Volume 25, 2018
|Number of page(s)||6|
|Published online||11 April 2018|
A national retrospective survey of anisakidosis in France (2010-2014): decreasing incidence, female predominance, and emerging allergic potential
Étude nationale rétrospective de l’anisakidose en France (2010-2014) : diminution de l’incidence, prédominance féminine et augmentation des allergies
Parasitology-Mycology Department, Cochin Hospital, Assistance Publique Hôpitaux de Paris, Paris Descartes University,
27 rue du Faubourg St Jacques,
2 CHU Lille, Parasitology-Mycology Laboratory, 59000 Lille, France
3 Université de Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019–UMR 8204 − CIIL − Center for Infection and Immunity of Lille, 59000 Lille, France
* Corresponding author: firstname.lastname@example.org
Accepted: 4 March 2018
A retrospective survey was carried out over the years 2010–2014 among all Parasitology laboratories of University hospitals in France (ANOFEL network). The objective was to estimate the incidence of anisakidosis in France as new culinary habits such as the consumption of raw fish (sushi) or undercooked fish are increasing. A total of 37 cases of anisakidosis were notified by all French laboratories: 7 proven cases with evidence of a worm, 12 possible cases with abdominal pain after consumption of raw fish with detection of anti-Anisakis precipitins, and 18 allergic cases defined as acute manifestations after consumption of fish, associated with specific IgE for Anisakis. The median age of affected individuals was 42 years (11-69) and there was a significant predominance of women (67%). Compared with previous surveys in France, this study indicates a decrease in clinical cases of anisakidosis and illustrates the emerging allergic potential of anisakids.
Une enquête rétrospective a été réalisée au cours des années 2010-2014 auprès des laboratoires de parasitologie des hôpitaux universitaires de France (réseau ANOFEL). L’objectif était d’estimer l’incidence de l’anisakidose en France depuis l’émergence de nouvelles habitudes culinaires comme la consommation de poissons crus (sushi) ou insuffisamment cuits. Les laboratoires français de Parasitologie ont ainsi notifié 37 cas d’anisakidose: 7 cas certains avec présence du ver, 12 cas possibles se caractérisant par des douleurs abdominales après consommation de poisson cru et la présence de précipitines anti-Anisakis et 18 cas allergiques définis comme des manifestations aiguës après consommation de poisson associées à des IgE spécifiques anti-Anisakis. L’âge médian des cas était de 42 ans (11-69) et il y avait une prédominance féminine significative (67 %). Par rapport aux enquêtes précédentes en France, cette étude indique une diminution des cas cliniques d’anisakidose mais illustre le potentiel allergique émergent des anisakidés.
Key words: Anisakidosis / Anisakiasis / human / Anisakis / incidence / allergy / fish
© H. Yera et al., published by EDP Sciences, 2018
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Anisakidosis is the infestation of humans by larvae of parasitic nematodes of the family Anisakidae whose adults live in the digestive tract of mammals such as cetaceans and pinnipeds [2,15,19,25]. Human infection occurs after ingestion of raw or poorly cooked fish. In humans, the larvae cannot develop in this unusual host (dead-end host), but their presence may result in acute symptoms (epigastric pain simulating gastric ulcer, caused by the fixation of a larva to the gastroduodenal mucosa), chronic symptoms (eosinophilic granuloma around a larva having penetrated the intestine and simulating a bowel tumor), or allergic symptoms (angioedema, acute recurrent or chronic urticaria, asthma, segmental bowel inflammation which may lead to obstruction, anaphylactic shock). The genera most often involved in human cases of infestation are Anisakis and Pseudoterranova. Most cases of anisakidosis are reported in Japan, Spain, the Netherlands and Germany . The annual incidence in most European countries is around 20 cases/year . In France, in 1989, Hubert et al.  reported an incidence of 8 cases/year (21 cases between January 1, 1985 and September 30, 1987) by surveying all Parasitology laboratories at University hospitals in mainland France. In 1995, Bourée et al. reported 25 cases that they had personally observed and identified 30 previously published cases . Sporadic cases of anisakidosis are still regularly diagnosed but few are published [4,8,34]. Former studies had shown that the prevalence of infestation of marine fishes by anisakids was variable, but may be high [3,22,23]. These data were confirmed by the recent program “Fish-Parasites” (ANR-10-ALIA-004), which evaluated the prevalence of anisakids in the 15 most consumed fish species in France [26,31]. In this work, 1795 fishes were sampled between 2011 and 2013 during fishery research campaigns and from fish sellers inland. No anisakids were isolated from 44% of all fish sampled, whereas 34% of all fish had anisakids only in their viscera and 24% had anisakids either in their fillets only or in their fillets and viscera. The most parasitized fish species were saithe (Pollachius virens), megrim (Lepidorhombus whiffiagonis), cod (Gadus morhua), anglerfish (Lophius piscatorius), whiting (Merlangius merlangius) and hake (Merluccius merluccius). Most nematodes, identified by molecular methods, belonged to the genus Anisakis, mainly A. simplex, but A. pegreffii, Pseudoterranova, Contracaecum and Hysterothylacium were also identified.
