Anisakiasis is a parasitic disease caused primarily by Anisakis spp. larvae in Asia and in Western countries. The aim of this study was to investigate the genotype of Anisakis larvae endoscopically removed from Middle Eastern Japanese patients and to determine whether mucosal atrophy affects the risk of penetration in gastric anisakiasis.
In this study, 57 larvae collected from 44 patients with anisakiasis (42 gastric and 2 colonic anisakiasis) were analyzed retrospectively. Genotyping was confirmed by restriction fragment length polymorphism (RFLP) analysis of ITS regions and by sequencing the mitochondrial small subunit (SSU) region. In the cases of gastric anisakiasis, correlation analyses were conducted between the frequency of larval penetration in normal/atrophic area and the manifestation of clinical symptoms.
Nearly all larvae were A. simplex seusu stricto (s.s.) (99%), and one larva displayed a hybrid genotype. The A. simplex larvae penetrated normal mucosa more frequently than atrophic area (p = 0.005). Finally, patients with normal mucosa infection were more likely to exhibit clinical symptoms than those with atrophic mucosa infection (odds ratio, 6.96; 95% confidence interval, 1.52–31.8).
Citation: Arai T, Akao N, Seki T, Kumagai T, Ishikawa H, Ohta N, et al. (2014) Molecular Genotyping of Anisakis Larvae in Middle Eastern Japan and Endoscopic Evidence for Preferential Penetration of Normal over Atrophic Mucosa. PLoS ONE 9(2): e89188. https://doi.org/10.1371/journal.pone.0089188
Editor: Masaru Katoh, National Cancer Center, Japan
Received: October 13, 2013; Accepted: January 16, 2014; Published: February 28, 2014
Copyright: © 2014 Arai et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by grants 25460513 (Japan Society for Promotion of Science) and 2250502 (Ministry of Health, Labour and Welfare). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Anisakiasis is a parasitic infection caused by nematodes, particularly Anisakis simplex, A. physeteris or Pseudoterranova decipiens . A total of 2,000 cases of Anisakiasis are reported every year worldwide, with more than 90% of the cases in Japan. The disease is contracted by eating raw or undercooked fish contaminated with the parasites. The first cases of anisakiasis were reported in the Netherlands, followed by widespread infestation in Japan . In the past decade, the incidence of anisakiasis has been increasing in several countries, including Austria and Italy –. Most patients are infected by A. simplex worldwide. Isolated cases of A. physeteris infection were identified in Japan and Spain , . Pseudoterranovasis has been reported primarily in the United States and Canada, with a few reports in south Japan and Europe , –.
Recent molecular studies using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis and sequencing of the internal transcribed spacer (ITS) region revealed that A. simplex consists of 3 major sibling species: A. simplex seusu stricto (s.s.), A. pegreffii, and A. simplex C –. In North and South Japan, A. simplex s.s. is the most common species. However, the source of infection has not been identified, and no study has investigated regional differences in Anisakis spp. in Central Japan .
Currently, the only effective treatment is the endoscopic removal of the live larvae from the gastric mucosa. Therefore, it is important to find the larvae quickly and remove them thoroughly. Only few studies examined endoscopic findings of gastric anisakiasis , . The Anisakis larvae are usually found in the greater curvature . However, they are often hidden in the gastric folds. Furthermore, the mucosa undergoes a series of morphological changes from the time of contaminated food ingestion to the endoscopic examination, including edema and tumor formation, which may hide the larvae . Furthermore, it is often hidden among the gastric folds with mucosal edema. For these reasons, the endoscopic detection and removal of all live larvae remains a challenge, and more information is required on the penetration sites.
To the best of our knowledge, no study has investigated whether the health status of the mucosa affects Anisakis penetration in the human stomach. A recent in vitro study showed that Anisakis penetrates agar gel more easily under acidic conditions . In the stomach, the pH of normal mucosa is lower than that of atrophic area . Therefore, we hypothesized that Anisakis may preferentially invade normal gastric mucosa. In this report, we genotyped Anisakis larvae removed from patients in Middle Eastern part of Japan and tested the impact of mucosal properties on larval penetration.
