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Toxoplasma gondii Infection in Seagull Chicks Is Related to the Consumption of Freshwater Food Resources

  • Oscar Cabezón ,

    ocabezon@yahoo.com

    Affiliations Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Facultat de Veterinaria, Universitat Autònoma de Barcelona, Bellaterra, Spain, Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

  • Marta Cerdà-Cuéllar,

    Affiliation Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

  • Virginia Morera,

    Affiliation Institut de Recerca de la Biodiversitat (IRBio) and Departament de Biologia Animal, Universitat de Barcelona, Barcelona, Spain

  • Ignacio García-Bocanegra,

    Affiliation Departamento de Sanidad Animal, Facultad de Veterinaria, UCO, Córdoba, Spain

  • Jacob González-Solís,

    Affiliation Institut de Recerca de la Biodiversitat (IRBio) and Departament de Biologia Animal, Universitat de Barcelona, Barcelona, Spain

  • Sebastian Napp,

    Affiliation Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

  • Maria P. Ribas,

    Affiliation Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Facultat de Veterinaria, Universitat Autònoma de Barcelona, Bellaterra, Spain

  • Berta Blanch-Lázaro,

    Affiliation Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Facultat de Veterinaria, Universitat Autònoma de Barcelona, Bellaterra, Spain

  • Xavier Fernández-Aguilar,

    Affiliations Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Facultat de Veterinaria, Universitat Autònoma de Barcelona, Bellaterra, Spain, Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

  • Noelia Antilles,

    Affiliation Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

  • Sergio López-Soria,

    Affiliation Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

  • Cristina Lorca-Oró,

    Affiliation Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

  • Jitender P. Dubey,

    Affiliation Animal Parasitic Diseases Laboratory, Beltsville Agricultural Research Center, Agriculture Research Service, United States Department of Agriculture, Beltsville, MD, United States of America

  • Sonia Almería

    Affiliations Departament de Sanitat i d’Anatomia Animals, Facultat de Veterinària, Universitat Autònoma de Barcelona, Bellaterra, Spain, Centre de Recerca en Sanitat Animal (CReSA) - Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain

Toxoplasma gondii Infection in Seagull Chicks Is Related to the Consumption of Freshwater Food Resources

  • Oscar Cabezón, 
  • Marta Cerdà-Cuéllar, 
  • Virginia Morera, 
  • Ignacio García-Bocanegra, 
  • Jacob González-Solís, 
  • Sebastian Napp, 
  • Maria P. Ribas, 
  • Berta Blanch-Lázaro, 
  • Xavier Fernández-Aguilar, 
  • Noelia Antilles
PLOS
x

Abstract

Understanding the spread of Toxoplasma gondii (T. gondii) in wild birds, particularly in those with opportunistic feeding behavior, is of interest for elucidating the epidemiological involvement of these birds in the maintenance and dissemination of the parasite. Overall, from 2009 to 2011, we collected sera from 525 seagull chicks (Yellow-legged gull (Larus michahellis) and Audouin’s gull (L. audouinii)) from 6 breeding colonies in Spain and tested them using the modified agglutination test (MAT) for the presence of antibodies against T. gondii. Chick age was estimated from bill length. Main food source of seagull chicks was evaluated using stable isotope analyses from growing scapular feathers. Overall T. gondii seroprevalence was 21.0% (IC95% 17.5–24.4). A generalized linear mixed-effects model indicated that year (2009) and food source (freshwater) were risk factors associated to the individual risk of infection by T. gondii, while age (days) was close to significance. Freshwater food origin was related to the highest seroprevalence levels, followed by marine origin, supporting freshwater and sewages as important routes of dispersion of T. gondii. Year differences could indicate fluctuating rates of exposure of seagull chicks to T. gondii. Age ranged from 4 to 30 days and seropositivity tended to increase with age (P = 0.07), supporting that seropositivity is related to T. gondii infection rather than to maternal transfer of antibodies, which in gulls is known to sharply decrease with chick age. This study is the first to report T. gondii antibodies in Yellow-legged and Audouin’s gulls, thereby extending the range of intermediate hosts for this parasite and underscoring the complexity of its epidemiology.

Introduction

Toxoplasma gondii is a zoonotic intracellular protozoan parasite of worldwide distribution [1]. Wild and domestic felids are the definitive hosts and therefore are the only known hosts that excrete oocysts in feces. Humans and virtually all warm-blooded species, including birds, can be intermediate hosts and become infected by the ingestion of food and water contaminated with sporulated T. gondii oocysts, by consumption of tissue cysts in infected animal tissues, or congenitally [1]. T. gondii has been also recently considered as a waterborne parasite, and has been detected in diverse water sources including those used as recreational and drinking for humans [2]. Contamination of near-shore waters by T. gondii oocysts has been proven to be a threat for several marine mammal species, such as the sea otters (Enhydra lutris) from the California coasts, USA [3]. Sewage is considered to be one of the main sources of T. gondii oocysts from land to coastal environments [4]. However, the role of freshwater runoffs and/or sewages in the epidemiology of T. gondii in the Iberian Peninsula, as well as its impact in the health status on the different warm blooded species linked to aquatic ecosystems, have not been yet evaluated.

Birds can be exposed to the parasite via ingestion of food or water contaminated with sporulated oocysts and with infected tissues, based on their feeding habits. Although it is not common, vertical infection by T. gondii has been reported in some bird species [5,6]. Indeed, T. gondii infection is prevalent in many domestic and wild avian species, although the epidemiological role of those species is poorly understood [1,5,7,8,9]. Birds are suspected to act as dispersive agents of T. gondii into isolated territories without felines [10]. For instance, seropositivity to T. gondii has been reported in Arctic fox (Alopex lagopus) and polar bear (Ursus maritimus) from the Svalbard Island (Norway) [10,11,12,13], apparently in the absence of felids. However, the effectiveness of wild birds as carriers of the parasite into isolated feline-free environments is not fully understood.

Among birds, scavenging species such as some seagulls, which regularly feed on refuse dumps and sewage water, would be good candidates to study their epidemiological importance in Toxoplasma infection, but have rarely been studied. Exploring the spread of T. gondii in wild birds and possible links with opportunistic feeding behavior can help understanding the role of birds in maintaining and disseminating parasites over large geographical areas [5,6]. The feeding habits and the ecological adaptability to anthropized habitats of Larus spp. make them suitable to be considered as sentinels for environmental public health risks.

In the present study, we assayed T. gondii antibodies in seagull chicks from several breeding colonies in Spain. Main aims of the study were (1) to assess the role of seagulls as intermediate hosts and reservoirs of T. gondii; (2) to explore factors related to the presence of antibodies against this protozoa parasite in seagulls, particularly in relation to their feeding habits and access to human waste.

Materials and Methods

Animals and Samples

From 2009 to 2011, 479 yellow-legged gull chicks (Larus michahellis) were sampled from the Ebro Delta (n = 102), three Mediterranean islands (Medes Islands, n = 96; Dragonera Island, n = 68; and Columbretes Islands, n = 143) and one Atlantic island (Ons Island, n = 70) of the Iberian Peninsula (Table 1; Supplementary data). In 2011, we also sampled 47 Audouin’s gull (Larus audouinii) chicks from Alboran Island (Western Mediterranean). Colonies were sampled in a single visit over 1 to 4 days. All colonies are close to inhabited territories with the exception of Alboran Island and Columbretes Island, both small islands located more than 50 km away from continental land. All breeding colonies, except the one at Ebro Delta, are located in feline-free islands, with no wild or domestic felids or watercourses.

A single fledgling from each brood was captured, blood sampled, measured, weighed and marked with paint. The animals were sampled in the field and released immediately after sampling. Since maternal antibody concentration decreases with age in seabird nestlings, including gulls [14,15], we estimated the age of each chick from bill length. In yellow-legged gulls bill growth is known to approach linearity from the first to the fifth week following the relationship: age (days) = bill length (mm)*0.963–22.34 (JGS unpublished data), resulting in a chick age ranging from 4 to 30 days. Blood was extracted from a tarsal or brachial vein using sterile syringes, collected in a 2 ml tubes without anticoagulant and maintained in a cooler while in the field. In the lab, the blood was centrifuged at 652 g for 15 min and the resulting sera were stored at -80°C until analysis. Six to eight breast feathers from each bird were also collected and stored in plastic bags until analyzed.

Sampling methods were in compliance with the Ethical Principles in Animal Research of the Universitat Autònoma de Barcelona and field permits were authorized by Generalitat de Catalunya, Govern de les Illes Balears, Generalitat Valenciana, Xunta de Galicia and Junta de Andalucia. All sampling procedures and/or experimental manipulations in the field were reviewed and approved as part of obtaining the field permit.

Stable Isotopes Analyses

Before analyses, feathers were cleaned washing them in a 0.25M sodium hydroxide solution, and all residues eliminated by rinsing them repeatedly with distilled water. Once cleaned, feathers were dried to constant mass in an oven at 46°C and grounded to powder in a freezer mill (Spex Certiprep 6750; Spex Industries Inc., Metuchen, New Jersey, USA), operating at liquid nitrogen temperature. The resulting feather powder was subsampled for Carbon and Nitrogen analyses (0.4 mg) and for Sulphur analyses (3.4 g), placed in tin capsules and crimped for combustion. The samples were oxidized in a Flash EA1112 (for C and N) and EA1108 (for S) coupled to a Delta C stable isotope mass spectrometer through a Conflo III interface (Thermo Finnigan, Bremen, Germany), which was used to determine the δ15N, δ13C and δ34S values. Isotope ratios are expressed in δ notation as per mil units (‰) according to the following equation (δX = [(Rsample/Rstandard)-1] x 1000) where X (‰) is 15N, 13C or 34S and Rsample is the corresponding ratio 15N/14N, 13C/12C or 34S /32S. We used atmospheric nitrogen (AIR), Vienna-Pee Dee Belemnite (V-PDB) and troilite from the Canyon Diablo Meteorite, as Rstandard for the 15N, 13C and 34S, respectively. International standards were inserted every 12 samples to calibrate the system and compensate for drift over time. Sample errors were estimated by replicating essays of the standard material, indicating a sample error of ± 0.1‰ for the C and ± 0.2‰ for the N and S, although these values might be higher for organic materials of high complexity, such as feathers. All isotopic analyses were performed at the isotopic ratio mass spectrometry facility at the “Serveis Científico-Tècnics” at Barcelona’s University.

Isotopic values of the food sources were obtained from spontaneous regurgitations from chicks and fish discarded from vessels, collected by Ramos et al. [16] in a previous study of the Mediterranean colonies and by Moreno et al. [17] for the Atlantic colony, and classified in four functional groups: marine, freshwater and terrestrial prey and dumpsite feeding for the Mediterranean colonies and three groups (marine and terrestrial prey and dumpsite feeding) for the Atlantic colony, as freshwater prey was not found in those regurgitates. Trophic enrichment values were also taken from published data following Ramos et al. [18].

To assess the contribution of each food group to the chicks’ diet a three-isotope Bayesian mixing model was used (SIAR, Stable Isotope Analysis in R [19]) in the R Environment (R Core Team, 2014). This model includes the standard deviation of the isotopic values as a variable, thus allowing the intracolony variability to be taken into account, and applies a Markov Chain Monte Carlo (MCMC) method with a Dirichlet distribution. We ran the model with 106 iterations, discarding the first 105 as a burn-in.

Serological test

Sera were examined by the modified agglutination test (MAT) to detect IgG antibodies, which in birds would be mainly IgY, against T. gondii. Sera were tested at 1:25, 1:50, 1:100 and 1:500 dilutions. Positive and negative controls were also included in all tests. Titres of 1:25 or higher were considered positive and those with doubtful results were re-examined. This technique has been previously evaluated in several bird species [5,20,21].

Definition of variables and Statistical analysis

Prevalence of antibodies against T. gondii was estimated from the ratio of positive to the total number of samples, with the exact binomial confidence intervals of 95% [22]. Due to the limited number of Audouin’s gulls sampled (n = 47), the associated risk factors could not be properly analyzed, so this analysis was restricted to yellow-legged gulls, the most abundant and widely distributed gull species in Spain. To test for the potential influence of seroprevalence on chick body condition we checked for normality and equality of variances and performed an ANCOVA analysis, with body mass as dependent variable, and sampling (year/locality) and seroprevalence status as factors. To obtain an indication of the relevance of sampling year, food source and age on the risk of a chick being seropositive, we first tested their association to seropositivity for T. gondii using chi-square (sampling year, food source) and ANOVA tests (age). Associations between T. gondii seroprevalence and the three explanatory variables were analyzed using a Generalized Linear Mixed Model (GLMM) with an underlying binomial distribution (log link). The colony was included as a random effect. Models were fitted by Laplace approximation, implemented in the glmer function of the lme4 package for R (http://CRAN.R-project.org/package=lme4) [23]. Inference was based on model comparison of nested models (ANOVA), and the process of model selection was based on the lowest Akaike information criterion (AIC) value. Statistical analyses were carried out in R software (http://www.r-project.org/).

Results

Overall seroprevalence (MAT ≥ 1:25) against T. gondii was 21.0% (CI95%: 17.5–24.0), with titres of 1:25 in 38.0% of the samples, 1:50 in 39.4% of the samples, 1:100 in 18.3% of the samples and 1:500 in 4.2% of the samples. The seroprevalence in yellow-legged chicks and in Audouin’s gull chicks were 22.8% of 479 chicks and 2.2% of 46 chicks, respectively (Table 1).

Mean age of yellow-legged gull chicks differed significantly among the 13 samplings (locality-year) (Table 1). Body mass differed significantly among colonies and with chick age, but did not differ between seropositive and seronegative chicks (ANCOVA, locality-year F12,452 = 5.79, P<0.001; age F1,452 = 674.37, P<0.001; seroprevalence status F1,452 = 0.44; P = 0.51; locality-year*infection status F11,452 = 0.59; P = 0.84).

Statistically significant differences between the seropositivity to T. gondii and the three explanatory variables (year, food source and age) were observed in the bivariate analysis. Significantly higher seropositivity was found in 2009 (43.3%; 65/150) compared to 2010 (12.5%; 20/160) and 2011 (14.2%; 24/169). Freshwater origin as main food source showed statistically higher risk of infection compared to marine origin (29.5% of 132 seagull chicks versus 20.2% of 347 seagull chicks, respectively). The ANOVA tests showed that seropositivity significantly increased with age (p <0.001).

The model with best AIC-value (463.6) indicated that year (2009) and food source (freshwater) were risk factors associated to the individual risk of infection by T. gondii, while age (days) was close to significance (Table 2).

thumbnail
Table 2. Results of the generalized linear mixed-effects model of risk factors associated to Toxoplasma gondii seroprevalence in seagulls in Spain.

http://dx.doi.org/10.1371/journal.pone.0150249.t002

Food resources according to their origin (marine, freshwater, terrestrial, refuse) fed by chicks from the different seagull colonies is indicated in Table 3.

thumbnail
Table 3. Diet reconstruction with Bayesian mixing model: percentage of use of main food sources for each breeding colony and year.

Given values are medians, with 95% credibility intervals in brackets. Values in bold represent the main food source; underlined values represent the secondary source.

http://dx.doi.org/10.1371/journal.pone.0150249.t003

Discussion

The present study shows the first data on seroprevalence of T. gondii in yellow-legged and Audouin’s gulls worldwide, and adds two new species of gulls to the list of possible intermediate host for T. gondii infection. Isolation of the parasite from tissues would be necessary to confirm the intermediate host role of these seagull species. Of the two species of seagull analyzed, Audouin’s gull is an endemic species from the Mediterranean, which is regarded as globally near threatened [24]. The T. gondii seroprevalence differences between the two seagull species seem not to be due to differences in feeding behavior since similar origin of food was observed in the colony from Audouin´s gull compared to the yellow-legged colonies in the Mediterranean areas (Table 1). These differences could be due to the fact that Audouin´s gull, which showed the lowest seroprevalence in the study, were sampled in Alboran Island, a small Mediterranean island located far from the continental land, and closer to the Northern African (64.82 Km) than to the Spanish (92.6 Km) coasts. However, since the two species were sampled in different colonies, it is not possible to confirm this hypothesis.

Seroprevalence of T. gondii antibodies in this study showed also statistically significant differences among sampling years. The highest seroprevalence in yellow legged seagull chicks was observed from samples collected during the first year of study compared to those from the next two years, although different dynamics were observed in some colonies among years. These results would indicate fluctuating rates of transmission of T. gondii as has been observed in other wildlife species in Spain [25]. The highest seroprevalence observed in 2009 was not related to a particular colony, since no significant differences in seroprevalence were observed among colonies that year, and the variations seemed to be independent of the origin of the diet. Temporal, year-to-year variations have also been explained by the effect of variable meteorological conditions on the level of infection in domestic [26] and wild species [27]. Although seroprevalence fluctuation in wildlife populations has been studied [28], further studies will be needed to explain seroprevalence of T. gondii antibodies fluctuations in wildlife species.

The presence of antibodies against T. gondii in seagull chicks of the colonies from unoccupied and feline-free islands can be explained by 1) the presence of maternal antibodies or 2) by horizontal infection of chicks while being fed by their progenitors. Even though in the present study seropositivity seemed to increase with age, which would support the second hypothesis, the association was not statistically significant at the 5% level. However, the p value was close to significance (p value of 0.075) and the best fitting model (lowest AIC) included age, indicating that this variable is relevant for the evaluation of the risk T. gondii infection in seagull chicks.

In birds, maternal antibodies accumulate in the oocyte during egg yolk formation and receptor-mediated absorption by the chick begins shortly before hatching [29]. However, these antibodies are usually considered to decay within few days or weeks after hatching in classical model species, such as quails and chickens [14]. In another gull species, the black-legged kittiwake (Rissa trydactila), the rate of decay is high and levels of antibodies are very low two weeks after hatching [30]. In our study, most yellow legged-gull chicks were sampled when they were older than ten days old. Moreover, if the antibodies of young seropositive chicks were the result of maternal transfer, seropositivity should decrease with age, but we found the opposite trend. Therefore, the pattern of antibodies in those colonies indicates that the main route of transmission of T. gondii in seagulls is horizontal as the exposure to the parasite occurs through the feeding of chicks. In addition, it has to be taken into account that at least in chickens, infection in hens very rarely results in egg infection, and when egg infection occurs, it generally produces egg mortality and clinical toxoplasmosis in chicks [31], thus preventing vertical infection to be successful.

To our knowledge, T. gondii has been isolated from black-headed gulls (L. ridibundus), while antibodies have been reported in ring-billed gulls (L. delawarensis) and in laughing gulls (L. atricilla) [1,32]. The overall seroprevalence observed in the present study is in line with that found in black-headed gulls (19.9% of 659) in China using the same diagnosis method but with a cut off titer of ≥ 1:5 [32]. Previous reports showed seroprevalence levels of 15.3% in 13 ring-billed gull and 6% in 33 laughing gulls [1]. Negative results were observed in 127 gulls (Larus spp.) from Norway and Sweden [33], and in 27 glaucous gulls (L. hyperboreus) from Svalbard Island in the high Arctic [11]. However, differences in seroprevalence among studies have to be compared carefully since techniques, species, geographical and/or climatological conditions varied among studies. Our results indicate widespread exposure of T. gondii in seagulls in the Iberian Peninsula, in agreement with previous studies in many wild bird species in the South of Europe [5,6,7,21,34].

As other intermediate hosts, seagulls can be infected with T. gondii by ingestion of sporulated oocysts, ingestion of bradyzoites in tissue cysts of other intermediate hosts or vertically. Toxoplasma gondii oocysts from cat feces are believed to be washed into sewage and fresh-water runoffs to the marine ecosystems [4], where oocysts remain infective for up to 24 months [35]. In the aquatic ecosystems, oocysts have proven to be accumulated by filter-feeding invertebrates or fishes [36,37], and that has been suggested as the route of transmission by which aquatic ecosystems are linked to warm-blooded animals. [3,38]. Also, high concentrations of oocysts of the parasite in water were also positively correlated with the proximity of human settlements and sewages [4].

In a recent study carried out in a large number of wild bird species with a large number of samples analyzed, the main risk factors associated with T. gondii seropositivity in wild birds in Spain were age and feeding behavior [5]. The diet reconstruction shows, as expected, a heavy dependence on marine sources for the colonies closer to important fishing grounds (Columbretes, Ons and Ebro Delta). In the particular case of the Ebro Delta, in which gulls have easy access to brackish and freshwater environments, freshwater prey has a relatively high importance as a secondary food source. In Medes Islands fisheries discards are not abundant, but the Empordà wetlands nearby provide a constant and predictable source of freshwater prey, and this is certainly reflected in the diet reconstruction. The opportunistic nature of this species is reflected in the changes in diet in the Dragonera colony after the covering of the local landfill reduced the availability of dumpsite-related food sources, and a rodent extermination intensive program that poisoned a great number of birds and drastically reduced the population [39]. Interestingly, our results detected the highest seroprevalence in colonies that had freshwater as their primary food source. Most of the seagull colonies in our study had access to the shore and coastal aquatic areas close to human settlements, which could increase the risk of exposure to this parasite [1]. The lowest seroprevalence in yellow-legged gulls was observed in the colonies from Ons Island, located in the Atlantic Ocean, where the main source of food was marine followed by refuse, and where freshwater and terrestrial food origin represented only a small percentage [17]. On the contrary, the highest seroprevalence was observed in the Mediterranean island of Medes with a freshwater source of food as the main diet. There was also higher prevalence of antibodies in the chicks that had marine as the secondary source of food. We can assume that the presence of T. gondii oocysts was high in filter feeding invertebrates or fish provided to the seagull chicks of our study during the first weeks of life. These data would indicate the aquatic environment as one of the main routes of transport and accumulation of T. gondii oocysts in the Mediterranean basin. This hypothesis is in agreement with previously reported T. gondii infection in several dolphin species from the Western Mediterranean sea [40,41].

The assessment of T. gondii infection in seagulls confirms the susceptibility to T. gondii infection and points these bird species as intermediate hosts. Therefore, as subclinical carriers, there would be no health limitations imposed by T. gondii infection on the seagull species analyzed. In addition, since Audouin´s gull is a migratory species, our results suggest that gulls can act as carriers of the parasite in their migrations, having the capability to introduce pathogens in remote islands as naïve territories and expose to other susceptible hosts. In this sense, our results identify the yellow-legged and Audouin´s gulls as a good sentinel species to monitor the presence of T. gondii due to their scavenging feeding behavior and the high population densities in certain geographic locations. However, in order to evaluate the role of these species in the dispersion of different T. gondii biotypes, information on the distance covered by each species during migration and molecular characterization of the parasite in migratory birds would be useful.

Supporting Information

S1 Table. Data about the chick gulls analyzed.

Species; MAT: results (positive/negative) of the analysis for the detection of antibodies against Toxoplasma gondii; Titer of the antibodies; year of sampling; age (in days) of the analyzed animal; colony of origin; main food source of the chick analyzed.

doi:10.1371/journal.pone.0150249.s001

(DOCX)

Acknowledgments

Thanks for the legal permissions to develop this work to the Dept. de Medi Ambient i Habitatge de la Generalitat de Catalunya; Conselleria de Medi Ambient i Mobilitat del Govern de les Illes Balears; Conselleria de Medi Ambient de la Generalitat Valenciana; Consejería de Medio Ambiente de la Junta de Andalucía; Conselleria do Medio Rural de la Xunta de Galicia; Parc Natural del Delta de l'Ebre, Parc Natural del Montgrí, les Illes Medes i el Baix Ter; Parc Natural illes Columbrets; Parc Natural de sa Dragonera; Parque Nacional Marítimo-Terrestre de las Islas Atlánticas; and to Mariano Paracuellos, Juan Carlos Nevado, José Antonio Fernandez Bouzas, Joan Mayol, Jose Vicente Escobar and the guarderia de Columbrets, for their help in logistics and sampling. The authors would also like to thank our many colleagues at University of Barcelona and the staff of CReSA for their help in the field. This study was partially supported by the Spanish MINECO grant AGL2012-39830-C02, CGL2009-11278/BOS and INIA grant FAU2008-00012-C02-01 and FEDER funds.

Author Contributions

Conceived and designed the experiments: OC MCC JGS JPD SA. Performed the experiments: MPR BBL XFA VM NA SLS CLO. Analyzed the data: OC IGB JGS SA MCC SN. Contributed reagents/materials/analysis tools: MCC JGS SA. Wrote the paper: OC JGS IGB SA SN.

