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Rodriguez-Fernandez, V.; Bruschi, F. Toxoplasma gondii in Marine Life of Italian Coasts. Encyclopedia. Available online: https://encyclopedia.pub/entry/52963 (accessed on 21 December 2024).
Rodriguez-Fernandez V, Bruschi F. Toxoplasma gondii in Marine Life of Italian Coasts. Encyclopedia. Available at: https://encyclopedia.pub/entry/52963. Accessed December 21, 2024.
Rodriguez-Fernandez, Veronica, Fabrizio Bruschi. "Toxoplasma gondii in Marine Life of Italian Coasts" Encyclopedia, https://encyclopedia.pub/entry/52963 (accessed December 21, 2024).
Rodriguez-Fernandez, V., & Bruschi, F. (2023, December 20). Toxoplasma gondii in Marine Life of Italian Coasts. In Encyclopedia. https://encyclopedia.pub/entry/52963
Rodriguez-Fernandez, Veronica and Fabrizio Bruschi. "Toxoplasma gondii in Marine Life of Italian Coasts." Encyclopedia. Web. 20 December, 2023.
Toxoplasma gondii in Marine Life of Italian Coasts
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This entry is adapted from the peer-reviewed paper 10.3390/parasitologia3040035

Coastal areas of Italy experience high anthropogenic pressure, with a population density estimated to be 360 people per km2. This is correlated with the production of sewage or surface runoff of water contaminated with Toxoplasma gondii oocysts and other pathogens that can in turn enter the food chain and become a public health concern.

Toxoplasma gondii detection environment Italian coast

1. Distribution of T. gondii in Italy

In Europe, animal husbandry biosecurity measures and good manufacturing practices in the meat industry have been considerably improved, shifting attention to the role of oocysts in the epidemiology of this parasite. In recent years, long-term observations of pregnant women showed that the infection cannot always be linked to known risk factors such as the consumption of cyst-contaminated meat. Environmental exposure to T. gondii oocysts can indeed be an important route for human infection [1]. More sensitive analytical methods have been developed for the detection of oocysts in soil and water samples, adding evidence on the spread of oocysts via shedding in the environment. The role of oocysts is no longer seen as secondary to tissue-cyst-based transmission.
Half of the game produced in Europe is estimated to be seropositive for T. gondii, and meat from game is identified as an important source of T. gondii infection for consumers, including venison and wild boar meat [2][3]. Moreover, atypical and recombinant genotypes have been detected in wild animals in northern and central Italy [4][5].
Different studies report the seroprevalence of T. gondii in livestock in different Italian regions. A recent study conducted in the north of Italy reports seropositivity in different animals: 42.9% in cats, 29.9% in sheep, 25% in roe deer, 21.8% in dogs, 18.7% in goats, 15.5% in wild boar, and 9.7% in pigs. The same study reports a seroprevalence of 20.4% on a screened population of 36,814 individuals, while, among pregnant women, toxoplasmosis was active in 0.39% of cases [6]. Overall, the seroprevalence among small ruminants in farms of central and northern Italy is 90.7% [7] and 68.4% in cattle farms [8]. In southern and insular regions of Italy, there is a similar epidemiological scenario, with a prevalence of 87% among small ruminants farmed in Sicily [9]. In Campania, a southern region, the prevalence among livestock is reported at 77.8% in sheep [10] and 13.7% in water buffalo [11]. A seroprevalence of 39.6% was found among wild boar in the south [12].
Most cats are infected by ingesting infected prey [13]. Up to one billion oocysts can be shed by a single cat over a 1–2-week period, and they can repeatedly shed oocysts during their lifetime [14]. According to a survey from FEDIAF [15], between 2020 and 2021, the total number of cats owned by Italian households increased by almost 27%, reaching a population of 10.2 billion. Official feline population data and cat censuses are difficult to gather since it is not always recognized as a public health concern. In Italy, cat registration and identification are carried out on a voluntary basis. A multi-center study carried out in 2021 including 987 cats distributed across the country estimated that 27.9% of cats were living in colonies, 69.2% had a private owner, and 2.9% were living in shelters [16]. Among owned cats, it has been shown that the majority are living in rural areas (67.8%), being kept outdoors and often in households with other pets [17]. The same survey estimated that 32% of cats in Italy do not attend a veterinary clinic [17]. However, few studies have been conducted at a national level to determine the T. gondii seroprevalence among domestic cats. In Europe, the prevalence among feral and stray cats ranges between 18.27% and 40.7%, varying with the age and lifestyle of the cat [18]. In Italy, a seroprevalence of 40.7% was estimated among stray cats, being higher in urban (45%) than suburban areas (35.7%) [19].
ISTAT reported a yearly average temperature of 15.6 °C for 2021, with an increase of +0.6 °C compared to the period 1981–2010 and +1 °C compared to the period 1971–2000. In total, the yearly precipitation accounted for 746 mm in 2021, but 2022 presented a very dry year, with 455 mm [20]. In the current year, precipitation has already reached 500 mm, and it is projected to be a rainy fall and winter. Climatic changes with periods of drought followed by intense periods of rain could facilitate the dispersion of oocysts, as previously stated.

