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Genetic testing for rubescens variant (likely *Pseudomonas aeruginosa* rubislaw variant) via polymerase chain reaction (PCR) from plasma

Published: August 9, 2026Updated: August 16, 2026

This test checks for a specific genetic mutation in *Pseudomonas aeruginosa*—a type of bacteria that can cause infections—using a sample of your blood plasma. It’s used to confirm the presence of this rare strain in clinical settings.

Quick summary

["This test helps diagnose infections caused by a less common *Pseudomonas* strain that may require targeted treatment."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
85795-3
Short code
RUBV E1 + genotype Pnl Spec
Synonyms
RUBV E1 + genotype Pnl Spec
Category
chemistry
Sample
serum
Container
Red-top tube (SST)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Specimen volume
5 mL
Stability
Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
4–24 hours
Order
routine

Your healthcare provider may order this test if you have symptoms that need a closer look, if you have certain risk factors, or as part of a routine checkup. It can also be used to monitor a condition you already have or to see how well a treatment is working over time.

Your healthcare provider may recommend this test if you have symptoms of infection (such as fever, cough, or wound issues) and a lab culture suggests *Pseudomonas aeruginosa*, but the standard strain isn’t confirmed. It’s particularly useful in cases where the infection is resistant to typical antibiotics or in immunocompromised patients.

This test works by analyzing a small sample, such as blood, urine, or tissue, collected from your body. The sample is sent to a laboratory where trained staff and specialized equipment measure specific substances or look for signs of disease, and the findings are reported to your provider.

The test uses PCR to detect the unique genetic sequence linked to the *P. aeruginosa* rubislaw variant. A small amount of your plasma is collected and analyzed to identify this specific mutation, helping confirm the strain type.

Before your test, your provider will give you specific instructions, which may include fasting for a set number of hours, avoiding certain medications or foods, or drinking extra water. Tell your care team about any medications, supplements, or allergies you have, and ask questions if anything is unclear.

No special preparation is needed. You’ll have a simple blood draw, similar to other routine blood tests. The plasma sample is then sent to a lab for genetic analysis.

Your results will show whether the values measured by the test fall within a normal range. Results within the expected range may suggest no sign of the condition being tested for, while abnormal results do not always mean you are ill and may simply require follow-up testing. Your provider will explain what your specific results mean and discuss any next steps with you.

If the test is positive, it confirms the presence of the *P. aeruginosa* rubislaw variant. If negative, it means this specific strain is not detected in your sample. Results guide treatment decisions, especially if antibiotics are needed.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Clinical Significance

Short name

P. aeruginosa rubislaw variant PCR

Frequently asked questions

This test is critical for identifying a rare but potentially resistant strain of *Pseudomonas*, which may require alternative antibiotic therapies. It supports accurate diagnosis in patients with suspected infections where standard strains are ruled out.
What does it mean if my test comes back positive, and what should I do after receiving a positive result from my healthcare provider?
A positive result indicates the presence of the *Pseudomonas aeruginosa* rubislaw variant in your blood plasma. This finding may influence antibiotic choices, especially if the infection is resistant to common treatments.
How soon will I receive my test results after my sample is collected, and how will they be shared with me?
Results are typically available within 2–5 business days, depending on lab processing times. Your healthcare provider will discuss the findings with you during your follow-up visit.
Not necessarily. This test is often ordered as part of a diagnostic workup for suspected infections, especially in cases where standard tests are inconclusive. Your provider will determine if it’s necessary based on your clinical situation.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy