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1.
Nat Prod Res ; 34(1): 158-161, 2020 Jan.
Article in English | MEDLINE | ID: mdl-30784309

ABSTRACT

A total of 1104 fish samples from markets of Sicily were analysed for the detection and species identification of Anisakidae nematodes. The preliminary analysis of the fish samples showed the presence of 2459 larvae. All the fish species revealed different prevalence of infestation, with a maximum of 100% for Lepidopus caudatus and a minimum of 4.5% in Sardina pilchardus. The 80% of the larvae examined by PCR-RFLP analysis belonged to Anisakis pegreffii species. The seasonal infestation trend of Anisakis was evaluated in all the fish sample examined. The results of the seasonal infestation trend showed a marked connection with the ecological aspects of the fish species examined. As far as we know, this work report for the first time important ecological aspects of Lepidopus caudatus specimens of South Mediterranean. This work could be useful to plan a seasonal fishing strategy aimed at reducing the health risks related to Anisakis.


Subject(s)
Anisakiasis , Fish Diseases/parasitology , Food Parasitology , Perciformes/parasitology , Seasons , Animals , Anisakiasis/parasitology , Anisakis/pathogenicity , Fishes/parasitology , Mediterranean Sea , Nematoda/genetics , Polymerase Chain Reaction , Prevalence , Seafood/parasitology , Sicily
3.
Int J Food Microbiol ; 292: 159-170, 2019 Mar 02.
Article in English | MEDLINE | ID: mdl-30599456

ABSTRACT

Anisakis spp. and Hysterothylacium spp. are nematodes that commonly parasitize several fish species. Nematode larvae can be recovered in coelomic cavity and viscera, but also in flesh and have an important economic and public health impact. A total of 1144 subjects of wild teleosts, 340 samples of cephalopods and 128 specimens of farmed fish collected from Apulia region were analysed for anisakid larvae detection by visual inspection of coelomic cavity and viscera and by digestion of the flesh. No nematode larvae were found in farmed fish and cephalopod molluscs. All examined wild-caught fish species were parasitized, except for 5 species for each of which only a few subjects belonging to the same batch were sampled, therefore the results are just indicative. A total of 6153 larvae were isolated; among these, 271 larvae were found in the muscular portion. Larvae were identified by morphological method as belonging to the genera Anisakis (97.2%) (type I and type II) and Hysterothylacium (2.8%). Both nematodes could be found in all fish species, except for round sardinella (Sardinella aurita), infected only by Hysterothylacium spp. and for Mediterranean scaldfish (Arnoglossus laterna), little tunny (Euthynnus alleteratus) and chub mackerel (Scomber japonicus) infected only with Anisakis spp.. A sample of 185 larvae was sent to the National Reference Centre for Anisakiasis (C.Re.N.A.) of Sicily for identification at the species level: 180 larvae belonged to the species A. pegreffii and 2 larvae to A. physeteris. The remaining 3 larvae were identified at genus level as Hysterothylacium. Statistical indices such as prevalence, mean intensity and mean abundance were calculated. Chub mackerel (S. japonicus) was the species with the highest prevalence and mean intensity. Moreover, the average and the median values of larvae per 100 g of edible part for each fish species were determined to estimate the consumer exposure to Anisakis spp.. The obtained values were then recalculated by referring to the edible part of all specimens (infected and non-infected) forming a single parasitized batch, getting more realistic and objective data useful for risk assessment. Our results indicate that the consumption of raw or undercooked wild fish caught off Apulian coasts could result in the acquisition of anisakiasis; on the contrary, farmed fish and cephalopods appear to be safer for the consumer.


