|LETTER TO EDITOR
|Year : 2021 | Volume
| Issue : 1 | Page : 101-103
Multicenter evaluation of xpert MTB/RIF ultra tests reporting detection of “Trace” of Mycobacterium tuberculosis DNA
Ester Mazzola1, Paola Dal Monte2, Claudio Piersimoni3, Annalisa Del Giudice4, Anna Camaggi5, Cristina Pedrotti6, Francesca Gurrieri7, Cristina Russo8, Claudio Farina9, Alessandra Lombardi10, Pietro Viggiani11, Elio Cenci12, Salvatore Nisticò13, Vanina Rognoni14, Eugenio Sala15, Paola Cichero16, Eliana Frizzera17, Vincenzina Monzillo18, Fulvia Morini19, Claudio Scarparo20, Emanuele Borroni16, Daniela M Cirillo16, Enrico Tortoli16
1 ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy
2 S. Orsola-Malpighi Polyclinic, Bologna, Italy
3 Ospedali Riuniti, Ancona, Italy
4 AO dei Colli, Naples, Italy
5 AOU Maggiore della Carità Hospital, Novara, Italy
6 APSS S. Chiara Hospital, Trento, Italy
7 ASST Spedali Civili, Brescia, Italy
8 Bambino Gesù Pediatric Hospital, Roma, Italy
9 Papa Giovanni XXIII Hospital, Bergamo, Italy
10 ASST Sacco Hospital, Milan, Italy
11 ASST della Valtellina e alto Lario, Sondalo, Italy
12 S. Maria della Misericordia Hospital, Perugia, Italy
13 Pugliese Ciaccio Hospital, Catanzaro, Italy
14 ASST Lodi, Lodi, Italy
15 S. Anna Hospital, Como, Italy
16 IRCCS S. Raffaele, Hospital, Milan, Italy
17 Centrale Hospital, Bolzano, Italy
18 IRCCS S. Matteo, Pavia, Italy
19 S. Gerardo Hospital, Monza, Italy
20 AULSS Serenissima, Mestre, Italy
|Date of Submission||29-Oct-2020|
|Date of Acceptance||30-Nov-2020|
|Date of Web Publication||28-Feb-2021|
Emerging Bacterial Pathogens Unit, San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Mazzola E, Monte PD, Piersimoni C, Giudice AD, Camaggi A, Pedrotti C, Gurrieri F, Russo C, Farina C, Lombardi A, