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Table 4 Diagnostic tests for important helminths that may cause persistent digestive disorders

From: Persistent digestive disorders in the tropics: causative infectious pathogens and reference diagnostic tests

Infectious pathogen

Diagnostic method

 

Microscopy

Stool culture

Immunology

Molecular biology (PCR)

Reference(s)

Cestodes

Diphyllobothrium latum

Stool microscopy: identification of eggs or proglottids

-

-

PCR and sequencing for species differentiation (for epidemiological purpose)

[77, 78]

 

· Wet preparation

    
 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Sedimentation techniques

    

Hymenolepis spp.

Stool microscopy

-

-

PCR in research settings (for epidemiological purpose)

[79]

 

· Kato-Katz method

    
 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Sedimentation techniques

    
 

· FLOTAC

    

Taenia spp.

Stool microscopy

-

· Coproantigen EIA

PCR for species differentiation

[80]

 

· Perianal egg detection

 

· Serology: detection of specific circulating antibodies against T. solium

  
 

· (Graham’s test applying adhesive tape)

    
 

· Examination of tapeworms from purges

    

Nematodes

Ascaris lumbricoides

Stool microscopy: egg detection

-

-

PCR in research settings (for epidemiological purpose)

[81–83]

 

· Kato-Katz method

    
 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Sedimentation techniques

    
 

· FLOTAC

    

Capillaria philippinensis

Stool microscopy: egg detection

-

-

-

[84, 85]

 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Sedimentation techniques

    
 

· (Kato-Katz method: great care is indicated to distinguish between T. trichiura and C. philippinensis eggs)

    

Hookworms (Ancylostoma duodenale, Necator americanus)

Stool microscopy: egg detection

Culture on Koga agar and subsequent microscopic identification of larvae

 

PCR mainly applied in research settings (for epidemiological purpose)

[81–83]

 

· Kato-Katz method

    
 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Sedimentation techniques

    
 

· FLOTAC

    

Strongyloides stercoralis

· Stool: microscopy following Baermann funnel concentration

Culture on Koga agar and subsequent microscopic identification of larvae

· ELISA tests detecting serum antibodies or faecal antigens

PCR applied in research settings (for epidemiological purpose) and increasingly used for individual patient management

[86, 87]

 

· Microscopy of sputum, bronchoalveolar lavage, duodenal aspirate, skin biopsy

 

· Indirect fluorescent antibody test

  

Trichuris trichiura

Stool microscopy: egg detection

-

-

-

[81, 82]

 

· Kato-Katz method

    
 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Sedimentation techniques

    
 

· FLOTAC

    

Trematodes

Intestinal flukes

Stool microscopy: egg detection

-

ELISA to detect worm-specific antibodies or antigens in serum or stool

PCR applied in research settings (for epidemiological purpose)

[88]

 

· Kato-Katz method

    
 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Stoll’s dilution

    
 

· Sedimentation techniques

    
 

· FLOTAC

    

Intestinal blood flukes: Schistosoma mansoni, S. intercalatum, S. japonicum, S. mekongi

Stool microscopy: egg detection

-

- ELISA to detect serum antibodies or worm-specific antigens in serum or urine

PCR applied in research settings for epidemiological purpose and increasingly used for individual patient management

[89]

 

· Kato-Katz method

 

- RDT to detect CCA or CAA antigen in serum or urine (for S. mansoni)

  
 

· Ethyl-acetate or formalin-ether-based concentration techniques

    
 

· Stoll’s dilution

    
 

· Sedimentation techniques

    
 

· FLOTAC (first experiences for S. mansoni)

    
 

Miracidium-hatching test from stool samples

    
  1. The laboratory techniques are divided into different categories and recommended tests for each pathogen are highlighted.