Figures
Abstract
Background
Schistosomiasis has decreased significantly in prevalence and intensity of infection in China, thus more accurate and sensitive methods are desperately needed for the further control of schistosomiasis. The present work aimed to assess the utility of the loop-mediated isothermal amplification (LAMP) for detection of light intensity infection or false-negative patients and patients post-treatment, targeting the highly repetitive retrotransposon SjR2 of Schistosoma japonicum.
Methodology/ Principal Findings
LAMP was first assessed in rabbits with low intensity infection (EPG<10). Then 110 patient sera from Hunan Province, China, and 47 sera after treatment by praziquantel were used to evaluate the diagnostic validity of LAMP. Meanwhile, 42 sera from healthy individuals in a non-endemic area, and 60 sera from "healthy” residents who were identified as being negative for feces examination and immuno-methods in an endemic area were also examined. The results showed that LAMP could detect S. japonicum DNA in sera from rabbits at 3rd day post-infection. Following administration of praziquantel, the S. japonicum DNA in rabbit sera became negative at 10 weeks post-treatment. Of 110 sera from patients, LAMP showed 95.5% sensitivity, and even for 41 patients with less than 10 EPG, the sensitivity of LAMP still reached to 95.1%. For 47 patients after treatment, the negative conversion rate of S. japonicum DNA in patient sera increased from 23.4%, 61.7% to 83.0% at 3 months, 6 months and 9 months post-treatment, respectively. No false-positive result was obtained for 42 human sera from non-endemic area, while for the 60 “healthy” individuals from endemic area, 10 (16.7%) individuals were positive by LAMP, which suggested that these individuals might be false-negative patients.
Conclusions/ Significance
The present study demonstrated that the LAMP assay is sensitive, specific, and affordable, which would help reduce schistosomiasis transmission through targeted treatment of individuals, particularly for those with negative stool examinations who may yet remain infected. The LAMP assay may provide a potential tool to support schistosomiasis control and elimination strategies.
Author Summary
Accurate diagnostic tests play a key role in patient management and control of schistosomiasis, especially in China where the prevalence and intensity of Schistosoma japonicum infection is low in recent years. The present study aimed to assess the utility of the loop-mediated isothermal amplification (LAMP) assay for detection of light intensity infection or false-negative patients and for the evaluation of chemotherapy effectiveness in patients, targeting the highly repetitive retrotransposon SjR2 of S. japonicum, using 110 serum samples of schistosomiasis patients. The results showed that the LAMP assay had high sensitivity of 95.1% for the diagnosis of S. japonicum infection with the lowest intensity (EPG<10). For the assessment of efficacy after treatment with praziquantel, the negative conversion rate increased from 23.4%, 61.7% to 83.0% at 3 months, 6 months and 9 months post-treatment by LAMP, whereas for ELISA and IHA, the negative conversion rate remains at a low level (25.5% by ELISA and 31.9% by IHA) even at 9 months after treatment. Our results demonstrated that the LAMP assay may provide a valuable tool for the diagnosis of Schistosoma infection, especially for cases of light infection which is coincident with the current endemic situation.
Citation: Xu J, Guan Z-X, Zhao B, Wang Y-Y, Cao Y, Zhang H-Q, et al. (2015) DNA Detection of Schistosoma japonicum: Diagnostic Validity of a LAMP Assay for Low-Intensity Infection and Effects of Chemotherapy in Humans. PLoS Negl Trop Dis 9(4): e0003668. https://doi.org/10.1371/journal.pntd.0003668
Editor: Aaron R. Jex, University of Melbourne, AUSTRALIA
Received: October 7, 2014; Accepted: March 2, 2015; Published: April 13, 2015
Copyright: © 2015 Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper.
