospirorchis clade as a sister taxon of Neospirorchis sp. Neogen 11 (KU601335). In the ML tree, two clades (I and II) could be identified within the genus Neospirorchis. Both clades received bootstrap corroboration. The phylogenetic relationships among the different Neospirorchis taxa were well resolved and received bootstrap corroboration in many cases. However, clade I was not found in the BI consensus tree. Hapalotrema mistroides Italy (LT617052) formed a clade with two other specimens assigned to the same species. This group received strong statistical corroboration by bootstrap and BI posterior probability values. Samples of H. mistroides were the sister group of Hapalotrema postorchis specimens, a phylogenetic relationship supported by both bootstrap and BI posterior probability values. Hapalotrema pambanensis and Learedius learedi were not monophyletic.

Fig. 3
figure 3

Phylogenetic analysis of spirorchiid flukes based on ITS2 sequences. The ML tree (-ln = 6007.5517) was computed with IQ-TREE program. The scale-bar represents 0.2 substitutions/state change per position. Numbers in black represent ultrafast bootstrap values (> 50%) expressed in percent; numbers in red refer to Bayesian Inference posterior probabilities presented in a compressed way (e.g. 1 instead of 1.00; .95 instead of 0.95) to allow a better readability of the figure

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The maximum likelihood tree obtained from the 28S multiple alignment is presented in Fig. 4. The BI consensus tree exhibited a fully congruent topology (data not shown). Most of the nodes received support by bootstrap and BI posterior probability values. The family Spirorchiidae was paraphyletic with respect to Schistosomatidae. Two main clades could be recognized within the spirorchiid flukes. A clade containing mostly species of the genera Carettacola, Amphiorchis, Hapalotrema and Learedius was a sister group of the Schistosomatidae. Within this clade, L. learedi (represented by three sequences) and H. pambanensis (represented by two sequences) were monophyletic. Indeed, Hapalotrema mehrai Rao,1976 is a junior synonym of H. pambanensis (Additional file 1: Table S1). The second major clade included various spirorchiid taxa. Neospirorchis sp. Italy (LT882716) grouped with the other taxa of the genus Neospirorchis. Similarly, H. mistroides Italy (LT882715) was a sister taxon to H. mistroides (KU892016).

Fig. 4
figure 4

Phylogenetic analysis of spirorchiid flukes based on 28S sequences. The ML tree (-ln = 10,754.3072) was computed with IQ-TREE program. The scale-bar represents 0.1 substitutions/state change per position. Numbers in black represent ultrafast bootstrap values (> 50%) expressed in percent; numbers in red refer to Bayesian Inference posterior probabilities presented in a compressed way (e.g. 1 instead of 1.00; .95 instead of 0.95) to allow a better readability of the figure

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The average p-distance among the ITS2 sequences of the Neospirorchis taxa was 0.128 ± 0.075. The p-distances ranged from 0 [Neospirorchis sp. Italy (LT617053) vs Neospirorchis sp. Neogen11 (KU601335)] to the maximum value of 0.291 observed in Neospirorchis sp. Neospirgen2 (KU600080) vs Neospirorchis sp. Neogen15 (KU601339). The average p-distance among taxa belonging to the Hapalotrema + Learedius clade was 0.122 ± 0.064. The range varied from 0 [H. mistroides Italy (LT617052) vs H. mistroides (GU937893)] to the maximum value of 0.195 observed in the pair H. mistroides (KY499798) vs H. synorchis (KM652618). Finally, within the genus Schistosoma, the average p-distance was 0.110 ± 0.072, while values ranged from 0 [Schistosoma japonicum (FJ852567) vs Schistosoma japonicum (FJ852566)] to 0.188 [Schistosoma japonicum (FJ852566) vs Schistosoma haematobium (U22165)].