Subject(s)
Fishes/parasitology , Food Contamination/analysis , Food Parasitology , Nematoda/isolation & purification , Seafood/parasitology , Animals , Anisakis/isolation & purification , Fisheries , Larva , Prevalence , Risk Assessment , Sicily
4.
Mycotoxin Res ; 35(1): 47-53, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30215192

ABSTRACT

Samples (n = 485) of raw (n = 394) or heat-treated (n = 91) milk of three different species (cow, n = 170; sheep, n = 133; donkey, n = 84), collected 2013-2016 in Western Sicily (Southern Italy), were analyzed for aflatoxin M1 (AFM1) by enzyme-linked immunosorbent assay (ELISA). Positive ELISA results were further analyzed by HPLC with fluorescence detection. Both methods had a detection limit for AFM1 in milk of 7 ng kg-1. ELISA yielded 12.9 and 5% positives in cows and sheep milk, respectively, all samples of donkey milk were negative. Levels of AFM1 were in most cases at 0.007-< 0.05 µg kg-1, only two samples (sheep milk) slightly exceeded the European Union maximum level of 0.05 µg kg-1. Only 6% of the samples were positive for AFM1 in a concentration range of 0.008-0.15 µg kg-1. Only milk samples collected directly from farms were positive. Overall, the levels were much lower than previously reported for Southern Italy cow and sheep milk samples purchased in retail stores. The results of this work indicate a continuous improvement of the feeding techniques on dairy farms of Southern Italy, which is essential to ensure consumers' protection.


Subject(s)
Aflatoxin M1/analysis , Food Contamination/analysis , Milk , Animals , Cattle , Chromatography, High Pressure Liquid , Dairying , Enzyme-Linked Immunosorbent Assay , Equidae , Female , Food Microbiology , Limit of Detection , Raw Foods/analysis , Sheep , Sicily
5.
Vet Parasitol ; 259: 13-16, 2018 Aug 15.
Article in English | MEDLINE | ID: mdl-30056978

ABSTRACT

We examined 151 European sea bass (Dicentrarchus labrax L.) samples from farms and fish markets of Sicily (Southern Italy) for Anisakidae larvae detection. All the samples were examined by visual inspection and modified chloro-peptic digestion. Two nematode larvae were found in the viscera of only one European sea bass sample from a farm located in Greece (FAO 37.3), giving a total prevalence of infestation of 0.7%. No other parasites were found after chloro-peptic digestion of the samples. The larvae were morphologically ascribed, at genus level, to morphotypes I and molecularly identified as Anisakis pegreffii. To the best if our knowledge, this is the first report on the presence of anisakid parasites in farmed European sea bass of Mediterranean Sea. Our findings suggest that the risk of exposure to Anisakidae nematodes in farmed European sea bass remains very low. However, further data on Mediterranean farms are needed to have a detailed risk analysis.


Subject(s)
Anisakiasis/veterinary , Anisakis/isolation & purification , Bass/parasitology , Fish Diseases/epidemiology , Animals , Anisakiasis/epidemiology , Anisakiasis/parasitology , Anisakis/genetics , Aquaculture , Fish Diseases/parasitology , Fisheries , Greece/epidemiology , Larva/physiology , Mediterranean Sea/epidemiology , Polymerase Chain Reaction , Sequence Analysis, DNA , Sicily/epidemiology
6.
J Parasitol ; 104(4): 398-406, 2018 08.
Article in English | MEDLINE | ID: mdl-29762080

ABSTRACT

Samples obtained from 11 teleost fish species collected in waters off of the Mediterranean coasts of Sicily, Italy, were examined for the presence of Hysterothylacium spp. larvae. In total, 3,017 fish samples were examined, and the larvae recovered were used in subsequent phylogenetic studies. Fifty-eight raphidascaridid parasitic nematodes were found in the examined fish, with prevalence values ranging from 0.2% in anchovies to 60% in forkbeard samples. Twenty-seven parasites were identified as Hysterothylacium fabri and Hysterothylacium aduncum by sequencing the following regions: the nuclear ribosomal internal transcribed spacer ( ITS) and the mitochondrial cytochrome c oxidase subunit II ( COXII). Two other larvae collected from Lophius piscatorius had very low identity scores, with ITS and COXII sequences reported in GenBank and high genetic distances (AY603539). Pairwise comparisons between the ITS region of the H. fabri isolated from fishes from Sicilian coastal waters and those isolated from the Mediterranean Sea, Turkey (KC852206), revealed genetic differences ranging from 0.015 to 0.018. Our H. aduncum samples had very low genetic differences to H. aduncum from the Adriatic Sea (KP979763, 0.00-0.003). The concatenated phylogenetic examination of the ITS- COXII sequences by using maximum likelihood analyses indicated 3 distinct clades supported by high bootstrap values. Further molecular identification and detailed morphological analyses are needed to clarify these results and confirm the diversity and relationships within Hysterothylacium.


Subject(s)
Ascaridida Infections/veterinary , Ascaridoidea/isolation & purification , Fish Diseases/parasitology , Amino Acid Sequence , Animals , Anisakiasis/complications , Anisakiasis/epidemiology , Anisakiasis/parasitology , Anisakiasis/veterinary , Anisakis/anatomy & histology , Anisakis/classification , Anisakis/genetics , Anisakis/isolation & purification , Ascaridida Infections/complications , Ascaridida Infections/epidemiology , Ascaridida Infections/parasitology , Ascaridoidea/anatomy & histology , Ascaridoidea/classification , Ascaridoidea/genetics , Base Sequence , DNA, Helminth/chemistry , DNA, Helminth/isolation & purification , DNA, Ribosomal Spacer/chemistry , Electron Transport Complex IV/chemistry , Electron Transport Complex IV/genetics , Fish Diseases/epidemiology , Fishes , Mediterranean Sea/epidemiology , Phylogeny , Sequence Alignment , Sicily/epidemiology
7.
Int J Food Microbiol ; 257: 75-79, 2017 Sep 18.
Article in English | MEDLINE | ID: mdl-28646669

ABSTRACT

Anisakids are parasitic nematodes responsible for a zoonosis that occurs following the ingestion of fish and fish products infected with larvae belonging to the genera Anisakis and Pseudoterranova. Rarely Contracaecum is found in association with gastric/intestinal illness, while Hysterothylacium is commonly considered not pathogenic. Although Real Time PCR assays have been recently used with the aim to detect and quantify these parasites in food products, methods applied did not undergo through extensive validation process, a feature highly desirable or mandatory in the case of testing laboratories accredited for the ISO EN 17025:2005. Here, a comprehensive study has been performed to validate a commercial kit based on multiplex real time PCR for the qualitative detection of Anisakis and Pseudoterranova. Inclusivity/exclusivity trials were carried out on DNA from species of the genera Anisakis, Pseudoterranova, Contracaecum, Hysterothylacium and Ascaris, on fish intentionally contaminated with Anisakis spp. and Pseudoterranova spp. and on marine organisms as fish, crustacean and squid to test the commercial kit on a large sample. The assay gave positive amplification for several Anisakis and Pseudoterranova species, while providing no signal for the members of the remaining genera. Each sample was correctly assigned either to Anisakis or Pseudoterranova, thus indicating that no cross-reaction occurred. The LOD was determined using two independent standard curves. Robustness was assayed by using two different thermocyclers in three distinct laboratories with different operators. The establishment of a validation dossier will permit the use of the commercial kit for the detection of Anisakis and Pseudoterranova DNA in fish and fish products intended for human consumption by public or private laboratories, following the requirements regarding the quality assurance processes described in the ISO EN 17025:2005.


Subject(s)
Anisakiasis/transmission , Anisakis/isolation & purification , Ascaridida Infections/transmission , Ascaridoidea/isolation & purification , Fish Diseases/parasitology , Fish Products/parasitology , Real-Time Polymerase Chain Reaction/methods , Animals , Anisakiasis/parasitology , Anisakis/classification , Anisakis/genetics , Ascaridida Infections/parasitology , Ascaridoidea/classification , Ascaridoidea/genetics , Fishes/parasitology , Humans , Larva/classification , Zoonoses/parasitology , Zoonoses/transmission
8.
Nat Prod Res ; 31(10): 1156-1162, 2017 May.
Article in English | MEDLINE | ID: mdl-27616200

ABSTRACT

The aim of this study was to investigate mercury accumulation in some species, caught in Mediterranean Sea, in the period between May and December 2015, and to compare it to the presence of Anisakis parasites. The samples were examined by direct mercury analyzer (DMA-80) for their Hg levels. The metal concentration was compared to the presence or the absence of Anisakis parasites. Significant differences in Hg concentration in analysed samples were observed. The low-infested fishes contained 1-6 larvae of parasites whereas the high-infested one had 7-83 larvae.


Subject(s)
Anisakis , Cephalopoda/metabolism , Fishes/metabolism , Fishes/parasitology , Mercury/metabolism , Water Pollution, Chemical , Animals , Fish Diseases/parasitology , Larva , Mediterranean Sea , Parasites , Sicily
9.
Parasitol Int ; 65(6 Pt A): 696-701, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27568095

ABSTRACT

In this study, 1029 fish and cephalopod samples came from Central-Western Mediterranean (FAO 37.1.1 and FAO 37.1.3) were analysed for Anisakidae larvae research with the aim to identify possible hybridisations between Anisakis pegreffii and Anisakis simplex s.s. species. A total of 1765 larvae were detected, with prevalence values between 8.1% and 100%. The morphologic analysis revealed characters attributable to morphotype I of Anisakis in 98.5% of the examined larvae, while 1.5% belonged to the morphotype II. PCR-based Restriction Fragment Length Polymorphism (PCR-RFLP) analysis of the entire ITS region (ITS1, 5.8S and ITS2) of nuclear ribosomal DNA (rDNA) was performed with HinfI and HhaI restriction enzymes. The majority of the larvae examined by PCR-RFLP were identified as A. pegreffii (71%), with a prevalence on horse mackerel from FAO 37.1.3, while 10% were identified as A. simplex s.s., 2% as A. physeteris and 17% as A. pegreffii×A. simplex s.s. hybrid genotype. The sequence analysis confirmed the hybridisation in the 85% of the larvae recognised as hybrid forms by PCR- RFLP, suggesting this form as the product of natural interspecific recombination due to the presence of sympatry areas. The presence of hybrid forms were mostly found in fish samples from FAO subzone 37.1.1. This is the first report of A. pegreffii x A. simplex s.s. hybrid genotype in fishes caught off the coasts of Sicily (Southern Italy). Finally, this study provided substantial information about the geographical distribution of Anisakidae family in Central-Western Mediterranean Sea.


Subject(s)
Ascaridoidea/genetics , Cephalopoda/parasitology , Chimera/genetics , Fish Diseases/parasitology , Perciformes/parasitology , Animals , Ascaridoidea/classification , Ascaridoidea/isolation & purification , Base Sequence , DNA, Ribosomal Spacer/genetics , Larva/genetics , Mediterranean Sea , Polymorphism, Restriction Fragment Length
10.
Acta Parasitol ; 61(2): 369-75, 2016 Mar.
Article in English | MEDLINE | ID: mdl-27078661

ABSTRACT

Anisakis and other parasites belonging to the Anisakidae family are organisms of interest for human health, because of their high zoonotic potential. Parasites belonging to this family can cause Anisakiasis, a parasitological disease caused by the ingestion of raw, infested fish products. Furthermore, evidence from the EFSA (European Food Safety Authority; EFSA 2010) has highlighted the allergological potential of nematodes belonging to the Anisakis genre. The detection and identification of Anisakidae larvae in fish products requires an initial visual inspection of the fish sample, as well as other techniques such as candling, UV illumination and artificial digestion. The digestion method consists of the simulation of digestive mechanics, which is made possible by the utilization of HCl and pepsin, according to EC Regulation 2075/2005. In this study, a new Anisakidae larvae detection method using a mechanical digestion system called Trichineasy® was developed. A total of 142 fish samples, belonging to 14 different species, were examined to validate the method. A reaction mixture with 100 g of sample, 10 g of pepsin (1:10000 NF) and 50 ml of 10% HCl at 36 ± 1°C for 20 minutes was evaluated to be the best condition for the digestion of fish samples. These parameters have also allowed the detection of viable larvae after digestion. The results confirm this instrumentation as a valuable and safe tool for the detection of Anisakidae larvae in fishery products.


