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First report of cestode infection in the crustacean Artemia persimilis from Southern Chilean Patagonia and its relation with the Neotropical aquatic birds

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First report of cestode infection in the crustacean Artemia persimilis from Southern Chilean Patagonia and its relation with the Neotropical aquatic birds https://t.co/JkLRdPJf3A https://t.co/5fwPGfuKlL
First report of cestode infection in the crustacean Artemia persimilis from Southern Chilean Patagonia and its relation with the Neotropical aquatic #birds https://t.co/bRhHTG5cQD @thePeerJ https://t.co/7XIu4pr4Ql
PEER-REVIEWED Ecology section
Note that a Preprint of this article also exists, first published April 1, 2019.

Introduction

Conservation of biodiversity is one of the greatest challenges in this century given the accelerated rate of species loss due to global threats such as habitat degradation, biological invasions, overexploitation and co-extinctions. Parasites are important components of biodiversity and they are exposed to the same threats as their hosts (Gómez & Nichols, 2013). However, maintenance of the parasite biodiversity has not been traditionally considered as a priority strategy (Dunn et al., 2009) despite the fundamental role of parasitic organisms as ecological and evolutionary drivers, biomarkers of the ecology of their hosts and of ecosystems health as well as the benefits they can provide for host populations (reviewed by Gómez & Nichols, 2013). Understanding the host-parasite relationships in a given ecosystem, either in terms of the host specificity, virulence, transmission pathways or life cycles, is essential to know and preserve its biodiversity. Parasites with complex life cycles, i.e., those that involve more than one host, which are usually part of a common food web, may be used as good indicators of the aquatic biodiversity (Hechinger & Lafferty, 2005) and can reflect the specific diet of the final host and their population dynamics.

Hypersaline wetlands (i.e., salinity > 50 g/L; sensu Hammer, 1986) are natural laboratories for biodiversity key-studies due to their relatively simple trophic webs (Gajardo, Sorgeloos & Beardmore, 2006). The brine shrimps of the genus Artemia Leach (Crustacea: Branchiopoda: Anostraca) have a main ecological role in hypersaline ecosystems, both as food resource for aquatic bird communities (Sánchez, Green & Castellanos, 2006; Varo et al., 2011) and as filter feeders controlling the primary production via regulating the abundance of phytoplankton and transparency of water column, with potential for cascading effects (Mohebbi, 2010; Belovsky et al., 2011; Sánchez et al., 2016). Furthermore, they act as intermediate hosts of helminth parasites of aquatic birds such as flamingos, grebes, gulls, shorebirds and ducks (Georgiev et al., 2005; Vasileva et al., 2009; Redón et al., 2015a). Previous studies on helminths of Artemia spp. from the Western Mediterranean and USA have demonstrated the participation of brine shrimps in the life cycles of 15 cestode species of the order Cyclophyllidea and unidentified nematode species of the family Acuariidae (Georgiev et al., 2005; Vasileva et al., 2009; Redón et al., 2015a).

Two species of Artemia have been described as native for the American continent: A. franciscana Kellogg, widely distributed across the continent, and A. persimilis Piccinelli & Prosdocimi, restricted to Argentina and Southern Chile (Triantaphyllidis, Abatzopoulos & Sorgeloos, 1998; De los Ríos-Escalante, 2013). Information about their parasites is rather limited; the only comprehensive study has demonstrated the participation of A. franciscana in the circulation of helminth parasites in the Great Salt Lake (Utah, USA) (Redón et al., 2015a). For South American Artemia populations, their role in the transmission of avian parasites has never been explored. The aim of the present study is to fill the gap of knowledge by presenting the first helminthological study of A. persimilis from Southern Chilean Patagonia, including spatiotemporal effects on the dynamics of infection. The sampling sites include two of the most austral populations of A. persimilis described to date in Chile (Gajardo et al., 2002; De los Ríos-Escalante, 2013).

Material and Methods

Study area and Artemia sampling

The study area comprises two hypersaline aquatic ecosystems in the Southern Chilean Patagonia (50°–53°S), i.e., the Region of Magallanes and Chilean Antarctica (Fig. 1). Los Cisnes lagoon (53°15′S, 70°22′W) is located on Tierra del Fuego Island close to its main town Porvenir. It occupies 25.3 ha and represents an important habitat for flamingos, swans, grebes and shorebirds. In 1982, it was declared Natural Monument to protect its high diversity of aquatic birds (c. 50 species, see CONAF, 2009; CONAF, 2014). Amarga lagoon (50°58′S, 72°43′W) is a lake of 2.5 km length, 1.1 km breadth and 2.6 m of depth (Campos et al., 1996). It is located in the Province of Última Esperanza, at the entrance of Torres del Paine National Park. This Biosphere Reserve harbours a great diversity and abundance of birds, with c. 118 avian species using the area as permanent residents or migratory species, including flamingos, ducks, grebes, swans and geese (Matus & Barría, 1999; CONAF, 2007).

Geographical distribution of the study sites in the Region of Magallanes and Chilean Antarctica.

Figure 1: Geographical distribution of the study sites in the Region of Magallanes and Chilean Antarctica.

(1) Amarga lagoon. (2) Los Cisnes lagoon.

The local populations of Artemia were identified as A. persimilis, a species previously considered endemic to Argentina (Triantaphyllidis, Abatzopoulos & Sorgeloos, 1998) but later discovered in the Southern Chile, i.e., in the Amarga lagoon (Gajardo et al., 1998) and in Los Cisnes lagoon (De los Ríos-Escalante, 2010). Our sampling was carried out in spring (November 2017) and autumn (April 2018). Salinity of the water was measured in situ with a portable refractometer ATAGO®. Artemia individuals were collected with a plankton hand net (180 µm mesh size), washed in fresh water to remove salt and fixed in 70% ethanol. Artemia samples were transported to the laboratory and preserved at 4 °C for future parasitological examination. Additional living specimens were transferred into plastic bottles of 5 l containing lake brine and transported to the laboratory for further examination. Field work was conducted under an authorization for research activities in protected wild areas (Permission No 025/2017) issued by the Department of Conservation of Biological Diversity, National Forest Corporation of Chile (CONAF).

Processing brine shrimp samples and helminth identification

A total of 800 brine shrimps (200 individuals per site and season, mostly adults), randomly selected, with sex ratio c. 1:1, were mounted in glycerol and examined under a compound light microscope Olympus BX50 for the presence of cestodes. After screening, some cysticercoids (i.e., the larval stage of cestodes developing in the intermediate host) were isolated and mounted as microscope slides in Berlese’s medium for a more detailed morphological examination and taxonomic identification. In addition to these quantitative samples, in order to base the morphological examinations and the identification on greater numbers of parasite specimens, we examined some further Artemia individuals; the number of the cysticercoids recorded is given below in the text for each species. However, these additional cysticercoids were not used for the calculation of the infection parameters, which were based on the quantitative samples only.

