Diagnostic Techniques for Soil-Transmitted Helminths – Recent Advances

Introduction

More than 1.5 billion people, comprising nearly a quarter of the global population, are infected with soil-transmitted helminths (STH).¹ The STH infections are widely distributed in tropical and subtropical areas of the world, with the highest prevalence reported from Sub-Saharan Africa, China, South America and Asia. More than 267 million children of preschool-age and 568 million school-age children reside in these areas and need therapeutic and preventive interventions.¹ These infections are most commonly reported in people residing in or travelling to regions with poor access to clean drinking water, sanitation and hygiene, usually in low or middle-income countries; or in vulnerable populations in high-income countries.² The World Health Organization (WHO) has recognized infections caused by four species of STHs, viz. Ascaris lumbricoides, hookworms (i.e., Necator americanus and Ancylostoma duodenale) and Trichuris trichiura among neglected tropical diseases (NTDs).¹ More recently, some areas in South East Asia have been reporting zoonotic hookworm Ancylostoma ceylanicum in addition to human hookworms.² Although Strongyloides stercoralis is not yet considered in this list of NTD by the WHO, it is also an important STH given the significant disease morbidity caused by it and its geographic overlap with the other STHs. More than 600 million people are estimated to be infected by S. stercoralis globally.¹

STH infections are usually clinically asymptomatic, though non-specific gastrointestinal symptoms and/or eosinophilia may be seen. Since STH seldom cause mortality, their impact on health is measured using disability-adjusted life years (DALYs). The STH infections account for a high global burden with substantial morbidity.^3,4 Recent data have shown that STH caused 2090 deaths in 2019 with 1.97 million (1.26–3.00) DALYs, in which hookworm disease was the predominant cause.⁵ In fact, the morbidity is directly proportional to the intensity of infection and debilitating outcomes such as anemia, intestinal obstruction, retarded physical or cognitive development are seen in heavily infected individuals, especially children.^6–8 Iron deficiency anemia caused by hookworm infection during pregnancy has been linked to adverse maternal-fetal outcomes, including premature and low birth weight babies, impaired lactation, etc.⁹

At the turn of the new millennium, preventive chemotherapy (PC) in school-age children was endorsed by the WHO for STH control and stipulated further in the 2012 London Declaration on NTDs, with the ultimate aim to break STH transmission.^10–12 The WHO recommends an integrated approach, which includes access to clean water, promote sanitation, hygiene and health education, along with mass drug administration to children, and with sustained efforts, STH elimination is expected to be achieved by 2030.¹¹ It should be noted that each STH species has distinct epidemiological features and age-dependent patterns of infection prevalence (maximum prevalence of A. lumbricoides and T. trichiura is usually seen in young children, whereas the peak prevalence of hookworms is observed in adolescence or early adulthood), reinfection rates (short-lived helminths reinfect more rapidly),¹² and varying sensitivity to albendazole,¹³ which could influence the efficacy of PC strategies.¹³ Moreover, adults are not targeted for PC and remain important reservoirs for reinfection of treated children. Although PC is implemented without the need to assess individual infection status, accurate prevalence estimates using high sensitivity diagnostics are important to ascertain the intensity of infection in different regions. Diagnostics also inform on the performance of control measures in terms of reduction in the prevalence and/or intensity of infections, which can guide the frequency of preventive chemotherapy.

Epidemiological evidence reveals an increased prevalence of STH infections associated with direct exposure to wastewater, sludge amended soil and/or eating vegetables irrigated with them.¹⁴ Thus, apart from the detection of clinical infections, the detection of STH in such samples is also important. In this review, we elaborate on the various tools for diagnosis of STH in clinical specimens, sewage and wastewater.

Conventionally, the STH diagnosis is carried out by the examination of stool or other gastrointestinal samples for STH eggs, larvae or adult worms by microscopy. However, choice of the diagnostic technique also depends upon whether it is being employed in a high or low endemic setting since highly sensitive techniques would be required for surveillance in low endemic areas, travelers from these regions or during the elimination phase.

Microscopy Based Methods

The detection of STH by microscopy, despite being simple and low cost, lacks reasonable sensitivity due to many factors which include intermittent excretion of parasite ova, low infection intensity below the limit of detection, improper transportation or storage of sample leading to parasite disintegration etc. The parasite morphology may become distorted due to storage or drug treatment. Thus, at least three fresh fecal specimens should be examined over 10 days and some parasite concentration techniques should be employed.^15–17 Various microscopy-based diagnostic tests for STH diagnosis are summarized in Figure 1.

