Characterization of the Taenia spp HDP2 sequence and development of a novel PCR-based assay for discrimination of Taenia saginata from Taenia asiatica
© González et al; licensee BioMed Central Ltd. 2010
Received: 12 February 2010
Accepted: 11 June 2010
Published: 11 June 2010
A previously described Taenia saginata HDP2 DNA sequence, a 4-kb polymorphic fragment, was previously used as the basis for developing PCR diagnostic protocols for the species-specific discrimination of T. saginata from T. solium and for the differentiation of T. saginata from T. asiatica. The latter was shown subsequently to lack the required specificity, so we undertook genetic studies of the HDP2 sequence from T. saginata and T. asiatica to determine why, and to develop a novel HDP2-PCR protocol for the simultaneous unambiguous identification of human taeniids. Sequencing and further analysis of the HDP2 DNA fragments of 19 Asiatic isolates of T. saginata and T. asiatica indicated that the HDP2 sequences of both species exhibited clear genomic variability, due to polymorphic variable fragments, that could correspond to the non-transcribed region of ribosomal DNA. This newly observed polymorphism allowed us to develop a novel, reproducible and reliable HDP2-PCR protocol which permitted the simultaneous discrimination of all T. saginata and T. asiatica isolates examined. This species-specific identification was based on, and facilitated by, the clear size difference in amplicon profiles generated: fragments of 1300 bp, 600 bp and 300 bp were produced for T. asiatica, amplicons of 1300 bp and 300 bp being obtained for T. saginata. Control T. solium samples produced one amplicon of 600 bp with the HDP2-PCR protocol. The assay has the potential to prove useful as a diagnostic tool in areas such as South East Asia where T. saginata, T. asiatica and T. solium coexist.
Human taeniasis results from intestinal infection with the adult tapeworms Taenia saginata, Taenia asiatica or Taenia solium. Ingestion of eggs of T. saginata and T. solium/ T. asiatica causes cysticercosis in cattle and pigs, respectively. Importantly, T. solium eggs can also infect man, giving rise to human cysticercosis, with the frequent localization of the metacestodes in the brain, causing potentially fatal neurocysticercosis (NCC) [1–3]. Infection with T. solium is therefore a serious public health problem, notably in endemic areas (Latin America, Africa, Asia), but also in non-endemic areas due to imported cases . Hence, and as an essential part of transmission control programs, there is an immediate and practical need for reliable and species-specific diagnosis of human taeniasis caused by T. saginata, T. asiatica and T. solium in order to identify tapeworm carriers, particularly those with T. solium, thus helping to avoid transmission of cysticercosis/NCC.
Until recently, species-specific diagnosis of taeniasis was unsatisfactory. Conventional clinical and morphological identification has low specificity and sensitivity . Moreover, adult worms of T. saginata and T. asiatica are frequently confused due to their morphological similarities . Copro-antigen diagnosis by ELISA, that detects parasite antigens in patient feces, is based on the use of polyclonal antibody reagents although it does not distinguish among the human intestinal taeniids [7, 8]. More recently, serological diagnosis for T. solium taeniasis has been reported with recombinant ES antigens [9, 10], but this assay not necessarily indicates active infection.
Various PCR approaches have been developed for species-specific identification of DNA from T. saginata, T. asiatica and T. solium [6, 11–26]. Thus, the previously described T. saginata HDP2 DNA sequence [12, 27], a 4-kb polymorphic fragment, was the basis for various PCR-based diagnostic protocols for the species-specific detection of T. saginata and T. solium taeniasis [12, 17, 25, 26], as well as for the specific differentiation of T. saginata and T. asiatica samples ; however, the developed HDP2-PCR protocol was later shown to lack the required specificity to discriminate T. saginata from T. asiatica.
Geographical origin of the 6 Taenia saginata and 13 Taenia asiatica samples analyzeda.
Sample code number and species*
#4, #8, #10, #14
#1, #3, #6, #9, #13, #15, #17, #18
Asia (country unknown)
PCR names, primer sequences and amplification conditions used.
PCR primer name
Amplification conditions (Taq polymerase; BIOTOOLS , Spain)
HDP2 PCR I:
94°C for 30 sec, 55°C for 30 sec, 72°C for 1 min, 72°C for 7 min (35 cycles)
HDP2 PCR II:
94°C for 30 sec, 56.5°C for 30 sec, 72°C for 2 min, 72°C for 7 min (35 cycles)
HDP2 PCR III:
94°C for 30 sec, 60°C for 30 sec, 72°C for 2 min, 72°C for 7 min (35 cycles)
To study the HDP2 DNA sequence organization in the 19 Asian T. saginata and T. asiatica isolates, 5 μg of each parasite gDNA was digested to completion with Cla I (Roche, Penzberg, Germany), as recommended by the manufacturer. Electrophoresis, Southern blotting, probe labeling, and hybridization procedures were carried out, with minor modifications, as previously described . The probe used was one fragment derived from the HDP2 sequence, previously named IPHDP2 , which is a variable fragment from the mid region of HDP2 (Fig. 1).
In addition, the HDP2 DNA sequence of the Taenia isolates were PCR-amplified with the PTs7S35F1/ HDP2R1 primers set (Fig. 1, Table 2), using 10 ng of gDNA from each parasite sample. After electrophoresis, the amplicons were visualized and purified using a QIAquick Gel Extraction Kit (Qiagen,, Valencia, CA). All the DNA fragments were automatically sequenced by standard Sanger chemistry using a Model 377 ABI PRISM system. We used a primer walking sequencing strategy involving PTs7S35F1, HDP2F2, HDP2R2 forward primers and HDP2R2, HDP2R1 reverse primers (Fig. 1). The DNA sequences obtained and their alignments were analyzed by Seqman II (DNASTAR) and Clustal W2  software packages. DNA sequence comparisons were carried out using the GenBank databases and BLASTn . The nucleotide sequences obtained from amplification of the HDP2 gDNA fragments of the Taenia isolates have been deposited in the EMBL/GenBank databases under the following accession numbers: FM212953-71.
To explore the contribution of nucleotide variability to the observed HDP2 sequence polymorphism, a fragment of 1896 bp from the IHDP2 region was obtained from all 19 Asian taeniid DNA samples using the HDP2 PCR II protocol. A comparison of all the IHDP2 fragments obtained [GenBank: FM212953-FM212971] by Clustal W2, revealed a high degree of homology, particularly in regard to the T. saginata isolates. Thus, alignment of the 1896 bp fragment from the control T. saginata HDP2 sequence [GenBank: AJ133740] with the amplified fragments from the Asian T. saginata samples yielded nucleotide identities from 99.6- 99.7%. Alignment of the control T. saginata HDP2 sequence with the T. asiatica fragments yielded 97.0-98.8% nucleotide identity. This, the Asian T. asiatica HDP2 fragments showed a sequence divergence of 0.1% to 2.1%, compared with divergence of 0.0-0.1% recorded for the Asian T. saginata isolates and the control Spanish T. saginata isolate, thereby confirming low nucleotide variability between the two cestode taxa. Consequently, this structural analysis suggested that the HDP2 sequence polymorphism could be explained by variable representation of partially repeated sequences in the mid region of the HDP2 fragment, IHDP2, rather than due to nucleotide sequence divergence.
Seqman II-alignment of the partial HDP2 DNA fragments for T. saginata and T. asiatica within the NTR of the rDNA sequences of T. saginata (pTSgr 3.1, pTSgr 2.4) and T. asiatica (pTTr 3.1) [21, 36], revealed that the sequences were identical. Accordingly, the HDP2 sequence could thus also represent a variable repetitive fragment, being part of the NTR from rDNA. Notably, the identities among the sequences were restricted to nucleotides 859-1049 and 1738-1868 of the HPD2 DNA plus strand; pTSgr 3.1 and pTTr 3.1 has a 0.7 kb internal fragment, whereas pTSgr 2.4 does not (Fig. 1). This genetic variability in the NTR of the rDNA of T. saginata and T. asiatica allowed us to design a PCR protocol (HDP2 PCR III) for the simultaneous differential identification of the two species (Fig. 1). The HDP2F2/HDP2R3 primer set was designed from this region in the mid variable central part of HDP2 (Fig. 1).
Using 10 ng of gDNA from the Asian isolates and control samples, and following the PCR conditions described in Table 2, unambiguous species-specific amplification was obtained for all the samples analyzed (Fig. 2c). Three amplicons were evident with the T. asiatica samples (1300 bp, 600 bp and 300 bp), and two amplicons were generated for T. saginata (a strong band of 1300 bp and a weak band of 300 bp); the control T.solium samples produced one amplicon (600 bp) (Fig. 2c). Therefore, the novel HDP2 PCR III yielded results similar to those of Yamasaki et al.  (Fig. 2b). These assays will prove particularly useful in areas such as South East Asia where T. saginata, T. asiatica and T. solium coexist [37, 38].
In conclusion, this study showed and defined genetic polymorphism in the HDP2 sequence of the human taeniid cestodes T. saginata and T. asiatica. An unexpected but, nevertheless notable finding, was that HDP2 may be a repetitive fragment of the NTR within taeniid rDNA. This could explain the success of the published PCR protocols derived from this sequence in the sensitive diagnosis of taeniasis and NCC [12, 13, 17, 25, 26, 39]. These findings were used to design a new HDP2 based PCR protocol, which demonstrated to be useful for the unambiguous discrimination of T. saginata from T. asiatica.
enzyme-linked immunosorbent assay
Polymerase chain reaction
a 4- kb polymorphic DNA fragment.
We would like to thank Prof. PC Fan (now deceased), Dr. J Cross and Prof. P Craig for supplying the Taenia isolates used for analysis. This work was also supported by a grant from FIS (97/0141 and 00/407) and the Spanish Ministry of Science and Innovation and the Instituto de Salud Carlos III within the Network of Tropical Diseases Research (RICET RD06/0021/0019). L.M. Gonzalez was sponsored by fellowships from the ISCIII and RICET.
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