Identification of cysticercoids was based on a comparison with the previous descriptions of cestode larvae that use branchiopods as intermediate hosts (Maksimova, 1973; Maksimova, 1976; Maksimova, 1981; Maksimova, 1989; Gvozdev & Maksimova, 1978; Georgiev et al., 2005; Vasileva et al., 2009; Redón et al., 2015a). Terminology of the cysticercoids follows Chervy (2002). The morphological examination of parasites (including measuring and preparation of drawings and photographs) was carried out using the facilities of IBER-BAS, Sofia, Bulgaria. Metrical data are given as a range, followed by the mean and number of observations (n) in parentheses. The measurements are in micrometres unless otherwise stated. Photographs were taken using Zeiss Axio Imager 2 light microscope equipped with differential interference contrast (DIC) and Jenoptik ProgRes® microscope camera incorporated. Drawings were prepared using Olympus BX51 microscope equipped with a drawing tube. The opensource graphic software, GIMP and Inkscape, were used for the image processing of illustrations.

Voucher specimens of cysticercoids have been deposited at the Invertebrate Collection of the Natural History Museum in Geneva (MHNG), Switzerland.

The specimens studied for each species were as follows:

  1. Confluaria podicipina: Los Cisnes lagoon, 29 November 2017, 5 cysticercoids, isolated and mounted in Berlese’s medium; MHNG-PLAT-122057, a cysticercoid isolated and mounted in Berlese’s medium; Amarga lagoon, 26 November 2017, 2 cysticercoids, one of them isolated and mounted in Berlese’s medium.

  2. Fimbriarioides (?) sp.: Los Cisnes lagoon, 29 November 2017, 6 cysticercoids, 17 April 2018, 7 cysticercoids; all cysticercoids mounted and measured in glycerol, subsequently 7 cysticercoids isolated and mounted in Berlese’s medium; MHNG-PLAT-122058, a cysticercoid isolated and mounted in Berlese’s medium; Amarga lagoon, 26 November 2017, 3 cysticercoids, 27 November 2017, 2 cysticercoids, 18 April 2018, 1 cysticercoid; all cysticercoids mounted and measured in glycerol, subsequently 2 cysticercoids isolated and mounted in Berlese’s medium.

  3. Flamingolepis sp.: Los Cisnes lagoon, 29 November 2017, 14 cysticercoids, mounted and measured in glycerol; subsequently 12 cysticercoids isolated and mounted in Berlese’s medium; MHNG-PLAT-122059, a cysticercoid isolated and mounted in Berlese’s medium.

  4. Wardium sp.: Los Cisnes lagoon, 29 November 2017, 2 cysticercoids mounted and measured in glycerol; subsequently both cysticercoids isolated and mounted in Berlese’s medium.

Parameters of infection and statistical analysis

Infection descriptors for each cestode species and for the overall infection were calculated according to Bush et al. (1997): prevalence (P%, number of infected individuals of the host population presented as percentage of the total number of examined individuals), mean intensity (MI, mean number of parasites per infected individual of the host population) and mean abundance (MA, mean number of parasites per examined individual of the host population, both infected and non-infected) In order to characterise the cestode community composition for each locality and season, we calculated the relative abundance (RA%, percentage of the number of individuals of a certain parasite species from the total number of individuals of all parasite species in the examined host population) for each parasite species.

Generalized linear models (GLMs) were performed to analyse prevalence of infection (total cestodes and Fimbriariodes (?) sp.) in relation to locality (Los Cisnes and Amarga lagoons), season (spring and autumn) and interactions between both factors. For Confluaria podicipina, we tested only the effect of the locality since this species was exclusively recorded in spring. A binomial error distribution and log link function were used in the model. GLM analyses were not performed for Flamingolepis sp. and Wardium sp. due to a quasicomplete separation of the observed data since infection was only detected in one locality and in one season. Instead, Z tests were used to analyse differences in the prevalence of Flamingolepis sp. between seasons and between localities. However, no statistical analyses were applied for Wardium sp. because only one infected individual was found. Non-parametrical Mann–Whitney U test was applied for testing temporal variations on the abundance of parasites and the intensity of infection. The same procedure was applied to analyse variations of these infection parameters between the localities within the same season. Non-parametric statistics were used owing to the lack of normality in the distributions of these parameters (even after transformations). Significance was assumed at p ≤ 0.05. Statistical analyses were performed using SPSS 15.0 for Windows (SPSS Inc. Chicago, IL, USA).

Results

Identification of helminth larvae

In the studied brine shrimps, we found larvae (cysticercoids) of cestodes belonging to four species and four genera of the family Hymenolepididae. They were identified at either the species level or the generic level on the basis of their morphology. The morphological characters of these larvae as well as the argumentation of our taxonomic identifications and possible associations with avian definitive hosts are presented in the following systematic survey.

Confluaria podicipina (Szymanski, 1905) (Figs. 2A, 3)

Cestode larvae from Artemia persimilis, Amarga lagoon (A, E) and Los Cisnes lagoon (B–F), Chile.

Figure 2: Cestode larvae from Artemia persimilis, Amarga lagoon (A, E) and Los Cisnes lagoon (B–F), Chile.

(A) Hook of Confluaria podicipina (Szymanski, 1905). (B, E) Hooks and cysticercoid of Fimbriarioides (?) sp. (C, F) Hooks and cysticercoid of Flamingolepis sp. 1. (D) Hook of Wardium sp. Drawing credit: Gergana P. Vasileva.

Remarks

We do not provide a complete description of cysticercoids from A. persimilis from Chile because they have morphological characters similar to those previously described for C. podicipina from Central Asia, Europe and North America (see Maksimova, 1981; Georgiev et al., 2005; Redón et al., 2015a): presence of an external envelope formed by the anterior part of the cercomer (Figs. 3A, 3B); invaginable rostellum armed with 10 aploparaksoid hooks (Figs. 2A, 3C, 3D); a very long and coiled cercomer, densely packed in a thin membranous envelope (Fig. 3A). The measurements of isolated cysticercoids in Berlese’s medium corresponded well to the previous data from A. parthenogenetica in Spain (Georgiev et al., 2005) and A. franciscana in USA (Redón et al., 2015a) (see Table 1). The only exception was the size of the external capsules of the cysticercoids, which was smaller in the specimens from Chile. Our results revealed less variations in the total size of the external capsule in the samples of C. podicipina from A. persimilis in comparison to those from USA and Spain, where we found cysticercoids of various sizes, including some specimens with intermediate measurements (Redón et al., 2015a). This difference was probably due to the smaller sample size of this parasite species in the present study. Despite the differences in the size of the external capsule, the morphology of the cysticercoids, the shape of their rostellar hooks and the remaining metrical data were similar to those reported in previous descriptions. On this basis, we identified these cysticercoids from A. persimilis as C. podicipina.

Confluaria podicipina (Szymanski, 1905) from Artemia persimilis, Los Cisnes lagoon (A) and Amarga lagoon (B–D), Chile (mounts in Berlese’s medium).
Figure 3: Confluaria podicipina (Szymanski, 1905) from Artemia persimilis, Los Cisnes lagoon (A) and Amarga lagoon (B–D), Chile (mounts in Berlese’s medium).
(A) Isolated cysticercoid with unpacked cercomer. (B) Fully developed cysticercoid with a part of unpacked cercomer. (C) Internal cysts. (D) Rostellar hooks.
Table 1:
Metrical data of cysticercoids of Confluaria podicipina (Szymanski, 1905) recorded in Artemia spp. from various localities.
All measurements in µm.
Host A. parthenogenetica A. franciscana A. persimilis
Locality Odiel marshes (Spain) Great Salt Lake (USA) Los Cisnes lagoon and Amarga lagoon (Chile)
References Georgiev et al. (2005) Redón et al. (2015a) Present study
Range Mean n Range Mean n Range Mean n
External length 195–255 215 9 144–313 212 15 113–185 135 5
capsule width 135–204 152 9 72–192 118 15 73–110 87 5
Cyst length 93–147 121 12 72–143 106 17 80–100 90 7
width 47–87 73 12 36–89 61 17 43–55 49 7
Scolex length 72–104 92 12 38–52 48 15 50–63 57 6
width 38–72 59 12 25–47 37 15 33–40 38 6
Suckers diameter 26–32 28 10 21–26 22 6 16–23 19 10
Rostellum length 42–47 46 7 23–31 27 10 25 25 3
width 18–23 20 3
Rostellar total length 21–24 22 12 19–21 20 11 18–21 19 10
hooks blade 11 11 10–12 11 10
handle 3–5 4 11 3–4 4 10
guard 5–6 6 11 5–6 6 10
DOI: 10.7717/peerj.7395/table-1

The species of the genus Confluaria Ablasov in Spasskaya, 1966 are specific parasites of grebes (Podicipediformes), recorded mostly from the Holarctic Region (Vasileva, Georgiev & Genov, 1999a; Vasileva, Georgiev & Genov, 1999b; Vasileva, Georgiev & Genov, 2000; Vasileva, Kornyushin & Genov, 2001; Vasileva, Skirnisson & Georgiev, 2008; Sitko & Heneberg, 2015). In South America, there are only two records of Confluaria spp.: C. capillaris (Rudolphi, 1810) in Tachybaptus dominicus (L.) in Brazil (Fuhrmann, 1906; Vasileva, Georgiev & Genov, 1999a) and an identified species of Confluaria reported from the Southern Silvery Grebe Podiceps occipitalis Garnot in the central Chile (González-Acuña et al., 2017). Until now, C. podicipina has been recorded in the Holarctic Region (Stock & Holmes, 1987; Vasileva, Georgiev & Genov, 2000). In North America (Alberta, Canada), Podiceps auritus (L.) and P. nigricollis have been reported as definitive hosts of C. podicipina (Stock & Holmes, 1987) and its confirmed intermediate host is A. franciscana (Redón et al., 2015a).

The present study is the first report of this species in the Neotropical Region and might be associated with grebe species distributed in Southern Patagonia. These are Silvery Grebe Podiceps occipitalis, Hooded Grebe Podiceps gallardoi Rumboll, White-tufted Grebe Rollandia rolland (Quoy & Gaimard), Pied-billed Grebe Podylimbus podiceps (L.) and the Great Grebe Podiceps major (Boddaert) (see Sylvester, 1995; Storer, 2000; CONAF, 2014). Based on its anatomical peculiarities (Fjeldså, 1983; Storer, 2000), feeding behaviour (Fjeldså, 1981) and diet (Wetmore, 1926), the most probable definitive host of C. podicipina in Patagonian lakes is P. occipitalis. The biological traits of this grebe species allow brine shrimps to be essential part of its feeding resources and it is the South-American grebe with dietary peculiarities similar to those of P. nigricollis (Mahoney & Jehl Jr, 1985; Storer, 2000). In contrast, Podylimbus podiceps feeds on crabs, crayfish and other hard-bodied animals; Rollandia rolland is a generalist, feeding on oligochaetes, crustaceans, fish and molluscs; Podiceps major is fish-eating; and P. gallardoi feeds on rather big amphipods, leaches and especially snails (Fjeldså, 1983; Storer, 2000).

Fimbriarioides (?) sp. (Figs. 2B, 2E, 4)

Description of cysticercoids (metrical data based on specimens mounted in Berlese’s medium): Diplocysticercoid. Outer envelope thin-walled, formed by packed cercomer, usually encircling internal cyst, often with irregular shape (Figs. 2E, 4B). Internal cyst lemon-shaped, thick-walled. Scolex almost oval, 195–210 ×163 − 195 (203 × 170, n = 5), with short apical protrusion. Suckers oval, muscular, unarmed; diameter 45–65 (56, n = 11). Rhynchus thick-walled, with distinct radial musculature (Fig. 2E). Rostellar sheath sac-like, 95–100 ×53 (98 ×53, n = 2); thin-walled (Fig. 2E). Rostellum invaginable, cup shaped, muscular, with apical invagination. Rostellar hooks resembling diorchoid, 10 in number. Each hook with long and straight handle with flattened, spatulate posterior end (Figs. 2B, 4C, 4D); blade sickle-shaped, slightly shorter than handle; guard short, with slightly bifurcated thickening (Figs. 2B, 4C). Measurements of rostellar hooks: total length 32–35 (33, n = 10), length of blade 13–15 (14, n = 10), length of handle 16–20 (17, n = 10), length of guard 3–4 (4, n = 10). Calcareous corpuscles concentrated anteriorly to scolex. Cercomer thick, long, usually forming compact additional thin-walled envelope surrounding cyst; unpacked cercomer thin-walled (Fig. 4A).

Additional measurements based on specimens in temporary glycerol mounts: diplocyst with outer envelope 200–315 ×155–265 (254 ×209, n = 6); internal cyst 175–215 ×130 − 155 (192 ×151, n = 13); scolex 118–130 ×98 − 125 (124 ×112, n = 9); diameter of suckers 38–53 (46, n = 21); rostellar sheath 75–108 ×45 − 60 (99 ×52, n = 7), rostellum 45–58 ×33 − 48 (49 ×41, n = 8); longest fragment of cercomer 470 ×88.

Fimbriarioides (?) sp. from Artemia persimilis, Los Cisnes lagoon (A, D) and Amarga lagoon (B, C), Chile.
Figure 4: Fimbriarioides (?) sp. from Artemia persimilis, Los Cisnes lagoon (A, D) and Amarga lagoon (B, C), Chile.
(A) Cysticercoid with smashed outer cyst and unpacked cercomer (temporary glycerol mount). (B) Acaudate diplocyst with fully developed cysticercoid (temporary glycerol mount). (C, D) Rostellar hooks of isolated cysticercoids (mounts in Berlese’s medium).

Remarks

There are 15 valid genera of the family Hymenolepididae characterised with 10 diorchoid rostellar hooks and parasitic in birds (see Czaplinski in Czaplinski & Vaucher, 1994; Mariaux et al., 2017). Among them, three genera possess invaginable rostellum, i.e., Fimbriaria Fröhlich, 1802, Fimbriarioides Fuhrmann, 1932 and Fimbriasacculus Alexander & McLaughlin, 1996 (see Czaplinski & Vaucher, 1994; Alexander & McLaughlin, 1996). They belong to the subfamily Fimbriariinae Wolffhügel, 1898 and include parasites of aquatic birds (mainly Anseriformes and Charadriiformes), accidentally Galliformes (Spasskaya, 1966; Czaplinski in Czaplinski & Vaucher, 1994).

The hooks of the cysticercoids from A. persimilis in Chile are characterised by a sickle-shaped blade, slightly shorter than the handle, a spatulate posterior end of handle and a slightly bifurcated thickening of the guard. This shape differs from the hooks of Fimbriaria spp., which have blades much shorter than handle and their guards are not bifid; a spatulate handle has been illustrated only for F. czaplinskii Grytner-Zięcina, 1994 (see Fig. 4 of Cielecka et al., 2011). In addition, data about the life cycle of Fimbriaria spp. indicate that they have freshwater life cycles that include mostly copepods, ostracods and amphipods as intermediate host (Jarecka, 1958; Spasskaya, 1966).

The hooks of the cysticercoids from A. persimilis resemble those of the species of Fimbriarioides (see Webster, 1943; Maksimova, 1976; Maksimova, 1989) and Fimbriasacculus (see Alexander & McLaughlin, 1996). Webster (1943) reported the presence of “long, bifid guard” in Fimbriarioides haematopodis Webster, 1943 and F. lintoni Webster, 1943. Maksimova (1989) also mentioned a peculiar structure of the rostellar hooks of F. spasskyi Maksimova, 1989, in which the blade and the guard form a “clamp-like” anterior part of the hook. A spatulate posterior end of the handle has been illustrated for two species of Fimbriarioides, i.e., F. tadornae Maksimova, 1976 (see Vasileva et al., 2009) and F. spasskyi as well as for Fimbriasacculus africanensis Alexander & McLaughlin, 1996 described from three species of Anatinae in South Africa (see Fig. 5 of Alexander & McLaughlin, 1996). Unfortunately, the generic differentiation between Fimbriarioides and Fimbriasacculus is based mainly on the strobilar morphology, which is not applicable to our study. There are no published records of species belonging to these genera from waterfowl in South America. By this reason, the generic identification of our larvae is somewhat conditional. We prefer to keep the identification of cysticercoids from A. persimilis as “Fimbriarioides (?) sp.” by two reasons: (i) the hooks of Fimbriasacculus have no bifurcation of the guard; (ii) the previous data on the life cycles of Fimbriarioides spp. confirm the role of branchiopods as their intermediate hosts (Maksimova, 1976; Vasileva et al., 2009). Another reason could be the fact that similar cysticercoids, i.e., diplocysticercoid (Chervy, 2002) have been recorded for Fimbriarioides intermedia (Fuhrmann, 1913) (see Belopolskaya, 1953).

Flamingolepis sp. from Artemia persimilis, Los Cisnes lagoon.
Figure 5: Flamingolepis sp. from Artemia persimilis, Los Cisnes lagoon.
(A, C) Fully developed cysticercoid with different stage of aggregation of the cercomer (temporary glycerol mounts). (B) Fully developed cysticercoid with focus on the morphology of the scolex, rostellum and the rostellar hooks (temporary glycerol mount). (D) Isolated cysticercoid (mount in Berlese’s medium). (E) Rostellar hooks of an isolated cysticercoid (mount in Berlese’s medium).

The present finding is the first geographical record of the genus Fimbriarioides in Chile and in South America. The list of possible definitive hosts of Fimbriarioides (?) sp. in Los Cisnes and Amarga lagoons includes the representatives of Anseriformes, i.e., shelducks (Tadorninae) Chloephaga rubidiceps Sclater and C. picta (Gmelin); dabbling ducks (Anatinae) Speculanas specularis (King), Anas georgica Gmelin, Lophonetta specularioides (King), Tachyeres patachonicus (King) and Mareca sibilatrix Poeppig (Garay, Johnson & Franklin, 1991; Matus & Barría, 1999).

Table 2:
Metrical data of cysticercoids of Flamingolepis spp. recorded in Artemia spp. Intermediate host and locality are also indicated.
All measurements are in m except where otherwise stated.
Source Robert & Gabrion (1991) Georgiev et al. (2005) Maksimova (1973) Present study
Intermediate hosts A. salina A. parthenogenetica A. salina A. persimilis
Locality France Spain Kazakhstan Chile
Flamingolepis spp. F. caroli F. liguloides F. flamingo F. dolguschini F. tengizi Flamingolepis sp.
Range Range Mean n Range Mean n Range Range Range Mean n
Cyst length 300 560–810 671 14 168–270 231 14 418 180 150–163 156 8
width 200 372–597 479 14 126–207 177 14 287 130 110–145 121 8
Scolex length 358–771 614 14 141–225 182 12 254 96 113–128 122 7
width 339–490 423 14 108–183 145 12 164 84 90–100 94 7
Suckers diameter 181–288 233 18 45–75 66 16 121 40–42 45–53 49 14
Rostellum length 446–485 465 14 108–180 119 5 100–125 114 8
width 116–149 125 14 33–48 43 5 23–28 25 8
Rostellar total length (TL) 110–130 186–201 189 15 55–61 57 15 184 53–54 45–50 49 15
hooks length of blade (Lb) 105–117 110 15 28–30 29 15 102 30 24–27 25 15
Ratio Lb/TL 0.56–0.60 0.58 15 0.47–0.53 0.5 15 app. 0.55 app. 0.56 0.50–0.54 0.52 15
Cercomer length (mm) 0.40–0.50 0.62–0.81 0.71 8 6.5–7.4 3 0.610 0.60* 1
DOI: 10.7717/peerj.7395/table-2

Notes:

Maximum length of the longest fragment of cercomer.

Flamingolepis sp. (Figs. 2C, 2F, 5)

Description of cysticercoids (metrical data based on specimens in Berlese’s medium; for some measurements see Table 2): Cercocysticercoid. Cyst elongate oval, with very thick wall, consisting of several layers; outer layer thick, with fine radial striations (Figs. 2F, 5A); numerous calcareous corpuscles situated in anterior part of cysticercoid. Scolex with conical apical protrusion and maximum width at level of suckers. Suckers unarmed, elliptical, with well-developed musculature. Rhynchus unarmed, thin-walled. Rostellar sheath thick-walled, 125–133 ×33 − 38 (130 ×36, n = 3), passing far beyond posterior margins of suckers; glandular cells presented in its cavity (Fig. 2F). Rostellum retractile, highly elongated, apical part with conical protrusion, posterior end usually coiled near bottom of rostellar sheath; walls thick, consisting of strong radial musculature (Figs. 2F, 5B, 5D); cavity with glandular cells. Rostellar hooks 8, skrjabinoid; each hook with long handle and very short guard; blade as long as handle or slightly longer, with smooth curvature; length of handle 21–24 (24, n = 15) (Figs. 2C, 5E). Cercomer considerably thick, coiled; cysticercoid with complete cercomer not available.

Additional measurements based on specimens in temporary glycerol mounts: Cyst 158–170 ×95 − 123 (164 ×111, n = 5); thickness of wall 7–12 (10, n = 5); scolex 118–125 ×73 − 96 (123 ×88, n = 5); diameter of suckers 43–50 (47, n = 16); rostellum 123–125 ×25 − 28 (125 ×26, n = 5); rostellar sheath 118–130 ×30 − 38 (123 ×35, n = 5); the longest available fragment of cercomer 40–75 wide and 600 long.

Remarks

According to the latest taxonomic revision of the family Hymenolepididae, only two genera possessing eight skrjabinoid rostellar hooks have been considered valid, i.e., Cladogynia Baer, 1938 and Sobolevicanthus Spasskii & Spasskaya, 1954 (Czaplinski in Czaplinski & Vaucher, 1994); the taxonomic concept of these two genera in the cited source postulated numerous generic synonymies based on the adoption of a few morphological criteria only (e.g., number and shape of hooks, presence of stylet in the male copulatory organ) and ignoring numerous further morphological and life-cycle characteristics, which have been used for distinguishing a number of well-defined hymenolepidid genera. By these reasons, most of the proposed synonymies have not been widely accepted and genera as Pararetinometra Stock & Holmes, 1982, Retinometra Spasskii, 1955 and Flamingolepis Spasskii & Spasskaya, 1954 are considered valid (Vasileva, Georgiev & Genov, 1996; Mariaux et al., 2017).

Judging on the presence of 8 skrjabinoid hooks and the extremely long retractile muscular rostellum, the cysticercoids from A. persimilis in Chile most closely resemble species of the genus Flamingolepis. Some other hymenolepidid genera parasitising aquatic birds have also similar characters, i.e., Cladogynia, Retinometra, Sobolevicanthus and Calixolepis Macko & Hanzelova, 1997. However, there are differences in the shape of hooks of the species of this group, despite the fact they all have been described as belonging to the “skrjabinoid type”. Compared to the hooks of the cysticercoids from Chile, the type species of Cladogynia, C. phoeniconaiadis (Hudson, 1934), has much bigger hooks with very long and thick base and much shorter blade (Baer, 1938). The majority of the species of the remaining three genera have hooks with a different proportion of their parts, i.e., the blades are much longer than the handles (Spasskaya, 1966; Maksimova, 1989). Moreover, the data about the life cycles of species of Retinometra and Sobolevicanthus indicated freshwater crustaceans (Copepoda, Ostracoda and Amphipoda) as intermediate hosts (Jarecka, 1960; Maksimova, 1989). Flamingolepis is the only hymenolepidid genus with 8 skrjabinoid hooks, which has been proven to use branchiopods as intermediate hosts. The definitive hosts are various species of Phoenicopteriformes. On this basis, we consider the above-described cysticercoids from A. persimilis as belonging to Flamingolepis.

Cysticercoids of five species of Flamingolepis have been recorded so far from Artemia spp. (Table 2). Judging on the length of hooks (45–50 µm), the cysticercoids from the present material are most similar to those of F. flamingo (Skrjabin, 1914) and F. tengizi Gvozdev & Maksimova, 1968, both parasitic in flamingos in Eurasia (Maksimova, 1989). F. flamingo has been recorded from A. salina and A. parthenogenetica in France (Robert & Gabrion, 1991; Sánchez et al., 2012) and Spain (Georgiev et al., 2005; Georgiev et al., 2007; Redón et al., 2011; Redón et al., 2015b; Sánchez et al., 2013). The cysticercoids from A. persimilis differ from those of F. flamingo by their greater size as well as by their bigger scolex (Table 2); furthermore, the cercomer of these cysticercoids is 40–75 µm wide while that of F. flamingo is only 8–12 µm wide (Georgiev et al., 2005). The cysticercoids of F. tengizi were described from two intermediate host species in Kazakhstan, i.e., A. salina (Maksimova, 1973) (Table 2) and the ostracod Eucypris inflata (Sars) (Gvozdev & Maksimova, 1978). The cysticercoid of F. tengizi described from A. salina differs from Flamingolepis sp. from Chile by the bigger cyst with thicker envelopes, the slightly bigger hooks with blades comprising more than 55% of the total hook length. The cysticercoids of the remaining three species of Flamingolepis differ significantly from the present material by the length of their hooks (Table 2).

In addition to the above mentioned species, which use brine shrimps in their life cycles, Flamingolepis includes two further species. F. megalorchis (Lühe, 1898) uses ostracods as intermediate hosts and has been characterised with bigger hooks compared with the present material (68–85 µm long, see Gvozdev & Maksimova, 1978). Another species is F. chileno Babero, Cattan & Jensen, 1981, described from Phoenicoparrus andinus (Philippi) in Chile (Babero, Cattan & Jensen, 1981), the only previously recorded species of Flamingolepis from South America. It is characterised by much bigger hooks (163–189 µm) with shape differing from that of the hooks of the cysticercoids from A. persimilis.

On the basis of the above mentioned remarks, we consider that the cysticercoids from A. persimilis from Patagonia do not fit the morphology and metrical characters of the described Flamingolepis spp. Most probably, these larvae belong to an undescribed species parasitizing flamingos. Its description requires examination of adult cestodes from their most probable definitive host, Chilean Flamingo Phoenicopterus chilensis Molina, which is abundant in hypersaline shallow lakes from Central Argentina to southern Chilean Patagonia (Battauz et al., 2013; Gibbons, Vilina & Cárcamo, 2007). The remaining two species of flamingos, Andean flamingo Phoenicoparrus andinus and James’ Flamingo Phoenicoparrus jamesi (Sclater), live in the high altitudes of the Andean plateaus of Peru, Chile, Bolivia and Argentina and the probability to be hosts of the species recorded in brine shrimps in Patagonia is low. Furthermore, P. andinus is primarily herbivorous, feeding on microalgae (Tobar et al., 2012).

Wardium sp. (Figs. 2D, 6)

Description of cysticercoids (metrical data based on specimens mounted in Berlese’s medium): Cercocysticercoid. Cyst lemon-shaped, thick-walled, 300–315 ×215 − 225 (n = 2). Scolex oval, 150–195 ×118 (n = 2), with maximum width at level of suckers (Fig. 6A). Suckers oval, unarmed, muscular, with diameter 43–65 (51, n = 6). Rhynchus short. Rostellar sheath deep, thin-walled, passing beyond level of posterior margins of suckers; 125 ×45 (n = 2). Rostellum invaginable, thick-walled, with apical enlargement and conically-tapering posterior part, 55–75 ×45 − 50 (n = 2) (Fig. 6A). Rostellar hooks aploparaksoid-like, 10 in number (Figs. 2D, 6C); blade sickle-shaped, slightly longer than guard; handle distinct, but very short, guard thick; base of hook comprised by well-developed epiphyseal thickening; total length of hooks 25–26 (25, n = 4), length of blade 12–13 (12, n = 4), length of base 18–19 (18, n = 4), distance between handle-tip and guard-tip 9–10 (10, n = 4). Calcareous corpuscles mostly concentrated in anterior part of the cyst. Cercomer 125 thick, length of longest fragment 1.4 mm. Cysticercoid with complete cercomer not available.