Funding: This study was funded by A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institution(No.YX13400214); the National Basic Research Program of China(973 Program, Grant No. 2007CB513100); Key Laboratory of Control and Prevention of Parasitic Disease of Healthy Ministry,No. wk014-001). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Schistosomiasis remains one of the most important chronic parasitic diseases in tropical regions and affects approximately 200 million people, despite the continued implementation of control measures [1]. Schistosomiasis japonica, caused by infection with Schistosoma japonicum, is mainly endemic in China. In areas where infection occurs, the prevalence and infection intensity is now low due to long-term and large-scale chemotherapy campaigns [2]. Methods that allow infections to be correctly diagnosed are a prerequisite for effective disease control. All present schistosomiasis control measures, including targeted treatment of all infected individuals, especially those with low-intensity infections, and large-scale surveillance of disease transmission are strongly dependent on sensitive and accurate diagnostic assays [3]. Indeed, the move to identify and evaluate highly sensitive diagnostics has become increasingly necessary as the prevalence and intensity of schistosome infections continues to decline worldwide [4]. The Kato-Katz fecal smear technique is the most commonly used method to diagnose schistosomiasis. However, various studies have shown that its sensitivity is less appropriate for low endemic areas, post-treatment situations, and for determination of incidence [5,6,7]. Moreover, traditional stool examinations always underestimate the prevalence of schistosomiasis due to their low diagnostic sensitivity [8]. Antibody detection methods generally have high sensitivities, but the slow reduction of specific antibody levels after treatment and the inability to discriminate between active and past S. japonicum infection constituted great disadvantages of the antibody-based assays [9,10]. Moreover, the level of antibodies persisted after treatment, which could not indicate whether the patients were cured or not [11,12]. In recent years, detection of circulating antigens, such as circulating anodic antigens (CAA) in serum or urine, seems a promising tool for diagnosis of Schistosoma infection [7,13]. A field study done by van Dam et al. [7], using lateral-flow assay for determination of CAA in urine and serum, showed that the method was at least 6 times more sensitive than triplicate Kato-Katz thick smears. However, due to the lack of “golden” standard reference test, different diagnostic methods are not comparable, thus a more sensitive standard is still needed [14].
With the development of molecular techniques, polymerase chain reaction (PCR)-based methods have shown great sensitivity and specificity for detection of Schistosoma DNA in a variety of samples [9,10,15–23]. However, the dependence on expensive apparatus and on specialized training in molecular biology restricts their widespread applications for field conditions. As an alternative, the loop-mediated isothermal amplification (LAMP) may provide a potential tool for diagnosis of schistosomiasis. The LAMP assay, firstly reported by Notomi et al. [24], has been rapidly accepted for detection of various pathogens, including Plasmodium falciparum, S. mansoni, S. haematobium and S. japonicum, due to its simplicity and rapidity [25–32]. This technique does not require sophisticated equipment for DNA amplification or for amplicon detection [33], which is of great value for field use. Our previous study established a LAMP assay based on the sequence of highly repetitive retrotransposon SjR2, which is able to detect 0.08 fg S. japonicum DNA, and 104 times more sensitive than conventional PCR [30].
To extend from our previous work, in this study, we assessed the utility of this LAMP assay for detection of light infection or false-negative patients of schistosomiasis and evaluation of chemotherapy efficacy, with the aim of providing a potential tool to support schistosomiasis control and elimination strategies.
Materials and Methods
Ethics statement
This study was funded by A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institution(No.YX13400214); the National Basic Research Program of China(973 Program, Grant No. 2007CB513100); Key Laboratory of Control and Prevention of Parasitic Disease of Healthy Ministry, No. wk014-001). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Establishment of light-infection rabbit models and sample collections
This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Committee on the Ethics of Animal Experiments of the Soochow University (Permit Number: 2007–13). All surgery was performed under sodium pentobarbital anesthesia, and all efforts were made to minimize suffering.
Schistosoma japonicum-infected snails (Oncomelania hupensis) were obtained from Jiangsu Institute of Parasitic Diseases, China. The living snails were putting into a breaker filled with 4/5 volume of water and then exposed to a light source to induce shedding of live S. japonicum cercariae.
Eight adult female New Zealand rabbits, weighing 2.0–2.5 kg, were randomly divided into four groups of two rabbits each. Each rabbit in Group 1 was percutaneously infected with 30 mixed sexual cercariae. On the 7th week post-infection, all the rabbits were sacrificed, and adult worms (male and female) were collected to confirm the real intensity of infection. Rabbits of group 2 and group 3 were given the same infective intensity as group1. Rabbits of group 4 administrated with saline were used as uninfected control. The faecal samples of rabbits for Kato-Katz egg examination were collected weekly from 1 week post-infection to 30 weeks post-infection. Rabbits in group 2 were treated with a single dose of 150 mg praziquantel per kilogram body weight on the 7th week post-infection. This dose was known to eliminate S. japonicum in our model [9,30]. Rabbits of group 3 remained as untreated control, and received no drug treatment. Blood samples from rabbits of group 2 to group 4 were collected on the 3rd day and then weekly until 30 weeks post-infection (Fig 1). Serum of each blood samples was separated by centrifugation (2,000 rpm for 10 min) after storage at 37°C for 2 h. All of the serum samples were stored at -20°C until use. On the 30th week post-infection, all of the rabbits were sacrificed, and the portal system and liver of the rabbits in group 2 were examined for evaluation of therapy efficacy.
