The Comparison of PCR Kits for the Detection of Erythrocytic Parasites on Filter Paper

Tao, Zhi-yong; Zhang, Pei-yi; Zhang, Lu; Li, Chun-cao; Hu, Rui; Zhu, Han-wu; Zhou, Bei; Wu, Kai; Li, Ling-xu; Yao, Da-wei; Cao, Yu-jie; Wang, Dao-jin; Zheng, Chen-chen; Fang, Run-qi; Hua, Xiu-min; Ni, Yi-xuan; Jin, Xiao-xia; Xia, Hui; Fang, Qiang

doi:https://doi.org/10.1155/2022/5715436

Journal of Tropical Medicine

On this page

Abstract Introduction Materials and Methods Results Discussion Data Availability Ethical Approval Conflicts of Interest Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2022 | Article ID 5715436 | https://doi.org/10.1155/2022/5715436

The Comparison of PCR Kits for the Detection of Erythrocytic Parasites on Filter Paper

Zhi-yong Tao,^1,2Pei-yi Zhang,^1,2Lu Zhang,^1,2Chun-cao Li,^1,2Rui Hu,^1,2Han-wu Zhu,³Bei Zhou,⁴Kai Wu,⁵Ling-xu Li,⁶Da-wei Yao,⁶Yu-jie Cao,^1,2and Dao-jin Wang² et al.

Academic Editor: Jianbing Mu

Received05 Apr 2022

Accepted11 Jul 2022

Published13 Aug 2022

Abstract

Dried blood spot (DBS) based PCR was considered an inexpensive and feasible method for detecting pathogens in the blood. The DBS carrier filter paper and PCR kits are crucial for accurate diagnosis. We evaluated 4 types of filter papers and 20 PCR kits for DBS samples. The PCR detecting Plasmodium results showed that the minimum detection limit of the 4 filter papers was 1 × 10² parasites/μL, and the positive rates of 20 PCR kits ranged from 0% to 100%. PCR results were satisfactory for detecting Plasmodium falciparum (P. falciparum) and Plasmodium. vivax (P. vivax) in archived DBS samples and Babesia gibsoni (B. gibsoni) in fresh pet DBS samples. Our results provided a useful reference for the detection of blood pathogens with DBS samples and direct PCR, especially for screening the cost-efficacy combination of filter paper and PCR kit in resource-limited areas.

1. Introduction

Plasmodium [1–3] and Babesia [4–8] are two major intraerythrocytic parasites causing human and animal infection, namely malaria and babesiosis. Both are life-threatening. Fast and accurate diagnosis of these diseases is crucial for the treatment of patients and to contain the spread of these vector-borne diseases. Microscopy is the most common method for laboratory diagnosis of blood parasitic infection, but low parasitemia infection may lead to misdiagnosis. Sometimes, the identification of species of Plasmodium or Babesia may not be possible due to morphological similarity. More importantly, Babesia is easily confused with early-stage Plasmodium [3, 6, 9, 10] and can lead to unsuccessful treatment with antimalarial drugs. PCR-based molecular diagnostic approaches are important supplementary methods for accurate diagnosis [11–15], but these methods are usually not feasible in resource-limited areas due to equipment requirements and cost.

Since the 1960s, dried blood spot (DBS) samples have been used in the clinical diagnostic analysis for blood testing, mainly for the screening of neonatal metabolic disorders and genetic abnormalities [16–20]. Many DBS-based experimental methods have been successfully developed, such as analysis methods for nucleic acids, lipids, and other substances. Qualitative and quantitative detection based on DBS PCR has been widely used in the screening of infectious diseases such as HIV, HBV, CMV, and so on. It is also of great importance in the detection of parasitic infections in the blood [21–24], especially for Plasmodium infection [1, 9, 25, 26].

Collecting whole blood on filter paper as dried blood spot samples was optimal for the storage and transportation of blood samples from the field site to the laboratory for centralized testing [17]. As a sampling tool for PCR molecular diagnosis and surveillance, the quality of filter paper is particularly important. Among many types of filter paper, Whatman 903 filter paper has FDA approval and is widely used. Currently, 903 filter paper is provided as a relatively expensive ready-to-use sampling card. Whatman CF12 filter paper is a cheaper form of square sheet filter paper and is currently listed as one item of 903 Proteinsaver cards by its new manufacturer Cytiva. CF 12 filter paper is globally available and marketed as 903 filter paper in China. However, a comparison of physical properties and molecular detection performance of CF12 and other filter papers was not usually done.