References

  1. 1. Dubey JP. Toxoplasmosis in animals and humans. 2ns ed. CRC Press. Boca Raton, FL; 2010.
  2. 2. Palos-Ladeiro M, Bigot A, Aubert D, Hohweyer J, Favennec L, Villena I, et al. Protozoa interaction with aquatic invertebrate: interest for watercourses biomonitoring. Environ Sci Pollut Res. 2013; 20: 778–789.
  3. 3. Shapiro K, Krusor C, Mazzillo FF, Conrad PA, Largier JL, Mazet JA, et al. Aquatic polymers can drive pathogen transmission in coastal ecosystems. Proc Biol Sci. 2014; 22: 281(1795).
  4. 4. Miller MA, Gardner IA, Kreuder C, Paradies DM, Worcester KR, Jessup DA, et al. Coastal freshwater runoff is a risk factor for Toxoplasma gondii infection of southern sea otters (Enhydra lutris nereis). Int J Parasitol. 2002; 32: 997–1006. pmid:12076629
  5. 5. Cabezón O, García-Bocanegra I, Molina-López R, Marco I, Blanco JM, Höfle U, et al. Seropositivity and risk factors associated with Toxoplasma gondii infection in wild birds from Spain. PLoS One. 2011; 6:e29549. doi: 10.1371/journal.pone.0029549. pmid:22216311
  6. 6. Mancianti F, Nardoni S, Mugnaini L, Poli A. Toxoplasma gondii in waterfowl: the first detection of this parasite in Anas crecca and Anas clypeata from Italy. J Parasitol. 2013; 99: 561–563. doi: 10.1645/12-34.1. pmid:23145510
  7. 7. Lopes AP, Sargo R, Rodrigues M, Cardoso L. High seroprevalence of antibodies to Toxoplasma gondii in wild animals from Portugal. Parasitol Res. 2010; 108: 1163–1169. doi: 10.1007/s00436-010-2158-6. pmid:21104273
  8. 8. Yu L, Shen J, Su C, Sundermann CA. Genetic characterization of Toxoplasma gondii in wildlife from Alabama, USA. Parasitol Res. 2013; 112: 1333–1336. doi: 10.1007/s00436-012-3187-0. pmid:23160892
  9. 9. Zöller B, Koethe M, Ludewig M, Pott S, Daugschies A, Straubinger RK, et al. Tissue tropism of Toxoplasma gondii in turkeys (Meleagris gallopavo) after parenteral infection. Parasitol Res. 2013; 112: 1841–1847. doi: 10.1007/s00436-013-3337-z. pmid:23408341
  10. 10. Sandström CA, Buma AG, Hoye BJ, Prop J, van der Jeugd H, Voslamber B, et al. Latitudinal variability in the seroprevalence of antibodies against Toxoplasma gondii in non-migrant and Arctic migratory geese. Vet Parasitol. 2013; 194: 9–15. doi: 10.1016/j.vetpar.2012.12.027. pmid:23339847
  11. 11. Prestrud KW, Asbakk K, Fuglei E, Mørk T, Stien A, Ropstad E, et al. Serosurvey for Toxoplasma gondii in arctic foxes and possible sources of infection in the high Arctic of Svalbard. Vet Parasitol. 2007; 150: 6–12. pmid:17950534
  12. 12. Sørensen KK, Mørk T, Sigurðardóttir O´G, Asbakk K, Akerstedt J, Bergsjø B, et al. Acute toxoplasmosis in three wild arctic foxes (Alopex lagopus) from Svalbard; one with co-infections of Salmonella Enteritidis PT1 and Yersinia pseudotuberculosis serotype 2b. Res Vet Sci. 2005; 78: 161–167. pmid:15563924
  13. 13. Jensen SK, Aars J, Lydersen C, Kovacs KM, Åsbakk K. The prevalence of Toxoplasma gondii in polar bears and their marine mammal prey: evidence for a marine transmission pathway? Polar Biol. 2010; 33: 599–606.
  14. 14. Garnier R, Ramos R, Staszewski V, Militão T, Lobato E, González-Solís J et al. Maternal antibody persistence: a neglected life history trait with implications from albatross conservation to comparative immunology. Proc R Soc B—Biol Sci. 2012; 279: 2033–2041.
  15. 15. Arnal A, Gómez-Díaz E, Cerdà-Cuéllar M, Lecollinet S, Pearce-Duvet J, Busquets N, et al. Circulation of a Meaban-like virus in yellow-legged gulls and seabird ticks in the western Mediterranean Basin. Plos One. 2014; 9:e89601. doi: 10.1371/journal.pone.0089601. pmid:24625959
  16. 16. Ramos R, Ramírez F, Sanpera C, Jover L, Ruiz X. Diet of Yellow-legged Gull (Larus michahellis) chicks along the Spanish Western Mediterranean coast: The relevance of refuse dumps. J Ornithol. 2009; 150: 265–272.
  17. 17. Moreno R, Jover L, Munilla I, Velando A, and Sanpera C. A three-isotope approach to disentangling the diet of a generalist consumer: the yellow-legged gull in northwest Spain. Mar Biol. 2010; 157: 545–553.
  18. 18. Ramos R, Ramírez F, Sanpera C, Jover L, Ruiz X. Feedinfg ecology of Yellow-legged gulls Larus michahellis in the western Mediterranean: a comparative assessment using conventional and isotopic methods. Marine Ecology Progress Seires. 2009; 377: 289–297.
  19. 19. Parnell AC, Inger R, Bearhop S, Jackson AL. Source partitioning using stable isotopes: Coping with too much variation. PLoS ONE. 2010; 5: 1–5.
  20. 20. Dubey JP. A review of Toxoplasmosis in wild birds. Vet Parasitol. 2002; 106: 121–153. pmid:12031816