Figure 1 Summary of the advantages (orange) and disadvantages (purple) of microscopy-based diagnostic tests for soil-transmitted helminths.

Wet Mount Preparation

A smooth, thin preparation of stool with saline and iodine is examined for larvae or eggs of helminths. The characteristics of various STH eggs or larvae are summarized in Figure 2.

Figure 2 Summary of direct microscopy findings in different STH.Notes: Images adapted from https://www.cdc.gov/dpdx/diagnosticprocedures/stool/morphcomp.html. Source: Centres for disease control and prevention [CDC], DPDx.

Kato–Katz Thick Smear¹⁶

Currently, the Kato–Katz (KK) method is a WHO-recommended “Gold standard” method for detection of STH eggs, and additionally for Schistosoma eggs especially when quantitation of eggs is desired. Several modifications of Kato–Katz are in use. Briefly, large particles are removed by pressing the feces through a mesh screen followed by transfer of a known amount of the sample on a slide through a template with a hole which holds a fixed amount of fecal material (e.g., a hole of 9 mm on a 1 mm thick template holds about 50 mg of feces). The template is removed and cellophane soaked in glycerol-methylene blue solution is used to cover the remaining sample. The slides should be kept at room temperature or in an incubator at 40°C (except for hookworms) to clear the fecal debris. Microscopic examination can best be performed after 24–48 hours. The helminthic eggs per gram of stool (EPG) is calculated as: No. of eggs in smear × 20 (for 50 mg template) to measure the infection intensity.¹⁷ T. trichiura, A. lumbricoides and Schistosoma eggs are easily detected and remain recognizable for months by the Kato–Katz method but it has a poor performance for the detection of hookworm infection since these eggs tend to disintegrate early (within 60 min) resulting in false-negative results.¹⁸ Moreover, S. stercoralis larvae also remain undetected. Although Kato–Katz is cost-effective and easy to perform, samples with low infection intensity and variable clearing/disintegration times may impede the concurrent detection of different STHs.¹⁶ A summary of representative studies evaluating the performance of Kato–Katz with other microscopy based methods is provided in Table 1.^18–29

Table 1 Summary of Representative Studies Evaluating the Performance of Kato–Katz Thick Smear Examination

Stool Parasite Concentration Methods

Microscopic detection of parasites can be improved by employing various techniques that concentrate the parasite in the sample and removes the fecal debris. These techniques are based on either the principle of flotation or centrifugal sedimentation.

Centrifugation Based Technologies

Formol ether or ethyl acetate concentration (FEC) method can be used for both fresh and preserved samples and allows recovery of parasites by centrifugation into a fecal pellet. Briefly, a small quantity of stool sample is allowed to pass through two layers of gauze into a conical tube containing 0.85% saline or 10% formalin and then mixed. Ethyl acetate is added to the fecal suspension for extraction of fat and debris and the tube is centrifuged (500 g for a minimum of 10 min) leaving the parasites in the sediment. The supernatant is decanted and the sediment is resuspended with saline or 10% formalin and examined as a wet preparation using 10x and 40x objectives, with or without iodine. Diluted formalin or sodium acetate-acetic acid-formalin (SAF) is used to inactivate the organisms and minimizes the risk of laboratory-acquired infection from feces. FEC stool samples can be examined in several hours or days after the sample is preserved in formalin. However, this method has deficiencies due to the use of ether which is explosive, irritates the respiratory tract and may be harmful to laboratory personnel in addition to being time-consuming.¹⁶ Nikolay et al. (2014) have performed a meta-analysis of sensitivity of various diagnostic techniques for STH in the absence of a true gold standard.³⁰ A few studies that have compared various microscopic techniques to Kato–Katz are presented in Table 1.

