# 20.109(S14):Diagnostic primer design (Day2)

(diff) ←Older revision | Current revision (diff) | Newer revision→ (diff)

20.109(S14): Laboratory Fundamentals of Biological Engineering

## Protocols

### Part 1: Writing Across the Curriculum (WAC) session

During the enzymatic incubation, you will have an introductory session with our writing faculty.

### Part 2: Explore existing microsporidia-specific primers

The reference primer set that you will use to amplify microsporidia DNA comes from a 1999 paper from Franzen lab (link). These primers anneal to the 5' end of the small subunit (SSU) rRNA gene.

Primer name Direction Sequence (5'-->3')
V1 Forward CACCAGGTTGATTCTGCCTGAC
PMP2 Reverse CCTCTCCGGAACCAAACCCTG

First, let's assess some basic properties of these primers. Then we'll calculate expected product sizes for several different species of microsporidia.

#### Primer properties

Integrated DNA Technologies, or IDT, sells DNA primers and offers free tools for analyzing them.

You'll also access the National Center for Biotechnology Information (NCBI), a resource that we have used in many different 20.109 modules. Here, you will rely on it for sequence information.

1. At the IDT website, under the heading SciTools, choose OligoAnalyzer.
2. Keeping the default settings, press the Analyze button and note the resulting length, G/C content, and melting temperature (Tm) of each primer.
• Based on our discussion so far of PCR, are the primer lengths sufficient for a reasonable expectation of sequence uniqueness?
• Are the G/C contents in the appropriate range?
3. Now measure and note the Tm with the following settings: [oligo] = 0.2 μM, monovalent salt = 10 mM, divalent salt = 2 mM.
4. For this amplification, the annealing temperature (Ta) we are using is 58 °C. Which salt conditions best match this Ta and why?
5. Using the appropriate salt conditions, do a self-dimer analysis on each primer and a hetero-dimer analysis of the two primers together.
• It should not be energetically favorable for the primer to dimerize. The delta G for dimers should at least be greater than -9 , and ideally be greater than -5 kcal/mol.
• Annealing of one primer to the 3' end of another primer (or itself) is particularly bad. Why?
6. Having a G or C (a "GC clamp") at the 3' end of each primer helps promote complete binding due to the relatively greater hydrogen bonding for GC versus AT. Note that 1-2 bases is best, while 3 or more consecutive GC bases might promote non-specific binding. Do the primers above have such clamps?
7. It's best to avoid long stretches of a single base, or even a single type of base (purine or pyrimidine). Are the primers above relatively random or do they break this rule?
8. Finally, you would like to test whether these primers bind to a unique site in the genome or instead are promiscuous binders.
• Head over to nucleotide BLAST and copy your first primer into the "Query" box.
• Under Choose Search SetOrganism, start typing Vittaforma corneae; the name should auto-complete as you type.
• Under Algorithm Parameters, be sure "Automatically adjust parameters for short input sequences" is checked.
• Click BLAST and wait for your results.
• The forward primer should identically match the gene that codes for small subunit RNA for its entire length. Find the first gene that is not for SSU rRNA. What is the name of the gene? How many basepairs does the match encompass? Do you expect this annealing site to be a major competitor in your PCR?
• Repeat for the reverse primer.
9. When you design your own primers below, you can perform all these same checks on them.

