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LSSP-PCR of Trypanosoma cruzi: how the single primer sequence affects the kDNA signature
© Segatto et al.; licensee BioMed Central Ltd. 2013
- Received: 27 December 2012
- Accepted: 25 April 2013
- Published: 2 May 2013
Low-stringency single specific primer PCR (LSSP-PCR) is a highly sensitive and discriminating technique that has been extensively used to genetically characterize Trypanosoma cruzi populations in the presence of large amounts of host DNA. To ensure high sensitivity, in most T. cruzi studies, the variable regions of the naturally amplified kinetoplast DNA (kDNA) minicircles were targeted, and this method translated the intraspecific polymorphisms of these molecules into specific and reproducible kDNA signatures. Although the LSSP-PCR technique is reproducible under strict assay conditions, the complex banding pattern generated can be significantly altered by even a single-base change in the target DNA. Our survey of the literature identified eight different primers with similar, if not identical, names that have been used for kDNA amplification and LSSP-PCR of T. cruzi. Although different primer sequences were used in these studies, many of the authors cited the same reference report to justify their primer choice. We wondered whether these changes in the primer sequence could affect also the parasite LSSP-PCR profiles.
To answer this question we compared the kDNA signatures obtained from three different and extensively studied T. cruzi populations with the eight primers found in the literature. Our results clearly demonstrate that even minimal modifications in the oligonucleotide sequences, especially in the 3′ or 5′ end, can significantly change the kDNA signature of a T. cruzi strain.
These results highlight the necessity of careful preservation of primer nomenclature and sequence when reproducing an LSSP-PCR work to avoid confusion and allow comparison of results among different laboratories.
- Trypanosoma cruzi
- kDNA signatures
- Genetic diversity
Chagas disease is caused by the protozoan Trypanosoma cruzi and has a variable clinical course ranging from symptomless infection to severe chronic disease with cardiovascular and/or gastrointestinal involvement. The factors influencing this clinical variability have not yet been elucidated, but both host and parasite genetic factors are likely important.
The biological, biochemical, and genetic diversity of T. cruzi strains have long been recognized, and over the years, numerous approaches have been used to characterize the parasites, such as multilocus enzyme electrophoresis (MLEE) [1, 2], kinetoplast DNA restriction fragment length polymorphisms (kDNA RFLP) , random amplified polymorphic DNA (RAPD) [4–6], low-stringency single specific primer PCR (LSSP-PCR) , multilocus microsatellite typing (MLMT) [8–11], and many other methods such as PCR of the mini-exon and rDNA genes , .
The extensive efforts to comprehend the intraspecific genetic polymorphisms and population structure of T. cruzi are justified by the correlation between genetic variation and the biological properties of the parasite, including geographical distribution, host specificity, and the clinical outcome of infection. Additional understanding of the relationship between T. cruzi variation and clinical outcome will likely lead to a better understanding of the molecular epidemiology of Chagas disease –.
In this context, LSSP-PCR targeting the sequence polymorphisms within the variable regions of T. cruzi kDNA – or the intergenic regions of the spliced-leader gene  allows direct profiling of the parasites present in the tissues of chronically infected patients , .
LSSP-PCR is an extremely simple, PCR-based technique that permits the detection of single or multiple mutations in gene-sized DNA fragments. Briefly, purified DNA fragments are subjected to PCR using high concentrations of a single specific oligonucleotide primer, large amounts of Taq DNA polymerase, and a very low annealing temperature. Under these conditions, the primer hybridizes specifically to its complementary region and nonspecifically to multiple sites within the DNA fragments in a sequence-dependent manner, producing a heterogeneous set of reaction products that constitutes a unique “gene signature profile” . In fact, LSSP-PCR has been used in many organisms and fields of genetics and molecular medicine to obtain rapid, cheap and sensitive detection of mutations and sequence variations –.
The first study to use LSSP-PCR on T. cruzi was performed by Vago and collaborators using a primer called S35 as a driver , . This primer was originally designed to amplify minicircle variable region sequences of T. cruzi. Many subsequent works cite these studies to justify the use of the chosen methodology, although the primer sequences published do not exactly match what was previously used. Although the LSSP-PCR technique is highly reproducible under strict conditions, the complex banding pattern obtained can be significantly altered by even a single-base change in the target DNA , which suggests that different primer sequences may also produce substantially different results.
Here, we surveyed the literature to catalogue the primer sequences used for T. cruzi kDNA analysis by LSSP-PCR and references cited by many research groups to assess the impact of the primer sequence on the parasite profiles. Our results clearly demonstrated that LSSP-PCR is a sensible and reproducible profiling technique, but minimal modifications in the oligonucleotide sequences, used in the second round of PCR, can significantly change the kDNA signature of T. cruzi strains.
Parasites and DNA extraction
Three T. cruzi populations were used: the CL Brener clone (T. cruzi VI), which was harvested from the CL strain isolated from a Triatoma infestans specimen; the Col1.7G2 clone (T. cruzi I), which was obtained from the Colombian strain and originally isolated from the blood of a chronic cardiac patient in Colombia; and the JG strain (T. cruzi II), a monoclonal population isolated from a chagasic patient with megaesophagus in Minas Gerais, Brazil.
For T. cruzi DNA extraction, the epimastigote forms of each parasite population were grown in liver infusion tryptose (LIT) medium containing 10% calf serum at 27–28°C. Once the culture contained 108 epimastigote forms, the parasite cells were harvested, washed three times in sterile phosphate buffered saline and lysed in the presence of proteinase K overnight at 56°C. Standard DNA extraction was performed with phenol/chloroform as previously described .
Low-stringency single specific primer polymerase chain reaction (LSSP-PCR)
The kDNA signatures were obtained using a two-step procedure. The first step consisted of the specific PCR amplification of fragments of approximately 330 bp from variable regions of T. cruzi kDNA minicircle molecules. This reaction was carried out in a final volume of 20 μl and contained 1.5 mM MgCl2, Green Go Taq Reaction Buffer pH 8.5 (Promega, Madison, Wisconsin, USA), 250 μM dNTPs, primers 121 or S35 (5′-AAATAATGTACGGGKGAGATGCATGA-3′) and 122 (5′-GGTTCGATTGGGGTTGGTGTAATATA-3′) at 1.0 μM, 1.0 U of Go Taq DNA Polymerase (Promega) and 1.0 ng of purified DNA template. Amplification was performed in a PT100 thermocycler (MJ Research) using an initial denaturation step at 94°C for 5 min followed by 35 amplification cycles of an annealing step at 60°C, extension at 72°C and denaturation at 94°C, each for 1 min. The final extension step was extended to 10 min. Five microliters of PCR products was visualized on a silver-stained 6% polyacrylamide gel as previously described .
Sequence of primers designed to analyze three T . cruzi populations by LSSP-PCR
Sequence (5′ → 3′)
LSSP-PCR reactions were performed in triplicate, and only the consistent bands were taken into account to build a reproducible profile of each T. cruzi population. The multiband profiles obtained by LSSP-PCR of the T. cruzi populations were scored by eye, and each amplification band was numbered as present (1) or absent (0). These data were recorded on DNA-POP software , which calculates the proportion of shared bands among samples. Additionally, the distances among the profiles obtained with the different primers were calculated using the Nei and Li coefficient . Phylogenetic trees were constructed based on genetic distance matrices obtained through UPGMA or primer sequences using the Treecon software program version 1.3b .
Average ratio of the proportion of shared bands among samples using the different primers
Mean proportion of shared bands
The application of LSSP-PCR to the characterization of the 330 bp variable portion of kDNA minicircle molecules produces complex banding patterns that allow identification of clones and strains from cultures or experimentally infected tissues with good discriminatory capacity . Furthermore, the large genetic diversity in kDNA signatures obtained confirms the applicability of this method to genetic characterization studies on naturally infected vectors and humans , . Differential tissue distribution of diverse clones of T. cruzi have been demonstrated in infected mice  and humans , . LSSP-PCR is also useful to identify the differential distribution of T. cruzi populations associated with disease reactivation .
Despite being widely used for T. cruzi studies, LSSP-PCR reproducibility has been questioned due to its low-stringency nature. However, we have observed in our laboratory over our ten years of experience that LSSP-PCR patterns are highly reproducible even when the experiments are performed on separate days by different workers or when different thermocyclers and electrophoretic runs are used. To achieve this standardized amplification conditions both the enzyme and primer sources, and a good quality DNA at an adequate concentration must be consistently used . Herein, we confirmed the high reproducibility of the technique by performing reactions at least three times on different days and obtaining highly stable profiles using different primers.
LSSP-PCR uses a single primer that hybridizes with high specificity to its complementary sequence incorporated into the amplicons during the first round of PCR, and also with low specificity but in a sequence-dependent manner to multiple sites within the amplified fragment during the second round. Thus the reaction yields a large number of products that can be resolved by electrophoresis to give rise to a multiband DNA fragment signature that reflects the DNA template sequence . Changes as small as a single base mutation could drastically alter the multiband pattern, producing new signatures that are diagnostic of the specific alterations , . In this context, we asked whether the primer sequence might also influence the kDNA complex band in pattern.
To that end, we evaluated eight primer sequences previously used in the literature with similar names or citations. Our results demonstrated that sets of primers with related sequences, but differing from one another by 1 to 7 bases, resulted in different kDNA signatures for the same strain. In fact, alterations in primer sequence as small as a unique base mutation affected the kDNA multiband patterns, especially changes in the 3′or 5′ regions.
On the other hand, when we analyzed the profiles obtained with the same primer for the three evaluated strains, we saw that they were completely different from one another despite of the primer used. This is extremely important since the main goal of LSSP-PCR is to detect genetic polymorphisms in T. cruzi isolates belonging to distinct populations such as in different distant endemic areas or outbreaks or different clones within the same population with different tropisms, for example.
In conclusion we demonstrate here the importance of primer sequence when performing LSSP-PCR, at least for T. cruzi kDNA. This is especially relevant because different researchers frequently reproduce published techniques, but if the primer sequences are not faithful, comparisons of LSSP-PCR results among laboratories are not feasible, contributing to the false idea that LSSP-PCR is a technique poorly reproducible. Additionally, cases where oligonucleotide sequences are intentionally changed should be followed also by changes in the primers’ names. This would be highly useful for all laboratories working on kDNA signatures, while avoiding confusion and improving the comparison of LSSP-PCR patterns among laboratories.
This work was supported by FAPEMIG, CNPq (MCTI/CNPq/MS-SCTIE - Decit N° 40/2012) and CAPES founding agencies. We thank Neuza A. Rodrigues for expert technical assistance.
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