Recently, a closed, single-use Parasep^® SF fecal parasite concentrator method has been developed by DiaSys Europe. This removes the sample debris and fat by a two-stage filtration matrix. This does not use any potentially harmful chemical agents and besides is user friendly, time-saving and cost-effective for diagnosis of helminth infections in large-scale epidemiological surveys.³¹ A modification of this method, the Mini Parasep^® SF fecal parasite concentrator has been developed. Although this modification has been evaluated extensively for protozoal infections, its performance for STH diagnosis is reported in only a handful of studies.^29–32 A clearer background with less fecal debris and a better yield of T. trichiura has been noted with Mini Parasep^®.^29,31–34 Additionally, the mean time for processing is much faster with Parasep^® than the conventional formol-ether-acetate concentration (4–5 min vs 10–15 min/sample), which is a significant time-saver. However, conventional FEC costs less than Parasep® (0.30 vs 0.9 USD /sample).³³ Higher sensitivity of Mini Parasep^® SF has been reported for A. lumbricoides, Kato–Katz for T. trichiura and McMaster for hookworm eggs.³⁴

Flotation-Based Technologies

Most parasite eggs have a specific gravity of 1.05–1.20 which allows them to float when the stool sample is mixed in a high specific gravity solution (range 1.18–1.27). The commonly used flotation solutions are zinc sulphate or brine solution. Successor technologies of the Cornell Wisconsin centrifugal flotation method, namely McMaster method and FLOTAC/Mini-FLOTAC, have shown promise.^17,28,35,36

McMaster Technique

This technique uses a counting chamber which enables a known volume of fecal suspension (2 × 0.15 mL) to be examined microscopically. The McMaster chamber has two compartments, each with a grid etched onto the upper surface. When filled with a suspension of feces in flotation fluid, much of the debris sinks while the eggs float to the surface under the grid, where they can easily be seen and counted relatively quickly. With a known weight of feces and volume of flotation fluid used to prepare the suspension, the EPG count can easily be derived by multiplying the number of eggs under the marked areas by a simple conversion factor.²¹ The McMaster method is inexpensive, easy and has been extensively used in veterinary parasitology and even in human studies for estimation of anthelmintic cure rates.³⁵ The overall diagnostic performances of the McMaster method and Kato–Katz is comparable for STHs according to a recent meta-analysis.³⁰ In a study by Periago et al., the Kato–Katz outperformed the McMaster method for all three STHs, especially for unfertilized A. lumbricoides egg detection.²¹ The reason for the poor performance of the flotation methods for detection of the unfertilized Ascaris eggs is because of their high specific gravity (SG = 1.18) and absence of lipoidal membrane that prevents the equilibration of the egg with the external flotation media causing the egg to sink instead of float in the saline.^21,22,36 This deficiency and the need for a special counting chamber are disadvantages of this technique.

FLOTAC

Centrifugal flotation is the basis of the FLOTAC technology and it consists of a cylindrical device with two flotation chambers of 5 mL capacity allowing analysis of more fecal material compared with Kato–Katz (100 mg vs 42 mg).^37–39 It has a high sensitivity with the additional advantage of being a closed system that protects the operators, preserves the sample and even allows repeated subsequent sample examinations. However, the methodological complexity and the need for a specific device for sample centrifugation may limit its applicability in laboratories with resource constraints. Mini-FLOTAC is a simplified version of this device without the centrifugation step.^{20,22,37–39} A recent meta-analysis revealed a sensitivity of approx. 92.7% for FLOTAC vs 42.8% for direct microscopy.³⁰ The Kato–Katz method had a sensitivity of 74–95% for detection of all STH in high infection intensity, which drops to 53–80% in settings of low infection intensity, with the poorest performance for A. lumbricoides and hookworms. The FLOTAC method has the highest sensitivity in settings of both low and high infection intensity; however, the average egg counts are significantly lower compared with the Kato–Katz method.^25,26,30 Therefore, validation of this method in varying epidemiological settings with different intensity of infections is needed before recommendation for large-scale community use.

Digitized Microscopy

To ensure the objective evaluation of current technologies and prioritization of products for use in STH control programs, a detailed framework has been formulated to link the program decision points with analogous target product profiles (TPPs).⁴⁰ Three opportunities for improvement in STH diagnosis were suggested: “First, integration of quality control/assurance for sample processing and egg counting; second, increasing the sample throughput, and; thirdly, internet connectivity to make test results accessible for remote interpretation.”⁴⁰ These technical requirements are met by FECPAK^G2, a tool developed for helminth eggs counting in fecal samples from sheep, cattle, horses, camels etc.⁴⁰ In FECPAK, stool sample dissolved in flotation solution is filled in a tube with a central pillar and the eggs are allowed to concentrate into one microscopic field of view. Then an attachment takes images of the eggs that have accumulated into a single viewing area and this digital image is saved and uploaded online.⁴¹ In a study by Moser et al. a sensitivity of 75.6%, 71.5% and 65.8% for A. lumbricoides, hookworm and T. trichiura detection, respectively, was observed for FECPAK^G2 which was much lower than the Kato–Katz method.⁴² However, with rigorous development, this could be an interesting epidemiological and diagnostic tool.

Lab-On-A-Disk Technology

Another technique with compliance to the TTPs is the lab-on-a-disk (LOD) technology. This is a microfluidic platform based on both the centrifugation and flotation of eggs for concentration within an imaging zone, followed by image capture.⁴³ This technique holds potential for point-of-care application, however, adequate training and education of the users and quality management aspects in terms of device calibration and maintenance must be ensured. A field evaluation of the LOD technology in human samples from Ethiopia revealed successful capture of STH eggs in the image viewing zone of the LOD device even in low infection intensity settings.⁴³ An almost perfect agreement with Mini-FLOTAC (Kappa score: 0.91) was seen; in fact, more eggs were counted in the LOD technique.

Culture-Based Methods

The use of parasite culture in STH infections is seldom the mainstay for diagnosis and is primarily applied in research settings, except for the recovery of S. stercoralis.^44–46 However, great care must be taken since larvae are infective and can be a biohazard for lab personnel. A summary of various larval detection methods used are shown in Table 2.

Table 2 Characteristics of Larval Detection Methods for the Diagnosis of Strongyloidiasis or Hookworm Infection

Serology Based Methods

Antibody Detection

Antibody detection in serum is not particularly useful for STH diagnosis except for S. stercoralis. Although indirect immunofluorescence microscopy (IFAT) and gelatin particle agglutination (GPAT) test have high sensitivity (81–98%) and specificity (74%), the requirement for a large amount of living, infective larvae limit their use.^44,47 Immunoblot analysis using antigens of S. stercoralis and S. ratti was used in a study in 2003 to overcome this drawback and had shown sensitivity ranging from 65–100%.⁴⁸ However, there are no further reports on evaluation of these tests and therefore their validity is questionable.

The crude extracts of filariform larvae, from S. stercoralis/S. venezuelensis or S. ratti have been used in several in-house Enzyme-linked Immunosorbent Assays (ELISAs) and commercial kits with sensitivity ranging from 73–100%⁴⁴ however, cross-reactivity with other nematodes, especially filarial worms, and poor performance in immunosuppressed individuals are observed.⁴⁹ The false-positive results in infections due to Echinococcus and Toxocara are less commonly seen with ELISA compared with IFAT. It is worth mentioning that the ELISA-based studies have been performed in case-control study designs using serum samples from patients with known strongyloidiasis compared with healthy controls and not with individuals harbouring other nematode infections, causing falsely high estimates of performance. Another concern is the overestimation of disease burden by serology versus underestimation by parasitological techniques since stool examination by itself is an imperfect gold standard. Although increased specificity of 13.3% on substitution of IgG with IgG4 in Strongyloides ELISA is seen, very few studies have focused on detection of other antibody isotypes.⁵⁰

The luciferase immunoprecipitation system (LIPS) has been developed using a recombinant Strongyloides antigen (NIE).^51,52 This is a rapid test (< 3 hours) and has a good sensitivity (97%) and specificity (100%) with no cross-reaction.⁵² Additionally, it uses recombinant antigen, enabling mass production and purification compared with the time-consuming preparation of crude antigen which depends on the collection of stool from infected humans/animals. Detection of IgG and IgG4 specific antibodies by using the luciferase-tagged recombinant Ss-NIE-1 protein of S. stercoralis by LIPS has shown a sensitivity and specificity of 93% and 95%, respectively.⁵³ Recently, a dipstick lateral flow assay using recombinant NIE (rNIE) and recombinant Ss1a (rSs1a) proteins was developed. It demonstrated a sensitivity of 91.3% and 100% specificity for serodiagnosis of strongyloidiasis and merits further evaluation.⁵⁴

Coproantigen Detection

Coproantigen detection could have the potential to be used in point-of-care immunoassay-based tests such as that for malaria. The detection of coproantigen of S. stercoralis by ELISA was reported to have good sensitivity and specificity but no further results of its evaluation are available.⁵⁵ Recently BA-1, an excretory-secretory product of A. lumbricoides, has been investigated as a coproantigen marker of infection by ELISA.⁵⁶ The Ascaris BA-1 ELISA had a lower limit of quantification of 2.74 ng/g stool and its evaluation in a panel of stool samples from school-aged children residing in Kenya revealed a sensitivity and specificity of 91.5% and 95.3%, respectively. Apart from the qualitative assessment of infection, quantitative reflection into the intensity of infection was also seen and a value of 18.2 ng/g stool of the ABA-1 was found to be the cut-off between low and moderate intensities of infection. It was also seen that the levels of ABA-1 strongly decreased after treatment. A commercial kit for the detection of Ascaris, hookworms and Trichuris antigens has been patented and marketed by IDEXX laboratories for veterinary use.⁵⁷

Recently, urinary biomarkers of A. lumbricoides infection, such as 2-methyl butyramide, 2-methyl pentanoyl carnitine (2-MPC) and 2-methyl-valeramide metabolites have also been evaluated.^58,59 Of these, 2-MPC has been found to have an accuracy of 85.7% for detection of infection with better performance (90.5% accuracy) for moderate to heavy infection.⁵⁸ A substantial reduction after albendazole treatment was also seen with a significant association between urine 2-MPC levels and worm/egg counts.⁵⁸ However, the same authors did not find this biomarker in infected Indonesian subjects.⁵⁹

Molecular Methods

Over the past decade, efforts to develop and evaluate molecular diagnostics for STH have gained momentum for epidemiologic studies to guide interventional strategies and diagnostics in travelers returning from endemic areas.⁶⁰ However, there is still a dearth of molecular platforms for the detection of STH. Part of the difficulty in estimation of the performance of molecular tests is the lack of an optimum gold standard, as generally the stool-based microscopic examination methods are used as reference standard albeit having a low sensitivity. There are still no clear cut relevant criteria to validate laboratory developed PCRs. The diagnostic reliability of molecular methods also depends on the efficiency of DNA extraction and sample preservation before sample testing. There are a lot of inhibitors in the stool samples that affect the sensitivity of PCR. Moreover, preservation of samples in formalin also inhibits the PCR. It should be noted that helminthic eggs, especially those of T. trichiura, are more difficult to break thus affecting the DNA extraction efficiency and PCR.^60,61 Ayana et al. (2019) compared four DNA extraction and preservation methods for the molecular detection and quantification of soil-transmitted helminths in fecal samples and found significant differences in DNA recovery⁶⁰. However, if the samples had been kept in the preservatives, there was no loss of sensitivity attributed to delay in DNA extraction which makes it suitable for collection of samples in preservatives from remote areas and their subsequent analysis at a distant laboratory.⁶⁰

Great strides in the sequencing of nematode genomes with the availability of nematode sequence data have facilitated the discovery and development of assays based on more sensitive and species-specific genomic targets.^61,62 Ribosomal sequences and mitochondrial targets such as cytochrome oxidase are found in most eukaryotic cells making them attractive target choices.⁶² In STH, a large portion of the genome is comprised of repetitive non-coding DNA elements, which are useful PCR targets for STH.⁶³ It should be noted that some types of repetitive DNA, such as simple short nucleotide repeats or sequence variation within the repeat, impact the suitability of repeat-based molecular assays.^63,64 The repeats can be variable-type (i.e., copy number is not consistent within species) or constant-type (copy number is consistent within species) and understanding this variation on a species-by-species basis and its impact on the sensitivity of any molecular assay is needed.⁶⁴ New target development for repeat-based qPCR assays is easier using new bioinformatic tools such as RepeatExplorer, TAREAN etc. which can help in amplifying as little as 20 ag (attogram) of genomic DNA.⁶³

The gene targets used in PCR to detect STH are shown in Table 3.

Table 3 Gene Targets Used for the Molecular Diagnosis of Soil Transmitted Helminths

The main advantage of PCR-based assays lies in their higher sensitivity and the ability to multiplex for detecting concurrent infections, although singleplex PCR is slightly more sensitive compared with multiplexed assays.^65,66 Use of quantitative PCR (qPCR) provides even more accurate prevalence estimates compared with microscopy and is amenable to multiplexing.^69,70 Moreover, since the frequency of mass drug treatment of a population is determined by the prevalence of disease in the community, which in turn is greatly dependent on the sensitivity of the diagnostic test used, quantitative PCR has a greater role to play for accurate estimates and also after completion of MDA, when it is critical to define a threshold under which recrudescence of disease can occur.⁶⁹ However, qPCR can be technically demanding, complex and expensive and there is lack of standardization across different laboratories. Further, it is not very straightforward to correlate copies of molecular target to egg numbers in feces and worm numbers in gut, as number of copies of that target and difference of ploidy among unfertilized and fertilized eggs varies.⁶⁹ These hurdles are increasingly being removed and there are efforts to commercialize these tests.