In recent years, the growing popularity of consumption of raw fish such as sushi, carpaccio or prepared by multiple other recipes has been observed in France. The number of “Japanese” restaurants or fast-food shops serving and/or delivering sushi has increased dramatically. The purchase of prepared raw fish by French households increased by 230% (762 to 2540 tons) between 2005 and 2014 . However, no recent data on the incidence of human anisakidosis are available in France. The objective of our study was to assess changes in annual incidence two decades after the first investigation published by Hubert et al. , using a similar methodology.
The incidence of the disease over the period 2010–2014 was estimated by a national survey among all hospital Parasitology laboratories in mainland France (ANOFEL network). A questionnaire was sent to the 35 French hospital Parasitology laboratories in January 2015. Questions were “Did you diagnose cases of anisakidosis in the period 2010–2014” and, if so, what was its type “esophageal, gastroduodenal, allergic, eosinophilic granuloma or another form”? If the answer was positive, a more detailed questionnaire was sent to laboratories to collect epidemiological and bioclinical data, including the results and methodology for serological testing. The Laboratory of Lille University hospital receives requests for the detection of anti-Anisakis precipitins by immunoelectrophoresis (IEP) from a private medical laboratory having a national network and carried out, over the survey period, 566 serology assays. When anti-Anisakis detection by IEP was positive, prescribers were interviewed to obtain epidemiological and bioclinical information. These cases were included among the cases reported by all the other hospital Parasitology laboratories. All the cases were classified as follows: a confirmed case of anisakidosis was defined as the identification of a worm in a digestive sample; a possible case of anisakidosis was defined as any abdominal pain after raw fish consumption and the presence of anti-Anisakis precipitins; and an allergic case of anisakidosis was defined as the occurrence of acute allergic manifestations following fish consumption and associated with the presence of anti Anisakis IgE.
All the 35 Parasitology laboratories participated in the survey. Overall, 37 cases (Table 1) were identified and classified into 7 confirmed cases of anisakidosis (19%), 12 possible (32%) and 18 allergic cases (49%). The incidence of anisakidosis was 0.62 cases/month or 7.4 cases/year (37 cases over 60 months). Excluding the 18 cases of allergic anisakidosis, the incidence was 0.31 cases/month or 3.8 cases/year (19 cases over 60 months). When considering only confirmed cases, it was 0.1 cases/month or 1.4 cases/year. Among the confirmed cases, an esophageal form manifested as a few days of retro-sternal burning that stopped when the patient expelled a worm while vomiting. Five gastroduodenal forms were characterized by the observation of one (or several) worm(s) during gastric fibroscopy (with allergic swollen lips in one case). The 7th confirmed case was a colonic form fortuitously diagnosed by the observation of larvae sections inside an eosinophilic granuloma removed during colonoscopy. In possible cases of anisakidosis, patients had epigastric or abdominal pain after raw fish consumption and assays of anti-Anisakis precipitins by IEP were positive. Cases of allergic anisakidosis were characterized by various cutaneous manifestations (pruritus, urticaria, swollen lips or swelling of the face) or by general malaise and, in one case, by anaphylactic shock. These forms were sometimes associated with acute epigastric or abdominal pain. The median age of affected individuals was 42 years (11–69) and there was a significant predominance of women (25 women versus 12 men, chi2 p < 0.05). The same predominance, though not significantly different, was also observed in allergic cases (13 women versus 5 men). Regardless of the clinical form, anti-Anisakis specific IgE were always detected when they were tested for, even in the absence of patent allergic manifestations (2 of 3 confirmed cases, 3 of 3 possible cases, and 18 of 18 allergic cases). Blood hypereosinophilia was sometimes mentioned but these data were not systematically evaluated. Confirmed cases of anisakidosis were treated by removal of the larvae