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Diagnosis of human nematode infections

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Pages 1363-1376 | Published online: 10 Jan 2014

References

  • Michael Katz, Dickson D. Despommier, Robert W. Gwadz. The nematodes. Parasitic Diseases. Springer US 1–64 (1989).
  • Gottstein B, Pozio E, Nöckler K. Epidemiology, diagnosis, treatment, and control of trichinellosis. Clin. Microbiol. Rev. 22, 127–145 (2009).
  • Zouré HG, Wanji S, Noma M et al. The geographic distribution of Loa loa in Africa: results of large-scale implementation of the Rapid Assessment Procedure for Loiasis (RAPLOA). PLoS Negl. Trop. Dis. 5, 1210 (2011).
  • Thanomsub BW, Chansiri K, Sarataphan N, Phantana S. Differential diagnosis of human lymphatic filariasis using PCR-RFLP. Mol. Cell. Probes. 14, 41–46 (2000).
  • Pravettoni V, Primavesi L, Piantanida M. Anisakis simplex: current knowledge. Eur. Ann. Allergy Clin. Immunol. 44, 150–156 (2012).
  • Schuster A, Lesshafft H, Reichert F et al. Hookworm-related cutaneous larva migrans in northern brazil: resolution of clinical pathology after a single dose of ivermectin. Clin. Infect. Dis. 57(8), 1155–1157 (2013)..
  • Upendra Y, Mahajan VK, Mehta KS, Chauhan PS, Chander B. Cutaneous larva migrans. Indian J. Dermatol. Venereol. Leprol. 79, 418–419 (2013).
  • WHO deworming for health and development. Report of the third global meeting of the partners for parasite control Geneva: World Health Organization (2005).
  • Chammartin F, Scholte RG, Guimarães LH, Tanner M, Utzinger J, Vounatsou P. Soil-transmitted helminth infection in South America: a systematic review and geostatistical meta-analysis. Lancet Infect. Dis. 13, 507–518 (2013).
  • de Silva NR, Brooker S, Hotez PJ, Montresor A, Engels D, Savioli L. Soil-transmitted helminth infections: updating the global picture. Trends Parasitol. 19, 547–551 (2003).
  • Hotez PJ, Bethony J, Bottazzi ME, Brooker S, Diemert D, Loukas A. New technologies for the control of human hookworm infection. Trends Parasitol. 22, 327–331 (2006).
  • Croker C, Reporter R, Redelings M, Mascola L. Strongyloidiasis-related deaths in the United States, 1991-2006. Am. J. Trop. Med. Hyg. 83, 422–426 (2010).
  • Jeong YJ, Kim KI, Seo IJ et al. Eosinophilic lung diseases: a clinical, radiologic, and pathologic overview. Radiographics 27, 617–637 (2007).
  • Ross AG, Olds GR, Cripps AW, Farrar JJ, McManus DP. Enteropathogens and chronic illness in returning travelers. N. Engl. J. Med. 368, 1817–1825 (2013).
  • Bethony J, Brooker S, Albonico M et al. Soil-transmitted helminth infections: ascariasis, trichuriasis, and hookworm. Lancet 6, 367 (2006).
  • Bouree P, Paugam A, Petithory JC. Anisakidosis: report of 25 cases and review of the literature. Comp. Immunol. Microbiol. Infect. Dis. 18(2), 75–84 (1995).
  • Moore DA, McCroddan J, Dekumyoy P, Chiodini PL. Gnathostomiasis: an emerging imported disease. Emerg. Infect. Dis. 9, 647–650 (2003).
  • Simón F, Siles-Lucas M, MorchónR et al. Human and animal dirofilariasis: the emergence of a zoonotic mosaic. Clin. Microbiol. Rev. 25, 507–544 (2012).
  • Gopinath TN, Lakshmi KP, Shaji PC, Rajalakshmi PC. Periorbital dirofilariasis-clinical and imaging findings: live worm on ultrasound. Indian J. Ophthalmol. 61, 298–300 (2013).
  • Pampiglione S, Rivasi F, Angeli G et al. Dirofilariasis due to Dirofilaria repens in Italy, an emergent zoonosis: report of 60 new cases. Histopathology 38, 344–354 (2001).
  • Guinier D, Morlevat F, L’Ollivier C, Dalle F, Bonnin A. An inguinal dirofilariasis mimicking a groin hernia. Presse Med. 41, 759–761 (2012).
  • Genchi C, Mortarino M, Rinaldi L, Cringoli G, Traldi G, Genchi M. Changing climate and changing vector-borne disease distribution: the example of Dirofilaria in Europe. Vet. Parasitol. 22, 176(4), 295–299 (2011).
