Volume 24, Number 8—August 2018
Dispatch
Capillaria Ova and Diagnosis of Trichuris trichiura Infection in Humans by Kato-Katz Smear, Liberia
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Kerstin Fischer, Abakar Gankpala, Lincoln Gankpala, Fatorma K. Bolay, Kurt C. Curtis, Gary J. Weil, and Peter U. Fischer
Abstract
We examined human stool samples from Liberia for soil-transmitted helminth ova by Kato-Katz smear and by quantitative PCR. Twenty-five samples were positive for Trichuris trichiura by smear but negative by quantitative PCR. Reexamination of samples showed that they contained Capillariaeggs that resemble T. trichiura in Kato-Katz smears.
Kato-Katz smears are the most commonly used diagnostic tool for detecting and quantifying soil-transmitted helminth (STH) infections in field surveys (1). Although this method has some shortcomings, its advantages are field suitability and fast microscopic enumeration of worm eggs. Whereas sensitivity is low for light infections because of the small amount of stool examined (≈41 mg), the specificity of Kato-Katz for diagnosis of Ascaris lumbricoides and Trichuris trichiura infection is considered to be high (2). In contrast, hookworm eggs are difficult to differentiate by morphology, but quantitative PCR (qPCR) enables differentiation among Necator americanus, Ancylostoma duodenale, and A. ceylanicum eggs (3–5).
Among helminth eggs found in human feces, the barrel-shaped eggs of T. trichiura worms are considered to be characteristic, with a length of 50–55 µm, a width of 22–24 µm, and clearly protruding bipolar plugs (6). Similar eggs of other members of the Trichiuridae family may be differentiated from T. trichiura eggs by size and morphology when observed at high magnification, but these eggs have rarely been found in human fecal samples (7–9). Therefore, the presence of eggs of zoonotic members of the Trichiuridae family is generally not considered a confounder for detecting T. trichiura by Kato-Katz smear.
To assess the effect of mass drug administration using ivermectin and albendazole for the elimination of lymphatic filariasis on STH prevalence and intensity, we collected stool samples over a period of 3 years in 2 different areas in Foya district (Lofa County) in northwestern Liberia and in Harper district (Maryland County) in southeastern Liberia (10). We examined a single stool sample per subject by microscopy (magnification ×100) with duplicate Kato-Katz smears (41 mg template). We preserved aliquots of randomly selected specimens on FTA cards (GE Healthcare, Little Chalfont, UK) or in RNAlater (ThermoFisher, Waltham, MA, USA) and shipped them to Washington University School of Medicine (St. Louis, MO, USA) for analysis by qPCR. Two experienced microscopists (L.G., A.T. Momolu) examined the samples by Kato-Katz smear in both study areas. For detection of STH by qPCR, we extracted DNA from ≈100 mg of stool and tested it as described by Pilotte et al. (5) with a Quantstudio 6 Flex Thermocycler (Applied Biosystems, Carlsbad, CA, USA) and TaqMan Fast Advanced Mastermix (Applied Biosystems). We used the following primers and probes to detect Schistosoma mansoni DNA: forward primer 5′-TGTGGGAGTCTTTGGTTGTT-3′, reverse primer 5′-CAACATGACTGGGAACAGGA-3′, probe 5′-AGGTTCAGGTGG/ZEN/GTGTGTTACGAA-31ABkFQ-3′.
We tested 353 stool samples from Foya district by Kato-Katz smear; 31 (8.8%) were positive for A. lumbricoides eggs, 231 (65.4%) for hookworm eggs, 27 (7.6%) for T. trichiura–like eggs, and 276 (78.2%) for S. mansoni eggs. We tested 225 samples from Harper district by Kato-Katz smear; 163 (72.4%) were positive for A. lumbricoides eggs, 65 (28.9%) for hookworm eggs, and 51 (22.7%) for T. trichiura eggs (Table 1). There was good agreement between the results of the Kato-Katz and qPCR tests for the specimens from Harper (80.5%–91.6%), but generally qPCR had higher sensitivity. Our results were consistent with results previously reported with samples from other areas (3,11). Agreement between the 2 diagnostic tests for samples from Foya ranged from 77.3% to 92.9%, but the sensitivity of the qPCR was unexpectedly low, a finding that was especially true for Ascaris and Trichuris infection (Table 1). Whereas samples positive for Ascaris by Kato-Katz but negative by qPCR had low egg counts, samples positive for Trichuris by Kato-Katz but negative by qPCR had higher counts; 7 samples contained >1,000 barrel-shaped eggs/g of stool (Table 2). We repeated DNA extraction and qPCR and also used an alternative qPCR for T. trichiura (3), but these tests did not improve the agreement between microscopy and qPCR results.