Discussion

Prevalence data and ecological considerations

Few studies on spirorchiidiasis in loggerhead turtles have been carried out [1, 4, 15, 16, 42]; these studies involve a small number of animals and apply different methodologies for parasite detection. Only two surveys carried out in Florida can be considered for a comparison with the current study due to having a similar diagnostic approach and sampling effort [1, 11]. The prevalence of infection observed in our study for both Hapalotrema sp. and Neospirorchis spp. appears to be lower than that recorded in the two previous studies. In the most recent survey [11], the high percentage of loggerhead sea turtles infected by both Hapalotrema spp. and Neospirorchis spp. (96 and 77%, respectively) demonstrated a wide diffusion of infection in the north-western Atlantic. In the present study, spirorchiidiasis does not appear to be widespread among loggerhead turtles feeding in the northern Adriatic grounds (prevalence of 15.5 and 6.0% for Hapalotrema and Neospirorchis, respectively). There was one case of infection by H. mistroides observed in one loggerhead turtle stranded along the coast of central-western Italy [22]; however, other surveys performed in last few decades did not detect these parasites in C. caretta in the central or eastern Mediterranean areas [43,44,45]. These results may be partly due to different research methodologies or to minor sampling effort. Nevertheless, this finding supports the hypothesis that spirorchiidiasis did not raise the attention of researchers for frequent and serious patterns of infection in the region, which differs from the descriptions for North Atlantic waters [15]. The differences in the spread of infection may be due to environmental factors, including the presence and distribution of the intermediate hosts. Involvement of a gastropod intermediate host in the life-cycle of marine spirorchiids has been already demonstrated [16, 30].

The detection of adult flukes in a few cases may have been due to poor sample quality, the small body size of these trematodes and the tendency, especially for Neospirorchis spp., to inhabit small vessels, as already shown by other authors [3, 4]. Therefore, it is commonly recognized that the diagnosis of spirorchiidiasis cannot rely only on the detection of adult specimens. Spirorchiid eggs have greater resistance to decomposition than adults both in carcasses and in the environment [46]. Faecal examination has been used to detect infections in sea turtles [1], although it is considered a diagnostic method lacking in specificity and sensitivity [25, 47]. In this study, copromicroscopic examination showed excellent agreement (k = 0.886) with the method used for searching for eggs in the spleen, a common site of egg deposition due to its role as a blood filtering organ [2]. The presence of eggs in the faeces is related to their migration through the intestinal walls and entrance into the gut lumen [12, 47], but not all species have the primary route of elimination via the gastrointestinal tract in all host species [4, 47]. Our positive results from the copromicroscopic exams were often associated with the presence of both Hapalotrema mistroides and Neospirorchis sp. eggs in the intestinal mucosa; therefore, copromicroscopic examination remains a valid and noninvasive diagnostic method in the case of infection by Hapalotrema mistroides and Neospirorchis spp. in C. caretta and is also feasible for use with live animals. Copromicroscopic analysis has additional limitations, such as recent infections (immature specimens) or low parasite burden, that could produce false negative results, and since different spirorchiid genera have similar eggs, molecular approaches remain essential for certainty in identification.

Our genetic analyses were performed on positive hosts to test the hypothesis that spirorchiidiasis was acquired inside the Mediterranean Basin. Two recent reports [16, 22] demonstrated the presence of H. mistroides infection in loggerhead sea turtle specimens from the western Mediterranean and the Tyrrhenian Sea. However, no genetic analyses were done in those studies, and considering that both Atlantic and Mediterranean turtles can be found in the western part of the basin, uncertainty about their origins remains. The three D-loop haplotypes found in the present study are common in loggerhead sea turtles from the Mediterranean Basin [48]; haplotype CC-A2.1 is the most frequent in all Mediterranean rookeries [48] and is found at low frequencies in Atlantic colonies [49]. Haplotype CC-A2.8 was observed in loggerhead turtles nesting in Crete [48] and feeding in Ionian waters [50], while haplotype CC-A32.1 is private of Greek nesting colonies [48]. The presence of individuals from these two Mediterranean nesting colonies in Adriatic waters has been documented by genetic studies [50,51,52] as well as by satellite tracking studies [53, 54]. Therefore, the positive animals seem to belong to the stock usually encountered in the northern Adriatic waters. Loggerhead sea turtles of the Mediterranean, particularly those of Greek origin, show intra-Mediterranean migratory pathways and select neritic feeding areas inside the basin to which they show strong fidelity [55], sometimes sharing the same foraging area with turtles of Atlantic origin (i.e. the Gulf of Gabès, Tunisia [53]). These points enhance the probability that the turtles (at least those carrying Greek haplotypes) acquired the infection inside the Mediterranean Sea along their migratory routes.

Pathogenic impact

Spirorchiidiasis in sea turtles from the Atlantic and Pacific Oceans has been found to be causal or contributory to death in many cases [3, 11, 16, 56]. In the Mediterranean Sea, except for scarce historical data, there is only one case report of a free-ranging loggerhead turtle [22] in which severe lesions by spirorchiids likely contributed to the death of the animal. Nevertheless, in the present study spirorchiidiasis never affected the general health status of the hosts and represented an occasional finding during necropsy. Most of the positive turtles were in a good or excellent nutritional condition, and only mild lesions were observed.

Two patterns of lesions were observed for type 1 and type 3 eggs in the intestine and were similar to that described by Stacy et al. [4] in C. caretta for Hapalotrema spp. and Neospirorchis spp., respectively. In Hapalotrema-infected hosts, the severity of the granulomatous reaction to egg masses was higher, with transmural and prominent lesions visible both on the intestinal mucosa and on the subserosal vessels. In our study, the mucosal and (rarely) submucosal layers were affected, and no lesions were evident from the external surface of the intestinal walls.

Spirorchiids are known to produce serious pathological lesions in the circulatory system of the host. Arteritis, aneurysms and disseminated thrombi are described in various districts in C. caretta infected by H. mistroides and Neospirorchis spp. [1, 4]. Some differences in the distribution of adult flukes and lesions are reported depending on the infecting species and genotypes [11]. In our study, most of the positive turtles had no lesions in the cardiovascular system except for a few cases with mild to moderate alterations at the emergence of the major vessels where adult specimens of H. mistroides were collected. Associations between Hapalotrema spp. (including H. mistroides) and endarteritis was already shown by Stacy et al. who also found parasites attached to the lesions [4].

Molecular and phylogenetic findings

The specimens assigned to the genus Neospirorchis sequenced in our study shared the same ITS2 haplotype, Neospirorchis sp. Italy (LT617053). The latter was identical to the Neospirorchis sp. Neogen11 (KU601335) sequence obtained from a specimen previously isolated from the gastrointestinal tract of a C. caretta specimen in Florida [11]. Similarly, all the specimens assigned to H. mistroides Italy (LT617052) had identical ITS2 sequences that differed from H. mistroides (GU937893) by a single base (A vs G) located outside of the aligned portion.

The 28S sequences of H. mistroides Italy LT882715 and H. mistroides KU892016 were also identical (Fig. 4). The high levels of sequence similarity were mirrored by the phylogenetic results (Figs. 3 and 4), where newly generated sequences grouped with the orthologous counterparts obtained from congeneric (Neospirorchis) or conspecific specimens (H. mistroides). Multiple sequences were available for both Neospirorchis spp. and H. mistroides. If our sequences do not belong to the genus Neospirorchis/ H. mistroides, these taxa become paraphyletic in the ITS2 analysis, a situation that is untenable. Thus, the phylogenetic analysis allowed the straightforward generic/specific assignment of the new sequences.

The level of molecular variation observed among the Neospirorchis ITS2 sequences was higher than that observed among the species included in the Hapalotrema + Learedius clade or within the genus Schistosoma. These results support the view that the Neospirorchis flukes parasitizing sea turtles belong to at least two distinct species.

The analysis performed on the ITS2 of H. pambanensis and L. learedi suggested a non-monophyly of these taxa. In our opinion, these results must be regarded as an artifact due to a mislabelling of the sequences submitted to GenBank. In favour of our hypothesis, there are the following considerations. First, Chapman et al. [25] generated and used this set of sequences in a previous phylogenetic analysis where both species were monophyletic. Unfortunately, they did not present the accession numbers of the sequences in their phylogenetic tree. Secondly, in our 28S tree, both taxa are also monophyletic. Thirdly, it is unrealistic that two distinct species would present identical ITS2 sequences considering the level of variation also observed in the present study for these molecular markers.

Conclusions

In this study, eggs or adults from two species of spirorchiids, H. mistroides and Neospirorchis sp., were observed in single or mixed infections and were identified by both morphological and molecular approaches. Hapalotrema mistroides was already described in loggerheads stranded along Egyptian [18, 19] and Italian coastlines [17, 22], whereas the genus Neospirorchis is described in this basin for the first time. Our study noted the importance of molecular approaches and phylogenetic studies as a good complement for resolving problems related to poorly preserved specimens and to provide evidence of cryptic speciation within the currently recognized spirorchiid species, as previously suggested by other authors [11, 25]. Although spirorchiidiasis is one of the oldest observations in sea turtle literature [17], this study provides prevalence data with pathological features of the infection for the first time inside the Mediterranean Basin and updates our knowledge on the species present. Low prevalence and mild lesions were observed in the samples, leading to the conclusion that spirorchiidiasis does not represent a cause of severe morbidity or mortality for turtles in the region. Data on C. mydas, also a resident species in the Mediterranean, are completely lacking, and studies performed in the western Mediterranean included a limited number of loggerhead sea turtles. Therefore, further investigations are necessary for more thorough knowledge of the ecopathology and spread of spirorchiidiasis in the Mediterranean Sea. Considering the results of the genetic analysis carried out on positive turtles and the current knowledge of the migratory routes of Mediterranean turtles, the hypothesis that infection by both Hapalotrema and Neospirorchis was acquired inside the Mediterranean Basin seems to be supported. The identity of the ITS2 sequences of Neospirorchis sp. Italy and Neogen-11 from Florida suggest the possibility that the infection was transmitted by Atlantic turtles to Mediterranean turtles through an infected intermediate host in a shared feeding ground. If this hypothesis is confirmed, this would highlight the importance of studying the roles of these areas as ecological key points for the spill over of pathogens between the two populations.

References

  1. Wolke RE, Brooks DR, George A. Spirorchidiasis in loggerhead sea turtles (Caretta caretta): pathology. J Wildl Dis. 1982;18:175–85.

    Article  CAS  PubMed  Google Scholar 

  2. Flint M, Patterson-Kane JC, Limpus CJ, Work TM, Blair D, Mills PC. Postmortem diagnostic investigation of disease in free-ranging marine turtle populations: A review of common pathologic findings and protocols. J Vet Diagn Investig. 2009;21(6):733–59.

  3. Gordon AN, Kelly WR, Cribb TH. Lesions caused by cardiovascular flukes (Digenea: Spirorchiidae) in stranded green turtles (Chelonia mydas). J Vet Pathol. 1998;35:21–30.

    Article  CAS  Google Scholar 

  4. Stacy BA, Foley AM, Greiner E, Herbst LH, Bolten A, Klein P, et al. Spirorchiidiasis in stranded loggerhead Caretta caretta and green turtles Chelonia mydas in Florida (USA): host pathology and significance. Dis Aquat Org. 2010;89(3):237–59.

    Article  PubMed  Google Scholar 

  5. Dailey MD, Fast ML, Balazs GH. A survey of the Trematoda (Platyhelminthes: Digenea) parasitic in green turtles, Chelonia mydas (L.) from Hawaii. Bull Southern California Acad Sci. 1992;91(2):84–91.

    Google Scholar 

  6. Graczyk TK, Aguirre AA, Balazs GH. Detection by ELISA of circulating anti-blood fluke (Carettacola, Hapalotrema and Learedius) immunoglobulins in Hawaiian green turtles (Chelonia mydas). J Parasitol. 1995;81(3):416–21.

    Article  CAS  PubMed  Google Scholar 

  7. Work TM, Balazs GH, Schumacher JL, Marie A. Epizootiology of spirorchiid infection in green turtles (Chelonia mydas), in Hawaii. J Parasitol. 2005;91:871–6.