Materials and Methods
From January 2011 to December 2012, 44 patients with anisakiasis visited three hospitals of Middle Eastern Japan (Kameda General Hospital, Kameda Clinic and Toukatsu Hospital). A total of 55 larvae were removed by upper gastrointestinal endoscopic examination and 2 larvae were removed by colonoscopy.
The collected larvae were sent to our laboratory and morphological observation was carried out under a light microscope. We identified the genus and stage of the larvae, as previously described , , .
Total DNA was extracted with the Get pure DNA Kit-Cell, Tissue (Dojindo, Japan) according to the manufacturer's instructions. The ITS region (ITS1, 5.8S and ITS2) of ribosomal DNA (rDNA) was amplified with the forward primer NC5 (5′-GTAGGTGAACCTGCGGAAGGATCATT-3′) and the reverse primer NC2 (5′-TTAGTTTCTTTTCCTCCGCT-3′) –. Mitochondrial small subunit (SSU) of ribosomal RNA (rRNA) was amplified with the forward primer MH3 (5′-TTGTTCCAGAATAATCGGCTAGACTT-3′) and the reverse primer MH4 (5′-TCTACTTTACTACAACTTACTCC-3′). The PCR reaction was performed as previously described . Each PCR product was digested by two restriction enzyme HhaI and HinfI (Takara, Japan) and evaluated based on previous reports –, –. To identify the hybrid genotype, the PCR products of the ITS and mitochondrial SSU regions were sequenced using the BigDye Terminator version 3.1 Cycle Sequencing kit (Applied Biosystems, USA) according to the manufacturer's instructions, and an ABI3100 automatic sequencer (Applied Biosystems, USA). Sequences were visualized using chromatograms, and were, manually corrected subsequently using the Finch TV software (Geospiza, USA).A BLAST search (National Center of Biotechnology Information public databases; http://blast.ncbi.nlm.nih.gov/Blast.cgi) was carried out to elucidate previously published sequences. Multiple sequence alignment was carried out using the Clustal W software .
Identification of the penetration sites
Upper gastrointestinal endoscopy or colonoscopy was performed in all patients. All endoscopic examinations were conducted with an electronic scope (OLYMPUS or FUJINON, Tokyo, Japan). In all cases of gastric anisakiasis, we carefully examined each area infected by Anisakis and documented whether each larva was found in normal or atrophic mucosa. Normal mucosa was defined as homogeneously reddish, smooth, and regular arrangement of collecting venules, whereas atrophic mucosa was defined as yellowish-pale tissue, with transparent blood vessels without biopsies .
Grading of gastric mucosa atrophy
The severity of gastric atrophy was determined based on the classification system of Kimura and Takemoto . This classification divides the extent of atrophy into closed type (C-type) and open type (O-type). The C-type is subdivided into C1, C2, and C3, while the O-type is subdivided into O1, O2, and O3. The atrophic border is observed in the distal antrum in the C1 type, the lower and middle parts of the corpus in the C2 type, and the upper part of the corpus in the C3 type. In the O1-type, the atrophic border is within the cardiac lesion. In the O-2 type, it lies beyond the cardiac lesion to the anterior and posterior walls of the body. In the O-3 type, the endoscopic atrophic area is widely spread with border lying along the greater curvature. The area ratio of normal mucosa to atrophic mucosa was estimated using the figure adapted from S Ito (1996)  with imaging application (Image-J software, National Institutes of Health, Bethesda, Maryland, USA). To determine the impact of atrophy on the larvae penetration sites, C-0 (normal) and O-3 (almost completely atrophic mucosa) were excluded because the ratio varies depending on the selective site of invasion. Theoretical expectation of larvae in each condition of mucosa (from C-1 to O-2) was calculated as follows; the observation number of Anisakis larvae multiplied by the area ratio of normal mucosa to atrophic mucosa.
Statistical analyses were performed using test for population proportion and Fisher's exact test (Statcel 3 software, OMS Publishing Inc., Saitama, Japan); p value of less than 0.05 was considered to be statistically significant.