2. Toxoplasma gondii: From Land to Sea

Anthropogenic pressure on the coastline increases pollution with sewage or surface runoff of water possibly contaminated with T. gondii oocysts. It has been demonstrated that the distribution of pet cats and feral cat colonies is linked to human settlements that can provide food and shelter, even when feral cats are not directly fed or taken care of [21]. This is probably the key factor in T. gondii epidemiology in marine environments, with feral and domestic cats as the sole source of oocysts [22]. After infection, a single cat can shed millions of oocysts within 1 week, and, as previously reported, they can remain viable in soil for up to one year [23].
Reports of infection among marine mammals are becoming more frequent worldwide [24][25][26][27][28]. Clinical symptoms and seroprevalence have been described in sea otters, seals, sea lions, manatees, walruses, and dolphins [24][25][26][27][28]. It was only in the early 2000s that it was possible to isolate T. gondii from brain and heart tissues of sea otters (Enhydra lutris) in the National Wildlife Health Center (NWHC) of Madison, Wisconsin (USA) [29]. In the waters of the European continent, T. gondii has been found in the common dolphin (Delphinus delphis), striped dolphin (Stenella coeruleoalba), common bottlenose dolphin (Tursiops truncatus), long-finned pilot whale (Globicephala melas), Risso’s dolphin (Grampus griseus), harbor porpoise (Phocoena phocoena), humpback whale (Megaloptera novaengliae), bearded seal (Erignathus barbatus), harbor seal (Phocavitulina), ringed seal (Pusa hispida) and grey seal (Halichoerus grypus) [29].
Novel routes of oocyst transmission involving suspended microplastics have been found [30]. Parasites can associate with microplastics in contaminated seawater, suggesting that they may facilitate pathogen entry into marine food webs. Parasites could therefore be incorporated into aggregates of nanoparticles and ingested by filter-feeding marine invertebrates that may not be able to capture freely moving parasites [30]. Moreover, microplastics have the capacity to float or sink. In the first case, by floating on the sea surface, they can travel large distances, which may facilitate the dispersion of pathogens far from the areas from where they came. In the second case, sinking particles will accumulate in the benthos, where pathogens will concentrate and filter-feeding invertebrates are more likely to ingest them [31].

3. Toxoplasma gondii in the Italian Sea Environment

3.1. Marine Mammals

Toxoplasma gondii constitutes a major zoonotic agent and a significant cause of clinical disease in wildlife such as abortion, pneumonia, or encephalitis. Specifically, this parasite has been associated with neurological disease and encephalitis in cetaceans, becoming a primary neurotropic pathogen for striped dolphins [32][33][34][35]. A recent meta-analysis on marine species affected with T. gondii in Europe shows a total prevalence of 13%. The most affected are marine fissipeds (53.1%), followed by mollusks (26.4%), fishes (21.8%), cetaceans (14.8%), and pinnipeds (2.8%) [36].
The majority of data on the presence of T. gondii in Italian waters is related to stranded marine mammals. The International Pelagos Sanctuary, which occupies circa 90,000 km2 of international waters between France, Italy, and the Principality of Monaco, is a valuable source of information on marine mammals. It was established in 1999 to protect cetaceans from the combined pressures of natural environmental fluctuations and human impacts. It constitutes the first transboundary marine protected area, being a region with a high biomass of diversified plankton that attracts all eight cetaceans present in the Mediterranean Sea. Stranded cetaceans have been registered and analyzed in recent decades in this area, providing information on the presence of T. gondii and other parasites affecting the health of marine mammals.

3.2. Fish

In Italy, some fish species, such as anchovies (E. encrasicolus), are consumed raw or following marination in lemon juice for a few hours, which is not enough to inactivate oocysts [37]. Moreover, most of the species consumed in Italy are demersal or benthopelagic, living on different types of seabeds (sand, mud, rocks, or seagrass beds). In this environment, T. gondii oocysts are more likely to settle, sometimes aided by aquatic invertebrates that facilitate settling and help benthos concentration.
Only one study has investigated the presence of T. gondii in fish from local markets, analyzing a total of 1293 individuals from 17 different species, pooled into 147 groups [22]. Samples were obtained by pooling intestines, gills, and skin/muscles. T. gondii DNA was found in 12 of 17 fish species tested with 32 positive samples out of 147 overall [22]. Of these samples, 16 were of the skin/muscle and 11 of intestines and gills [22]. Fish was purchased at MAAS (Sicily Agro-Food Markets), which is the biggest market in Sicily, and in other small-size fisheries that sell fish from the area FAO 37.2.2.

3.3. Shellfish

There have been four studies analyzing shellfish in Italy in the last ten years, one regarding crustaceans and three regarding bivalves. The study on crustaceans collected Atlantic blue crab (Callinectes sapidus) from Lesina Lagoon and analyzed hemolymph, gills, stomach, hepatopancreas, and gonads using PCR. T. gondii was mostly found in the gills (n = 4), hemolymph (n = 2), and stomach (n = 1) [38].
Of the three studies analyzing bivalves in Italy, two focused on Mediterranean mussels (Mytilus galloprovincialis). In the study by Marangi et al., 53 samples from Turkey and 60 from Foggia food markets (Italy) were analyzed using qPCR targeting the B1 gene [39]. While all the samples from Italy were negative, 7 out of 53 (13.2%) mussel DNA samples from Turkey tested positive for T. gondii, and the type I genotype was confirmed [39]. In the study by Santoro et al., they analyzed 382 samples of M. galloprovincialis sampled in seven production sites in the Gulf of Naples and 27 farmed Mediterranean mussels obtained from a mollusk depuration plant in Corigliano Calabro (Calabria region) [40]. Digestive glands were used for the detection of the T. gondii B1 gene using qPCR. T. gondii DNA was detected in 39 out of 382 (10.2%) Mediterranean mussels from 6 out of 7 sampling sites in the Gulf of Naples and 4 out of 27 individuals from the mollusk depuration plant in Corigliano Calabro [40].
Only one study analyzed edible farmed shellfish. The study collected a total of 1734 individuals divided into 62 pooled samples: 109 Crassostrea gigas (6 pools of gills), 660 Mytilus galloprovincialis (22 pools), 804 Tapes decussatus (28 pools), and 161 Tapes philippinarum (6 pools) [41]. T. gondii DNA was detected by both nested PCR and real-time FLAG assay in 2 pooled samples out of 62 (3.2%) [41].

