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. 2020 Oct 28;21(21):7981. doi: 10.3390/ijms21217981

Table 15.

Publications found in the US National Library of Medicine National Institutes of Health (NCBI-PubMed) reporting the standardisation of the LAMP technique as a useful tool for diagnosing schistosomiasis in the definitive host.

Parasite Gene Extracted/Spiked/Natural DNA Sample Sample Size Sensitivity Reference
S. mansoni
S. intercalatum
S. haematobium
S. bovis
ITS-1 Extracted DNA Adult worms - S. mansoni and S. intercalatum: 1 pg
S. haematobium: 0.1 pg
S. bovis: 10 pg
[149]
S. mansoni Mitochondrial minisatellite DNA region Extracted/natural DNA Cutaneous and hepatic biopsies and appendix biopsy 3 ND [150]
S. mansoni Sm1-7 repeat fragment Natural DNA Human urine and stool 111 ND [151]
S. mansoni Mitochondrial minisatellite DNA region Spiked/natural DNA Human urine 28 0.01 fg [152]
S. haematobium IGS Natural DNA Human urine 172 ND [153]
S. mansoni Sm1- 7 repeat fragment Extracted/natural DNA Human faeces 383 32 fg [154]
S. mansoni Mitochondrial minisatellite DNA region Natural DNA Human faeces 427 ND [155]
S. haematobium is IGS Spiked/natural DNA Egyptian strain, NR-31682/human urine samples 94 1 fg [156]
S. japonicum Retrotransposon SjR2 Natural DNA Human serum 110 ND [157]
S. mansoni Mitochondrial minisatellite DNA Experimentally infected DNA Mice faeces - 1 fg [158]
S. japonicum Highly repetitive retrotransposon (SjR2) Natural DNA Rabbit faeces 6 0.08 fg [159]