At present, in order to facilitate the rapid control of many infectious diseases, there is a need for efficient and convenient nucleic acid collection and detection methods in the field. Existing PCR test requires a long detection time, and samples such as throat swabs and blood need to be extracted for nucleic acid before testing, which increases the overall diagnosis time. Moreover, the cost of nucleic acid extraction and detection is high, and some underdeveloped regions do not have proper nucleic acid extraction equipment and laboratory settings. Therefore, there was an urgent need for the development of rapid detection methods.

Direct PCR is one of the most valued rapid molecular detection techniques. Before 1993, direct PCR was used in the field of microbiology, for which the sample processing is very simple [19]. For example, colony PCR is a typical rapid method for screening colonies. Most direct PCR is based on the use of a genetically modified DNA polymerase, which makes it possible for bypassing nucleic acid extraction before PCR amplification, saving experimental materials and time. Moreover, it reduces the possibility of human error and sample cross-contamination [1]. The requirements for polymerase are high, not only in the tolerance to interferential components but also in the compatibility with the buffer of PCR reaction.

There are potent PCR inhibitors in crude samples such as blood, which can cause false negative PCR results [27]. Several major inhibitory components in blood have been characterized, that is, hemoglobin, immunoglobulin G, and lactoferrin. The mechanism is related to the inactivation or inhibition of Taq DNA polymerase, which may reduce the efficiency and usability of direct PCR based on filter paper blood samples [28, 29].

We purchased four types of filter papers commercially available in mainland China and evaluated them in terms of weight, thickness, blood absorption performance, positive rates, and price. A total of 20 commercially available PCR kits, mainly for direct PCR of blood samples, were selected and tested using DBS samples. The aim of this research is to evaluate the cost-effectiveness of DNA polymerases that were suitable for molecular diagnosis of blood infection in DBS samples.

2. Materials and Methods

2.1. Filter Papers

Whatman CF12 (GE healthcare, UK), Advantec 545 (Advantec Group, Tokyo, Japan), and Jesiman Filter Paper (Jesiman New Material Co. Ltd., Wuhan, China) were purchased from the Taobao platform in China (https://taobao.com), and Gel Blot Paper was purchased from Sangon Biotech Co. Ltd. (Shanghai, China). Supplementary Table S1 details this information.

2.2. The Preparation of DBS Filter Paper Samples Containing Plasmodium parasites

Collect EDTA-K2 anticoagulated blood from mice infected with P. yoelii. Adjust the parasitemia to 1 × 10⁵ parasites/μL, and 1, 10¹, 10², 10³, 10⁴, and 10⁵ parasites/µL blood samples were obtained by tenfold serial dilution with EDTA-K2 anticoagulated whole blood. Blood was absorbed by four types of filter papers to prepare DBS samples, each spot contains 50 µL of blood. The blood spot preparation schematic diagram is shown in Figure 1.

Plasmodium falciparum 3D7 (P. falciparum) dried blood spots: four levels of parasite density blood samples (1 and 10¹ to 10³ parasites/µL) were obtained by tenfold serial dilution and absorbed on CF12 filter paper.

The DBS samples were placed on a clean bench and dried for 48 h. The filter papers were stored in a sealed plastic bag with silica gel desiccant.

2.3. Self-Made Blood Collection Card

The self-made blood collection cards are made with CF12 filter paper, consisting of upper and lower cover and enclosed sampling filter (see Supplementary Figure S1). It was placed upright to dry the blood samples after collection and to protect the DBS samples during transportation. Each DBS sampling card was individually packaged with silica gel desiccant in a plastic bag and stored at room temperature.

2.4. DBS Samples of Malaria-Infected Blood

Our laboratory has established a repository of malaria samples obtained over decades of research. Preserved DBS samples of Plasmodium vivax (P. vivax) infected blood were collected in Wuhe County, China, between 2009 and 2014, stored at −20°C. The DBS samples of P. falciparum-infected blood were collected from imported cases mostly from African countries, between 2010 and 2013, and stored at room temperature.