References

  1. Conrad, P.; Miller, M.; Kreuder, C.; James, E.; Mazet, J.; Dabritz, H.; Jessup, D.; Gulland, F.; Grigg, M. Transmission of Toxoplasma: Clues from the study of sea otters as sentinels of Toxoplasma gondii flow into the marine environment. Int. J. Parasitol. 2005, 35, 1155–1168.
  2. EFSA Panel on Biological Hazards (BIOHAZ). Scientific Opinion on the public health hazards to be covered by inspection of meat from farmed game. EFSA J. 2013, 11, 3264.
  3. World Health Organization. WHO Estimates of the Global Burden of Foodborne Diseases: Foodborne Disease Burden Epidemiology Reference Group 2007–2015. World Health Organization: Geneva, Switzerland, 2015. Available online: https://apps.who.int/iris/handle/10665/199350 (accessed on 20 October 2023).
  4. Battisti, E.; Zanet, S.; Trisciuoglio, A.; Bruno, S.; Ferroglio, E. Circulating genotypes of Toxoplasma gondii in Northwestern Italy. Vet. Parasitol. 2018, 253, 43–47.
  5. Rocchigiani, G.; Nardoni, S.; D′Ascenzi, C.; Nicoloso, S.; Picciolli, F.; Papini, R.A.; Mancianti, F. Seroprevalence of Toxoplasma gondii and Neospora caninum in red deer from Central Italy. Ann. Agric. Environ. Med. 2016, 23, 699–701.
  6. Dini, F.; Morselli, S.; Marangoni, A.; Taddei, R.; Maioli, G.; Roncarati, G.; Balboni, A.; Dondi, F.; Lunetta, F.; Galuppi, R. Spread of Toxoplasma gondii among animals and humans in Northern Italy: A retrospective analysis in a One-Health framework. Food Waterborne Parasitol. 2023, 32, e00197.
  7. Gazzonis, A.L.; Zanzani, S.A.; Villa, L.; Manfredi, M.T. Toxoplasma gondii infection in meat-producing small ruminants: Meat juice serology and genotyping. Parasitol. Int. 2020, 76, 102060.
  8. Gazzonis, A.L.; Marino, A.M.F.; Garippa, G.; Rossi, L.; Mignone, W.; Dini, V.; Giunta, R.P.; Luini, M.; Villa, L.; Zanzani, S.A.; et al. Toxoplasma gondii seroprevalence in beef cattle raised in Italy: A multicenter study. Parasitol. Res. 2020, 119, 3893–3898.
  9. Vesco, G.; Buffolano, W.; La Chiusa, S.; Mancuso, G.; Caracappa, S.; Chianca, A.; Villari, S.; Currò, V.; Liga, F.; Petersen, E. Toxoplasma gondii infections in sheep in Sicily, southern Italy. Vet. Parasitol. 2007, 146, 3–8.
  10. Fusco, G.; Rinaldi, L.; Guarino, A.; Proroga, Y.T.R.; Pesce, A.; Giuseppina, D.M.; Cringoli, G. Toxoplasma gondii in sheep from the Campania region (Italy). Vet. Parasitol. 2007, 149, 271–274.
  11. Ciuca, L.; Borriello, G.; Bosco, A.; D’Andrea, L.; Cringoli, G.; Ciaramella, P.; Maurelli, M.P.; Di Loria, A.; Rinaldi, L.; Guccione, J. Seroprevalence and Clinical Outcomes of Neospora caninum, Toxoplasma gondii and Besnoitia besnoiti Infections in Water Buffaloes (Bubalus bubalis). Animals 2020, 10, 532.
  12. Sgroi, G.; Viscardi, M.; Santoro, M.; Borriello, G.; D′Alessio, N.; Boccia, F.; Pacifico, L.; Fioretti, A.; Veneziano, V.; Fusco, G. Genotyping of Toxoplasma gondii in wild boar (Sus scrofa) in southern Italy: Epidemiological survey and associated risk for consumers. Zoonoses Public Health 2020, 67, 805–813.
  13. Dubey, J.P. Toxoplasmosis of Animals and Humans, 2nd ed.; CRC Press: Boca Raton, FL, USA, 2009.
  14. Dubey, J.P.; Miller, N.L.; Frenkel, J.K. The Toxoplasma gondii oocysts from cat feces. J. Exp. Med. 1970, 132, 636–662.
