Literature DB >> 16355510

Angiostrongyliasis, Mainland China.

Xiao-Guang Chen, Hua Li, Zhao-Rong Lun.   

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Year:  2005        PMID: 16355510      PMCID: PMC3366736          DOI: 10.3201/eid1110.041338

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


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To the Editor: The first case of angiostrongyliasis caused by Angiostrongylus cantonensis in mainland China was reported in 1984; only 3 cases were reported between then and 1996 (). Recently, however, cases of angiostrongyliasis have increased rapidly because of its natural focus and a change in human dietary patterns. For example, snails have become a popular food in many regions of this country. Nearly 100 cases of angiostrongyliasis have been reported in mainland China, including 2 outbreaks (,). From 1994 to 2003, 84 cases of angiostrongyliasis were documented in mainland China. Of all the cases, 29 were reported individually, and 55 were reported from the 2 outbreaks that occurred in Zhejiang and Fujian. Sixty-three of the 84 patients had eaten raw or undercooked snails, 5 had eaten raw crabs, 1 swallowed tadpoles, and several pediatric patients had close contact with snails. Some researchers believe that the larvae of A. cantonensis can be released from mollusks into slime fluid and contaminate produce and other objects as they crawl. However, Liang et al. () reported finding no larvae in body fluid washed from 23 Achatina fulica that were infected with A. cantonensis. Therefore, whether slime fluid plays a role in human infection remains unclear. The clinical symptoms of the patients from the 2 outbreaks of angiostrongyliasis that occurred in China are shown in the Table. Eosinophilia is a typical characteristic of eosinophilic meningitis or meningoencephalitis caused by A. cantonensis. In our study, eosinophilia was detected in 79 of 84 patients. Therefore, clinical patients with eosinophilic meningitis or meningoencephalitis with eosinophilia should be presumptively considered to be infected with A. cantonensis and parasitologic or serologic tests should be performed. The parasitologic detection rate of A. cantonensis infection in humans is low; because this parasite is found in the human central nervous system (CNS) and the tiny larvae often stick to meninges or nerve root, a false-negative result is often shown when cerebrospinal fluid is examined. In the 84 cases reported in this article, worms were isolated from only 8 patients (9.5%), whereas 64 cases were diagnosed as angiostrongyliasis by immunologic methods. The most common immunologic methods used to diagnosis angiostrongyliasis in this country are indirect fluorescent antibody test, immunoenzymatic staining technique, and enzyme-linked immunosorbent assay. All antigens used in these methods were prepared from whole adult worms. Reports indicated that serologic cross-reaction occurred between trichinosis and angiostrongyliasis when whole-worm lysate was used as the antigen (). In addition, whole-worm antigens cannot discriminate between new and previous infection, or monitor the efficacy of the treatment. Therefore, finding potential diagnostic antigens will be essential to solving this problem and applying recombinant antigens may achieve this goal. A cDNA library from the larvae of A. cantonensis was constructed and screened with acute infection sera, and a diagnostic antigen that can detect early infection of A. cantonensis (3 weeks) was identified ().
Table

Clinical characteristics of patients with angiostrongyliasis in 2 outbreaks in China*

CharacteristicsOutbreak 1 (%)Outbreak 2 (%)
No. of patients478
No. of male patients (%)24 (51)8 (100)
Age, y
Median3212
Range6–5811–13
Incubation (day)
Median10.356
Range1–275–7
Symptoms†, no. (%)
Headache44 (93.6)8 (100)
Nuchal rigidity or neck pain06 (75.0)
Fatigue7 (14.9)7 (87.5)
Vomiting9 (19.1)8 (100)
Paresthesias30 (63.8)3 (37.5)
Muscle pain43 (91.5)8 (100)
Fever27 (57.4)3 (37.5)
Cough4 (8.5)0
Somnolence4 (8.5)7 (87.5)
Skin eruption10 (21.3)0
Skin itch13 (27.7)0
Laboratory detection
No. positive/no. examined (%)
Eosiniphils in cerebrospinal fluid23/25 (92)8/8 (100)
Eosinophils in blood23/25 (92)8/8 (100)
Serologic diagnosis21/25 (84)NT
Pathogenic testND1/8‡ (12.5)

*NT, not tested; ND, not detected.
†No patients had visual disturbance or photophobia, hyperesthesias, muscle weakness, or diarrhea.
‡Two larvae were found in cerebrospinal fluid.

*NT, not tested; ND, not detected.
†No patients had visual disturbance or photophobia, hyperesthesias, muscle weakness, or diarrhea.
‡Two larvae were found in cerebrospinal fluid. Some researchers considered that anthelminthics, such as albendazole, ivermectin, mebendazole, and pyrantel, did not affect A. cantonensis but noted that the death of worms in the CNS might exacerbate neurologic symptoms (). However, many studies in mainland China showed that anthelminthics can relieve symptoms and reduce the duration of disease. For example, Wang et al. () reported that albendazole could relieve the symptoms of angiostrongyliasis and suggested that it can be used to treat the disease. Lin et al. () also reported that in 8 patients who were treated with 20 mg/kg albendazole for 9 days, the symptoms and signs of acute angiostrongyliasis were rapidly relieved in 3–6 days. All of these patients had recovered by 10 days after treatment, and no side effects were observed. Angiostrongyliasis is an emerging foodborne public health problem in mainland China. However, most clinicians are not familiar with this disease and little is known about the prevalence of A. cantonensis in China. Thus, more studies should be conducted on the biology, epidemiology, and clinical characteristics of angiostrongyliasis, and more effective diagnostic methods and treatments for A. cantonensis should be developed.
  4 in total

1.  [A clinical research for eosinophilic meningoencephalitis caused by angiostrongyliasis].

Authors:  X Wang; H Huang; Q Dong; Y Lin; Z Wang; F Li
Journal:  Zhonghua Nei Ke Za Zhi       Date:  1999-05

2.  An outbreak of eosinophilic meningitis caused by Angiostrongylus cantonensis in travelers returning from the Caribbean.

Authors:  Trevor J Slom; Margaret M Cortese; Susan I Gerber; Roderick C Jones; Timothy H Holtz; Adriana S Lopez; Carlos H Zambrano; Robert L Sufit; Yuwaporn Sakolvaree; Wanpen Chaicumpa; Barbara L Herwaldt; Stuart Johnson
Journal:  N Engl J Med       Date:  2002-02-28       Impact factor: 91.245

3.  [Epidemiological study on group infection of Angiostrongylus cantonensis in Changle City].

Authors:  Jin-xiang Lin; You-song Li; Kai Zhu; Bao-jian Chen; You-zhu Cheng; Jin-cai Lin; Yi Cao; Ri-zhong Chen
Journal:  Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi       Date:  2003

4.  [Epidemiological investigation on an outbreak of angiostrongyliasis cantonensis in Wenzhou].

Authors:  D Y Xue; Y Z Ruan; B C Lin; R Y Zheng; J Q Fang; Q X Zhao; M F Li; C W Pan
Journal:  Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi       Date:  2000
  4 in total
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1.  First Evidence of Angiostrongyliasis Caused by Angiostrongylus cantonensis in Guadeloupe, Lesser Antilles.

Authors:  Céline Dard; Jean-Eudes Piloquet; Yvonne Qvarnstrom; LeAnne M Fox; Helmi M'kada; Jean-Christophe Hebert; Didier Mattera; Dorothée Harrois
Journal:  Am J Trop Med Hyg       Date:  2017-04-06       Impact factor: 2.345

2.  PCR-based detection of Angiostrongylus cantonensis in tissue and mucus secretions from molluscan hosts.

Authors:  Yvonne Qvarnstrom; James J Sullivan; Henry S Bishop; Robert Hollingsworth; Alexandre J da Silva
Journal:  Appl Environ Microbiol       Date:  2006-12-28       Impact factor: 4.792

3.  Control measures for slug and snail hosts of Angiostrongylus cantonensis, with special reference to the semi-slug Parmarion martensi.

Authors:  Robert G Hollingsworth; Kathleen Howe; Susan I Jarvi
Journal:  Hawaii J Med Public Health       Date:  2013-06

Review 4.  Pathways for transmission of angiostrongyliasis and the risk of disease associated with them.

Authors:  Robert H Cowie
Journal:  Hawaii J Med Public Health       Date:  2013-06

5.  The effect of temperature on the development of Angiostrongylus cantonensis (Chen 1935) in Pomacea canaliculata (Lamarck 1822).

Authors:  Shan Lv; Xiao-Nong Zhou; Yi Zhang; He-Xiang Liu; Dan Zhu; Wei-Gang Yin; Peter Steinmann; Xian-Hong Wang; Tie-Wu Jia
Journal:  Parasitol Res       Date:  2006-05-03       Impact factor: 2.289

6.  Preliminary molecular characterization of the human pathogen Angiostrongylus cantonensis.

Authors:  Hualiang He; Mei Cheng; Xiao Yang; Jinxiu Meng; Ai He; Xiaoying Zheng; Zhuoya Li; Pengjuan Guo; Zhihua Pan; Ximei Zhan
Journal:  BMC Mol Biol       Date:  2009-10-25       Impact factor: 2.946

Review 7.  Update on eosinophilic meningoencephalitis and its clinical relevance.

Authors:  Carlos Graeff-Teixeira; Ana Cristina Arámburu da Silva; Kentaro Yoshimura
Journal:  Clin Microbiol Rev       Date:  2009-04       Impact factor: 26.132

8.  Invasive freshwater snail, China.

Authors:  Qiao-Ping Wang; Xiao-Guang Chen; Zhao-Rong Lun
Journal:  Emerg Infect Dis       Date:  2007-07       Impact factor: 6.883

9.  Real-Time Polymerase Chain Reaction Detection of Angiostrongylus cantonensis DNA in Cerebrospinal Fluid from Patients with Eosinophilic Meningitis.

Authors:  Yvonne Qvarnstrom; Maniphet Xayavong; Ana Cristina Aramburu da Silva; Sarah Y Park; A Christian Whelen; Precilia S Calimlim; Rebecca H Sciulli; Stacey A A Honda; Karen Higa; Paul Kitsutani; Nora Chea; Seng Heng; Stuart Johnson; Carlos Graeff-Teixeira; LeAnne M Fox; Alexandre J da Silva
Journal:  Am J Trop Med Hyg       Date:  2015-11-02       Impact factor: 2.345

10.  Infectivity of gastropod-shed third-stage larvae of Angiostrongylus vasorum and Crenosoma vulpis to dogs.

Authors:  William Robbins; Gary Conboy; Spencer Greenwood; Roland Schaper
Journal:  Parasit Vectors       Date:  2021-06-07       Impact factor: 3.876

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