during fibroscopy (5 cases) or with albendazole (2 cases). Possible cases were sometimes treated with albendazole (2 cases) or ivermectin (1 case). Antihistamines and local or systemic corticosteroids were prescribed to treat allergic cases (5 cases), as well as albendazole (5 cases). When the data were available, fish incriminated by patients were salmon (8 cases), anchovies (5 cases), tuna and mackerel (4 cases for each species), cod and herring (3 cases for each), sea bream and hake (2 cases each), and other fish (3 cases). The distribution of fish species according to the different forms of anisakidosis is given in Table 2. Finally, the geographic distribution of cases showed that 35% of cases were observed in Paris and suburbs, 35% in other regions and only 29% in coastal regions.
Number of cases of anisakidosis (confirmed, possible or allergic) identified in France, 2010–2014.
Fish incriminated in the occurrence of cases of anisakidosis identified in France, 2010–2014. For some cases, the species was unknown. For one case several species were possible.
Our study is the first to estimate the incidence of anisakidosis in France since the survey by Hubert et al. published in 1989 , who identified 21 cases over a nearly 3-year period, including 10 confirmed anisakidosis cases and 11 patients with positive serology and having abdominal pain after eating raw fish, which could be considered as possible cases. No cases of allergic anisakidosis were identified since this clinical form was not known in 1989 and specific anti-Anisakis IgE assays were not available. In our study, over a 5 year-period (2010–2014), 37 cases were observed. Excluding the cases of allergic anisakidosis, we identified 19 cases over 60 months (0.31 cases/month), while 21 cases over 33 months (0.63 cases/month) were identified by Hubert et al. in 1989 . When considering only confirmed cases, the monthly incidence of anisakidosis was 0.3/month in the former survey compared to 0.1 cases/month in our study. Consequently, our survey demonstrates a decrease in the incidence of parasitological cases over the past 25 years. Conversely, we found that the allergic potential of anisakids was emerging. This emergence was also confirmed by the analysis of data from the French National Allergy-Vigilance Network which reported, during the period 2010–2014, six severe cases of allergy to anisakids, whereas no cases were reported in the 2001–2008 period . The emergence of allergy to anisakids has also been reported in international studies indicating an association between allergy to Anisakis and urticaria, or other allergic manifestations [2,6,12,22,25]. These aspects are well known in Spain or in Italy [1,21]. In France, allergic manifestations to anisakids have been reported [10,22], but their precise incidences still need to be evaluated. The analysis of a nationwide hospital medical information database (PMSI) database identified, between 1997 and 1999, 19 cases of anisakidosis for which the disease was recorded as the main reason for hospitalization . The analysis of the same database (PMSI) during the period 2010–2014 identified 19 hospitalized cases for which anisakidosis was reported as the main diagnosis of hospitalization . Therefore, the incidence of anisakidosis had decreased between these two periods: an average of 6.3 cases/year in the period 1997–1999 vs 3.8 cases/year in the period 2010–2014. This tendency to a decrease in cases had already been found by Petithory in 2007 . This author identified 25 cases between 1977 and 1991 (2 cases/year) and only 6 cases between 1992 and 2005 (1 case every 2 years). A European Directive of 1991 requiring deep-freezing of fish sold to be consumed raw was suggested as the reason underlying the decreasing incidence. The low incidence of human disease contrasts with the very high prevalence of anisakids found in fish and the recent modifications of culinary habits leading to higher consumption of raw fish. The high prevalence sometimes reported in fish directly examined at sea or bought from fishermen reflects the natural status of infection of fish, but not necessarily consumer exposure. Several causes may explain this discrepancy. At the level of sea professionals, anisakids are a major concern because they can lead to removal from sale and destruction of heavily parasitized batches. When preparing fillets, fishmongers