    Article  PubMed  Google Scholar 

  8. Santoro M, Morales JA, Rodríguez-Ortíz B. Spirorchiidiasis (Digenea: Spirorchiidae) and lesions associated with parasites in Caribbean green turtles (Chelonia mydas). Vet Rec. 2007;161(14):482–6.

    Article  CAS  PubMed  Google Scholar 

  9. Glazebrook JS, Campbell RS, Blair D. Studies on cardiovascular fluke (Digenea: Spirorchiidae) infections in sea turtles from the Great Barrier Reef, Queensland, Australia. J Comp Pathol. 1989;101:231–50.

  10. Luhman M. Two new trematodes from the loggerhead turtle (Caretta caretta). J Parasitol. 1935;21:274–6.

    Article  Google Scholar 

  11. Stacy BA. Spirorchiid trematodes of sea turtles in Florida: Associated disease, diversity and life cycle studies. PhD Thesis, University of Florida. 2008. Available: http://etd.fcla.edu/UF/UFE0024049/stacy_b.pdf.

  12. Greiner EC. Parasites of marine turtles. In: Wyneken J, Lohmann KJ, Lutz JA, editors. The biology of sea turtles. Volume 3. USA: CRC Press; 2013. p. 427–446.

  13. Platt TR, Blair D. Redescription of Hapalotrema mistroides (Monticelli, 1896) and Hapalotrema synorchis Luhman, 1935 (Digenea: Spirorchidae), with comments on other species in the genus. J Parasitol. 1998;84:594–600.

    Article  CAS  PubMed  Google Scholar 

  14. Manter HW, Larson MI. Two new blood flukes from a marine turtle, Caretta caretta. J Parasitol. 1950;36(6):595.

  15. Jacobson ER, Homer BL, Stacy BA, Greiner EC, Szabo NJ. Chrisman, et al. Neurological disease in wild loggerhead sea turtles Caretta caretta. Dis Aquat Org. 2006;70(1–2):139–54.

    Article  CAS  PubMed  Google Scholar 

  16. Cribb TH, Crespo-Picazo JL, Cutmore SC, Stacy BA, Chapman PA, Garcìa-Pàrraga D. Elucidation of the first definitively identified life cycle for a marine turtle blood fluke (Trematoda: Spirorchidae) enables informed control. Int J Parasitol. 2017; https://doi.org/10.1016/j.ijpara.2016.11.002.

  17. Monticelli FS. Di un ematozoo della Thalassochelys caretta Linn. Int Mschr Anat Physiol. 1896;13:141–72.

    Google Scholar 

  18. Looss A. Weitere Beiträge zur Kenntniss der Trematoden Fauna Aegyptens, Zugleich Versuch einer natürlichen Gliederung des Genus Distomum Retzius. Zool Jb-r Abt Syst. 1899;12:521–784.

    Google Scholar 

  19. Looss A. Ueber neue und bekannte Trematoden aus Seeschildkröten. Nebst Erörterungen zur Systematik und Nomenclatur. Zool. Jb-r. Abt. Syst., Oekol. Geogr. Tiere. 1902;16:411–894.

    Google Scholar 

  20. Gohar N. Liste des trematodes parasites et de leurs hotes vertebres signales dans la Vallee du Nil. Ann Parasitol Hum Comp. 1934;12:322–31.

    Google Scholar 

  21. Gohar N. Liste des trematodes parasites et de leurs hotes vertebres signales dans la Vallee du Nil. (Suite et fin.). Ann Parasitol Hum Comp. 1935;13:80–90.

    Google Scholar 

  22. Santoro M, Di Nocera F, Iaccarino D, Lawton SP, Cerrone A, degli Uberti B, et al. Pathology and molecular analysis of Hapalotrema mistroides (Digenea: Spirorchiidae) infecting a Mediterranean loggerhead turtle Caretta caretta. Dis Aquat Org. 2017;124:101–8.