Figure. Helminth eggs found in stool samples from persons in Lofa County, Liberia. A, B) Eggs of Trichuris trichiurain samples positive for T. trichiura by Kato-Katz smear and by qPCR. C–F)...
To check further whether Kato-Katz–positive, qPCR-negative stool samples contained T. trichiura eggs, we examined direct smears of stool samples preserved in RNAlater by microscopy (magnification ×100 and ×400) (Figure). The samples positive by qPCR contained eggs (6 measured)with typical T. trichiura morphology; these eggs had a mean (±SD) length of 52 µm (±2.4 µm) and width of 25.5 µm (±1.3 µm). In contrast, qPCR-negative samples contained eggs (31 measured) with a mean (±SD) length of 51.8 µm (±1.5 µm) and width of 32.7 µm (±2.1 µm). The qPCR-negative samples also had less pronounced plugs and a thick, striated shell, features that are consistent with eggs of Capillaria hepatica (syn. Calodium hepaticum) and some other Capillaria species (Trichuridae). Eggs of C. philippinensis or C. aerophila that have been observed in human stool samples previously were either smaller or larger than the Capillaria eggs found in Lofa (12,13). Because polar plugs of these eggs are less prominent than those of T. trichiura, and because their shapes are sometimes more oval or round, they can also be confused with A. lumbricoides eggs by low-power microscopy, especially if only a few eggs were detected (Figure).
Members of the subfamily Capillaridae are animal parasites with somewhat divergent life cycles, and most do not infect humans. Pseudoinfections with C. hepatica occur; eggs found in stool are present because they were consumed in infected animal liver. However, actual infections with C. hepatica do not lead to the passing of eggs in stool (9). Other species such as C. philippinensis cause true infections (and autoinfection) with eggs found in stool; the infection is linked to consumption of raw fish. Human capillariasis has not been reported from Liberia, and only isolated case reports have been published from sub-Saharan Africa (7–9). We performed DNA sequencing to better characterize the Capillaria species found in Foya. Using the primers Kt875351.1 (5′-CCCTAGTTGCGACTTTAAACGA-3′) and Capillaria 18S1R (5′- TCCACCAACTAAGAACGGCC-3′), we were able to amplify and sequence a 288-bp portion of the 18S rDNA from T. trichiura qPCR-negative samples that contained only eggs morphologically identified as Capillaria spp. (GenBank accession no. MG859285). The DNA fragment was 100% identical to orthologs of C. hepatica (accession no. MF287972.1), Aonchotheca putorii (C. putorii) (accession no. LC052356.2), and Pearsonema plica(C. plica) (accession no. MF621034.1), Capillaria worm species that have varying life cycles and host species but that are only 95% identical to the ortholog of T. trichiura.
The life cycle and the medical importance of the Capillaria species found in humans in northwestern Liberia remain to be elucidated. In our study some subjects showed high Capillaria egg loads that may indicate a true infection rather than pseudoinfection. However, transient high egg counts have been reported in persons with pseudoinfections (7). Whereas consumption of bush meat in Foya is common, consumption of raw or undercooked fish, which is necessary for transmission of C. philippinesis, is rare.
This study shows that Capillaria eggs similar to those of C. hepatica are not uncommon in stool samples collected in Liberia. These eggs can be misidentified by Kato-Katz smear as T. trichiura or as A. lumbricoides, which can confound results of STH surveys. The misidentification can also lead to an incorrect assumption that antihelminthic treatment was ineffective. Our results also illustrate the value of qPCR for validating Kato-Katz test results and for explaining unexpected findings.
Ms. Fischer is a medical technician and staff scientist at the Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA. For the last 20 years, her research has focused on medical helminthology and tropical medicine.
Acknowledgments
We thank Emanuel B. Gray and Aaron T. Momolu for their expert help during field work, as well as Laura Rinaldi and Guiseppe Cringoli for their advice concerning animal Capillaria species.
The study was funded in part by grant GH5341 from the Bill & Melinda Gates Foundation.
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