The research was approved by the Ethical Committee of Tokyo Medical and Dental University, Kameda Medical Center, and Toukatsu Hospital, respectively. All cases were adult and all subjects were required to give written informed consent, and where such approval was not forthcoming, the subject concerned was excluded from the study.
Characteristics of the patients
A total of 42 patients diagnosed with gastric anisakiasis and 2 patients with colonic anisakiasis were admitted in the three Middle Eastern Japan hospitals during the study period. The onset of symptoms was 1.4±1.1 days (range: 0–5 days) before admission to a hospital (Table 1). The sources of infection were raw or undercooked edible fish, including sardine (33%), mackerel (28%), and yellowtail snapper (21%). Interestingly, 11 cases were asymptomatic for anisakiasis. Four patients were admitted for a follow-up examination on gastric or colon cancer after endoscopic treatment, five patients we screened for gastric cancer by detailed endoscopic examination, and two patients were admitted for a follow-up examination on gastroesophageal reflux disease.
Morphological and genotyping of Anisakis larvae
In total, 55 larvae were removed by gastrointestinal endoscopy and 2 larvae by colonoscopy. Macroscopic examination revealed that all larvae belonged to the genus Anisakis sp. (Table 2). No Pseudoterranova type lava was found. Fifty-six larvae were identified at the 3rd larval stage, and one larva exhibited the characteristics of the 4th larval stage, with shedding of part of its outer cuticle and absence of mucron and boring tooth, as reported previously , . There were no morphological differences between the symptomatic isolates and asymptomatic isolates. The RFLP profiles obtained by digestion of the ITS region (HhaI and HinfI) showed that 99% of the larvae were A. simplex s.s. (550–430 and 620–250 bp), and one larva had a hybrid genotype (550–430 bp and 620–370–300–250 bp) (Figure 1). This observation was consistent with a hybrid genotype as reported previously . To confirm the diagnosis, the ITS region and mitochondrial SSU regions were further examined by sequence analysis. The sequencing of the ITS region supported the presence of heterozygotes (C/T) at position 240 and 256. Mitochondrial SSU alignment revealed that the sequence of the hybrid was consistent with that of A. simplex s.s, but different from that of A. pegreffii at positions 30, 32, and 429 (see Table 3), which indicated the female parent of hybrid was A. simplex s.s..
Restriction with HhaI produced two fragments of 550 bp and 430 bp in Hybrid genotype and A. simplex s. s.. HinfI produced four fragments of 620 bp, 370 bp, 300 bp, and 250 bp in Hybrid genotype, whereas produced two fragments of 620 bp and 250 bp in A. simplex s. s.. Lanes: 1, Hybrid genotype; 2, A. simplex s. s.; L, 100-bp ladder.
Correlation between mucosal status on larval penetration
For this analysis, the larvae from patients who were prescribed antacid medicines were excluded because they may affect the morphology of the gastric mucosa. Accordingly, a total of 45 larvae from 35 patients were included. First, we identified a statistically significant correlation between clinical symptoms and penetration site (p = 0.014; Table 4). Patients with infected normal mucosa were more likely to exhibit symptoms (odds ratio, 6.96; 95% confidence interval, 1.52–31.8) than those with infected atrophic mucosa. Also, we tested whether the larvae preferentially infected normal or atrophic mucosa. Statistically significant correlation was found between the penetration sites and normal mucosa by test for population proportion (p = 0.005) (Table 5). Thus, we suggested that A. simplex s.s. tends to penetrate normal mucosa than atrophic area, regardless of the extent of background atrophic gastritis.
Anisakiasis is a major issue in Japan due to the nutritional habits of the general population. The medical record of the patients included in this study revealed that they consume a large variety of raw or undercooked edible fishes as sashimi or sushi. Because this habit is deeply rooted in the culture of the country, the current focus is to improve the efficiency of endoscopic removal of the larvae implanted in the gastrointestinal wall. The present study identified the genotype of the larvae affecting the Middle Eastern Japanese population, and offers invaluable information on the distribution of the larvae in the gastric mucosa.
In Southern and Northern Japan, the major etiological agent of human anisakiasis was identified as A. simplex s.s. . The present study identified the same parasite in 99% of the larvae isolated from Middle Eastern Japanese patients with gastric anisakiasis. Interestingly, 1 larva exhibited a hybrid genotype, which is the first report for human anisakiasis. The larva with the hybrid genotype was collected from a patient who ate trout and was infected with three larvae by gastrointestinal endoscopy; this patient had abdominal pain. The existence of a hybrid genotype was explained as the result of natural interspecies hybridization between A. simplex s.s. and A. pegreffii , , . In the previous study, hybrid genotypes were detected in Blue whiting, Scomber japonicas, and Scomber scombrus , .We hypothesized that the hybrid genotype could parasite in various marine fish. There was no morphological difference between A. simplex s.s. and the hybrid genotype. Moreover, we didn`t find the pathogenic characteristics between A. simplex s.s. and the hybrid genotype. Further studies are required to characterize the hybrid genotype.
These data suggest that A. simplex s.s. is the causative agent of anisakiasis everywhere in Japan. Incidentally, A. simplex s.s. larvae was reported to penetrate muscle tissue more easily than A. pegreffii larvae in edible fish , . Therefore, the predominance of gastric infection by A. simplex s.s. does not necessarily reflect the relative abundance of these parasites in the ocean.
The present study also addressed the challenging task of locating and removing all Anisakis larvae lodged in the gastric mucosa of a patient. Close endoscopic examination of the infected areas revealed that the larvae penetrated normal mucosa significantly more often than the atrophic area. A recent study suggests that regional pH differences may be responsible for this behavior. They showed that A. simplex s.s. larvae penetrated agar gel more efficiently at lower pH, and survived longer in gastric juice than A. pegreffii larvae . These data are consistent with the lower pH measured in normal gastric mucosa than in atrophic gastric mucosa . A recent report suggests that the use of narrow band imaging improves the detection of Anisakis larvae in the gastrointestinal wall . Therefore, when endoscopic examination for anisakiasis is conducted, it is very important to examine normal mucosa very carefully using narrow band imaging.
We also report the puzzling observation that patients with Anisakis larvae lodged in normal mucosa exhibited clinical symptoms more frequently than those infected in atrophic area. This is an alarming observation because patients already facing digestive complications causing extensive mucosal atrophy may not manifest the typical clinical symptoms. These patients may have undiagnosed anisakiasis for years and suffer from unexplained complications. For example, a recent case-control study showed that prior Anisakis infection is an independent risk factor for upper gastrointestinal bleeding, and amplifies 3-fold the adverse effects of non-steroidal anti-inflammatory drugs (NSAIDs) on the joints . Therefore, patients who have received treatment for anisakiasis should be monitored closely when they are prescribed NSAIDs for a chronic condition.
It is still unclear why patients with Anisakis larvae infecting their normal gastric mucosa are more likely to exhibit clinical symptoms than those with atrophic mucosa infections. Several reports mentioned that symptomatic anisakiasis is caused by an allergic response , . Accordingly, clinicians noted the efficacy of corticosteroids therapy for gastric and intestinal anisakiasis . Since this is a retrospective study, anti-Anisakis IgE antibody was not determined. Future studies comparing serum IgE levels between symptomatic and asymptomatic patients may shed some light on the mechanisms of anisakiasis.
Thus, after treatment of anisakiasis, it may be necessary to follow-up when the patients take NSAIDs. In conclusion, the present study showed that A. simplex s.s. is the predominant etiological agent for anisakiasis in Japan, and the larvae preferentially penetrate normal gastric mucosa. Careful endoscopic examination of normal mucosa, particularly in the greater curvature of the gastric body, will improve detection of the larvae and treatment efficiency. Finally, since patients with widespread atrophic mucosa may not manifest the clinical symptoms of anisakiasis, routine endoscopic screening could potentially avoid unexplainable complications and adverse reactions to common medications.