2.5. Animal Blood Samples

Self-made blood collection cards were sent to the pet hospitals located in three cities: Bengbu, Changsha, and Nanjing. DBS samples were collected from dogs. After complete drying, DBS samples were sent back to our lab for detection of Babesia infection.

2.6. Pretreatment of Blood Spots before PCR Reaction

Two pieces of dried blood spots (equivalent to 3–5 µL of whole blood) were punched with a 1.5 mm puncher and placed in one PCR reaction tube. To remove the hemoglobin in the sample and dust floating on the surface of the blood spots, 70 µL of sterilized ultrapure water was added to each tube, and the reaction tubes were incubated at 50°C for 5 min, 21°C for 15 s, 50°C for 1.5 min, and 21°C for 15 s. The supernatant in the tubes was then aspirated and discarded.

2.7. Primers Used for PCR Detection of Pathogens

The target of nested PCR for Plasmodium was 18S rRNA. Genus-specific primers rPLU6 and rPLU5 were used for the first round of amplification, and the amplified products were used for the second round of amplification, in which the primers used were species-specific for P. falciparum and P. vivax. The target gene for the detection of Babesia gibsoni was 18S rRNA. The sequences of all primers used in this research are shown in Supplementary Table S2.

2.8. The Information of 20 Commercial DNA Polymerases

All 20 DNA polymerases were purchased from Labgic Technology Co. Ltd. (Hefei, China), and the purchasing information is shown in Supplementary Table S3.

2.9. PCR Conditions

For each PCR, all reagent components were added according to their product instructions. For different PCR, the detailed programs were listed in Supplementary Tables S4–S6. The annealing temperatures were set according to the Tm value of each primer pair, and the extension times are set according to the expected fragment length and the enzyme elongation speed. All PCR reactions were carried out on an S1000 Thermal Cycler (Bio-Rad, USA).

3. Results

3.1. The Characteristics of Four Types of Filter Papers

We compared the general properties of the four types of filter papers available from the mainland China market, including thickness, weight, and blood absorption ability. The results showed that there were differences in the absorption time and the diameter of the blood spots when using healthy human blood and laboratory mice blood. For the absorption time of 50 μL whole blood by different filter papers, CF12 and 545 filter papers only take 3–5 seconds, which was significantly faster than the other two filter papers. CF12 and 545 filter papers formed more regular blood spots and were less prone to leakage (see Table 1). The Sangon Gel Blot paper could not completely absorb 50 μL of blood in a short time, and the blood sample was seen to spread unevenly in the filter paper, while no similar diffusion and leakage occurred in the other three filter papers (see Figure 2).

(a)

(b)

3.2. Detection Limits and Positive Rates of Direct PCR on Four Types of Filter Papers

A high-fidelity polymerase (Tks Gflex, TAKARA R060Q) based PCR was used to determine the detection limit for Plasmodium in the dried blood spots of four filter papers. The detection target was a 134 bp fragment of P. yoelii 17XNL 18srRNA gene. The results showed that the minimum detection limit of all four filter papers was 1 × 10² parasites/μL.

For comparison of the efficiency of different filter papers for DBS-based PCR, we purchased 20 commercial DNA polymerases for PCR detection of erythrocytic parasites in the DBS sample. The Plasmodium genus-specific primer rPLU6/5 was used to amplify a 1,003 bp fragment of P. yoelii in the DBS sample. The results showed positive rates of four filter papers that ranged from 56.7% to 63.3% (see Table 2), and the chi-square test showed no significant difference between the four filter papers ().

3.3. The Results of 20 DNA Polymerases for Detection of Plasmodium Genes in DBS

For comparing the performance of 20 polymerases, serial diluted P. yoelii 17XNL DBS samples on four filter papers were tested. The results showed that the positive rates ranged from 0% to 100% (see Table 2). Five PCR kits can detect all Plasmodium samples with different parasite densities on four types of filter papers.

3.4. Cost-Effectiveness Analysis of 20 DNA Polymerases

In order to screen cost-effective DNA polymerases, both unit price and positive rate need to be considered. As well known, the less template DNA in samples, the more difficult to amplify, the cost-effective criteria were established according to the difficulty of amplification: 1 point for positive of 10³ parasites, 10 points for 10² parasites, and 100 points for 10¹ parasites (see Table 3). Eight DNA polymerases with positive rates from 80% to 100% were selected for the subsequent experiments.

3.5. Performance Comparison of DNA Polymerases for Detection of P. falciparum

Blood samples of cultured P. falciparum were tenfold serial diluted (1–10³ parasites/µL) by normal mice blood and DBS samples were prepared using CF12 filter paper. Eight selected DNA polymerases were tested for detection of P. falciparum using nested PCR techniques. The first-round primers rPLU5/6 were genus-specific, and the second-round primers rFAL1/2 were P. falciparum-specific. One microliter of first-round PCR product was used as the template DNA in the second-round PCR. The results showed that the following five DNA polymerases: Beyotime HemoTaq, NEB Hemo Klen Taq, TAKARA MightyAmp, TOYOBO KOD FX Neo, and Sangon Direct PCR Kit, were better for P. falciparum, with all positive rates at 100% (detailed amplification results are listed in Supplementary Table S7). These five DNA polymerases were selected for subsequent detection of clinical samples.

3.6. Direct PCR Results of Human Malaria Parasites in DBS Sample

Forty-one positive DBS samples of human malaria were retrieved from our laboratory archive and were analyzed by direct PCR using five cost-effective polymerases. The original filter papers used for preserving blood samples were not uniform: some of them were obvious thinner or thicker; some were prepared with an FTA card. Also, the density of parasites in each DBS sample was unclear. These samples consisted of 21 P. falciparum and 20 P. vivax. The results showed that the following three polymerases can detect both malaria parasites at 100% positivity rates: TAKARA MightyAmp, TOYOBO KOD FX Neo, and Sangon Direct PCR Kit. The regions from which these samples were taken and the results of the amplification of the five DNA polymerases are shown in Supplementary Table S8.

3.7. DBS-Sample-Based Direct PCR for Detection of Babesia in Dog Blood

In order to verify whether DBS direct PCR is suitable for detecting Babesia in dog blood, self-made CF12 blood collection cards were used to collect dog blood in three regional veterinary hospitals. DBS samples were sent back to our laboratory for the batch test. After receiving the samples, the direct PCR test was conducted by using only the MigthyAMP kit. The results showed that two positive samples were detected from Bengbu dog blood DBS samples. Sequencing of PCR product and Giemsa’s stain confirmed that the two dogs were infected with Babesia gibsoni. The detailed results are shown in Supplementary Table S9.

4. Discussion

Due to limited resources in many tropical countries, it may not be possible to meet the basic storage requirements for blood samples for laboratory diagnostics. Many studies have shown that a variety of substances were stable in DBS and could be preserved for longer periods than traditional methods. DBS was considered an alternative to blood samples for the detection of antibodies or nucleic acid in resource-limited areas and in populations where venous blood collection, preservation, and transportation were difficult. However, differences in the nature of the filter papers could influence the analytic results, and the compatibility with key reagents and their uneven performance can also cause variable results of a DBS-based assay.

In this study, four commercially available filter papers were compared in terms of their performance in absorbing blood, price, and suitability for nucleic acid detection using 20 DNA polymerases. The Whatman CF12 and Advantec 545 filter papers exhibited excellent blood absorption properties and were more convenient for preparation but were relatively expensive. The comparison of nucleic acid detection performance showed that there was no significant difference in the positivity and detection limits between the four filter papers. And the results from the archived DBS samples made with a variety of filter papers for P. falciparum also showed that DBS samples made with much thinner filter paper can be effectively detected by direct PCR. The results of this experiment suggest that common laboratory filter paper could also provide nucleic acid detection support when there was no high-quality filter paper available.

The nucleic acids in DBS samples can be extracted by commercial kits with higher purity, but a relatively larger volume of eluent is needed, and the final concentration of DNA may be quite low. In this experiment, the amplification was carried out by using two pieces of punched filter paper placed directly in the PCR tube during the reaction. The punched DBS sample was treated with a mild and simple wash procedure, which can remove partial inhibitors in the blood and retain enough nucleic acids for successful detection in the sample, which helps improve the results, reduce cost, and save time.