Subject(s)
Anisakis/isolation & purification , Fish Products/parasitology , Food Microbiology/methods , Specimen Handling/methods , Animals , Hydrochloric Acid/metabolism , Larva , Pepsin A/metabolism , Temperature , Time Factors
11.
Bioinorg Chem Appl ; 2016: 5408014, 2016.
Article in English | MEDLINE | ID: mdl-27127456

ABSTRACT

A number of ninety-six hair samples from Sicilian fishermen were examined for total mercury detection by an Inductively Coupled Plasma Mass Spectrometry (ICP-MS) method. The mercury levels obtained were compared with mercury levels of 96 hair samples from a control group, in order to assess potential exposure to heavy metals of Sicilian fishermen due to fish consumption and closeness to industrial activities. Furthermore, the mercury levels obtained from hair samples were sorted by sampling area in order to verify the possible risks linked to the different locations. The overall mean concentration in the hair of the population of fishermen was 6.45 ± 7.03 µg g(-1), with a highest value in a fisherman of Sciacca (16.48 µg g(-1)). Hair mercury concentration in fishermen group was significantly higher than in control group (p < 0.01). There was no significant difference in hair total mercury concentrations between sampling areas (p > 0.05). The results of this study indicate a greater risk of exposure to mercury in Sicilian fishermen, in comparison to the control population, due to the high consumption of fish and the close relationship with sources of exposure (ports, dumps, etc.).

12.
Ital J Food Saf ; 4(1): 4090, 2015 Feb 03.
Article in English | MEDLINE | ID: mdl-27800374

ABSTRACT

In this work a total of 949 fish samples were analysed for the identification of nematode larvae belonging to the Anisakidae family. Biomolecular application for the identification of Anisakidae larvae can be an optimal instrument for the traceability of fish products, described on the Reg. EC 178/2002. Results confirm a correlation between geographical distribution of fishes and presence of specific Anisakid larvae. FAO 37 zone (Mediterranean sea) showed a prevailing distribution of Anisakis pegreffii and a minimal presence of A. simplex s.s. in hybrid form with Anisakis pegreffii. FAO 27 zone showed a prevailing distribution of A. simplex s.s. in fish like Brosme (Brosme brosme) and infestation prevalence of Pseudoterranova krabbei and P. decipiens s.s. in Gadus morhua. Obtained results validate the hypothesis that molecular biology methods for identifying Anisakidae larvae are effective traceability markers of fish products.

13.
Ital J Food Saf ; 3(2): 1719, 2014 Apr 17.
Article in English | MEDLINE | ID: mdl-27800344

ABSTRACT

One of the parasite diseases associated with the consumption of raw fish that occurs with some frequency is the anisakiasis, a human disease caused by the accidental ingestion of larval nematodes of the genus Anisakis, family Anisakidae. At the National Reference Centre for Anisakiasis (C.Re.N.A.) from October 2012 to February 2013, a number of 231 bony fish (Trichiuridae, Engraulidae, Scombridae and Clupeidae) were received from different fishing sites in Sicily. Anisakis pegreffii is the main species detected in fish, as identified by molecular analysis based on polymerase chain reaction-restriction fragment length polymorphism, while Anisakis simplex sensu stricto was found only in Scomber scombrus caught in the Mediterranean Sea (Fishing Areas 37), in the Spanish coast (Fishing Areas 37) and in the Atlantic Ocean (Fishing Areas 34). Larvae of the genus Pseudoterranova were found only in fish caught in the Norwegian Sea.

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