#### Product sizes

1. One microsporidia species that can infect humans is called Encephalitozoon hellem, or E hellem. Find the NCBI accession number AF118143, which shows the SSU rRNA gene sequence for one strain of E hellem.
2. To continue with the exercise below, you might find it convenient to paste this sequence intoApE (A plasmid Editor, created by M. Wayne Davis at the University of Utah), which is found on your desktop.
• Look for the forward primer in this sequence. At what basepair do you find it?
• Within ApE, you can use command-F to find matches to sequence fragments.
• Note: V1-PMP2 are designed to broadly target many different species of microsporidia. As you plan your search strategy, keep in mind that any particular strain might have some mismatches to the primer sequence.
• Look for the reverse primer. (What will you have to do to the primer sequence to make it match the coding strand DNA?) At what basepair do you find it?
• Does the sequence have any mismatches to the primer? How many? What about E hellem accession number AF039229?
• What is the total product size expected for each E hellem strain? Are they the same?
3. Another species of interest is Vittaforma corneae, or V corneae. Repeat the exercise above for accession number JX049115.
• Note: The above accession number will lead you to a partial sequence! For design purposes later, you may need to find the complete sequence.
• Is the product size the same as for E hellem? If different, by how much?
• On a typical DNA gel, do you expect to be able to tell apart fragments of this size? If you have no experience with such gels, talk with the teaching faculty.
4. Search on your own for the rRNA gene sequence of the species cuniculi, another member of the genus Encephalitozoon. What product size do you find here?

### Part 3: Design novel microsporidia-specific primers

Sign up for the specificity or sensitivity challenge in the table on today's Talk page. Half of the class should try each challenge. You and your partner are designing one primer set together. You may design primers either to the SSU rRNA gene or the polar tube protein. An accession number for the latter to help get you started is AY171240. Shoot for a Tm of 58 ± 1 if possible.

In diagnostics, a two-stage identification system is often used. First, clinicians look for a quick yes/no -- is the organism there? In this stage, sensitivity is prioritized: one would like as few false negatives as possible, even if that means some false positives come up, because the latter can always be excluded in the second stage. Next, clinicians would like to know precisely what species has infected the patient, for both acute treatment of that patient and long-term tracking of infection prevalence across patients. In this stage, specificity is prioritized.

Professor Runstadler takes a very similar approach to flu screening in his lab. All bird samples are broadly checked for flu infection using primers against highly conserved regions of the virus. Samples that come up positive are screened for human-pathogenic strains such as H2, specifically against the "2" version of hemagglutinin. These samples must be handled with extra precautions to avoid infection of lab personnel.

#### Important note for both challenges

As you work, remember to keep in mind that the forward and reverse primer bind to different strands of DNA. You may find it easiest to work with only the coding strand sequence at first, and then take the complement (for one of the primers -- which one?) during the very last step of your design. When you are happy with your primers, please add them to the table on the "Talk" page, with each primer written from 5' to 3' -- this direction is the standard way that primers are written on an order form.

Feel free to use free software to help guide your design such as that from NCBI or the P3 program.

#### Specificity challenge

Assume that the V1/PMP2 primer set is appropriate for a first-stage diagnostic. Design a second-stage diagnostic that can specifically identify V corneae from a complex mixture. In reality, your complex mixture will include only one other strain of microsporidia, E hellem, which you want to avoid amplifying. You will test your primer set against each organism separately and a mixture of the two, and compare your results with the default primer set.

Occasionally, co-infection with multiple strains of an organism may occur. If you are able to design primers that better resolve V corneae and E hellem when they coexist in one solution -- that is, the expected products differ by more than 40 bp -- this could also be an interesting approach to the challenge!

#### Sensitivity challenge

This challenge will require somewhat more luck than the one above. Your goal is to design primers that can detect a lower DNA concentration than V1-PMP2 can. The default primer set reliably amplifies less than 1 ng in a 50 μL reaction, which is near the lower limit expected for basic PCR. You might be able to improve the amplification somewhat by designing primers that vary according to the parameters you explored in Part 2. These days, folks often ask computers to design several primers for them, and then empirically test which primer set works best. Today we ask you to take the role of the computer and see how you stack up.

For the purposes of this exercise, you should design broadly functional primers that can target either E hellem or V corneae. Note that the latter species produces a substantial amount of off-target PCR product (incorrect size) in addition to the expected PCR product when using V1-PMP2. Thus, the primers you design might end up improving a specificity of sorts -- not for targeting a particular species, but for targeting a particular site in the genome (of one or more species).