Collection of field serum samples
One hundred and ten serum samples positive for S. japonicum infection determined by triplicate Kato-Katz stool examinations were obtained from 30 females and 80 males living in endemic areas in Hunan Province, China. Written consent letters were obtained from all participants. Ethical approval was obtained from the village (local government), county (anti-schistosomiasis office) and provincial (schistosomiasis headquarters) authorities. Five mL blood sample was collected from each participant, and about 2 mL serum was obtained from each blood sample. Then the serum samples were divided into 3 groups according to the eggs per gram of feces (EPG): 93 samples with <100 EPG, 13 samples with 100–400 EPG, 4 samples with >400 EPG. According to the new classification in China, which sets 100 EPG as the lower limit for a heavy infection; 40–99 EPG denotes a moderate infection, while 40 EPG is the upper limit for a light infection [34], the 93 samples with less than 100 EPG was divided again: 10 samples with 40–99 EPG, 42 samples with 10–39 EPG, 41 samples with < 10 EPG (Table 1). All the 110 cases were treated with praziquantel (single oral dose of 40 mg/kg), two stool samples were obtained from each participant at the 3rd month, the 6th month and the 9th month post-treatment, respectively, and each sample was subjected to triplicate Kato-Katz thick smears to evaluate the effectiveness of chemotherapy. Meanwhile, 2 mL serum samples were collected from the study population accordingly. However, only 47 serum samples from the participants had the complete data records. Forty-two serum samples from uninfected individuals collected from Wuxi, Jiangsu Province, China were used as negative control to evaluate the specificity of the LAMP assay. Meanwhile, 60 serum samples from individuals living in fishing villages in endemic areas, which were negative for fecal eggs by triplicate Kato-Katz thick smears, and also negative for serology diagnosis by triplicate IHA and ELISA tests, were used to evaluate the validity of the LAMP assay.
DNA extraction
DNA from all of the collected serum samples was extracted using the method described previously [9]. Briefly, 200 μl sera were dissolved in 400 μl serum lysis buffer, incubated 20 min at 55°C, and then extracted with phenol–chloroform–isoamyl alcohol (25:24:1) and precipitated with dehydrated alcohol.
IgG-enzyme linked immunosorbent assay (IgG-ELISA)
Serum samples were tested for anti-Schistosoma antibodies by IgG-ELISA. Serology was performed according to the protocol described by Xia et al. [9]. Sera were considered positive when the OD value exceeded the mean±3 SD absorbance of sera from non-infected samples.
Indirect hemagglutination assay (IHA)
Indirect hemagglutination kit containing human erythrocytes coated with soluble egg antigen is commercially available from the Anhui Provincial Institute of Parasitic Diseases (Wuhu, China). The test procedure followed a previous study [2]. The test result was considered positive when a positive reaction appeared at a titer 1:10.
LAMP
The LAMP assay was based on a previously study targeting the highly repetitive retrotransposon SjR2 of S. japonicum (GeneBank Accession no. AF412221) [9,30,35], with slight modifications. The LAMP assay was carried out with a total of 25 μl reaction mixture containing 2.5 μl 10×Bst-DNA polymerase buffer, 6 mmol/L MgSO4, 1.4 mmol/L dNTP, 0.2mmol/L F3, B3, 1.6 mmol/L FIP, BIP, 0.8 mol/L betain, 8 U Bst-DNA polymerase, and 5 μl template DNA. The reaction mixture was incubated at 64°C for 90 min. The LAMP amplification results were identified by adding 5 μl 1:80 diluted 10000×SYBR Green I after incubation, positive reactions were detected by an orange to green color change visible under normal light.
Data management and statistical analysis
Diagnostic sensitivity, specificity, PPV and NPV were calculated using the following formulae:
- Sensitivity = True positives/(True positives+False negatives)
- Specificity = True negatives/(True negatives+False positives)
- Positive predictive value (PPV) = True positives/(True positives+False positives)
- Negative predictive value (NPV) = True negatives/(True negatives+False negatives)
The SPSS 19.0 software was used for data analysis.
Results
Confirmation of real intensities of infection and therapy efficacy in rabbit models
On average, 3 female and 10 male adult worms (3 pairs of worms) were collected in rabbits of Group 1, and the mean EPG of the rabbits infected with 30 cercariae was 16, which is very low intensity infection. In addition, for fecal examinations of the rabbits, the eggs could not be found untill 7 weeks post-infection from group 1 to group 3. No adult worms were found in the portal system and liver of the rabbits in group 2, indicating thoroughly treatment of the rabbits in group 2. While for the rabbits without praziquantel treatment, 3 female and 18 male adult worms were found, and egg-granulomas were clearly observed (Table 2).
Serum DNA detection in rabbit models with light infection of S. japonicum
ELISA and IHA examination of rabbit serum samples gave positive results at 5 weeks and 4 weeks post-infection, respectively, and the antibody sustained at high level even at 23 weeks post-treatment (30 weeks post-infection, Table 2). Whereas the S. japonicum DNA was detectable by LAMP at the 3rd day post-infection in serum of rabbit model with very low intensity infection (EPG = 16, Table 2, Fig 2). Following administration of praziquantel, the detection of S. japonicum DNA in rabbit sera became negative at 10 weeks post-treatment (17 weeks post-infection, Table 2, Fig 3).
Serum samples were collected at 3 days (3d) and 1–7 weeks (1w–7w) post-infection. Tube N, serum of non-infected rabbits; tube P, DNA of S. japonicum adult worm (positive control).
Serum samples were collected from 15weeks to 20 weeks post-infection (8–13 weeks post-treatment). Tube N, serum of non-infected rabbits (negative control); tube P, DNA of S. japonicum adult worm (positive control).
Validity of LAMP for diagnosis of schistosomiasis in humans
Of the 110 patient serum samples with confirmed S. japonicum infection by stool examination, the sensitivity and specificity of LAMP assay was 95.5% and 100%, respectively. Whereas, the sensitivity and specificity of ELISA and IHA was 84.6% and 85.7%, and 91.8% and 88.1%, respectively. There was significant difference between the sensitivity of LAMP and ELISA (χ2 = 7.273, P = 0.007). Table 3 shows the PPV and NPV of the three detection methods, and the LAMP assay had the highest PPV (100%) and NPV (89.4%). Although all the three methods showed 100% sensitivity for patients with high-intensity infections (EPG>400), LAMP assay had higher sensitivity (95.7%) than ELISA (83.9%) and IHA (93.4%) for patients with <100 EPG(χ2 = 7.627, P = 0.022, Table 4). For 42 patients with 10–39 EPG, the detection rate of LAMP achieved 97.6%, which was significantly higher than the two immunoassays(χ2 = 6.157, P = 0.046, Table 5). Even for 41 patients excreting <10 EPG, which was very low-intensity infection, the sensitivity of LAMP assay sustained at a high level (95.1%), and only 2 cases were missed (Table 5).
After treatment with praziquantel, all the stool samples were negative for faecal eggs by triplicate Kato-Katz method. However, the negative conversion rate of S. japonicum specific SjR2 DNA detected by LAMP assay increased remarkably from 23.4%, 61.7% to 83.0% at 3 months, 6 months and 9 months post-treatment, while for the two immunoassays, the negative conversion rate of antibodies sustained at a low level even after 9 months post-treatment (Table 6). Statistical analysis showed that there was significant difference between LAMP and the two immunodiagnostics for the negative conversion rate of S. japonica at 6 months and 9 months post-treatment (χ2 = 17.63 and 37.43, both P value <0.0001).
Additionally, 42 serum samples of individuals from non-endemic areas, and 60 serum samples of residents in endemic areas who were identified with negative results for all the three commonly used diagnostic methods, including triplicate stool examinations, IHA and ELISA tests, were used to assess the validity of LAMP assay for field diagnosis of schistosomiasis. No positive result was observed for 42 uninfected human serum samples, indicating an excellent specificity of LAMP assay (Table 7). However, for the 60 serum samples from residents in endemic areas, which were negative for faecal eggs and serological methods, 10 (16.7%) samples were positive diagnosed by LAMP assay (Table 7), which might be missed by the commonly used diagnostic methods, such as Kato-Katz method, IHA and ELISA.
Discussion
Diagnosis is central to control of schistosomiasis [36]. The prevention and control of the disease need rapid and reliable diagnostic techniques to identify target population accurately for treatment [37]. However, the currently available diagnostic assays are not ideal, since the search for eggs in stools and detection of circulating antigens lack sensitivity in low prevalence and post-treatment situations, and antibody detection lacks specificity [38], and cannot distinguish current and cured infections, which results in the difficulties in determining prevalence, identifying true infected individuals for selective chemotherapy and assessing the effectiveness of intervention including follow-up of chemotherapy [34,39,40,]. Our results further demonstrated the limitations of the direct parasitological technique (Kato-Katz method) and antibody detection assays (ELISA and IHA). In rabbit models infected with S. japonicum cercariea, we did not find faecal eggs until 7 weeks post-infection, and for the two immunoassays, the earliest positive detection result was obtained at 4 weeks post-infection. Our rabbit experiment results confirmed that both the stool examination and antibody detection methods could not give early diagnosis at the beginning of S. japonicum infection. Moreover, 4 egg-positive cases were negative for antibodies by ELISA and IHA, with ages ranging from 43 to 65, indicating that antibody detections were insufficient for diagnosis of schistosomiasis in patients of older ages, due to immune down-regulation in chronic infection stages [7,41]. However, DNA amplification assays, which had identical diagnostic value with that of parasitological methods, may provide alternative approaches for sensitive and specific diagnosis of schistosomiasis. Lier et al. [21] reported a real-time PCR assay for detection of low intensity S. japonicum infections in a pig model. Subsequently, this method was used in a clinical trial. This real-time PCR assay detected slightly more positive faecal samples than the microscopy method, but was consistently negative in serum and urine samples [22]. To our knowledge, most of the PCR-based methods were focused on the detection of specific Schistosoma DNA in faeces, all of these methods could be seen as improvements on the stool examination approach [7], thus the sensitivity was influenced by the large day-to-day egg fluctuations in infected individuals [42]. In general, serum and urine samples are easier to obtain and more accepted in many populations than faecal samples, and unlike eggs in faecal samples, schistosome DNA would be equally distributed throughout the serum of the patient, resolving the restrictions of uneven distributions of eggs in stool samples [43]. Therefore, the detection of Schistosoma DNA from serum samples would be more accurate in field conditions. In our previous study, we found that the S. japonicum DNA in host serum primarily comes from the residual body of dead schistosomula in the first 4 weeks post-infection, while during the spawning stage of the female schistosome, the parasite DNA mainly comes from the disintegration of inactive eggs [44]. Furthermore, a 230-bp sequence from the highly repetitive retrotransposon SjR2 was identified in our previous study, and showed high sensitivity and specificity for detecting S. japonicum DNA in sera of rabbit model and patients [9]. Although PCR-based methods have the potential for sensitive and specific detection of schistosomiasis, the dependence on expensive apparatus restricts their wide application in the field.
Unlike PCR, LAMP assay does not require amplification cycles by thermocycling or amplicon detection by electrophoresis. Given these features, LAMP is potentially useful for work in the field and has already used in rural laboratories in developing areas for the diagnosis of tuberculosis [45]. Our previous study established a LAMP assay targeting S. japonicum SjR2, and the method was capable of detecting as little as 0.08 fg S. japonicum DNA, which was 104 times more sensitive than common PCR assay. In particular, the LAMP assay was able to detect S. japonicum DNA in rabbit sera at 1 week post-infection, and become negative at 12 weeks post-treatment [30]. However, the rabbit models used in our previous study were of high and moderate intensity infections, and the detection of S. japonicum DNA in low-intensity infections is more consistent with the current epidemiological situation.
In this study, the utility of LAMP assay was firstly assessed in rabbit models with very low grade intensities of infection (EPG = 16). It was able to detect S. japonicum DNA in serum at 3 days post-infection, and the detection results became negative at 10 weeks post-treatment, indicating that the LAMP method was useful for diagnosis of schistosomiasis, especially with low-intensity infection, and had potential for evaluation of chemotherapy effectiveness.
Then the field diagnostic value of the LAMP method, and its ability for evaluation of effectiveness of drug treatments was tested using 110 patient serum samples with confirmed S. japonicum infection by stool examination. Meanwhile, two of the most extensively used immunoassays (ELISA and IHA) in the field were also used to assess the validity of the LAMP assay for diagnosis of schistosomiasis. Our detection results showed that the LAMP assay performed better than the commonly used immunoassays in terms of higher sensitivity in patients with low-intensity infection (Table 4 and Table 5). After treatment with praziquantel, the negative seroconversion rate of IHA and ELISA sustained at low levels, while for the LAMP assay, the negative conversion rate of S. japonicum DNA in serum increased from 23.4%, 61.7% to 83.0% after 3 months, 6 months and 9months post-treatment (Table 6). All of the results confirmed that the LAMP assay was efficient for diagnosis of cases with low-intensity infections, and had potential for assessment of effectiveness of drug treatment.
Finally, 60 residents living in endemic areas with negative detection results of Kato-Katz, IHA and ELISA, were recognized as “healthy” residents, and were employed to assess the ability of LAMP assay for accurate diagnosis of schistosomiasis. Of the 60 serum samples from “healthy” individuals, 10 (16.7%) were diagnosed as positive by LAMP assay (Table 7), who might had been missed by parasitological methods, indicating that traditionally used methods lack sensitivity for diagnosis of individuals with low intensity infections. A field study done by Xu et al. [3] further confirmed our results. In this study, of 1371 enrolled residents, parasitological detection identified only 74 (5%) individuals as being egg-positive by Kato-Katz thick smears, of whom all the individuals were also positively diagnosed by LAMP detection of SjR2 DNA. More importantly, additional 368 (27%) individuals were positive for SjR2 DNA [3]. Professor Clive Shiff of Johns Hopkins Bloomberg School of Public Health, USA, commented on this paper as “New diagnostics reform infectious parasite epidemiology” [12]. The comment suggested that continuous surveillance to predict any resurgence of infection by accurate and sensitive measuring methods is highly recommended. It is very important to help reduce schistosomiasis transmission through targeted treatment of individuals, particularly those people who are presumed to be free of infection (false-negative) may actually remain infected and capable of infecting snails when their faeces get into the water.
In conclusion, the LAMP assay with rapidity, simplicity, sensitivity and specificity is suitable not only for case detections, but also for disease surveillance in schistosomiasis-endemic areas. Application of this method may improve the identification of cases with low-intensity infections and targeted treatment, which is of great significance for schistosomiasis control and elimination programmes.
Acknowledgments
We are grateful to Professor Zhongdao Wu for excellent technical assistance and improvement of our manuscript.
Author Contributions
Conceived and designed the experiments: JX CMX. Performed the experiments: JX ZXG BZ YYW YC. Analyzed the data: JX CMX. Contributed reagents/materials/analysis tools: JX YYW YC HQZ YKH CMX. Wrote the paper: JX CMX XQZ. Revised the paper: XQZ CMX.
References
- 1.
World Health Organisation (WHO). WHO fact sheet on Schistosomiasis. WHO Geneva, 2013. http://www.who.int/mediacentre/factsheets/fs115/en/
- 2. Zhou XN, Guo JG, Wu XH, Jiang QW, Zheng J, et al. (2007) Epidemiology of schistosomiasis in the People's Republic of China, 2004. Emerg Infect Dis 13: 1470–1476. pmid:18257989
- 3. Xu XD, Zhang YB, Lin DD, Zhang JJ, Xu J, et al. (2014) Serodiagnosis of Schistosoma japonicum infection: genome-wide identification of a protein marker, and assessment of its diagnostic validity in a field study in China. Lancet Infect Dis 14: 489–497. pmid:24656567
- 4. Bergquist R, Yang GJ, Knopp S, Utzinger J, Tanner M. (2015) Surveillance and response: Tools and approaches for the elimination stage of neglected tropical diseases. Acta Trop 141(Pt B):229–234. http://dx.doi.org/10.1016/j.actatropica.2014.09.017 pmid:25301340
- 5. Allam AF, Kader O, Zaki A, Shehab AY, Farag HF. (2009) Assessing the marginal error in diagnosis and cure of Schistosoma mansoni in areas of low endemicity using Percoll and PCR techniques. Trop Med Int Health 14: 316–321. pmid:19278527
- 6. Lin DD, Liu JX, Liu YM, Hu F, Zhang YY, et al. (2008) Routine Kato-Katz technique underestimates the prevalence of Schistosoma japonicum: A case study in an endemic area of the People’s Republic of China. Parasitol Int 57: 281–286. pmid:18485807
- 7. van Dam GJ, Xu J, Bergquist R, de Dood CJ, Utzinger J, et al. (2015) An ultra-sensitive assay targeting the circulating anodic antigen for the diagnosis of Schistosoma japonicum in a low-endemic area, People’s Republic of China. Acta Trop 141(Pt B):190–197. http://dx.doi.org/10.1016/j.actatropica.2014.08.004 pmid:25128703
- 8. Gordon CA, Acosta LP, Gray DJ, Olveda RM, Jarilla B, et al. (2012) High Prevalence of Schistosoma japonicum Infection in Carabao from Samar Province, the Philippines: Implications for Transmission and Control. PLoS Negl Trop Dis 6(9): e1778. pmid:23029571
- 9. Xia CM, Rong R, Lu ZX, Shi CJ, Xu J, et al. (2009) Schistosoma japonicum: A PCR assay for the early detection and evaluation of treatment in a rabbit model. Exp Parasitol 121: 175–179. pmid:19027005
- 10. Pontes LA, Dias-Neto E, Rabello A. (2002) Detection by polymerase chain reaction of Schistosoma mansoni DNA in human serum and feces. Am J Trop Med Hyg 66: 157–162. pmid:12135287
- 11. Zhu Y, Hua W, Xu M, He W, Wang X, et al. (2012) A novel immunodiagnostic assay to detect serum antibody response against selected soluble egg antigen fractions from Schistosoma japonicum. PloS one 7: e44032. pmid:22952862
- 12. Shiff C. (2014) New diagnostics reform infectious parasite epidemiology. Lancet Infect Dis 14: 446–448. pmid:24656566
- 13. van Dam GJ, de Dood CJ, Lewis M, Deelder AM, van Lieshout L, et al. (2013) A robust dry reagent lateral flow assay for diagnosis of active schistosomiasis by detection of Schistosoma circulating anodic antigen. Exp Parasitol 135: 274–282. pmid:23850995
- 14. Utzinger J, N’Goran EK, Caffrey CR, Keiser J. (2011) From innovation to application: social-ecological context, diagnostics, drugs and integrated control of schistosomiasis. Acta Trop 120 (Suppl 1): S121–S137. pmid:20831855
- 15. Hamburger J, He-Na Abbasi I, Ramzy RM, Jourdane J, Ruppel A. (2001) Polymerase chain reaction assay based on a highly repeated sequence of Schistosoma haematobium: a potential tool for monitoring schistosome infested water. Am J Trop Med Hyg 65: 907–911. pmid:11791997
- 16. Pontes LA, Oliverira MC, Katz N, Dlas-Neto E, Rabello A. (2003) Comparison of a polymerase chain reaction and the Kato-Katz technique for diagnosing infection with Schistosoma mansoni. Am J Trop Med Hyg. 68: 652–656. pmid:12887022
- 17. Sandoval N, Siles-Lucas M, Lopez Aban J, Perez-Arellano JL, Garate T, et al. (2006a) Schistosoma mansoni: a diagnostic approach to detect acute schistosomiasis infection in a murine model by PCR. Exp Parasitol. 114: 84–88. pmid:16571353
- 18. Sandoval N, Siles-Lucas M, Perez-Arellano JL, Carranza C, Puente S, et al. (2006b). A new PCR-based approach for the specific amplification of DNA from different Schistosoma species applicable to human urine samples. Parasitology 133: 581–587.
- 19. Suzuki T, Osada Y, Kumagai T, Hamada A, Okuzawa E, et al. (2006) Early detection of Schistosoma mansoni infection by touchdown PCR in a mouse model. Parasitol Int. 55: 213–218. pmid:16822708
- 20. Lier T, Simonsen GS, Haaheim H, Hjelmevoll SO,Vennervald BJ, et al. (2006) Novel real-time PCR for detection of Schistosoma japonicum in stool. Southeast Asian J Trop Med Public Health. 37: 257–264. pmid:17124983
- 21. Lier T, Johansen MV, Hjelmevoll SO, Vennervald BJ, Simonsen GS. 2008. Real-time PCR for detection of low intensity Schistosoma japonicum infections in a pig model. Acta Trop 105: 74–80. pmid:18036505
- 22. Lier T, Simonsen GS, Wang T, Lu D, Haukland HH, et al. (2009) Real-time polymerase chain reaction for detection of low-intensity Schistosoma japonicum infection in China. Am J Trop Med Hyg. 81: 428–432. pmid:19706908
- 23. ten Hove BJ, Verweij JJ, Vereecken K, Polman K, Dieye L, et al. (2008) Multiplex real-time PCR for the detection and quantification of Schistosoma mansoni and S. haematobium infection in stool samples collected in northern Senegal. Trans R Soc Trop Med Hyg 102: 179–185. pmid:18177680
- 24. Notomi T, Okayama H, Masubuchi H, Yonekawa T, Watanabe K, et al. (2000) Loop-mediated isothermal amplification of DNA. Nucleic Acids Res 28: E63. pmid:10871386
- 25. Poon LL, Wong BW, Ma EH, Chan KH, Chow LM, et al. (2006) Sensitive and inexpensive molecular test for falciparum malaria: detecting Plasmodium falciparum DNA directly from heat-treated blood by loop-mediated isothermal amplification. Clin Chem 52: 303–306. pmid:16339303
- 26. Poschl B, Waneesorn J, Thekisoe O, Chutipongvivate S, Karanis P. (2010) Comparative diagnosis of malaria infections by microscopy nested PCR, and LAMP in northern Thailand. Am J Trop Med Hyg 83: 56–60. pmid:20595478