  21. 21. Molina-López R, Cabezón O, Pabón M, Darwich L, Obón E, Lopez-Gatius F, et al. High seroprevalence of Toxoplasma gondii and Neospora caninum in the Common raven (Corvus corax) in the Northeast of Spain. Res Vet Sci. 2012; 93: 300–302. doi: 10.1016/j.rvsc.2011.05.011. pmid:21645913
  22. 22. Thrusfield M. Veterinary Epidemiology. 3rd ed. Oxford (UK): Blackwell Science Ltd, Blackwell Publishing company; 2007.
  23. 23. Zuur A, Ieno EN, Walker N, Saveliev AA, Smith GM. Mixed effects models and extensions in ecology with R. Springer Science & Business Media; 2009.
  24. 24. International Union for Conservation of Nature and Natural Resources—IUCN; 2014. Available: http://www.iucnredlist.org
  25. 25. Fernández-Aguilar X, Alzaga V, Villanúa D, Cabezón O, García-Bocanegra I, Dubey JP, et al. Epidemiology and prevalence of Toxoplasma gondii infection in the Iberian hare (Lepus granatensis). Vet Parasitol. 2013; 196: 194–198. doi: 10.1016/j.vetpar.2013.01.061. pmid:23462253
  26. 26. Afonso E, Thulliez P, Gilot-Fromont E. Local meteorological conditions, dynamics of seroconversion to Toxoplasma gondii in cats (Felis catus) and oocyst burden in a rural environment. Epidemiol Infect. 2010; 138: 1105–1113. doi: 10.1017/S0950268809991270. pmid:19961642
  27. 27. Gotteland C, Aubert D, Gibert P, Moinet M, Klein F, Game Y, et al. Toxoplasmosis in natural populations of ungulates in France: prevalence and spatiotemporal variations. Vector Borne Zoonotic Dis. 2014; 14: 403–413. doi: 10.1089/vbz.2013.1304. pmid:24745359
  28. 28. Garnier R, Graham AL. Insights from parasite-specific serological tools in eco-immunology. Integr Comp Biol. 2014; 54: 363–376. doi: 10.1093/icb/icu022. pmid:24760794
  29. 29. Rose ME, Orlans E. Immunoglobulins in the egg, embryo and young chick. Dev Comp Immunol. 1981; 5: 15–20. Review. pmid:7009243
  30. 30. Staszewski V, Gasparini J, McCoy KD, Tveraa T, Boulinier T. Evidence of an interannual effect of maternal immunization on the immune response of juveniles in a long-lived colonial bird. J Anim Ecol. 2007; 76: 1215–1223. pmid:17922718
  31. 31. Dubey JP. Toxoplasma gondii infections in chickens (Gallus domesticus): prevalence, clinical disease, diagnosis and public health significance. Zoonoses Public Health. 2010, 57: 60–73.
  32. 32. Miao Q, Han JQ, Xiang X, Yuan FZ, Liu YZ, Duan G, et al. Prevalence of antibody to Toxoplasma gondii in black-headed gulls (Chroicocephalus ridibundus), Dianchi Lake, China. J Wildl Dis. 2014; 50: 717–719. doi: 10.7589/2014-01-016. pmid:24807354
  33. 33. Kapperud G. Survey for toxoplasmosis in wild and domestic animals from Norway and Sweden. J Wildl Dis. 1978; 14: 157–162. pmid:650778
  34. 34. Darwich L, Cabezón O, Echeverria I, Pabón M, Marco I, Molina-López R, et al. Presence of Toxoplasma gondii and Neospora caninum DNA in the brain of wild birds. Vet Parasitol. 2012; 183: 377–381. doi: 10.1016/j.vetpar.2011.07.024. pmid:21831525
  35. 35. Lindsay DS, Dubey JP. Long-term survival of Toxoplasma gondii sporulated oocysts in seawater. J Parasitol. 2009; 95: 1019–1020. doi: 10.1645/GE-1919.1. pmid:20050010
  36. 36. Massie GN, Ware MW, Villegas EN, Black MW. Uptake and transmission of Toxoplasma gondii oocysts by migratory, filter-feeding fish. Vet Parasitol. 2010; 169: 296–303. doi: 10.1016/j.vetpar.2010.01.002. pmid:20097009
  37. 37. Lindsay DS, Collins MV, Mitchell SM, Wetch CN, Rosypal AC, Flick GJ, et al. Survival of Toxoplasma gondii oocysts in Eastern oysters (Crassostrea virginica). J Parasitol. 2004; 90: 1054–1057. pmid:15562605
  38. 38. Chadwick EA, Cable J, Chinchen A, Francis J, Guy E, Kean EF, et al. Seroprevalence of Toxoplasma gondii in the Eurasian otter (Lutra lutra) in England and Wales. Parasit Vectors. 2013; 6: 75. doi: 10.1186/1756-3305-6-75. pmid:23510234
  39. 39. Steigerwald EC, Igual JM, Payo-Payo A, Tavecchia G. Effects of decreased anthropogenic food availability on an opportunistic gull: evidence for a size-mediated response in breeding females. Ibis. 2015; 157: 439–448.
  40. 40. Resendes AR, Almería S, Dubey JP, Obón E, Juan-Sallés C, Degollada E, et al. Disseminated toxoplasmosis in a Mediterranean pregnant Risso's dolphin (Grampus griseus) with transplacental fetal infection. J Parasitol. 2002; 88: 1029–1032. pmid:12435153
  41. 41. Cabezón O, Resendes AR, Domingo M, Raga JA, Agustí C, Alegre F, et al. Seroprevalence of Toxoplasma gondii antibodies in wild dolphins from the Spanish Mediterranean coast. J Parasitol. 2004; 90: 643–644. pmid:15270114