Rapid detection of Giardia intestinalis and ... · Rapid detection of Giardia intestinalis and...
Transcript of Rapid detection of Giardia intestinalis and ... · Rapid detection of Giardia intestinalis and...
Rapid detection of Giardia intestinalis and Cryptosporidium spp. in stool samples using an antigen-
based detection approach : evaluation of a new commercial immunochromatographic strip test
Introduction & purpose
Materials & methods
Results
Acknowledgements We are grateful to CORIS BioConcept for providing the
reagents used in this study.
Microscopy is the gold standard for routine
laboratory diagnosis in faecal parasitology but
there is a growing interest for alternative methods
to overcome the limitations of microscopic
examination, which is time-consuming and
dependent on the operator’s skills and expertise
[1,2].
In this context, antigen-based detection using
rapid detection tests (RDTs) could represent
attractive alternatives.
Purpose
To evaluate a new immunochromatographic strip
test (Crypto-Giardia K-SeT®, Coris BioConcept,
Belgium) for the simultaneous detection of both
Giardia intestinalis and Cryptosporidium spp.
antigens from stool specimens.
ØEvaluation performed using a reference panel of
184 cryopreserved human stool samples [2]:
q 134 positive samples (Table 1)
q 50 negative samples
q Each sample previously determined by a
standardized protocol (microscopy+/-PCR) [2]
ØEach sample was tested blindly to the results
of microscopy
ØVisual reading performed after 15 min (Figure 1).
ØDiscrepancies with microscopy were investigated
by specific PCR assays
ØDetermination of sensitivity and specificity
Ø Correct agreement with microscopy (Table 2).
Ø Four false-negative samples.
Ø One false-positive (PCR/microscopy negative).
This RDT facilitates the detection of G. intestinalis
and Cryptosporidium spp. from stool samples, being
easy to use and time-saving compared to
microscopy (45 min for processing 15 samples).
A prospective evaluation of its performances in routine
diagnosis is currently undergoing.
Table 1: Diversity of the gastrointestinal
parasites included in the reference panel
(n= 134)
Genus/Species N=
Giardia intestinalis 37
Cryptosporidium spp. 30
C. parvum/C. hominis 28
C. felis 1
C. meleagridis 1
Other gastrointestinal parasites
Entamoeba coli 35
Endolimax nana 20
E. histolytica/E. dispar 16
Entamoeba hartmanni 4
Blastocystis sp. 15
Schistosoma mansoni 4
Iodamoeba bütschlii 3
Cystoisospora belli 2
Hookworms 2
Hymenolepis nana 1
Trichuris trichiura 1
Taenia sp. 1
Dientamoeba fragilis 1
Sarcocystis hominis 1
Chilomastix mesnili 1
Pentatrichomonas intestinalis 1
Enterocytozoon bieneusi 1
Table 2: Antigen detection findings for Giardia intestinalis
Conclusions
Gardia intestinalis Cryptosporidium spp.
Microscopy
+ -
Crypto-Giardia K-SeT® + 33 1
- 4 146
Se= 89.2%, Sp= 99.3% Microscopy
+ -
Crypto-Giardia K-SeT® + 26 0
- 4 154
Se = 86.7%, Sp = 100%
Ø Correct agreement with microscopy (Table 3).
Ø Four false-negative samples.
Ø Both C. meleagridis and C. felis detected (n=2).
Each sample was tested blindly. This test
appeared time-saving due to a reduced
turnaround time.
No cross-reactivity with other gastro-
intestinal parasites included in the reference
panel was observed.
Individual results for G. intestinalis and
Cryptosporidium spp. are presented below.
Table 3: Antigen detection findings for Cryptosporidium spp.
Figure 1: The Crypto-Giardia K-SeT diagnostic test (here positive for G. intestinalis)
C: Control-band, Cr: Crypto-specific band; Gi: Giardia-specific band
1Laboratoire de Parasitologie-Mycologie, CHU de Nantes ; 2Laboratoire de Parasitologie-Mycologie, CHU de Dijon ; 3Service de Parasitologie-Mycologie-Médecine Tropicale, CHU de Tours; 4Laboratoire de Parasitologie-Mycologie, AP-HP, Hôpital Bichat, Paris ; 5Laboratoire de
Parasitologie-Mycologie, CHU de Clermont-Ferrand ; 6Laboratoire de Parasitologie-Mycologie, CHU de Nice ; 7Laboratoire de Parasitologie-Mycologie, CHU de Nancy ; 8Laboratoire de Parasitologie-Mycologie, CHU d’Angers ; 9Laboratoire de Parasitologie-Mycologie, AP-HP Hôpital Henri
Mondor, Créteil ; 10Laboratoire de Parasitologie-Mycologie, CHU de Montpellier ; 11Laboratoire de Parasitologie-Mycologie, CHU de Poitiers ; 12Laboratoire de Microbiologie, CH de la Roche-sur-Yon.
For more information, please contact:
GOUDAL A.1, LAUDE A., VALOT S.2, DESOUBEAUX G.3, ARGY N.4, NOURRISSON C.5, POMARES C.6, MACHOUART M.7, LE GOVIC Y.8,
DALLE F.2, BOTTEREL F.9, BOURGEOIS N.10, CATEAU E.11, LETERRIER M.12, LAVERGNE RA.1, LE PAPE P. 1, MORIO F1.
References:
[1] Becker et al., Clin Microbiol Infect. 2015 Jun;21(6):591.e1-10.
[2] Laude et al., Clin Microbiol Infect. 2016 Feb;22(2):190.e1-8.