In a recent study to evaluate the diagnostic performance of Kato–Katz, Mini-FLOTAC, FECPAK G2 and qPCR, all diagnostic techniques showed a sensitivity of ≥90% for all of the moderate-to-heavy intensity STH infections. However, only qPCR had a sensitivity that was superior to a single Kato–Katz for all STHs or infections of very low intensity. For qPCR, there was a positive significant correlation between the egg counts of a single Kato–Katz and the DNA concentration. qPCR is the only method that could be considered in the phase that aims to seek confirmation for cessation of program.³⁵ In addition, pooling of samples has been tested as a strategy to reduce cost and time and found to be cost-effective, time and labour saving without loss of sensitivity or accuracy.⁷¹

A newer molecular tool, Loop-mediated amplification assay (LAMP) is a single-step method amplifying target DNA sequences isothermally.^72–76 It only requires a heat block or incubator/water bath and is more tolerant of biological inhibition. For improving sensitivity, fluorescent probes, DNA-functionalized gold nanoparticles etc. can be used. However, due to difficulties in primer design, false positives and carry over-cross contamination, further validation of LAMP assays is needed. Recently, a colorimetric isothermal assay using SmartAmp2 primer was developed to identify STH by targeting the amplification of a specific sequence of the β-tubulin gene visualized by hydroxy naphthol blue (HNB) dye in LAMP format.⁷³ The unique asymmetrical primer design makes this a very specific assay with easy visual result inspection, empowering its development as a portable tool for field surveys.

Other Aids in Clinical Diagnosis

Low hemoglobin, low ferritin and eosinophilia (>600 μL or >6% of the thin-layer chromatography) can be used as indirect indicators of STH infection.¹⁶ Occult blood in stool has been used as a surrogate marker of chronic hookworm infection.⁷⁷ In ascariasis, Charcot-Leyden crystals and eosinophils may be found in the sputum. In the case of S. stercoralis, duodenal material may be examined for the presence of larvae using the string test (or entero-test capsule).⁴⁴ The use of other investigations such as diagnostic radiology, histopathology, and intra-dermal skin tests have also been reported but are seldom used routinely.¹⁶

Choosing the Right Diagnostic Technique

Despite considerable progress to control STH over several decades, we are still far from identifying a fully adequate diagnostic test. In general, the consensus is still to strive towards the development of novel sensitive technologies or further optimize the current methods. To choose from the present armamentarium of diagnostic assays, a few aspects which merit consideration are the diagnostic performance, cost-effectiveness, ease of performance, rapidity and in-field applicability. Apart from the performance of the technique per se, adequate training and stringent quality-control/quality-assurance measures greatly improve the performance of any diagnostic assay. Importantly, different phases of STH control programs would require different techniques; microscopy would suffice to map prevalence in a geographic area but more sensitive molecular tests will be required for post MDA surveillance and to measure success of control programs.

Detection of STH in Environmental Samples

The detection of STH eggs and quantification in other sample types such as wastewater, sludge, plants, etc., is also important for control of these infections. Unfortunately, due to differences in the moisture content and amount of solids or soil particles etc. in the environmental samples, there is significant heterogeneity in the detection of STHs from these samples.⁷⁸ The conventional microscopic techniques are largely insensitive, time-consuming and labor intensive for environmental samples. Thus, various modifications of traditional methods and newer molecular technologies are now being increasingly applied. Due to dilution in the environment, helminth egg concentrations in wastewater are normally very low, necessitating the use of large volumes (1–10 L) for detection. The major hurdle for the molecular detection of STH eggs is the extraction of the nucleic acid of good quantity and quality due to the hardy eggshells, and high amounts of suspended solids or PCR inhibitors in most of the samples. A high concentration of STH may be seen in sludge, biosolids and compost since eggs attach to particulate material, and thus usually around 2–5 g dry weight of sludge is sampled. An adequate amount of soil sample varies from 10–50 g of dry soil, mostly from the top 0–5 cm layer. Higher egg recovery and less variation in egg count are observed in sand than from clay and silt.⁸⁰ For vegetable samples, the preferred weight is 100–250 g (lower for grass). It should be noted, however, that even with the same volumes of sample, the concentration of helminth eggs differs regionally depending on the local prevalence of infection and solid content in the sample.⁷⁸ Also, it is important to determine the number of viable STH eggs for risk estimation per international guidelines.^78–81 A schematic diagram depicting the steps involved in the detection of STH from environmental samples is shown in Figure 3.