We thank Kaoru Fueda from the Department of Human Ecology, Okayama University for conducting the statistical analyses. We also thank Hiromu Sugiyama and Hiroshi Yamasaki from the Department of Parasitology, National Institute of Infectious Disease for PCR work. We express our gratitude to the staff of the Department of Gastroenterology (Kameda Medical Center and Toukatus Hospital).
Conceived and designed the experiments: TA NA NO. Performed the experiments: TA NA. Analyzed the data: TA NA HI NO T. Seki NH. Contributed reagents/materials/analysis tools: TA NA TK NH SN KY MH T. Shiratori MK HF EI MN SS TY NS MS TT. Wrote the paper: TA NA NO.
- 1. Hochberg NS, Hamer DH (2010) Anisakidosis: Perils of the deep. Clin Infect Dis 51: 806–812.
- 2. Nawa Y, Hatz C, Blum J (2005) Sushi delights and parasites: the risk of fishborne and foodborne parasitic zoonoses in Asia. Clin Infect Dis 41: 1297–1303.
- 3. Kapral C, Haditsch M, Wewalka F, Schatzlmayr W, Lenz K, et al. (2009) [The first case of anisakiasis acquired in Austria]. Z Gastroenterol 47: 1059–1061.
- 4. Mattiucci S, Paoletti M, Borrini F, Palumbo M, Palmieri RM, et al. (2011) First molecular identification of the zoonotic parasite Anisakis pegreffii (Nematoda: Anisakidae) in a paraffin-embedded granuloma taken from a case of human intestinal anisakiasis in Italy. BMC Infect Dis 11: 82.
- 5. Me. Audicana MT, Kennedy MW (2008) Anisakis simplex: from obscure infectious worm to inducer of immune hypersensitivity. Clin Microbiol Rev 21: : 360–379, table of contents.
- 6. Mercado R, Torres P, Maira J (1997) Human case of gastric infection by a fourth larval stage of Pseudoterranova decipiens (Nematoda, Anisakidae). Rev Saude Publica 31: 178–181.
- 7. Sohn WM, Seol SY (1994) A human case of gastric anisakiasis by Pseudoterranova decipiens larva. Korean J Parasitol 32: 53–56.
- 8. Cavallero S, Nadler SA, Paggi L, Barros NB, D'Amelio S (2011) Molecular characterization and phylogeny of anisakid nematodes from cetaceans from southeastern Atlantic coasts of USA, Gulf of Mexico, and Caribbean Sea. Parasitol Res 108: 781–792.
- 9. D'Amelio S, Mathiopoulos KD, Santos CP, Pugachev ON, Webb SC, et al. (2000) Genetic markers in ribosomal DNA for the identification of members of the genus Anisakis (Nematoda: ascaridoidea) defined by polymerase-chain-reaction-based restriction fragment length polymorphism. Int J Parasitol 30: 223–226.
- 10. Umehara A, Kawakami Y, Araki J, Uchida A (2007) Molecular identification of the etiological agent of the human anisakiasis in Japan. Parasitol Int 56: 211–215.
- 11. Kakizoe S, Kakizoe H, Kakizoe K, Kakizoe Y, Maruta M, et al. (1995) Endoscopic findings and clinical manifestation of gastric anisakiasis. Am J Gastroenterol 90: 761–763.
- 12. Lee EJ, Kim YC, Jeong HG, Lee OJ (2009) [The mucosal changes and influencing factors in upper gastrointestinal anisakiasis: analysis of 141 cases]. Korean J Gastroenterol 53: 90–97.
- 13. Kojima F, Kasane U, Shuji F (2012) [Evaluating Method of the Penentration Capacity of Anisakis Larvae with Agar. Clin Parasitol]. C Parasitology 23: 64–65.
- 14. Marotta F, Hayakawa K, Mikami Y, Morello P, Sugai M, et al. (1990) Relationship between gastrin cell number, serum, antral mucosa and luminal gastrin concentration and gastric acidity in antral atrophic gastritis. Gut 31: 279–281.