It is known that PCR inhibitors are present in the blood, and requirements for reagents used in direct PCR of blood samples were high, especially polymerases. In this experiment, we compared the performance and cost-effectiveness of 20 commercially available DNA polymerases for DBS direct PCR. This technique does not need DNA extraction, simplifies the sample processing steps, and reduces the chance of possible contamination in the extraction step. Our results showed that most of the DNA polymerases can detect blood parasites in filter paper samples with high levels of parasite density (10³ parasites/µL), and some of them reach their minimum detection limits as the density of parasite decreases. Among all polymerases tested, five polymerases, Beyotime HemoTaq, NEB Hemo Klen Taq, TAKARA MightyAmp, TOYOBO KOD FX Neo, and Sangon Direct PCR Kit, gave better results and were more resistant to inhibitors in the blood. However, some polymerases may not be suitable for DBS PCR. Furthermore, the experimental results of direct PCR on archived human malaria DBS samples showed that all five DNA polymerases had high detection rates, and the three DNA polymerases, TAKARA MightyAmp, TOYOBO KOD FX Neo, and Sangon Direct PCR Kit, had 100% positive rates for both human malaria tests.

In order to perform large-scale screening, the cost per test must be taken into account. By scoring the PCR results to compare the cost-efficiency of direct PCR reagents, the method used in this study can be used as a useful reference for regions with limited resources to evaluate kits that were available locally and to facilitate large-scale screening of pathogens. In the reaction system for PCR, we followed the product instructions without modification. In fact, after optimization of direct PCR conditions for each primer and template, the performance of polymerases may be improved to some extent.

This study suggests that a simple PCR nucleic acid detection technique based on filter paper and direct PCR kits with high sensitivity is suitable for the detection of pathogen genes within the blood, especially in resource-limited epidemic areas, and provides an economical and convenient option for large-scale screening of human and animal infectious disease by collecting filter paper blood samples in field sites and transporting them back to laboratories that are equipped to perform bulk testing.

Data Availability

The data that support the findings of this study are available in the manuscript as well as in the supplementary materials of this article.

Ethical Approval

All animal experiments were approved by the Experimental Animal Management and Ethics Committee of Bengbu Medical College, Bengbu, China (BBMC2021-195). The usage of archived dried blood samples was approved by the Institutional Review Board of Wuhan Center for Disease Control and Prevention (WHCDCIRB-K-2021013), Chenzhou Center for Disease Control and Prevention (20211218), Jiangsu Institute of Parasitic Diseases (IRB00004221), and the Biomedical Ethics Committee of Anhui Medical University.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Authors’ Contributions

Zhi-yong Tao and Qiang Fang contributed to conceptualization, methodology, writing, editing, validation, and resource; Pei-yi Zhang contributed to data acquisition, methodology, writing, data curation, and visualization; Lu Zhang, Chun-cao Li, and Rui Hu contributed to sample processing and data acquisition; Han-wu Zhu, Bei Zhou, Kai Wu, Ling-xu Li, and Da-wei Yao contributed to sample collection and resource; Yu-jie Cao, Dao-jin Wang, Chen-chen Zheng, and Run-qi Fang contributed to sample processing and sample collection; Xiu-min Hua, Yi-xuan Ni, Xiao-xia Jin, and Hui Xia contributed to reviewing and validation. Zhi-yong Tao and Pei-yi Zhang contributed equally.

Acknowledgments

The authors thank the staff of the Bengbu Pet Clinic, for their assistance in collecting samples. The authors also thank the undergraduate students of Bengbu Medical College who participated in the Innovation Training Program for taking care of laboratory animals. This work was supported by grants from the Key Joint projects of Bengbu City and Bengbu Medical College (BYLK201828), the National and Anhui Provincial College Student’s Innovation and Entrepreneurship Training Program (202110367025 and S202010367023), the Scientific Innovation Project for Graduate Student of Bengbu Medical College (Byycxz20004), and the Key Program and the Major Project of Natural Science Project of Anhui Higher Education Institutions (KJ2020A0567 and KJ2021ZD0077).