  • Perret-Court A, Coulibaly B, Ranque S et al. Intradural dirofilariasis mimicking a Langerhans cell histiocytosis tumor. Pediatr. Blood Cancer 53, 485–487 (2009).
  • Magnaval JF, Glickman LT, Dorchies P, Morassin B. Highlights of human toxocariasis. Korean J. Parasitol. 39, 1–11 (2001).
  • Gavignet B, Piarroux R, Aubin F, Millon L, Humbert P. Cutaneous manifestations of human toxocariasis. J. Am. Acad. Dermatol. 59, 1031–1042 (2008).
  • Katchanov J, Nawa Y. Helminthic invasion of the central nervous system: many roads lead to Rome. Parasitol. Int. 59, 491–496 (2010).
  • Hochberg NS, Park SY, Blackburn BG et al. Distribution of eosinophilic meningitis cases attributable to Angiostrongylus cantonensis, Hawaii. Emerg. Infect. Dis. 13; 1675–1680 (2007).
  • Wang QP, Lai DH, Zhu XQ, Chen XG, Lun ZR. Human angiostrongyliasis. Lancet Infect. Dis. 8, 621–630 (2008).
  • Lima AR, Mesquita SD, Santos SS et al. Alicata disease: neuroinfestation by Angiostrongylus cantonensis in Recife, Pernambuco, Brazil. Arq Neuropsiquiatr. 67,1093–1096 (2009).
  • do Espírito-Santo MC, Pinto PL, da Mota DJ, Gryschek RC. The first case of Angiostrongylus cantonensis eosinophilic meningitis diagnosed in the city of São Paulo, Brazil. Rev. Inst. Med. Trop. Sao Paulo. 55: 129–132 (2013).
  • Herman JS, Chiodini PL. Gnathostomiasis, another emerging imported disease. Clin. Microbiol. Rev. 22, 484–492 (2009).
  • Leder K, Weller PF. Eosinophilia and helminthic infections. Baillieres Best Pract. Res. Clin. Haematol. 13, 301–317 (2000).
  • Vidal JE, Sztajnbok J, Seguro AC. Eosinophilic meningoencephalitis due to Toxocara canis: case report and review of the literature. Am. J. Trop. Med. Hyg. 69, 341–343 (2003).
  • Basáñez MG, Pion SD, Churcher TS, Breitling LP, Little MP, Boussinesq M. River blindness: a success story under threat? PLoS Med. 3, 371 (2006).
  • Mawhorter SD. Eosinophilia caused by parasites. Pediatr. Ann. 23, 409–413 (1994).
  • Ehrhardt S, Burchard GD. Eosinophilia in returning travelers and migrants. Dtsch. Arztebl. Int. 105, 801–807 (2008).
  • Moneret-Vautrin DA. Is the seric eosinophil cationic protein level a valuable tool of diagnosis in clinical practice? Rev. Med. Interne. 27, 679–683 (2006).
  • Slom TJ, Cortese MM, Gerber SI et al. An outbreak of eosinophilic meningitis caused by Angiostrongylus cantonensis in travelers returning from the Caribbean. N. Engl. J. Med. 346, 668–675 (2002).
  • Ramirez-Avila L, Slome S, Schuster FL et al. Eosinophilic meningitis due to Angiostrongylus and Gnathostoma species. Clin. Infect. Dis. 48, 322–327 (2009).
  • Lee JY, Kim BJ, Lee SP et al. Toxocariasis might be an important cause of atopic myelitis in Korea. J. Korean Med. Sci. 24, 1024–1030 (2009).
  • Watanabe N, Bruschi F, Korenaga M. IgE: a question of protective immunity in Trichinella spiralis infection. Trends Parasitol. 21, 175–18 (2005).
  • Karthikeyan K, Thappa DM. Cutaneous larva migrans. Indian J. Dermatol. Venereol. Leprol. 68, 252–258 (2002).
  • Capó V, Despommier DD. Clinical aspects of infection with Trichinella spp.. Clin. Microbiol. Rev. 9, 47–54 (1996).
  • Dreyer G, Fernandes-Silva E, Alves S, Rocha A, Albuquerque R, Addiss D. Patterns of detection of Strongyloides stercoralis in stool specimens: implications for diagnosis and clinical trials. J. Clin. Microbiol. 34, 2569–2571 (1996).
  • Requena-Méndez A, Chiodini P, Bisoffi Z, Buonfrate D, Gotuzzo E, Muñoz J. The laboratory diagnosis and follow up of strongyloidiasis: a systematic review. PLoS Negl. Trop. Dis. 7, e2002 (2013).