  15. FEDIAF. European Pet Food, Annual Report 2023. Available online: www.europeanpetfood.org (accessed on 15 November 2023).
  16. Genchi, M.; Vismarra, A.; Zanet, S.; Morelli, S.; Galuppi, R.; Cringoli, G.; Lia, R.; Diaferia, M.; di Regalbono, A.F.; Venegoni, G.; et al. Prevalence and risk factors associated with cat parasites in Italy: A multicenter study. Parasites Vectors 2021, 14, 475.
  17. Carvelli, A.; Iacoponi, F.; Scaramozzino, P. A Cross-Sectional Survey to Estimate the Cat Population and Ownership Profiles in a Semirural Area of Central Italy. BioMed Res. Int. 2016, 2016, e3796872.
  18. Dubey, J.P. Feline toxoplasmosis and coccidiosis: A survey of domiciled and stray cats. J. Am. Vet. Med. Assoc. 1973, 162, 873–877.
  19. Papini, R.; Sbrana, C.; Rosa, B.; Saturni, A.M.; Sorrentino, A.M.; Cerretani, M.; Raffaelli, G.; Guidi, G. Serological survey of Toxoplasma gondii infections in stray cats from Italy. Rev. Med. Vet. 2006, 157, 193–196.
  20. Vignani, D.; Budano, F. Istat, Istituto Nazionale di Statistica. Temperatura e Precipitazione delle Città Capoluogo Negli Anni 1971–2021. Report, 17 May 2023. Available online: www.istat.it (accessed on 20 October 2023).
  21. Horn, J.A.; Mateus-Pinilla, N.; Warner, R.E.; Heske, E.J. Home range, habitat use, and activity patterns of free-roaming domestic cats. J. Wildl. Manag. 2011, 75, 1177–1185.
  22. Marino, A.M.F.; Giunta, R.P.; Salvaggio, A.; Castello, A.; Alfonzetti, T.; Barbagallo, A.; Aparo, A.; Scalzo, F.; Reale, S.; Buffolano, W.; et al. Toxoplasma gondii in edible fishes captured in the Mediterranean basin. Zoonoses Public Health 2019, 66, 826–834.
  23. Lélu, M.; Villena, I.; Dardé, M.-L.; Aubert, D.; Geers, R.; Dupuis, E.; Marnef, F.; Poulle, M.-L.; Gotteland, C.; Dumètre, A.; et al. Quantitative Estimation of the Viability of Toxoplasma gondii Oocysts in Soil. Appl. Environ. Microbiol. 2012, 78, 5127–5132.
  24. Baker, R.E.; Mahmud, A.S.; Miller, I.F.; Rajeev, M.; Rasambainarivo, F.; Rice, B.L.; Takahashi, S.; Tatem, A.J.; Wagner, C.E.; Wang, L.-F.; et al. Infectious disease in an era of global change. Nat. Rev. Microbiol. 2022, 20, 193–205.
  25. Cabezón, O.; Hall, A.; Vincent, C.; Pabón, M.; García-Bocanegra, I.; Dubey, J.; Almería, S. Seroprevalence of Toxoplasma gondii in North-eastern Atlantic harbor seal (Phoca vitulina vitulina) and grey seal (Halichoerus grypus). Vet. Parasitol. 2011, 179, 253–256.
  26. Michael, S.A.; Howe, L.; Chilvers, B.L.; Morel, P.; Roe, W.D. Seroprevalence of Toxoplasma gondii in mainland and sub-Antarctic New Zealand sea lion (Phocarctos hookeri) populations. N. Z. Vet. J. 2016, 64, 293–297.
  27. Terracciano, G.; Fichi, G.; Comentale, A.; Ricci, E.; Mancusi, C.; Perrucci, S. Dolphins Stranded along the Tuscan Coastline (Central Italy) of the “Pelagos Sanctuary”: A Parasitological Investigation. Pathogens 2020, 9, 612.
  28. VanWormer, E.; Carpenter, T.E.; Singh, P.; Shapiro, K.; Wallender, W.W.; Conrad, P.A.; Largier, J.L.; Maneta, M.P.; Mazet, J.A.K. Coastal development and precipitation drive pathogen flow from land to sea: Evidence from a Toxoplasma gondii and felid host system. Sci. Rep. 2016, 6, 29252.
  29. Cole, R.A.; Lindsay, D.S.; Howe, D.K.; Roderick, C.L.; Dubey, J.P.; Thomas, N.J.; Baeten, L.A. Biological and Molecular Characterizations of Toxoplasma gondii Strains Obtained from Southern Sea Otters (Enhydra lutris nereis). J. Parasitol. 2000, 86, 526–530.
  30. Zhang, E.; Kim, M.; Rueda, L.; Rochman, C.; VanWormer, E.; Moore, J.; Shapiro, K. Association of zoonotic protozoan parasites with microplastics in seawater and implications for human and wildlife health. Sci. Rep. 2022, 12, 6532.
  31. De-la-Torre, G.E. Microplastics: An emerging threat to food security and human health. J. Food Sci. Technol. 2020, 57, 1601–1608.
  32. Di Guardo, G.; Mazzariol, S. Toxoplasma gondii: Clues from stranded dolphins. Vet. Pathol. 2013, 50, 737.
  33. Dubey, J.P.; Murata, F.H.A.; Cerqueira-Cézar, C.K.; Kwok, O.C.H.; Grigg, M.E. Recent epidemiologic and clinical importance of Toxoplasma gondii infections in marine mammals: 2009–2020. Vet. Parasitol. 2020, 288, 109296.
  34. Giorda, F.; Crociara, P.; Iulini, B.; Gazzuola, P.; Favole, A.; Goria, M.; Serracca, L.; Dondo, A.; Crescio, M.I.; Audino, T.; et al. Neuropathological Characterization of Dolphin Morbillivirus Infection in Cetaceans Stranded in Italy. Animals 2022, 12, 452.
  35. Pintore, M.D.; Mignone, W.; Di Guardo, G.; Mazzariol, S.; Ballardini, M.; Florio, C.L.; Goria, M.; Romano, A.; Caracappa, S.; Giorda, F.; et al. Neuropathologic findings in cetaceans stranded in Italy (2002–2014). J. Wildl. Dis. 2018, 54, 295–303.
  36. Ahmadpour, E.; Rahimi, M.T.; Ghojoghi, A.; Rezaei, F.; Hatam-Nahavandi, K.; Oliveira, S.M.R.; Pereira, M.d.L.; Majidiani, H.; Siyadatpanah, A.; Elhamirad, S.; et al. Toxoplasma gondii Infection in Marine Animal Species, as a Potential Source of Food Contamination: A Systematic Review and Meta-Analysis. Acta Parasit. 2022, 67, 592–605.
  37. Dumètre, A.; Dardé, M.L. How to detect Toxoplasma gondii oocysts in environmental samples? FEMS Microbiol. Rev. 2003, 27, 651–661.
  38. Marangi, M.; Lago, N.; Mancinelli, G.; Antonio, O.L.; Scirocco, T.; Sinigaglia, M.; Specchiulli, A.; Cilenti, L. Occurrence of the protozoan parasites Toxoplasma gondii and Cyclospora cayetanensis in the invasive Atlantic blue crab Callinectes sapidus from the Lesina Lagoon (SE Italy). Mar. Pollut. Bull. 2022, 176, 113428.
  39. Marangi, M.; Giangaspero, A.; Lacasella, V.; Lonigro, A.; Gasser, R.B. Multiplex PCR for the detection and quantification of zoonotic taxa of Giardia, Cryptosporidium and Toxoplasma in wastewater and mussels. Mol. Cell. Probes 2015, 29, 122–125.
  40. Santoro, M.; Viscardi, M.; Boccia, F.; Borriello, G.; Lucibelli, M.G.; Auriemma, C.; Anastasio, A.; Veneziano, V.; Galiero, G.; Baldi, L.; et al. Parasite Load and STRs Genotyping of Toxoplasma gondii Isolates from Mediterranean Mussels (Mytilus galloprovincialis) in Southern Italy. Front. Microbiol. 2020, 11, 355. Available online: https://www.frontiersin.org/articles/10.3389/fmicb.2020.00355 (accessed on 8 August 2023).
  41. Putignani, L.; Mancinelli, L.; Del Chierico, F.; Menichella, D.; Adlerstein, D.; Angelici, M.; Marangi, M.; Berrilli, F.; Caffara, M.; di Regalbono, D.F.; et al. Investigation of Toxoplasma gondii presence in farmed shellfish by nested-PCR and real-time PCR fluorescent amplicon generation assay (FLAG). Exp. Parasitol. 2011, 127, 409–417.
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