- 15. Quiazon KM, Yoshinaga T, Ogawa K, Yukami R (2008) Morphological differences between larvae and in vitro-cultured adults of Anisakis simplex (sensu stricto) and Anisakis pegreffii (Nematoda: Anisakidae). Parasitol Int 57: 483–489.
- 16. Murata R, Suzuki J, Sadamasu K, Kai A (2011) Morphological and molecular characterization of Anisakis larvae (Nematoda: Anisakidae) in Beryx splendens from Japanese waters. Parasitol Int 60: 193–198.
- 17. Abollo E, Paggi L, Pascual S, D'Amelio S (2003) Occurrence of recombinant genotypes of Anisakis simplex s.s. and Anisakis pegreffii (Nematoda: Anisakidae) in an area of sympatry. Infect Genet Evol 3: 175–181.
- 18. Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 22: 4673–4680.
- 19. Yagi K, Aruga Y, Nakamura A, Sekine A (2005) Regular arrangement of collecting venules (RAC): a characteristic endoscopic feature of Helicobacter pylori-negative normal stomach and its relationship with esophago-gastric adenocarcinoma. J Gastroenterol 40: 443–452.
- 20. Ito S, Azuma T, Murakita H, Hirai M, Miyaji H, et al. (1996) Profile of Helicobacter pylori cytotoxin derived from two areas of Japan with different prevalence of atrophic gastritis. Gut 39: 800–806.
- 21. Martin-Sanchez J, Artacho-Reinoso ME, Diaz-Gavilan M, Valero-Lopez A (2005) Structure of Anisakis simplex s.l. populations in a region sympatric for A. pegreffii and A. simplex s.s. Absence of reproductive isolation between both species. Mol Biochem Parasitol 141: 155–162.
- 22. Umehara A, Kawakami Y, Matsui T, Araki J, Uchida A (2006) Molecular identification of Anisakis simplex sensu stricto and Anisakis pegreffii (Nematoda: Anisakidae) from fish and cetacean in Japanese waters. Parasitol Int 55: 267–271.
- 23. Suzuki J, Murata R, Hosaka M, Araki J (2010) Risk factors for human Anisakis infection and association between the geographic origins of Scomber japonicus and anisakid nematodes. Int J Food Microbiol 137: 88–93.
- 24. Quiazon KM, Yoshinaga T, Ogawa K (2011) Experimental challenge of Anisakis simplex sensu stricto and Anisakis pegreffii (Nematoda: Anisakidae) in rainbow trout and olive flounder. Parasitol Int 60: 126–131.
- 25. Arizono N, Yamada M, Tegoshi T, Yoshikawa M (2012) Anisakis simplex sensu stricto and Anisakis pegreffii: biological characteristics and pathogenetic potential in human anisakiasis. Foodborne Pathog Dis 9: 517–521.
- 26. Taranto D, Sessa G, Tortora R, Tremolaterra F (2011) Narrow band imaging enhancement could improve gastric anisakis detection. Dig Liver Dis 43: e5.
- 27. Ubeira FM, Anadón AM, Salgado A, Carvajal A, Ortega S, et al. (2011) Synergism between prior Anisakis simplex infections and intake of NSAIDs, on the risk of upper digestive bleeding: a case-control study. PLoS Negl Trop Dis 5: e1214.
- 28. Caballero ML, Asero R, Antonicelli L, Kamberi E, Colangelo C, et al. (2013) Anisakis Allergy Component-Resolved Diagnosis: Clinical and Immunologic Differences between Patients from Italy and Spain. Int Arch Allergy Immunol 162: 39–44.
- 29. Tachibana M, Yamamoto Y (1986) [Serum anti-Anisakis IgE antibody in patients with acute gastric anisakiasis]. Nihon Shokakibyo Gakkai Zasshi 83: 2132–2138.
- 30. Ramos L, Alonso C, Guilarte M, Vilaseca J, Santos J, et al. (2005) Anisakis simplex-induced small bowel obstruction after fish ingestion: preliminary evidence for response to parenteral corticosteroids. Clin Gastroenterol Hepatol 3: 667–671.