Figure 3 A schematic diagram depicting the steps involved in the detection of STH from environmental samples. *phase extraction may be performed after flotation step.

Briefly, the samples need to be homogenized first to break down coarse material into finer particles, followed by separation of eggs from particles using different solutions (mainly anionic detergents). Then the samples are filtered, thereby allowing eggs to pass through for further analysis. The samples are concentrated by sedimentation or flotation. Phase extraction to remove lipid/ether soluble material from samples may be performed after flotation using ethyl acetate and diethyl ether (for lipophilic extraction) and sulphuric acid and acetoacetic acid buffer (for hydrophilic extraction). The exposure time should be minimal to reduce the adverse impact of chemicals on egg morphology and recovery.

After this, the viable STH eggs per sample are assessed. The viability assessment can be done by incubation for larval development, which is time-consuming and is subject to observer expertise. Viable and non-viable eggs can also be differentiated by using vital stains. Another emerging and rapid method is based on differential integrity of viable and non-viable cell membranes by using the BacLight LIVE/DEAD Viability Kit that was initially developed for the enumeration of viable bacteria.⁸²

Recently, image analysis software or systems have been developed to identify and quantify helminth eggs in wastewater using various image processing tools and pattern recognition algorithms.⁸² These have a reported sensitivity of 80–90% and a specificity of 99% depending on the total suspended solids content of the wastewater samples and the time taken to examine each sample is less than a minute. It should be remembered that even when such software is used, the eventual identification still depends on proper sample processing. Improving the optics with provision for better quality images could potentially make use of smartphones by enabling the consultation of remotely located experts to interpret the tests, especially for surveys in remote and low-income areas.

Molecular methods such as real-time PCR (qPCR), digital/ droplet PCR (ddPCR) etc. also allow the accurate detection of STH eggs in environmental samples.⁷⁶ The application of ddPCR in poultry water samples revealed a better performance compared with qPCR and culture-based methods for the detection of zoonotic pathogens.^82,83 However, further research on the optimization of chip-based PCR or ddPCR in environmental samples is warranted. Another approach is flow cytometry, which is based on the differentiation of eggs based on sizes.⁷⁸ In fact, fluorescent staining may even enable us to determine the stage of egg development or viability. However, the cost of equipment and the need for trained staff may cause hindrance in the application of this technique.

Conclusion

STH infections have a substantial socio-economic impact and entail huge physical and developmental consequences for infected populations. The microscopic examination of stool is an acceptable measure for the assessment of infection levels in high-intensity endemic areas. The sensitivity of microscopy-based techniques can be improved greatly by properly training the involved laboratory staff. However, the major challenge of conventional techniques is that they are time-consuming and involve cumbersome procedures in sample analysis. Less cumbersome and more sensitive FLOTAC techniques may be useful in such areas. However, in areas of low endemicity, or during the elimination phase, the relevance of microscopy-based methods is limited and more sensitive molecular techniques such as PCR may be needed. qPCR with its ability to provide estimation of intensity of infection has been demonstrated to be of potential, especially when cessation of intervention by mass drug administration is considered or for surveillance of STH in low endemic areas or travelers returning from endemic regions. Moreover, the molecular techniques are important to detect new/emerging species. However, more rigorous studies are required to accurately relate qPCR data to worm burden.

Future Perspective

The development of new diagnostic methods with broad-spectrum applicability in different sample matrices is imperative for STH detection. Although the development of molecular tools has numerous advantages in the context of sensitivity, ease of performance, reproducibility and automation, they still have many shortfalls; the most important being high cost which limits applicability in regions where sophisticated equipment and adequate user training is not possible. However, pooling of samples and cost-effective modifications of existing molecular methods are being attempted to circumvent problems associated with PCR.

There may be a potential for antibody/ antigen detection but these need to be evaluated in the field. Development of new techniques, digitization/automation of procedures, implementation of clear protocols, identification of novel biomarkers and multiplexing hold promise for STH diagnosis. Additionally, rigorous multi-centric validation of new diagnostic assays, particularly in low endemic settings, is imperative.