often work on candling-tables and are able to cut the sides and, thus, eliminate the most patent parasites. European health regulations are also very strict and precise. They prohibit the marketing of fish intended to be eaten raw for catering if it has not been cured by appropriate measures such as freezing [19,24]. In addition, many sushis are prepared with farmed fish which, in general, are not parasitized . Specialized television programs have promoted preventive methods (such as freezing) which are also popularized on the internet. However, it is uncertain whether these methods are used by individual consumers. Finally, concerning allergies, freezing or heating does not avoid allergy to anisakids as some allergens are thermo-tolerant [23,30,32]. The fish species incriminated in the occurrence of anisakidosis cases were salmon (8 cases), anchovies (5 cases), mackerel, and tuna (4 cases each). Although the latter are usual sources of infection by anisakids, the frequent incrimination of salmon was rather surprising as most salmon consumed in France are Atlantic farmed salmon which are usually not parasitized . Wild Pacific salmon of the genus Oncorhynchus are also consumed in France and were sources of diphyllobothriosis . These Pacific salmon are known to host anisakids; Setyobudi et al. examined 120 Pacific salmon and found that all were parasitized with a high level of anisakid larvae, mostly found in muscles . In our survey, we were not able to obtain more details on the origin of the salmon. Analysis of the geographical distribution of cases does not show any regional predominance. We are not aware of different regional culinary habits concerning fish preparations in France, and most fish are distributed and sold all over the country by several networks of supermarkets. Therefore, parasitized fish can be found everywhere. We did not find the marked geographic differences found in Italy, where sensitization rates showed marked geographic differences (range: 0.4-12.7%), being highest along the Adriatic and Tyrrhenian coasts, where homemade marinated anchovies are an age-old tradition. In inland centers in northern Italy, the prevalence was directly related to the number of inhabitants. Interestingly, the analysis of the impact of immigration on the prevalence of Anisakis hypersensitivity showed that about 60% of sensitized subjects in Milan and Turin came from southern Italy or from non-European countries. . Our survey also showed a significant predominance of cases in women. This female predominance was not known and was not found in the study of Hubert et al. . Women may consume some pieces of raw fish during the domestic preparation of fish dishes and consequently be more exposed to the parasite than men. There are no data showing that French women consume more raw fish than men. A 2006 Japanese study showed that older women were the heaviest sushi consumers . However, such differences were not found in an analysis of a recent population survey carried out in the United States to examine differences in the consumption of various types of foods between men and women . A predominance of anisakidosis in women is mentioned by Sohn et al.  in Korea (45.8% men versus 54.2% women). Interestingly, sex hormones have been reported to play a possible role in the homeostasis of immunity as women could be more susceptible to allergic diseases  and this could explain the slight predominance of women having allergic forms in our study. However, our study has some limitations. There are certainly many asymptomatic cases, or cases involving people with very few symptoms who do not consult physicians for their illness. Furthermore, confirmed cases can be diagnosed only by the observation of the larva, which limits this diagnosis to departments practicing endoscopy. Our study shows the emergence of allergy to the anisakids. However, the detection of Anisakis simplex-specific IgE is questionable because multiple cross reactions, through the allergen Ani s 3 (tropomyosin), can be observed between anisakids and mites, crustaceans, and molluscs. The detection of IgE directed against a very specific antigenic fraction (Ani s 1) is available in the expensive multi-testImmunoCAP® ISAC . Recent data have shown a strong correlation between the results of this test and those from western blot analysis of ES or crude antigens .
