Understanding and Interpreting Testing for Clostridium difficile

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Understanding and Interpreting Testing for Clostridium difficile

Postby roy » Wed Mar 21, 2018 5:27 am

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Understanding and Interpreting Testing for Clostridium difficile

Daniel A. Solomon Danny A. Milner, Jr

Open Forum Infectious Diseases, Volume 1, Issue 1, 1 March 2014, ofu007,https://doi.org/10.1093/ofid/ofu007

Published:

 

16 May 2014


 

Abstract

Understanding and interpreting the molecular tests for Clostridium difficile is challenging because there are several different types of assays and most laboratories combine multiple tests in order to assess for presence of disease. This learning unit demonstrates the basic principles of each test along with its strengths and weaknesses, and illustrates how the tests are used in clinical practice.

Topic:

 laboratoryclostridium difficile

Issue Section:

 BRIEF REPORTS

A 68-year-old woman received a dose of clindamycin prior to a routine dental procedure. The next day she developed watery diarrhea. Testing for Clostridium difficile is reported as follows: “Antigen” positive, “Toxin” negative, “PCR” pending.

How do you interpret these results, and why are there so many tests?

If you feel confused when trying to interpret tests for antibiotic-associated Clostridium difficile, rest assured you are not alone. There are multiple different assays, and most microbiology laboratories utilize a combination of these tests to optimize for sensitivity and specificity, control cost, and ensure a rapid turnaround time to avoid delays in therapy. This learning unit is designed to help (1) you understand the value and limitations of the various tests and (2) demonstrate how they are used together in clinical practice.

An essential concept to understand is that not all C difficile bacteria cause the prototypical diarrheal illness. If all C difficile resulted in disease, testing would be easy, and we would simply pick the test that performs best at detecting the presence of bacteria in the stool or the colon! Whether the bacteria causes clinical symptoms depends on both bacterial and host factors.

After adhering to the colonic mucosa, pathogenic C difficile releases 2 different toxins, toxin A and toxin B, that are directly cytotoxic to the colonic epithelial cells and cause indirect destruction by activating an inflammatory response in the host. However, not all strains of C difficile are equipped with the gene that produces toxin, and bacteria that do not produce toxin are not pathogenic [1]. Furthermore, even toxigenic strains of C difficile can live harmlessly in the colon without producing toxin. A complex balance of host factors, including immune function, exposure to medications such as antibiotics or immunosuppressants, and the host microbiome, mediates whether a toxigenic organism actively produces toxin [2]. Understanding this balance is particularly important because the prevalence of asymptomatic carriers–patients who have toxigenic C difficile but no toxin production–is rising, especially among patients in healthcare settings. Prospective screening studies have shown that up to 12%–14% [3, 4] of patients admitted to the hospital are colonized with toxigenic strains of C difficile, and that number may be even higher in long-term care facilities [5].

So when we test for C difficile what are we actually testing for? The presence of any bacteria, the presence of toxigenic bacteria, the presence of the toxin itself, or the activity of toxin on human cells? The answer is that it depends on the test you are sending. The four most commonly used tests are described below and summarized in Table 1.

Table 1.

Summary of laboratory tests for C difficile

Laboratory Test Sensitivity Specificity Time to results Comment ELISA for Antigen High Low Rapid Cannot distinguish between toxigenic and non-toxigenic strains ELISA for Toxin Low High Rapid Easy to perform; poor sensitivity PCR for toxigenic genes High High Rapid Cannot distinguish between active infection and asymptomatic carriage; more expensive than ELISA Cytotoxin Assay High High Slow (24-48hrs) Gold standard; requires tissue culture facility 


Test: Enzyme-linked immunosorbent assay (ELISA) for the glutamate dehydrogenase (GDH) antigen

What it tests for: The presence of C difficile organisms

Commonly known as the antigen test, this test uses antibodies to test for presence of the GDH enzyme, a protein preserved in all C difficile bacteria. It is an excellent screening test because it has sensitivity greater than 90%, a rapid turnaround time of 15–45 minutes, and it is inexpensive. However, this assay does not assess for toxin production, and because the GDH is present in all bacterial cells, it cannot even distinguish between toxigenic and non-toxigenic strains of the bacteria, so its specificity for active disease is poor [6].

Test: Polymerase chain reaction

What it tests for: The presence of toxigenic C difficile organisms

Polymerase chain reaction (PCR) is a highly sensitive laboratory technique that uses DNA primers to amplify copies of a targeted gene in a test sample. Clostridium difficile PCR is designed to amplify 2 different genes that are specific to toxigenic strains of C difficile: tcdB, which encodes for toxin B, and tcdC, which encodes for a toxin regulatory pathway. Clostridium difficile bacteria that do not produce toxin do not carry this gene, so it is specific for toxigenic strains of C difficile [7, 8].

