Multi-parallel qPCR provides increased sensitivity and diagnostic breadth for gastrointestinal parasites of humans: field-based inferences on the impact of mass deworming
Мультипараллельная qPCR обеспечивает повышенную чувствительность и более широкий диагностический охват кишечных паразитов человека: полевые выводы о влиянии массовой дегельминтизации
2016-01-25
SCID: 54.1/8b7cswnh
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Kato-Katz methoddiagnostic sensitivitymass dewormingmulti-parallel qPCRsoil-transmitted helminths
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Abstract (AI)
BACKGROUND: Although chronic morbidity in humans from soil transmitted helminth (STH) infections can be reduced by anthelmintic treatment, inconsistent diagnostic tools make it difficult to reliably measure the impact of deworming programs and often miss light helminth infections. METHODS: Cryopreserved stool samples from 796 people (aged 2-81 years) in four villages in Bungoma County, western Kenya, were assessed using multi-parallel qPCR for 8 parasites and compared to point-of-contact assessments of the same stools by the 2-stool 2-slide Kato-Katz (KK) method. All subjects were treated with albendazole and all Ascaris lumbricoides expelled post-treatment were collected. Three months later, samples from 633 of these people were re-assessed by both qPCR and KK, re-treated with albendazole and the expelled worms collected. RESULTS: Baseline prevalence by qPCR (n = 796) was 17 % for A. lumbricoides, 18 % for Necator americanus, 41 % for Giardia lamblia and 15% for Entamoeba histolytica. The prevalence was <1% for Trichuris trichiura, Ancylostoma duodenale, Strongyloides stercoralis and Cryptosporidium parvum. The sensitivity of qPCR was 98% for A. lumbricoides and N. americanus, whereas KK sensitivity was 70% and 32%, respectively. Furthermore, qPCR detected infections with T. trichiura and S. stercoralis that were missed by KK, and infections with G. lamblia and E. histolytica that cannot be detected by KK. Infection intensities measured by qPCR and by KK were correlated for A. lumbricoides (r = 0.83, p < 0.0001) and N. americanus (r = 0.55, p < 0.0001). The number of A. lumbricoides worms expelled was correlated (p < 0.0001) with both the KK (r = 0.63) and qPCR intensity measurements (r = 0.60). CONCLUSIONS: KK may be an inadequate tool for stool-based surveillance in areas where hookworm or Strongyloides are common or where intensity of helminth infection is low after repeated rounds of chemotherapy. Because deworming programs need to distinguish between populations where parasitic infection is controlled and those where further treatment is required, multi-parallel qPCR (or similar high throughput molecular diagnostics) may provide new and important diagnostic information.
Key Findings
1
At baseline, qPCR estimated prevalence at 17% for Ascaris lumbricoides, 18% for Necator americanus, 41% for Giardia lamblia, and 15% for Entamoeba histolytica.
2
For A. lumbricoides and N. americanus, qPCR sensitivity was 98%, compared with 70% and 32%, respectively, for Kato-Katz.
3
Kato-Katz may be inadequate for surveillance where hookworm or Strongyloides are prevalent or helminth intensities are low after repeated chemotherapy; qPCR intensity correlated with worm expulsion and Kato-Katz measurements.
4
Multi-parallel qPCR detected eight gastrointestinal parasites and provided broader diagnostic coverage than the two-stool, two-slide Kato-Katz method.
5
qPCR detected Trichuris trichiura and Strongyloides stercoralis infections missed by Kato-Katz, as well as Giardia and Entamoeba infections undetectable by Kato-Katz.
Research Object
Human gastrointestinal parasite infections in stool samples from residents of four villages in western Kenya, before and after mass albendazole deworming
Research Subject
Diagnostic sensitivity and breadth of multi-parallel qPCR versus Kato-Katz, and the measured impact of deworming on parasite prevalence and infection intensity
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2016-01-25
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