In conclusion, our survey shows that in France half of the cases of human anisakidosis are allergic forms; the other half is divided into confirmed and possible cases. We also showed a predominance of cases in women. Sometimes, although this could not be precisely quantified, clinical forms may be combined: confirmed cases with allergic manifestations, possible cases sensitized to anisakids and allergic cases with epigastric pain a few hours after consumption of raw fish. It is not possible to assess the level of underestimation in the total number of cases because some uncertainties remain: the number of asymptomatic cases, the number of patients who do not consult a physician, the number of specific analyses prescribed to confirm anisakidosis when patients are seen in medical departments, and the number of allergic forms without digestive symptoms which are potentially misclassified as fish allergy. For these reasons, a better evaluation of the risk of anisakids for public health is needed in France.
The authors declare that they have no conflicts of interest in relation to this article.
We would like to thank the following members of the French association of hospital practitioners and teachers in Parasitology-Mycology “ANOFEL” for their help in supplying information about the patients with anisakidosis who were included: Bernard Cimon (Angers), Frédéric Grenouillet (Besançon), Laurence Delhaes (Bordeaux), Dorothée Quinio (Brest), Michel Vergnaud (Caen), Françoise Botterel (Créteil), Frédéric Dalle (Dijon), Hélène Fricker-Hidalgo (Grenoble), Marie-Laure Dardé (Limoges), Martine Wallon (Lyon), Coralie L’Ollivier (Marseille), Marie Machouart (Nancy), Pierre Marty (Nice), Fabrice Le Pape (Nantes), Sandrine Houze (Paris-Bichat), Luc Paris (Paris-Pitié Salpêtrière), Christophe Hennequin (Paris-Saint Antoine), Nisen Abuaf (Paris-Tenon), Dominique Toubas (Reims), Florence Robert-Gangneux (Rennes), Loïc Favennec (Rouen), Pierre Flori (Saint-Etienne), Odile Villard (Strasbourg), Judith Fillaux (Toulouse), Jacques Chandenier (Tours) and Patrice Bourée (Paris). We also thank Naïla Touabet-Azouzi for helping us at the beginning of the survey. In addition, acting for a healthier population, the Hauts-de-France region partially funded this work (ArCIR dynamique 2013 program, ABCFish project, grant No. 13003283). We also thank Pr Boualem Sendid (Lille) for providing us with the results of Anisakis antibodies assays. Finally, we mention that the idea of this work emerged during the “FishParasite” French ANR program initiated by the late Eduardo Dei-Cas and driven by Cécile-Marie Aliouat.
- AAITO-IFIACI Anisakis Consortium. 2011. Anisakis hypersensitivity in Italy: prevalence and clinical features: a multicenter study. Allergy, 66, 1563-1569. [Google Scholar]
- Audicana, MT, Kennedy, MW. 2008. Anisakis simplex: from obscure infectious worm to inducer of immune hypersensitivity. Clinical Microbiological Review, 21, 360-379. [CrossRef] [PubMed] [Google Scholar]
- Bourée, P., Paugam, A., Petithory, J.C. 1995. Anisakidosis: report of 25 cases and review of the literature. Comparative Immunology, Microbiology and Infectious Diseases, 18, 75-84. [CrossRef] [PubMed] [Google Scholar]
- Brunet J, Pesson B, Royant M, Lemoine JP, Pfaff AW, Abou-Bacar A, Yera H, Fréalle E, Dupouy-Camet J, Merino-Espinosa G, Gómez-Mateos M, Martin-Sanchez J, Candolfi E. 2017, Molecular diagnosis of Pseudoterranova decipiens s.s in human, France. BMC Infectious Diseases, 6, 397. [CrossRef] [Google Scholar]
- Chen W, Mempel M, Schober W, Behrendt H, Ring J. 2008. Gender difference, sex hormones, and immediate type hypersensitivity reactions. Allergy, 63, 1418-1427. [CrossRef] [PubMed] [Google Scholar]