- 27. Lucchi NW, Demas A, Narayanan J, Sumari D, Kabanywanyi A, et al. (2010) Real-time fluorescence loop mediated isothermal amplification for the diagnosis of malaria. PLoS One 5: e13733. pmid:21060829
- 28. Abbasi I, King CH, Muchiri EM, Hamburger J. (2010) Detection of Schistosoma mansoni and Schistosoma haematobium DNA by Loop-Mediated Isothermal Amplification: Identification of Infected Snails from Early Prepatency. Am J Trop Med Hyg 83: 427–432. pmid:20682894
- 29. Kumagai T, Furushima-Shimogawara R, Ohmae H, Wang TP, Lu S, et al. (2010) Detection of Early and Single Infections of Schistosoma japonicum in the Intermediate Host Snail, Oncomelania hupensis, by PCR and Loop-Mediated Isothermal Amplification (LAMP) Assay. Am J Trop Med Hyg 83: 542–548. pmid:20810818
- 30. Xu J, Rong R, Zhang HQ, Shi CJ, Zhu XQ, et al. (2010) Sensitive and rapid detection of Schistosoma japonicum DNA by loop-mediated isothermal amplification (LAMP). Int J Parasitol 40: 327–331. pmid:19735662
- 31. Wang C, Chen L, Yin X, Hua W, Hou M, et al. (2011) Application of DNA-based diagnostics in detection of schistosomal DNA in early infection and after drug treatment. Parasit Vectors 4:164. pmid:21864384
- 32. Fernandez-Soto P, Gandasegui Arahuetes J, Sanchez Hernandez A, Lopez Aban J, Vicente Santiago B, et al. (2014) A Loop-Mediated Isothermal Amplification (LAMP) Assay for Early Detection of Schistosoma mansoni in Stool Samples: A Diagnostic Approach in a Murine Model. PLoS Negl Trop Dis 8: e3126. pmid:25187956
- 33. Mori Y, Nagamine K, Tomita N, Notomi T. (2001) Detection of loop-mediated isothermal amplification reaction by turbidity derived from magnesium pyrophosphate formation. Biochem Biophys Res Commun 289: 150–154. pmid:11708792
- 34. Utzinger J, Zhou XN, Chen MG, Bergquist R. (2005) Conquering schistosomiasis in China: the long march. Acta Trop 96: 69–96. pmid:16312039
- 35. Laha T, Brindley PJ, Smout MJ, Verity CK, McManus DP, et al. (2002) Reverse transcriptase activity and untranslated region sharing of a new RTE-like, non-long terminal repeat retrotransposon from the human blood fluke, Schistosoma japonicum. Int J Parasitol 32:1163–1174. pmid:12117499
- 36. Zhu YC. (2005) Immunodiagnosis and its role in schistosomiasis control in China: a review. Acta Trop 96: 130–136. pmid:16143288
- 37. Wang W, Li Y, Li H, Xing Y, Qu G, et al. (2012) Immunodiagnostic efficacy of detection of Schistosoma japonicum human infections in China: a meta analysis. Asian Pac J Trop Med 5: 15–23. pmid:22182637
- 38. Rabello A, Pontes LA, Dias-Neto E. (2002) Recent advances in the diagnosis of Schistosoma infection: the detection of parasite DNA. Mem Inst Oswaldo Cruz 97 (Suppl. I): 171–172. pmid:12426615
- 39. Zhou YB, Zheng HM, Jiang QW. (2011) A diagnostic challenge for schistosomiasis japonica in China: consequences on praziquantel-based morbidity control. Parasit Vectors 4: 194. pmid:21981948
- 40. Doenhoff MJ, Chiodini PL, Hamilton JV. (2004) Specific and sensitive diagnosis of schistosome infection: can it be done with antibodies? Trends Parasitol 20: 35–39. pmid:14700588
- 41. van Lieshout L, Panday UG, De Jonge N, Krijger FW, Oostburg BF, et al. (1995) Immunodiagnosis of schistosomiasis mansoni in a low endemic area in Surinam by determination of the circulating antigens CAA and CCA. Acta Trop 59: 19–29. pmid:7785523
- 42. Engels D, Sinzinkayo E, Gryseels B. (1996) Day-to-day egg count fluctuation in Schistosoma mansoni infection and its operational implications. Am J Trop Med Hyg 54: 319–324. pmid:8615440
- 43. Wichmann D, Panning M, Quack T, Kramme S, Burchard GD, et al. (2009) Diagnosing schistosomiasis by detection of cell-free parasite DNA in human plasma. PLoS Negl Trop Dis 3: e422. pmid:19381285
- 44. Xu J, Liu AP, Guo JJ, Wang B, Qiu SJ, et al. (2013) The sources and metabolic dynamics of Schistosoma japonicum DNA in serum of host. Parasitol Res 112:129–133. pmid:22983220
- 45. Boehme CC, Nabeta P, Henostroza G, Raqib R, Rahim Z, et al. (2007) Operational feasibility of using loop-mediated isothermal amplification for diagnosis of pulmonary tuberculosis in microscopy centers in developing countries. J Clin Microbiol 45: 1936–1940. pmid:17392443