  • Katz N, Chaves A, Pellegrino J. A simple device for quantitative stool thick smear technique in Schistosomiasis mansoni. Rev. Inst. Med. Trop. 14, 397–400 (1972).
  • Carvalho GL, Moreira LE, Pena JL, Marinho CC, Bahia MT, Machado-Coelho GL. A comparative study of the TF-Test®, Kato-Katz, Hoffman-Pons-Janer, Willis and Baermann-Moraes coprologic methods for the detection of human parasitosis. Mem. Inst. Oswaldo Cruz. 107, 80–84 (2012).
  • Willis HH. A simple levitation method for the detection of hook worm ova. Med. J. Aust. 2, 375–376 (1921).
  • Bouhoum K, Schwartzbrod J. Quantification of helminth eggs in waste water. Zentralbl. Hyg. Umweltmed. 188, 322–330 (1989).
  • Carvalho GL, Moreira LE, Pena JL, Marinho CC, Bahia MT, Machado-Coelho GL. Moraes coprologic methods for the detection of human parasitosis. Mem. Inst. Oswaldo Cruz. 107, 80–84 (2012).
  • Garcia L. Diagnostic medical parasitology (5th Edition). ASM Press, Washington, DC, USA (2007).
  • Inês Ede J, Souza JN, Santos RC et al. Efficacy of parasitological methods for the diagnosis of Strongyloides stercoralis and hookworm in faecal specimens. Acta. Trop. 120, 206–210 (2011).
  • Barda BD, Rinaldi L, Ianniello D et al. Mini-FLOTAC, an innovative direct diagnostic technique for intestinal parasitic infections: experience from the field. PLoS Negl. Trop. Dis. 1, 7 (2013).
  • Cringoli G, Rinaldi L, Maurelli MP, Utzinger J. FLOTAC: new multivalent techniques for qualitative and quantitative copromicroscopic diagnosis of parasites in animals and humans. Nat Protoc. 5, 503–515 (2010).
  • Cheesbrough M. District Laboratory Practice in Tropical Countries, Part 1. (2nd Edition). Cambridge University Press, Cambridge, UK 454 (2005).
  • Walther M, Muller R. Diagnosis of human filariases (except onchocerciasis). Adv. Parasitol. 53, 149–193 (2003).
  • Noireau F, Apembet JD. Comparison of thick blood smear and saponin haemolysis for the detection of Loa loa and Mansonella perstans infections. J. Trop. Med. Hyg. 93, 390–392 (1990).
  • Olsen A, van Lieshout L, Marti H et al. Strongyloidiasis--the most neglected of the neglected tropical diseases? Trans. R. Soc. Trop. Med. Hyg. 103, 967–972 (2009).
  • del Rey-Moreno A, Valero-López A, Gómez-Pozo B et al. Use of anamnesis and immunological techniques in the diagnosis of anisakidosis in patients with acute abdomen. Rev. Esp. Enferm. Dig. 100, 146–152 (2008).
  • Chye SM, Chang JH, Yen CM. Immunodiagnosis of human eosinophilic meningitis using an antigen of Angiostrongylus cantonensis L5 with molecular weight 204 kD. Acta. Trop. 75, 9–17 (2000).
  • van Doorn HR, Koelewijn R, Hofwegen H et al. Use of enzyme-linked immunosorbent assay and dipstick assay for detection of Strongyloides stercoralis infection in humans. J. Clin. Microbiol. 45, 438–442 (2007).
  • Boscolo M, Gobbo M, Mantovani W et al. Evaluation of an indirect immunofluorescence assay for strongyloidiasis as a tool for diagnosis and follow-up. Clin. Vaccine Immunol. 14, 129–133 (2007).
  • Silva LP, Barcelos IS, Passos-Lima AB, Espindola FS, Campos DM, Costa-Cruz JM. Western blotting using Strongyloides ratti antigen for the detection of IgG antibodies as confirmatory test in human strongyloidiasis. Mem. Inst. Oswaldo Cruz. 98, 687–691 (2003).
  • Sato Y, Toma H, Kiyuna S, Shiroma Y. Gelatin particle indirect agglutination test for mass examination for strongyloidiasis. Trans. R. Soc. Trop. Med. Hyg. 85, 515–518 (1991).
  • Sithithaworn J, Sithithaworn P, Janrungsopa T, Suvatanadecha K, Ando K, Haswell-Elkins MR. Comparative assessment of the gelatin particle agglutination test and an enzyme-linked immunosorbent assay for diagnosis of strongyloidiasis. J. Clin. Microbiol. 43, 3278–3282 (2005).