Supplementary Materials

The supplementary materials contain nine tables showing filter papers and DNA polymerases purchasing details; sample collecting information; and PCR primers, conditions, and results. In addition, Supplementary Figure S1 shows the self-made blood collection card based on CF12 filter paper. (Supplementary Materials)

References

D. F. Echeverry, N. A. Deason, J. Davidson et al., “Human malaria diagnosis using a single-step direct-PCR based on the Plasmodium cytochrome oxidase III gene,” Malaria Journal, vol. 15, no. 1, p. 128, 2016.
View at: Publisher Site | Google Scholar
G. Snounou, S. Viriyakosol, X. P. Zhu et al., “High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction,” Molecular and Biochemical Parasitology, vol. 61, no. 2, pp. 315–320, 1993.
View at: Publisher Site | Google Scholar
B. A. Mathison and B. S. Pritt, “Update on malaria diagnostics and test utilization,” Journal of Clinical Microbiology, vol. 55, no. 7, pp. 2009–2017, 2017.
View at: Publisher Site | Google Scholar
P. J. Kelly, C. Xu, H. Lucas et al., “Ehrlichiosis, babesiosis, anaplasmosis and hepatozoonosis in dogs from St. Kitts, West Indies,” PLoS One, vol. 8, no. 1, Article ID e53450, 2013.
View at: Publisher Site | Google Scholar
G. R. Healy and T. K. Ruebush, “Morphology of Babesia microti in human blood smears,” American Journal of Clinical Pathology, vol. 73, no. 1, pp. 107–109, 1980.
View at: Publisher Site | Google Scholar
E. G. Vannier, M. A. Diuk-Wasser, C. Ben Mamoun, and P. J. Krause, “Babesiosis,” Infectious Disease Clinics of North America, vol. 29, no. 2, pp. 357–370, 2015.
View at: Publisher Site | Google Scholar
A. Rehman, N. Abbas, T. Saba, Z. Mehmood, T. Mahmood, and K. T. Ahmed, “Microscopic malaria parasitemia diagnosis and grading on benchmark datasets,” Microscopy Research and Technique, vol. 81, no. 9, pp. 1042–1058, 2018.
View at: Publisher Site | Google Scholar
M. S. Bang, C. M. Kim, S. H. Pyun, D. M. Kim, and N. R. Yun, “Molecular investigation of tick-borne pathogens in ticks removed from tick-bitten humans in the southwestern region of the Republic of Korea,” PLoS One, vol. 16, no. 6, Article ID e0252992, 2021.
View at: Google Scholar
P. Boonma, P. R. Christensen, R. Suwanarusk, R. N. Price, B. Russell, and U. Lek-Uthai, “Comparison of three molecular methods for the detection and speciation of Plasmodium vivax and Plasmodium falciparum,” Malaria Journal, vol. 6, p. 124, 2007.
View at: Google Scholar
Y. Zhang, A. F. Xu, J. Q. Zhang et al., “Differential diagnosis of a case of Babesia microti infection previously misdiagnosed as malaria,” Chinese Journal of Parasitology & Parasitic Diseases, vol. 38, no. 4, pp. 445–448, 2020.
View at: Google Scholar
X. H. Zhai, D. W. Yao, and W. H. He, “PCR diagnosis of a case of canine Babesia gibsoni,” Animal Husbandry & Veterinary Medicine, vol. 43, no. 12, pp. 80-81, 2011.
View at: Google Scholar
C. A. F. Bora, A. Varghese, C. K. Deepa et al., “Sequence and phylogenetic analysis of the thrombospondin-related adhesive protein gene of Babesia gibsoni isolates in dogs in South India,” Parasitology International, vol. 86, Article ID 102477, 2022.
View at: Publisher Site | Google Scholar
M. N. Singh, O. K. Raina, M. Sankar et al., “Molecular detection and genetic diversity of Babesia gibsoni in dogs in India,” Infection, Genetics and Evolution, vol. 41, pp. 100–106, 2016.
View at: Publisher Site | Google Scholar
M. T. E. P. Allsopp and B. A. Allsopp, “Molecular sequence evidence for the reclassification of some Babesia species,” Annals of the New York Academy of Sciences, vol. 1081, no. 1, pp. 509–517, 2006.
View at: Publisher Site | Google Scholar
W. P. Guo, G. C. Xie, D. Li, M. Su, R. Jian, and L. Y. Du, “Molecular detection and genetic characteristics of Babesia gibsoni in dogs in Shaanxi Province, China,” Parasites & Vectors, vol. 13, no. 1, p. 366, 2020.
View at: Publisher Site | Google Scholar
C. Williams, L. Weber, R. Williamson, and M. Hjelm, “Guthrie spots for DNA-based carrier testing in cystic fibrosis,” Lancet, vol. 332, no. 8612, p. 693, 1988.
View at: Publisher Site | Google Scholar
R. Guthrie and A. Susi, “A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants,” Pediatrics, vol. 32, no. 3, pp. 338–343, 1963.
View at: Publisher Site | Google Scholar
K. Chan and J. M. Puck, “Development of population-based newborn screening for severe combined immunodeficiency,” The Journal of Allergy and Clinical Immunology, vol. 115, no. 2, pp. 391–398, 2005.
View at: Publisher Site | Google Scholar
D. C. Jinks, M. Minter, D. A. Tarver, M. Vanderford, J. F. Hejtmancik, and E. R. B. McCabe, “Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening,” Human Genetics, vol. 81, no. 4, pp. 363–366, 1989.
View at: Publisher Site | Google Scholar
A. L. Nagy, R. Csáki, J. Klem et al., “Minimally invasive genetic screen for GJB2 related deafness using dried blood spots,” International Journal of Pediatric Otorhinolaryngology, vol. 74, no. 1, pp. 75–81, 2010.
View at: Publisher Site | Google Scholar
D. L. Fink, J. Kamgno, and T. B. Nutman, “Rapid molecular assays for specific detection and quantitation of Loa loa microfilaremia,” PLoS Neglected Tropical Diseases, vol. 5, no. 8, Article ID e1299, 2011.
View at: Publisher Site | Google Scholar
D. Mumba, E. Bohorquez, J. Messina et al., “Prevalence of human african trypanosomiasis in the democratic republic of the Congo,” PLoS Neglected Tropical Diseases, vol. 5, no. 8, Article ID e1246, 2011.
View at: Google Scholar
K. Katakura, C. Lubinga, H. Chitambo, and Y. Tada, “Detection of Trypanosoma congolense and T. brucei subspecies in cattle in Zambia by polymerase chain reaction from blood collected on a filter paper,” Parasitology Research, vol. 83, no. 3, pp. 241–245, 1997.
View at: Publisher Site | Google Scholar
H. Tani, Y. Tada, K. Sasai, and E. Baba, “Improvement of DNA extraction method for dried blood spots and comparison of four PCR methods for detection of Babesia gibsoni (Asian genotype) infection in canine blood samples,” Journal of Veterinary Medical Science, vol. 70, no. 5, pp. 461–467, 2008.
View at: Publisher Site | Google Scholar
B. Singh, J. Cox-Singh, A. O. Miller, M. S. Abdullah, G. Snounou, and H. Abdul Rahman, “Detection of malaria in Malaysia by nested polymerase chain reaction amplification of dried blood spots on filter papers,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 90, no. 5, pp. 519–521, 1996.
View at: Publisher Site | Google Scholar
G. W. Long, S. L. Hoffman, L. Fries, and G. H. Watt, “Polymerase chain reaction amplification from Plasmodium falciparum on dried blood spots,” The American Journal of Tropical Medicine and Hygiene, vol. 52, no. 4, pp. 344–346, 1995.
View at: Publisher Site | Google Scholar
M. B. Kermekchiev, L. I. Kirilova, E. E. Vail, and W. M. Barnes, “Mutants of Taq DNA polymerase resistant to PCR inhibitors allow DNA amplification from whole blood and crude soil samples,” Nucleic Acids Research, vol. 37, no. 5, p. e40, 2009.
View at: Publisher Site | Google Scholar
C. A. Kreader, “Relief of amplification inhibition in PCR with bovine serum albumin or T4 gene 32 protein,” Applied and Environmental Microbiology, vol. 62, no. 3, pp. 1102–1106, 1996.
View at: Publisher Site | Google Scholar
W. A. Al-Soud, L. J. Jönsson, and P. Râdström, “Identification and characterization of immunoglobulin G in blood as a major inhibitor of diagnostic PCR,” Journal of Clinical Microbiology, vol. 38, no. 1, pp. 345–350, 2000.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2022 Zhi-yong Tao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

328

Downloads

569

Citations