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In silico vs in vitro analysis of primer specificity for the detection of Gardnerella vaginalis, Atopobium vaginae and Lactobacillus spp.

Ana Henriques, Tatiana Cereija, António Machado and Nuno Cerca*

Author Affiliations

CEB-IBB, Centro de Engenharia Biológica - Instituto de Biotecnologia e Bioengenharia, Universidade do Minho, Campus de Gualtar, 4710-057, Braga, Portugal

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BMC Research Notes 2012, 5:637  doi:10.1186/1756-0500-5-637

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1756-0500/5/637


Received:4 September 2012
Accepted:14 November 2012
Published:15 November 2012

© 2012 Henriques et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Bacterial vaginosis (BV) is a common pathology of women in reproductive age that can lead to serious health complications, and is associated with shifts in the normal microflora from predominance of Lactobacillus spp. to a proliferation of other anaerobes such as G. vaginalis and A vaginae, which can be detected by PCR. The optimal PCR pathogen detection assay relies mainly on the specificity and sensitivity of the primers used.

Findings

Here we demonstrate that in silico analytical testing of primer specificity is not a synonym to in vitro analytical specificity by testing a range of published and newly designed primers with both techniques for the detection of BV-associated microorganisms.

Conclusions

By testing primer in vitro specificity with a sufficient range of bacterial strains, we were able to design primers with higher specificity and sensitivity. Also by comparing the results obtained for the newly designed primers with other previously published primers, we confirmed that in silico analysis is not sufficient to predict in vitro specificity. As such care must be taken when choosing the primers for a detection assay.

Keywords:
Primer specificity; Primer sensitivity; In silico primer testing; In vitro primer testing; G. vaginalis; A. vaginae; Lactobacillus spp.

Findings

Bacterial vaginosis (BV) is one of the most common vaginal disorders of women in reproductive age and is reported to be linked to increased risks of pre-term labor, HIV infection, postoperative infection and inflammatory pelvic disease [1]. It has been recognized that this pathology is caused by a shift in the microbial ecosystem colonizing the vagina of healthy women; from a Lactobacillus spp. dominated microbial population to the proliferation of other anaerobic microorganisms such as Gardnerella vaginalis, Atopobium vaginae, Mobiluncus spp. among others [2-4]. The etiology of BV remains unknown but a recent study reported that microbial biofilms, complex tridimensional structures that are known to be highly resistant to antimicrobial chemotherapy [5], may play a fundamental role in BV [6]. It has been described that G. vaginalis may account for 60 to 90% of the BV biofilm mass, while A. vaginae may account for 1 to 40% and Lactobacillus spp. for 1 to 5% [7]. While trying to confirm these findings, in biofilms from vaginal samples of Portuguese women, using a quantitative PCR approach, we came across some difficulties related with primer specificity, despite the increase in the number of published papers regarding the use of molecular tools, such as PCR, for the detection of BV-associated microorganism [8-11]. In order to assess the usefulness of the primers for the detection of our target microorganisms used we decided to test the analytical specificity (% of non-target organisms detected) and sensitivity (% of target organisms detected) of the primers used. Being a quick and inexpensive method, in silico analysis of primer specificity and sensitibity has been widely used. However this technique poses some limitations, already described for other applications, namelly significant differences between the in silico prediction for primer specificity/sensitivity and the actual in vitro results [8,9].

To our knowledge the analytical comparison of primer in silico and in vitro specificity/sensitivity for primers designed for the detection of BV-associated microorganisms has not been studied and with the increase in the use of molecular techniques for the study of BV such information becomes relevant.

We began by selecting primers previously described in the literature specific for Lactobacillus spp. [12,13], G. vaginalis[8,14] and A. vaginae[11,15]. The reported primers specificity was mainly determined by in silico analysis using sequence alignment such as BLAST [16]. Whenever in vitro specificity was reported, often published details of such specificity determinations were scarce. When confirming primer specificity, using a few collection strains, and the same conditions reported in the literature, we found that some in silico primer specificity did not correspond to the in vitro specificity (data not shown). To address this, we selected the best primers that we could find in the literature and repeated the in silico specificity analysis using ProbeMatch [17]. We also designed new primers (using VectorNTI, version 11.0 and sequences available in the GeneBank databases) (Table 1).

Table 1. In silico analysis of primer specificity of the primers used in this study

During in silico analysis of the selected primers, we found two main problems: (i) the selected published primers for G. vaginalis were designed for the 16S rRNA-encoding DNA and 23S rRNA-encoding DNA intergenic region [8,14] and there are no available databases which include this region that could be used for the in silico analysis; (ii) some of the primers for A. vaginae and Lactobacillus spp. showed low sensitivity in silico. In order to confirm our in silico analysis, in vitro testing of primer specificity was performed, initially with 3 strains of each target (G.vaginalis, A. vaginae and Lactobacillus spp., details in Additional file 1: Table S1), using DyNAnzyme PCR Master Mix 2x (Finnenzymes, Thermo Scientific, Finland). The initial amplification conditions comprised 40 cycles with the following temperatures each cycle: 94°C for 30 seconds, 60°C for 30 seconds, and 72°C for 1 minute. Amplified products were analysed in a 1% agarose gel and stained with Midori Green nucleic acid dye (Nippon Genetics Europe GmbH, Germany). Results of the PCR at 60°C showed low sensitivity and specificity for Lactobacillus spp. primers, and as such we decided to optimize this detection with the aim of obtaining a greater specificity. The annealing temperature was then adjusted to 62°C, and the number of strains increased to a total of 12 target strains (per group) and up to 34 non-target strains (including Pseudomonas aeruginosa, Staphylococcus epidermidis, Streptococcus agalactiae, Enterococcus faecalis, Escherichia coli and Staphylococcus cohnii) (Table 2). We used different annealing temperatures, in order to observe the effect that this variation would have in primer sensitivity and specificity, which is information that could facilitate the use of these primers in combination (for multiplex PCR assays for example) for quick and effective PCR detection assay.

Additional file 1. Table S1. Description of name and origin of strains used in this study for the in vitro testing of primer specificity and sensitivity.

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Table 2. In vitro analysis of primer specificity of the primers used in this study

When comparing in silico predictions against in vitro results, we found considerable differences in specificity and sensitivity values. Despite the fact that theoretical melting temperature of the A. vaginae primers designed in this study was 60°C, at this temperature primer specificity was very low. Only with higher annealing temperature (66°C), we could achieve reasonable specificity (91.2%) and sensitivity (100%) values. The primers for Lactobacillus spp. were the ones with the lowest specificity. Of note, some of the primers previously reported as specific were found to be non-specific (0%) despite an in silico prediction of 81% of specificity. A lower specificity was expected since these primers were designed for the identification of a genus, which results in a higher inherent genetic variability than primers for the identification a species. However, the accentuated decrease between in silico and in vitro primer specificity was not anticipated. The primers described by Pepin et al. (10) revealed the highest specificity for A. vaginae (Table 2), probably due to the previous in vitro specificity analysis against at least 20 isolates that was performed by the authors [10]. Although A. vaginae primers demonstrated an overall lower specificity, they proved to be highly sensitive, being able to detect all the targets used (Table 2). It is worth to note that the primer designed for this study for the detection of G. vaginalis proved to have a higher sensitivity than that of published primers, and that contrary to the results obtained for the other target microorganisms, the in silico prediction of sensitivity and specificity was similar to the in vitro results obtained.

It is interesting to note that in silico analysis for primers specificity was not a good predictor of in vitro primer specificity, something already reported by other researchers [8,9], in silico predictions do not take into account the chemical reactions/limitations that can occur in the PCR tube and as such cannot truly approximate experimental events. In most articles describing the detection of BV-associated microorganisms the primer specificity testing is described as being performed in silico[10-15]. This work confirms the importance of proper in vitro analysis of primer specificity, as the in silico analysis can sometimes underestimate the possible cross reaction with non-sense strains or species which are not yet sequenced, as is the case of most of the strains present in vaginal environment. Furthermore, the new G. vaginalis and A. vaginae primers reported here have high in vitro specificity, demonstrating its potential for use in clinical microbiology.

Competing interests

The authors declare that they have no competing interests in this work. The funding organization did not play any role in the design of the experiments and article drafting.

Authors’ contributions

This an original work that has not been published elsewhere. The experiments were designed by NC and AH, the in vitro analysis was done by AH and TC, primer design and in silico analysis was done by AM. AH drafted the manuscript, and all authors critically reviewed and agreed with the present manuscript.

Acknowledgements

This work was supported by European Union funds (FEDER/COMPETE) and by national funds (FCT) under the project with reference FCOMP-01-0124-FEDER-008991 (PTDC/BIA-MIC/098228/2008). AM acknowledges the FCT individual fellowship SFRH/BD/62375/2009.

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