  • Bon B, Houze S, Talabani H et al. Evaluation of a rapid enzyme-linked immunosorbent assay for diagnosis of strongyloidiasis. J. Clin. Microbiol. 48, 1716–1719 (2010).
  • Schaffel R, Nucci M, Carvalho E, Braga M, Almeida L, Portugal R, Pulcheri W. The value of an immunoenzymatic test (enzyme-linked immunosorbent assay) for the diagnosis of strongyloidiasis in patients immunosuppressed by hematologic malignancies. Am. J. Trop. Med. Hyg. 65, 346–350 (2001).
  • Sudarshi S, Stümpfle R, Armstrong M et al. Clinical presentation and diagnostic sensitivity of laboratory tests for Strongyloides stercoralis in travellers compared with immigrants in a non-endemic country. Trop. Med. Int. Health. 8, 728–732 (2003).
  • Yori PP, Kosek M, Gilman RH et al. Seroepidemiology of strongyloidiasis in the Peruvian Amazon. Am. J. Trop. Med. Hyg. 74, 97–102 (2006).
  • de Savigny DH, Voller A, Woodruff AW. Toxocariasis: serological diagnosis by enzyme immunoassay. J. Clin. Pathol. 32, 284–288 (1979).
  • Jacquier P, Gottstein B, Stingelin Y, Eckert J. Immunodiagnosis of toxocarosis in humans: evaluation of a new enzyme-linked immunosorbent assay kit. J. Clin. Microbiol. 29, 1831–1835 (1991).
  • Fillaux J, Magnaval JF. Laboratory diagnosis of human toxocariasis. Vet. Parasitol. 193, 327–336 (2013).
  • Gómez-Morales MA, Ludovisi A, Amati M, Cherchi S, Pezzotti P, Pozio E. Validation of an enzyme-linked immunosorbent assay for diagnosis of human trichinellosis. Clin. Vaccine Immunol. 15, 1723–1729 (2008).
  • Rocha A, Braga C, Belém M et al. Comparison of tests for the detection of circulating filarial antigen (Og4C3-ELISA and AD12-ICT) and ultrasound in diagnosis of lymphatic filariasis in individuals with microfilariae. Mem. Inst. Oswaldo Cruz. 104, 621–625 (2009).
  • Simonsen PE, Magesa SM. Observations on false positive reactions in the rapid NOW Filariasis card test. Trop. Med. Int. Health 9, 1200–1202 (2004).
  • More SJ, Copeman DB. A highly specific and sensitive monoclonal antibody-based ELISA for the detection of circulating antigen in bancroftian filariasis. Trop Med Parasitol. 41, 403–406 (1990)
  • Rocha A, Addiss D, Ribeiro ME, Norões J, Baliza M, Medeiros Z, Dreyer G. Evaluation of the Og4C3 ELISA in Wuchereria bancrofti infection: infected persons with undetectable or ultra-low microfilarial densities. Trop. Med. Int. Health 1, 859–864 (1996).
  • Weil GJ, Lammie PJ, Weiss N. The ICT filariasis test: a rapid-format antigen test for diagnosis of bancroftian filariasis. Parasitol. Today 13, 401–404 (1997).
  • Braga C, Dourado MI, Ximenes RA et al. Field evaluation of the whole blood immunochromatographic test for rapid bancroftian filariasis diagnosis in the northeast of Brazil. Rev. Inst. Med. Trop. Sao Paulo. 45, 125–129 (2003).
  • Chandrasena TG, Premaratna R, Abeyewickrema W, de Silva NR. Evaluation of the ICT whole-blood antigen card test to detect infection due to Wuchereria bancrofti in Sri Lanka. Trans. R. Soc. Trop. Med. Hyg. 96, 60–63 (2002).
  • Iqbal J, Sher A. Determination of the prevalence of lymphatic filariasis among migrant workers in Kuwait by detecting circulating filarial antigen. J. Med. Microbiol. 55, 401–405 (2006).
  • Rahmah N, Taniawati S, Shenoy RK et al. Specificity and sensitivity of a rapid dipstick test (Brugia Rapid) in the detection of Brugia malayi infection. Trans. R. Soc. Trop. Med. Hyg. 95, 601–604 (2001).
  • Supali T, Rahmah N, Djuardi Y, Sartono E, Rückert P, Fischer P. Detection of filaria-specific IgG4 antibodies using Brugia Rapid test in individuals from an area highly endemic for Brugia timori. Acta. Trop. 90, 255–261 (2004).
  • Intapan PM, Maleewong W, Sawanyawisuth K, Chotmongkol V. Evaluation of human IgG subclass antibodies in the serodiagnosis of angiostrongyliasis. Parasitol. Res. 89, 425–429 (2003).