- Daschner A, Pascual CY. 2005. Anisakis simplex: sensitization and clinical allergy. Current Opinion in Allergy and Clinical Immunology, 5, 281-285. [CrossRef] [PubMed] [Google Scholar]
- De Silva D, Yamao M. 2006. A yen for sushi: an analysis of demographic and behavioral patterns of sushi consumption in Japan. Journal of Foodservice, 17, 63-76. [CrossRef] [Google Scholar]
- Dupouy-Camet J, Gay M, Bourgau O, Nouchi A, Léger E, Dei-Cas E. 2014. L’atteinte œsophagienne : une complication rare de l’anisakidose à Pseudoterranova. Presse Médicale, 43, 81-83. [CrossRef] [Google Scholar]
- Dupouy-Camet J, Touabet-Azouzi N, Fréalle E, Van Cauteren D, Yera H, Moneret-Vautrin A. Incidence de l’anisakidose en France. Enquête rétrospective 2010-2014. 2016. Bulletin Epidémiologique Hebdomadaire, 5-6. 64-70. Retrieved 8 January 2018 from http://www.invs.sante.fr/beh/2016/5-6/2016_5-6_1.html [Google Scholar]
- Eldin de Pécoulas P, Paugam A., Bourée P. 2014. Anisakiose et allergie : une association morbide négligée ? Revue Francophone des Laboratoires, 464, 89-95. [CrossRef] [Google Scholar]
- European Food Safety Authority. 2010. Scientific opinion on risk assessment of parasites in fishery products. EFSA panel on biologic hazards (BIOHAZ). EFSA Journal, 8, 1543. [Google Scholar]
- Falcão H, Lunet N, Neves E, Iglésias I, Barros H. 2008. Anisakis simplex as a risk factor for relapsing acute urticaria: a case-control study. Journal of Epidemiology and Community Health, 62, 634-637. [CrossRef] [PubMed] [Google Scholar]
- FranceAgriMer, 2015. Consommation des produits de la pêche et de l’aquaculture, 2014. pp.28 Retrieved 8th of January 2018 from http://www.franceagrimer.fr/content/download/38313/352902/file/STA-MER-CONSO%202014-mai2015.pdf [Google Scholar]
- INVS. 2004. Morbidité et mortalité dues aux maladies infectieuses d’origine alimentaire en France Institut de Veille Sanitaire St Maurice, France Retrieved 8th of January 2018 from http://invs.santepubliquefrance.fr/publications/2004/inf_origine_alimentaire/inf_origine_alimentaire.pdf. [Google Scholar]
- Hochberg NS, Hamer DH, 2010. Anisakidosis: Perils of the deep. Clinical Infectious Diseases, 51, 806-812 [CrossRef] [Google Scholar]
- Hubert B, Bacou J, Belveze H. 1989. Epidemiology of human anisakiasis: incidence and sources in France. American Journal of Tropical Medicine and Hygiene, 40, 301-303. [CrossRef] [Google Scholar]
- Lunestad BT. 2003. Absence of nematodes in farmed Atlantic salmon (Salmo salar L.) in Norway. Journal of Food Protection. 66, 122-124. [CrossRef] [PubMed] [Google Scholar]
- Martínez-Aranguren RM, Gamboa PM, García-Lirio E, Asturias J, Goikoetxea MJ, Sanz ML, 2014. In vivo and in vitro testing with rAni s 1 can facilitate diagnosis of Anisakis simplex allergy. Journal of Investigational Allergology and Clinical Immunology, 24, 431-438. [Google Scholar]
- Mattiucci S & D’Amelio S. 2014. Anisakiasis, in Helminth Infections and their Impact on Global Public Health, Bruschi F, Editor. Springer-Verlag: Wien. P., 325-365. [Google Scholar]
- Mattiucci S, Colantoni A, Crisafi B, Mori-Ubaldini F, Caponi L, Fazii P, Nascetti G, Bruschi F. 2017. IgE sensitization to Anisakis pegreffii in Italy: Comparison of two methods for the diagnosis of allergic anisakiasis. Parasite Immunology, 39 (7). DOI: 10.1111/pim.12440. [CrossRef] [Google Scholar]
- Moro Moro, M., Tejedor Alonso, M.A., Esteban Hernández, J, Múgica García M.V., Rosado Ingelmo, A., Vila Albelda, C., 2011. Incidence of anaphylaxis and subtypes of anaphylaxis in a general hospital emergency department. Journal of Investigational Allergology and Clinical Immunology, 21, 142-149. [Google Scholar]