    Article  CAS  PubMed  Google Scholar 

  23. Snyder SD, Clopton RE. New methods for the collection and preservation of spirorchiid trematodes and polystomatid monogeneans from turtles. Comp Parasitol. 2005;72(1):102–7.

  24. Platt TR. Family Spirorchiidae Stunkard, 1921. In: Gibson DI, Jones A, Bray RA, editors. Keys to the Trematoda. Volume 2. Wallingford, UK: CABI Publishing; 2002. pp. 453–467.

  25. Chapman PA, Cribb TH, Blair D, Traub RJ, Kyaw-Tanner MT, Flint M, et al. Molecular analysis of the genera Hapalotrema Looss, 1899 and Learedius Price, 1934 (Digenea: Spirorchiidae) reveals potential cryptic species, with comments on the validity of the genus Learedius. Syst Parasitol. 2015;90:67–79.

    Article  PubMed  Google Scholar 

  26. Chapman PA, Traub RJ, Kyaw-Tanner, Owen H, Flint M, Cribb TH, Mills PC. Terminal restriction fragment length polymorphism for the identification of spirorchiid ova in tissues from the green sea turtle, Chelonia mydas. PLoS One. 2016;11(8):e0162114.

  27. Poppi L, Marchiori E. In: Poppi L, Di Bello A, editors. Dissection techniques and notions. Venice, Italy: Sea turtle management manual. Genesi design; 2015. p. 288–334.

    Google Scholar 

  28. Landis JR, Koch GG. The measurement of observer agreement for categorical data. Biometrics. 1977;33:159–74.

    Article  CAS  PubMed  Google Scholar 

  29. Abreu-Grobois FA, Horrocks J, Formia A, Leroux, R., Velez-Zuazo, X., Dutton, P., et al. New mtDNA D-loop primers which work for a variety of marine turtle species may increase the resolution capacity of mixed stock analysis. In: Frick M, Panagopoulou A, Rees AF, Williams K, editors. Book of abstracts. Twenty-sixth Annual Symposium on Sea Turtle Biology and Conservation. Athens: International Sea Turtle Society; 2006. pp.179. Available: http://www.nmfs.noaa.gov/pr/pdfs/species/turtlesymposium2006_abstracts.pdf.

  30. Stacy BA, Frankovich T, Greiner E, Alleman AR, Herbst LH, Klein P, et al. Detection of spirorchiid trematodes in gastropods tissues by polymerase chain reaction: preliminary identification of an intermediate host of Learedius learedi. J Parastol. 2010;96(4):752–7.

    Article  Google Scholar 

  31. Olson PD, Cribb TH, Tkach VV, Bray RA, Littlewood DTJ. Phylogeny and classification of the Digenea (Platyhelminthes: Trematoda). Int J Parasitol. 2003;33(7):733–55.

    Article  CAS  PubMed  Google Scholar 

  32. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990;215:403–10.

    Article  CAS  PubMed  Google Scholar 

  33. Snyder SD. Phylogeny and paraphyly among tetrapod blood flukes (Digenea: Schistosomatidae and Spirorchiidae). Int J Parasitol. 2004;34:1385–92.

    Article  CAS  PubMed  Google Scholar 

  34. Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 2013;30:772–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Li W, Cowley A, Uludag M, Gur T, McWilliam H, Squizzato S, Park YM, Buso N, Lopez R. The EMBL-EBI bioinformatics web and programmatic tools framework. Nucleic Acids Res. 2015;43:W580–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol. 2013;30:2725–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Felsenstein J. Inferring phylogenies. Sunderland (MA): Sinauer Associates; 2004.

    Google Scholar 

  38. Nguyen LT, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 2015;32:268–74.

    Article  CAS  PubMed  Google Scholar 

  39. Kalyaanamoorthy S, Minh BQ, Wong TKF, von Haeseler A, S Jermiin LS. ModelFinder: Fast model selection for accurate phylogenetic estimates. Nature Methods. 2017;doi:https://doi.org/10.1038/nmeth.4285.

  40. Minh BQ, Nguyen MAT, von Haeseler A. Ultrafast approximation for phylogenetic bootstrap. Mol Biol Evol. 2013;30:1188–95.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Ronquist FM, Teslenko P, van der Mark D, Ayres A, Darling S, Höhna B, et al. 2011. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol. 2011;61:539–42.

    Article  Google Scholar 

  42. Chen H, Kuo RJ, Chang TC, Hus CK, Bray RA, Cheng IJ. Fluke (Spirorchiidae) infections in sea turtles stranded on Taiwan: prevalence and pathology. J Parasitol. 2012;98(2):437–9.

    Article  PubMed  Google Scholar 

  43. Manfredi MT, Piccolo G, Meotti C. Parasites of Italian sea turtles. II. Loggerhead turtles (Caretta caretta Linnaeus, 1758). Parassitologia. 1998;40:305–8.

    CAS  PubMed  Google Scholar 

  44. Gračan R, Bursic M, Mladineo I, Kucinic M, Lazar B, Lackovic G. Gastrointestinal helminth community of loggerhead sea turtle Caretta caretta in the Adriatic Sea. Dis Aquat Org. 2012;99:227–36.

    Article  PubMed  Google Scholar 

  45. Santoro M, Badillo JF, Mattiucci S, Nascetti G, Bentivegna F, Insacco G, et al. Helminth communities of loggerhead turtles (Caretta caretta) from Central and Western Mediterranean Sea: The importance of host's ontogeny. Parasitol Int. 2010;59:367–75.

    Article  PubMed  Google Scholar 

  46. Dailey MD, Morris R. Relationship of parasites (Trematoda: Spirorchidae) and their eggs to the occurence of fibropapillomas in the green turtle (Chelonia mydas). Can J Fish Aquat Sci. 1995;52:84–9.

    Article  Google Scholar 

  47. Chapman PA, Owen H, Flint M, Soares Magalhães RJ, Traub RJ, Cribb TH, Kyaw-Tanner, Mills PC. Molecular epidemiology and pathology of spirorchiid infection in Green Sea Turtle (Chelonia mydas). Int J Parasitol Parasite Wildl. 2017;6:39–47.

    Article  Google Scholar 

  48. Clusa M, Carreras C, Pascual M, Demetropoulos A, Margaritoulis D, Rees AF, et al. Mitochondrial DNA reveals Pleistocenic colonisation of the Mediterranean by loggerhead turtles (Caretta caretta). J Exp Mar Biol Ecol. 2013;439:15–24.

    Article  Google Scholar 

  49. Shamblin BM, Bolten AB, Abreu-Grobois FA, Bjorndal KA, Cardona L, Carreras C, et al. Geographic patterns of genetic variation in a broadly distributed marine vertebrate: New insights into loggerhead turtle stock structure from expanded mitochondrial DNA sequences. PLoS One. 2014;9(1):e85956.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Garofalo L, Mastrogiacomo A, Casale P, Carlini R, Eleni C, Freggi D, et al. Genetic characterization of central Mediterranean stocks of the loggerhead turtle (Caretta caretta) using mitochondrial and nuclear markers, and conservation implications. Aquat Conserv. 2013;23(6):868–84.

    Article  Google Scholar 

  51. Clusa M, Carreras C, Pascual M, Gaughran SJ, Piovano S, Giacoma C, et al. Fine-scale distribution of juvenile Atlantic and Mediterranean loggerhead turtles (Caretta caretta) in the Mediterranean Sea. Mar Biol. 2014;161:509–19.

    Article  Google Scholar 

  52. Yilmaz C, Turkozan O, Bardakci F, White M, Kararaj E. Loggerhead turtles (Caretta caretta) foraging at Drini Bay in northern Albania: genetic characterisation reveals new haplotypes. Acta Herpetol. 2012;7:155–62.

    Google Scholar 

  53. Zbinden JA, Bearhop S, Bradshaw P, Gill B, Margaritoulis D, Newton J, Godley BJ. Migratory dichotomy and associated phenotypic variation in marine turtles revealed by satellite tracking and stable isotope analysis. Mar Ecol Prog Ser. 2011;421:291–302.