  • Eamsobhana P, Yoolek A, Punthuprapasa P, Suvouttho S. A dot-blot ELISA comparable to immunoblot for the specific diagnosis of human parastrongyliasis. J. Helminthol. 78, 287–91 (2004).
  • Eamsobhana P, Yoolek A, Kreethapon N. Blinded multi-laboratory evaluation of an in-house dot-blot ELISA kit for diagnosis of human parastrongyliasis. Southeast Asian J. Trop. Med. Public Health 34, 1–6 (2003).
  • Anantaphruti MT. Immunodiagnosis of gnathostomiasis. J. Trop. Med. Parasitol. 25, 83–90 (2002).
  • Parola P, Caumes E. Gnathostomiasis. Med. Trop. 65, 9–12 (2005).
  • Parola P, Bordmann G, Brouqui P, Delmont J. Eosinophilic pleural effusion in gnathostomiasis. Emerg. Infect. Dis. 10, 1690–1691 (2004).
  • Anantaphruti MT, Nuamtanong S, Dekumyoy P. Diagnostic values of IgG4 in human gnathostomiasis. Trop. Med. Int. Health. 10, 1013–1021 (2005).
  • Audicana MT, Kennedy MW. Anisakis simplex: from obscure infectious worm to inducer of immune hypersensitivity. Clin. Microbiol. Rev. 21, 360–379 (2008).
  • del Pozo MD, Moneo I, de Corres LF, Audicana MT, Muñoz D, Fernandez E, Navarro JA, García M. laboratory determinations in Anisakis simplex allergy. J. Allergy Clin. Immunol. 97, 977–984 (1996).
  • García M, Moneo I, Audicana MT et al. The use of IgE immunoblotting as a diagnostic tool in Anisakis simplex allergy. J. Allergy Clin. Immunol. 99, 497–501 (1997).
  • Lorenzo S, Iglesias R, Leiro J, Ubeira FM, Ansotegui I, García M, Fernández de Corres L. Usefulness of currently available methods for the diagnosis of Anisakis simplex allergy. Allergy 55, 627–633 (2000).
  • Ten Hove RJ, van Esbroeck M, Vervoort T, van den Ende J, van Lieshout L, Verweij JJ. Molecular diagnostics of intestinal parasites in returning travellers. Eur. J. Clin. Microbiol. Infect. Dis. 28, 1045–1053 (2009).
  • Whitty CJ, Carroll B, Armstrong M, Dow C, Snashall D, Marshall T, Chiodini PL. Utility of history, examination and laboratory tests in screening those returning to Europe from the tropics for parasitic infection. Trop. Med. Int. Health 5, 818–823 (2000).
  • Verweij JJ, Canales M, Polman K et al. Molecular diagnosis of Strongyloides stercoralis in faecal samples using real-time PCR. Trans. R. Soc. Trop. Med. Hyg. 103, 342–346 (2009).
  • Basuni M, Muhi J, Othman N et al. A pentaplex real-time polymerase chain reaction assay for detection of four species of soil-transmitted helminths. Am. J. Trop. Med. Hyg. 84, 338–343 (2011).
  • Janwan P, Intapan PM, Thanchomnang T, Lulitanond V, Anamnart W, Maleewong W. Rapid detection of Opisthorchis viverrini and Strongyloides stercoralis in human fecal samples using a duplex real-time PCR and melting curve analysis. Parasitol. Res. 109, 1593–1601 (2011).
  • Taniuchi M, Verweij JJ, Noor Z et al. High throughput multiplex PCR and probe-based detection with Luminex beads for seven intestinal parasites. Am. J. Trop Med. Hyg. 84, 332–337 (2011).
  • Foissac M, Million M, Mary C et al. Subcutaneous infection with Dirofilaria immitis nematode in human, France. Emerg. Infect. Dis. 19, 171–172 (2013).
  • Latrofa MS, Dantas-Torres F, Annoscia G, Genchi M, Traversa D, Otranto D. A duplex real-time polymerase chain reaction assay for the detection of and differentiation between Dirofilaria immitis and Dirofilaria repens in dogs and mosquitoes. Vet. Parasitol. 30, 181–185 (2012).
  • Eamsobhana P, Wanachiwanawin D, Dechkum N, Parsartvit A, Yong HS. Molecular diagnosis of eosinophilic meningitis due to Angiostrongylus cantonensis (Nematoda: Metastrongyloidea) by polymerase chain reaction-DNA sequencing of cerebrospinal fluids of patients. Mem. Inst. Oswaldo Cruz. 108, 116–118 (2013).

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