A highly sensitive and specific test sounds ideal, so why don't we just use this test alone? First, it is relatively expensive. Given the frequency with which we test for C difficile, ELISA is a more cost-effective screening tool. Second, although it can distinguish between toxigenic and non-toxigenic strains of the bacteria, it still does not test for active toxin production, so it picks up asymptomatic carriers of disease. Moreover, in patients who have active C difficile and complete an adequate course of antibiotic therapy, the PCR often remains positive, so it is a challenging test to interpret in patients who have had C difficile in the past.

Test: ELISA for toxin

What it tests for: The presence of toxin

Using the same technique as the antigen test, this assay uses antibodies to detect the presence of C difficile toxin A or toxin B. The specificity of this test is nearly perfect, and it is therefore an excellent test to confirm active disease. Similar to the antigen test, this test can be performed quickly (15–45 minutes) and is inexpensive. The pitfall of the toxin assay is its low sensitivity (75%), so it results in a high rate of false negatives [9].

Test: Cytotoxin neutralization assay

What it tests for: Toxin activity

A functional assay that tests for cytopathic effect on human tissue cells, this is our gold standard laboratory test. The specimen is prepared by centrifuging liquid stool samples, harvesting the supernatant, and then inoculating different dilutions onto a monolayer of human foreskin cells in cell culture. The sample is then monitored at different time intervals for cytotoxicity. If cell disruption is observed, a C difficile antitoxin is added to a second cell culture with the patient sample and monitored for absence of cytotoxicity. The combination, cytotoxicity, and abrogation by antitoxin specific to C difficile, is diagnostic.

The unique value of this test is that it simulates the clinically important outcome: is there a toxic effect on human cells? It is highly specific and sensitive and, historically, was the preferred test for most laboratories. The downside of this test is that it takes a long time–clinicians may have to wait up to 48 hours before results are reported (or even longer over a weekend), which leads to delays in therapy and hospital workflow. Furthermore, performing and interpreting the test is work intensive, and it relies on the technique of laboratory technicians, introducing an element of user variability [10]. With the addition of cheaper and faster tests, the cytotoxin assay has fallen out of favor, but there is a still a role for its use in complicated cases when alternative tests are confusing or contradictory. In any situation in which a new testing modality is being validated, cytotoxicity assay should be used as the gold standard.

So how are these tests actually used in clinical practice? First, you should be careful to order C difficile testing only for patients with appropriate clinical history, which should include loose or poorly formed stools and/or diarrhea. Because each single test has individual pitfalls, most laboratories combine multiple tests to optimize sensitivity and specificity as well as ensure that results are delivered to clinicians in a timely manner. Below is a typical algorithm that combines several tests.

Step 1: ELISA for GDH antigen and ELISA for toxin (Figure 1) [11]


Depiction of combined Antigen and Toxin ELISA assay with test interpretation.

When used together, these tests provide a powerful screening test. They are inexpensive, rapid, and when their results are concordant they have both a high sensitivity and high specificity. If both tests are positive, the assay is reported as positive and no further tests are required. If both tests are negative, the assay is reported as negative and no further tests are required. Here is where it gets a bit complicated: if the antigen is positive, but the toxin is negative, the assay is reported out as indeterminate. There are several possible explanations for an indeterminate result:

The patient has non-toxigenic C difficile, and the toxin test was a true negative.

The patient is an asymptomatic carrier of toxigenic C difficile, and the toxin test was a true negative, but does not have active disease.

The patient has active toxigenic C difficile and the toxin test was a false negative.

In this case, we utilize a third test to act as a tie breaker.

Step 2: PCR

If the PCR is positive, we can determine with certainty that the patient has toxigenic C difficile, and the final interpretation is positive. It is important to recall that the PCR still does not distinguish between active disease and asymptomatic carriage. This point of distinction remains a challenge in the diagnosis of C difficile, and it serves as an important reminder that testing must be interpreted in the clinical context. If you suspect that the test is identifying asymptomatic carriage in your patient, it might be helpful to ask your laboratory to dig up the old cytotoxin assay to test for disease activity.

If you are still scratching your head, you may be tempted to abandon laboratory testing altogether and enlist the help of Cliff, the adorable 2-year-old beagle, who has been trained to sniff out toxigenic strains of C difficile [12]. Unfortunately, his effectiveness runs into the same pitfalls as the PCR–he cannot distinguish between active C difficile and asymptomatic colonization. There is not yet enough data for us to endorse the mythical combination of pet therapy and 4-legged C difficile testing as a scalable, cost-effective technique.

Note

Potential conflicts of interest. All authors: No reported conflicts.

All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

https://academic.oup.com/ofid/article/1 ... 07/2280544

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