    Article  Google Scholar 

  54. Schofield G, Hobson VJ, Fossette S, Lilley MKS, Katselidis KA, Hays G. Fidelity to foraging sites, consistency of migration routes and habitat modulation of home range by sea turtles. Divers Distrib. 2010;16:840–53.

    Article  Google Scholar 

  55. Casale P, Freggi D, Basso R, Vallini C, Argano R. A model of area fidelity, nomadism, and distribution patterns of loggerhead sea turtles (Caretta caretta) in the Mediterranean Sea. Mar Biol. 2007;152(5):1039–49.

    Article  Google Scholar 

  56. Flint M, Patterson-Kane JC, Limpus CJ, Mills PC. Health surveillance of stranded Green Turtles in Southern Queensland, Australia (2006–2009): an epidemiological analysis of causes of disease and mortality. EcoHealth. 2010;7(1):135–45.

    Article  PubMed  Google Scholar 

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Acknowledgements

We are grateful to Rita Lorenzini and Pietro Calderini of the Istituto Zooprofilattico Sperimentale delle Regioni Lazio e Toscana; Sauro Pari and Valeria Angelini of the Cetacean Foundation (Riccione); Franco Zuppa (WWF Area Marina Protetta di Miramare); Giuseppe Palmisano and Emanuele Zanetti for their logistic support, and Federica Bertuzzo for precious help in performing turtle necropsies and analysis of data.

Funding

This work was financially supported by a Research Project of Padova University (Prot. CPDA149521/14).

Availability of data and materials

The data supporting the conclusions of this article are included within the article. Sequences of Hapalotrema mistroides Italy and Neospirorchis sp. Italy have been deposited in the GenBank database under the accession numbers LT617052 and LT617053 (ITS2), respectively, and LT882715 and LT882716 (28S), respectively. The D-loop haplotypes of the turtles were already described and deposited in the Archie Carr Center for Sea Turtle Research database (ACCSTR; http://accstr.ufl.edu/files/cclongmtdna.pdf).

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Authors and Affiliations

  1. Department of Animal Medicine, Production and Health, University of Padova, Viale dell’Università, Legnaro, Italy

    Erica Marchiori, Rudi Cassini, Cinzia Tessarin & Federica Marcer

  2. Department of Comparative Biomedicine and Food Science, University of Padova, Viale dell’Università, Legnaro, Italy

    Enrico Negrisolo & Lisa Poppi

  3. Istituto Zooprofilattico Sperimentale delle Regioni Lazio e Toscana, Centro di Referenza Nazionale per la Medicina Forense Veterinaria, Rieti, Italy

    Luisa Garofalo

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Contributions

EM contributed to the conceptualization of the study, performed necropsies, parasitological and histopathological analysis and was a major contributor in writing and editing the paper. EN contributed to conceptualization of molecular and phylogenetic studies, performed phylogenetic studies, provided molecular studies on parasites sequences and secondary structure of ITS2 and was a major contributor in writing and editing the paper. RC made statistical analyses and contributed in editing the manuscript. LG made genetic analysis on turtles mtDNA and drafted the corresponding part of the manuscript. LP provided the collaborations for the collection of turtles carcasses, performed necropsies, and histopathological analyses and contributed in editing the pathological findings. CT made molecular analysis on parasite samples and collaborated in editing the paper. FM contributed to the conceptualization of the study, performed parasitological analyses and the necropsies, was a major contributor in drafting and editing the manuscript, coordinated the project and provided funding for the study. All authors read and approved the final manuscript.

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Additional file

Additional file 1: Table S1.

List of fluke taxa analysed in the present study with GenBank accession numbers, sources, hosts and localities. (DOCX 67 kb)

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Marchiori, E., Negrisolo, E., Cassini, R. et al. Cardiovascular flukes (Trematoda: Spirorchiidae) in Caretta caretta Linnaeus, 1758 from the Mediterranean Sea. Parasites Vectors 10, 467 (2017). https://doi.org/10.1186/s13071-017-2396-x

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Parasites & Vectors

ISSN: 1756-3305

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