Wardium sp. from Artemia persimilis, Los Cisnes lagoon.
Figure 6: Wardium sp. from Artemia persimilis, Los Cisnes lagoon.
(A) Fully developed cysticercoid (temporary glycerol mount). (B) Isolated cysticercoid (mount in Berlese’s medium). (C) Rostellar hooks of an isolated cysticercoid (mount in Berlese’s medium).

Additional measurements based on specimens mounted in temporary glycerol mounts: Cyst 300–312 ×202 − 205 (n = 2); scolex 150 ×120 (n = 1); suckers 45–64 (51, n = 6); rostellar sheath 113 ×48 (n = 1); rostellum 50 ×43 (n = 1).

Remarks

The present material corresponds to the cysticercoids of the genus Wardium described previously from A. franciscana in Great Salt Lake, USA (Redón et al., 2015a). The shape and the measurements of the cyst, the suckers and rostellum are very similar. The rostellar hooks possess the same shape and epiphyseal thickening. The length of the hooks is also similar, i.e., 25–26 µm in cysticercoids from A. persimilis versus 24–26 µm in Wardium sp. from A. franciscana. Based on these similarities, we identify the cysticercoids from the present material as Wardium sp. and consider it as conspecific to the specimens from A. franciscana in USA. The exact identification of the species is difficult because of the small number of cysticercoids, e.g., two larvae per each of the localities (USA and Chile). The small sample makes difficult to obtain a representative range of the measurements and the intraspecific variability. Nevertheless, the detailed comparison of the rostellar hooks of the cysticercoids of Wardium sp. with the known species of Wardium Mayhew, 1925 and Branchiopodataenia Bondarenko & Kontrimavichus, 2004 revealed that none of the species of these two genera can be matched with the hooks of the cysticercoids of Wardium sp. (see Redón et al., 2015a).

Several species of Wardium and Branchiopodataenia have been recorded so far in South America. However, none of them has rostellar hooks with shape and length similar to these of the cysticercoids from Chile. These species are: Branchiopodataenia arctowskii (Jarecka & Ostas, 1984) from Larus dominicanus Lichtenstein from the King George Island (Antarctica) (the hooks are 14–20 µm long with elongate handle, but without epiphyseal thickening, see Bondarenko & Kontrimavichus, 2004a; Bondarenko & Kontrimavichus, 2004b); Wardium neotropicale Deblock & Vaucher, 1997 from Himantopus melanurus (Vieillot) in Paraguay (hooks are 9 µm long) (see (Bondarenko & Kontrimavichus, 2006)); W. paucispinosum Labriola & Suriano, 2000 described from Larus maculipennis in Argentina (hooks are 13–18 µm long, see Labriola & Suriano, 2000); and W. tinamoui (Olsen, 1970) from Nothoprocta perdicaria (Kittlitz) in Chile (16.6 µm long, see Bondarenko & Kontrimavichus, 2006). W. semiductilis Szidat, 1964, recorded from L. maculipennis and L. dominicanus from Argentina (Szidat, 1964), has hooks of completely different shape (assuming diorchoid, see Szidat, 1964) and a different shape of scolex, possessing a very long rhynchus.

The definitive hosts of the species of Wardium and Branchiopodataenia include mostly aquatic birds of the order Charadriiformes (Spasskaya, 1966; Bondarenko & Kontrimavichus, 2006). The list of potential hosts at Southern Chile includes species of this order such as Pluvianellus socialis Gray, Charadrius falklandicus Latham, C. modestus Lichtenstein, Vanellus chilensis (Molina), Haematopus leucopodus, Larus dominicanus (Garay, Johnson & Franklin, 1991; Matus & Barría, 1999). In addition, some of charadriiform birds migrate through both North and South America, e.g., Limosa haemastica (L.) (see Lepage, 2019), and they also might be hosts of these cestodes.

Spatial and temporal variations of cestode infections

Among examined 800 brine shrimp individuals (640 adults and 160 juveniles), 92 were infected by cestodes (P = 11.5%). Despite most of the infected Artemia individuals were adults (n = 88), infection was also detected in 2.5% of juveniles (n = 4). A total of 98 cestode larvae were identified in A. persimilis from the two localities in the Southern Chile, with the majority of them (>87%) found at Los Cisnes lagoon (Table 3). The cysticercoids were identified as belonging to four species of four genera of the family Hymenolepididae. Two of these species, Fimbriarioides (?) sp. and C. podicipina, were recorded at both localities. The other two, Flamingolepis sp. and Wardium sp. were found at Los Cisnes lagoon only. The total intensity ranged from 1 to 3 cysticercoids; 94.6% of the infected individuals harboured one cysticercoid. The brine shrimp individuals infected with 2 and 3 cysticercoids were 4.3% (4 individuals) and 1.1% (1 individual), respectively. Single species infections were recorded in 87 host individuals. Multiple species infections were found in 5 brine shrimps: 4 individuals from Los Cisnes from the November sample (3 individuals harbouring Flamingolepis sp. plus C. podicipina and 1 individual infected with Flamingolepis sp. and Fimbriarioides (?) sp.) as well as 1 individual from Amarga from the November sample containing Fimbriarioides (?) sp. plus C. podicipina.

Table 3:
Descriptive parameters of cestodes in brine shrimps Artemia persimilis from two hypersaline ecosystems in Southern Chile.
Cestode species Number of cysticercoids Prevalence (%) Intensity Abundance
Range Mean ± SE Relative (%) Mean ± SE
Los Cisnes lagoon
Confluaria podicipina 10 2.5 1 1.00 ± 0.00 11.6 0.025 ± 0.01
Fimbriarioides (?) sp. 19 4.8 1 1.00 ± 0.00 22.1 0.048 ± 0.01
Flamingolepis sp. 56 13.8 1–2 1.02 ± 0.01 65.1 0.140 ± 0.02
Wardium sp. 1 0.3 1 1.00 1.2 0.003 ± 0.00
Overall infection 86 20.3 1–3 1.06 ± 0.01 0.215 ± 0.02
Amarga lagoon
Confluaria podicipina 2 0.5 1 1.00 ± 0.00 16.7 0.005 ± 0.00
Fimbriarioides (?) sp. 10 2.5 1 1.00 ± 0.00 83.3 0.025 ± 0.01
Overall infection 12 2.8 1–2 1.09 ± 0.02 0.030 ± 0.01
DOI: 10.7717/peerj.7395/table-3

Notes:

SE

standard error

The cestode community in Los Cisnes lagoon was dominated by the parasite of flamingos, Flamingolepis sp. (RA = 65.1%), followed by Fimbriarioides (?) sp. (Table 3). The later species was the most abundant in the cestode community in brine shrimps at Amarga lagoon (RA = 83.3%). C. podicipina was recorded exclusively in spring. Fimbriarioides (?) sp. was the only cestode species recorded in both seasons (Table 4).