- Petithory JC. 2007. Données nouvelles sur l’anisakidose. Bulletin de l’Académie Nationale de Médecine (Paris), 191, 53-65. [Google Scholar]
- Petithory JC. 2008. Actualités sur l’anisakidose. Revue Française des Laboratoires, 399, 87-93. [CrossRef] [Google Scholar]
- Pozio E. 2013. Integrating animal health surveillance and food safety: the example of Anisakis. Scientific and Technical Review of the Office International des Epizooties (Paris), 32, 487-496. [CrossRef] [Google Scholar]
- Pravettoni V, Primavesi L, Piantanida M. 2012. Anisakis simplex: current knowledge. European Annals of Allergy and Clinical Immunology, 44, 150-156. [PubMed] [Google Scholar]
- Seesao Y. 2015. Caractérisation des Anisakidae dans les poissons marins : développement d’une méthode d’identification par séquençage à haut-débit et étude de prévalence. Thèse de doctorat en Biologie. Université Lille 2. [Google Scholar]
- Setyobudi E, Jeon CH, Lee CH, Seong KB, Kim JH. 2011. Occurrence and identification of Anisakis spp. (Nematoda: Anisakidae) isolated from chum salmon (Oncorhynchus keta) in Korea. Parasitology Research. 108, 585-592. [CrossRef] [PubMed] [Google Scholar]
- Shiferaw B, Verrill L, Booth H, Zansky SM, Norton DM, Crim S, Henao OL. 2012. Sex-based differences in food consumption: Foodborne Diseases Active Surveillance Network (FoodNet) Population Survey, 2006-2007. Clinical Infectious Disease, 54 Suppl 5, S453-S457. [CrossRef] [Google Scholar]
- Sohn WM, Na BK, Kim TH, Park TJ. 2015. Anisakiasis: Report of 15 gastric cases caused by Anisakis Type I larvae and a brief review of Korean anisakiasis cases. Korean Journal of Parasitology, 53, 465-470. [CrossRef] [Google Scholar]
- Ventura MT, Tummolo RA, Di Leo E, D’Ersasmo M, Arsieni A. 2008. Immediate and cell-mediated reactions in parasitic infections by Anisakis simplex. Journal of Investigational Allergology and Clinical Immunology 18(4), 253-259. [Google Scholar]
- Verrez-Bagnis V, Seesao Y, Thebault A, Gay M, Aliouat-Denis CM, Le Fur B, Cuzzucoli D, Cos I, Jérôme, M, Kolypczuk L, Bruzac S, Audebert C, Dei-Cas E, Viscogliosi E. and the “Fish-Parasites” consortium. 2015. Prevalence of nematodes (Anisakidae) in fish species most consumed in France. Abstract book of the 5th Trans-Atlantic Fisheries Technology conference, Nantes, France. Retrieved 8 January 2018 from http://wwz.ifremer.fr/taft2015/content/download/90381/1110052/file/book%20of%20abstracts%20final.pdf [Google Scholar]
- Vidacek S, de las Heras C, Solas MT, Mendizábal A, Rodriguez-Mahillo AI, Tejada M. 2010. Antigenicity and viability of Anisakis larvae infesting hake heated at different time-temperature conditions. Journal of Food Protection, 73, 62-68. [Google Scholar]
- Yera H, Estran C, Delaunay P, Gari-Toussaint M, Dupouy-Camet J, Marty P. 2006. Putative Diphyllobothrium nihonkaiense acquired from a Pacific salmon (Oncorhynchus keta) eaten in France; genomic identification and case report. Parasitology International. 55, 45-49. [Google Scholar]
- Yera H, Fréalle E, Dupouy-Camet J. 2016. Molecular confirmation of Anisakis pegreffii as a causative agent of anisakidosis in France. Digestive and Liver Disease, 48, 970. [Google Scholar]
Cite this article as: Yera H, Fréalle É, Dutoit E, Dupouy-Camet J. 2018. A national retrospective survey of anisakidosis in France (2010-2014): decreasing incidence, female predominance, and emerging allergic potential. Parasite 25, 23
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