Table 4:
Temporal variations of cestode infection in Artemia persimilis in two localities from Southern Chile.
Los Cisnes lagoon Amarga lagoon
Cestode species Spring 2017 (S = 55 g/L) Autumn 2018 (S = 51 g/L) Spring 2017 (S = 86 g/L) Autumn 2018 (S = 81 g/L)
Confluaria podicipina P (%) 5.0* 0.0 1.0 0.0
MI ±  SE 1.00 ± 0.00 0.00 1.00 ± 0.00 0.00
MA ±  SE 0.05 ± 0.02* 0.00 0.01 ± 0.01 0.00
RA (%) 13.5 33.3
Fimbriarioides (?) sp. P% 3.5 6.0 2.0 3.0
MI ±  SE 1.00 ± 0.00 1.00 ± 0.00 1.00 ± 0.00 1.00 ± 0.00
MA ±  SE 0.04 ± 0.01 0.06 ± 0.02 0.02 ± 0.01 0.03 ± 0.01
RA (%) 9.5 100 66.7 100
Flamingolepis sp. P% 27.5* 0.0 0.0 0.0
MI ±  SE 1.02 ± 0.02 0.00 0.00 0.00
MA ±  SE 0.28 ± 0.03* 0.00 0.00 0.00
RA (%) 75.7
Wardium sp. P% 0.5 0.0 0.0 0.0
MI ±  SE 1.00 0.00 0.00 0.00
MA ±  SE 0.01 ± 0.01 0.00 0.00 0.00
RA (%) 1.4
Overall infection P% 34.5* 6.0 2.5 3.0
MI ±  SE 1.07 ± 0.04 1.00 ± 0.00 1.20 ± 0.03 1.00 ± 0.00
MA ±  SE 0.37 ± 0.04* 0.06 ± 0.02 0.03 ± 0.01 0.03 ± 0.01
No. of cestode specimens 74 12 6 6
No. of Artemia individuals examined 200 200 200 200
DOI: 10.7717/peerj.7395/table-4

Notes:

P (%)

prevalence

MI

mean intensity

MA

mean abundance

RA (%)

relative abundance

SE

standard error

S

salinity measured in situ

Spatiotemporal variations at p level 0.05 are shown according to Z-test (for prevalences) and Mann–Whitney U test (for intensities and abundances).

Indicates significant differences between seasons.
Indicates significant differences between sites in the same month.

GLM performed on total cestode prevalence showed a significant effect of locality (Table S1). Values were higher at Los Cisnes lagoon than at Amarga lagoon (Table 4 and Table S1). The interaction between locality and season was also significant, denoting a higher prevalence in spring in Los Cisnes lagoon but not in Amarga lagoon (Table S1 and Table 4). GLM for Fimbriarioides (?) sp. showed no significant effects of either locality or season (Table S1). For C. podicipina (recorded exclusively in spring), a significant positive effect of Los Cisnes lagoon was detected (B = 1.630, χ 2 Wald = 4.390, p = 0.036).

Significant difference for prevalence of Flamingolepis sp. was detected between seasons in Los Cisnes lagoon, registering higher values in spring (Z = 7.840, p < 0.001; Table 4). The overall abundance and the abundance of C. podicipina and Flamingolepis sp. were also significantly higher in spring than in autumn at Los Cisnes lagoon (Mann–Whitney tests, p < 0.001; Table 4 and Table S2). However, no seasonal differences were detected in Amarga lagoon for either total abundance or any cestode species (Mann–Whitney tests, p > 0.157; Table S2). Comparing between both localities in the same season, significant differences were detected for the prevalence of Flamingolepis sp. (Z = 7.840, p < 0.001) as well as for the overall abundance (Mann–Whitney, p < 0.001; Table S2) and the abundance of C. podicipina and Flamingolepis sp. in spring (Mann–Whitney test, p < 0.019; Table S2), with lower values in Amarga lagoon (Table 4). In contrast, for Fimbriarioides (?) sp., differences in abundance between localities were not statistically significant (Mann–Whitney test, p > 0.148, Table S2 and Table 4).

No seasonal variations were detected for the intensity of the overall infection in Los Cisnes lagoon (Mann–Whitney test, U = 390, p = 0.395) or Amarga lagoon (Mann–Whitney test, U = 12, p = 0.273) nor between localities in the same season (Mann–Whitney tests, p > 0.302; Table 4).

Discussion

Species composition of cestode larvae in relation to the avian communities

The present study provides the first evidence that A. persimilis participates in the life cycles of four cestode species of the family Hymenolepididae. These include: C. podicipina, a specific parasite of grebes; Flamingolepis sp., an unidentified cestode parasitic in flamingos; Fimbriarioides (?) sp. and Wardium sp., two unidentified species that could be parasitic in ducks or charadriiform birds.

Previous studies in the Western Mediterranean and North America have revealed that the prevalence of avian cestodes in brine shrimps may depend on the seasonal presence of definitive hosts at certain hypersaline wetlands (Georgiev et al., 2005; Georgiev et al., 2014; Sánchez et al., 2013; Redón et al., 2015a). On this basis, we could expect that the peculiarities of parasite communities in brine shrimps from Los Cisnes and Amarga lagoons are due to the differences between the avian communities of the two wetlands. Unfortunately, the information on the population dynamics of aquatic birds at both sampling sites in the Southern Chile is very limited.

Los Cisnes lagoon is an area with diverse habitats (Fuentes-González & Gajardo, 2017). This wetland is formed by a lagoon with a long peninsula protruded into it and surrounded by several temporary shallow water bodies and muddy areas used as feeding places for charadriiforms such as White-rumped Sandpiper Calidris fuscicollis, Baird’s Sandpiper C. bairdii, Two-banded Plover Charadrius falklandicus, Rufous-chested Plover C. modestus and the Magellanic Plover Pluvianellus socialis. Other frequent birds in the lagoon are Podiceps occipitalis, P. gallardoi and Phoenicopterus chilensis, particularly in winter and spring (CONAF, 2014; Roesler, 2015). The Amarga lagoon is a shallow hypersaline lake at the eastern border of the Torres del Paine National Park. The following species are among the most abundant birds year-round: Black-necked Swan Cygnus melancoryphus, Coscoroba Swan Coscoroba coscoroba, Upland Goose Chloephaga picta, several species of dabbling ducks, grebes Rollandia roland and Podiceps occipitalis (see Garay, Johnson & Franklin, 1991) as well as the flamingo Phoenicopterus chilensis, especially in spring (Campos et al., 1996; Matus & Barría, 1999). This avian diversity at the two examined wetlands is in agreement with the species composition of cestode larvae in A. persimilis found in the course of the present study. The most abundant cestode species in brine shrimps in Los Cisnes lagoon are Flamingolepis sp. (parasite of flamingos) and Fimbriarioides (?) sp., probably parasitic in shelducks (Tadorninae) or dabbling ducks (Anatinae). Data from dietary studies confirm that the most probable definitive host of Flamingolepis sp. is the Chilean Flamingo, which is feeding mainly on brine shrimps (Hurlbert, López & Keith, 1984) and other invertebrates (such as copepods, cladocers, rotifers, ostracods), and to a lesser extent on bacteria and microalgae (Polla et al., 2018).

The specific parasite of grebes C. podicipina was present at both sampling sites. However, comparing with data from previous studies in Spain and USA (Georgiev et al., 2005; Redón et al., 2011; Redón et al., 2015a), the prevalence, mean abundance and mean intensity of C. podicipina from A. persimilis in Chile are lower. For example, the prevalence in A. persimilis from Los Cisnes is 2.5% versus 28.7% in a population from A. parthenogenetica from Spain (Redón et al., 2011) and 27.4–40.6% in A. franciscana from the Great Salt Lake (Redón et al., 2015a). These dissimilarities could be due to differences in the abundance of the grebe populations at the sampling sites, P. nigricollis in the Holarctic and, most probably, P. occipitalis in the Neotropical Region. The high infection parameters at Great Salt Lake can be explained by the fact that the second largest staging population of P. nigricollis in North America (over 1 million grebes) occurs there (Redón et al., 2015a).

The low prevalence of larvae of parasites of charadriiform birds such as Wardium sp. as well as the lack of cysticercoids of the family Dilepididae were unexpected. However, further studies including (austral) summer and winter months might provide more parasitological data on cestodes of charadriforms since many Nearctic species arrive to South America for wintering during austral summer (i.e., from December to February). With the diversity of shores and shallow waters at both sampling sites and the variety of shorebirds inhabiting them (Garay, Johnson & Franklin, 1991; Matus & Barría, 1999), it could be expected that A. persimilis may play a role as an intermediate host for more cestode species, especially dilepidids occurring as adults in shorebirds (Georgiev et al., 2005; Redón et al., 2015a).

Spatial and temporal variations of cestode communities and bird communities

We have found that the two studied localities significantly differ concerning the overall cestode infection in A. persimilis, with higher prevalence of infection in Los Cisnes lagoon. Seasonal effects on the prevalence have been detected only for Los Cisnes lagoon, there being a significant locality ×season interaction. The present study has revealed both spatial and temporal variations in the prevalence and mean abundance of two species, Flamingolepis sp. and C. podicipina (Table 4), and therefore variations of the overall cestode abundance. The seasonal abundance of Flamingolepis sp. in spring samples from Los Cisnes lagoon may be explained by the abundance of Chilean flamingos, which are one of the main Artemia predators in Patagonian hypersaline wetlands (Campos et al., 1996). It is also considered as a common summer resident at Torres del Paine National Park (Garay, Johnson & Franklin, 1991). C. podicipina has been recorded only in spring at both localities, a fact suggesting the presence of grebes in a certain short period only. The most probable definitive host, P. occipitalis, is a resident bird at the two localities but it migrates to the Atlantic Coast and to Paraguay in non-breeding seasons (Matus & Barría, 1999), which might explain the lack of cysticercoids of C. podicipina in the autumn samples. Cysticercoids of Fimbriarioides (?) sp. were recorded at both localities and both seasons; its infection parameters did not demonstrate apparent seasonal trends (Table 4). This could be explained by the presence of waterfowl during the entire annual cycle at both sampling sites, especially the shelducks Cloephaga picta and C. poliocephala, as well as various dabbling ducks (Garay, Johnson & Franklin, 1991; Matus & Barría, 1999).

The limited amount of information on the population dynamics of aquatic birds at both sites demands further studies for a more comprehensive knowledge of host-parasite interactions in the “cestode –Artemia –aquatic birds” system in the hypersaline habitats in the austral part of Chile.

Contribution to the cestode fauna of the Neotropical aquatic birds

Previous surveys on helminth parasites from aquatic birds in southern South America are scarce, with a few studies from the last decades including parasites of gulls (Larus dominicanus and L. maculipennis), cormorants (Phalacrocorax olivaceus), grebes (Podiceps occipitalis, P. major and P. gallardoi) and swans (Cygnus melanocoryphus) (see Torres et al., 1991; Torres et al., 1993; González-Acuña et al., 2009; González-Acuña et al., 2010; González-Acuña et al., 2017; Núñez et al., 2017b). The available data on the helminth fauna associated to Chilean Flamingo are very limited, consisting of two reports of nematodes from captive birds in the San Francisco Zoo (Fox et al., 1974) and two further nematodes from Central Argentina (Núñez et al., 2017a). The data about cestodes from grebes in Chile are limited to a few cestode taxa recorded in several grebe species (for review, see Storer, 2000). The Neotropical Region has been considered as not sufficiently studied area in terms of the diversity of the avian cyclophyllidean cestodes (Mariaux et al., 2017). In this sense, our results contribute to the knowledge of the diversity of cestodes of aquatic birds in the region, providing the first geographical records of C. podicipina and the genus Fimbriarioides for the Neotropics. We also believe that Flamingolepis sp. from A. persimilis represents a new undescribed species, most probably a specific parasite of the Chilean Flamingo. In addition, the present work shows that hypersaline wetlands and their most conspicuous inhabitant (Artemia) are an excellent model system for parasitological studies and a useful tool to evaluate and monitor aquatic biodiversity (including hosts and parasites) or to explore the “hidden fauna” (avian endoparasites). The Magallanes and Chilean Antarctica Region is a pristine area and its hypersaline wetlands provide habitat for diverse aquatic birds. Thus we could expect that further studies on parasites of various groups of crustaceans can also contribute to increase the knowledge of avian cestode diversity in the region.

Conclusions

The present study provides the first evidence for the transmission of avian cestode parasites using brine shrimps as intermediate hosts in the Neotropical Region. It demonstrates the role of A. persimilis in the life cycles of at least four cestode species of the family Hymenolepididae parasitic in aquatic birds. These are specific parasites of grebes and flamingos as well as two unidentified species, most probably parasitic in ducks or charadriiform birds. Despite the lack of data on the adult cestodes, our finding represents the first data of the occurrence of a specific cestode parasite of flamingo (Flamingolepis sp.) transmitted via brine shrimps in hypersaline ecosystems of the Southern Chilean Patagonia. A more comprehensive research of wildlife parasite diversity of aquatic birds in South America is needed for better knowledge of the parasite life cycles and the factors affecting the host-parasite interactions.

Supplemental Information

Results from GLM of the effects of season, locality and their interaction on the prevalence of cestode infection using a binomial error distribution and a logit link function (0 = non infected; 1 = infected)

Localities are Los Cisnes and Amarga lagoons. Seasons are spring and autumn. Total cestode prevalence and prevalence for Fimbriarioides (?) sp. were analysed. Estimates for “Amarga lagoon”, “spring” and Los Cisnes * spring, Amarga * autumn, and Amarga * spring interactions are not included because they were aliased but they are effectively zero. Significant effects are indicated in bold.

DOI: 10.7717/peerj.7395/supp-1

Results for Mann-Whitney tests for the abundance of cestodes in A. persimilis between localities and seasons

Abundance for the overall infection and for each cestode species is presented. CIS, Los Cisnes lagoon; AMA, Amarga lagoon; S, spring; A, autumn. Significant p-values at 0.05 level are indicated in bold.

DOI: 10.7717/peerj.7395/supp-2

Metrical data of cestode cysticercoids found in the crustacean intermediate host Artemia persimilis in Chile

DOI: 10.7717/peerj.7395/supp-3

Raw data of cestode infection in the crustacean intermediate host Artemia persimilis in Chile

DOI: 10.7717/peerj.7395/supp-4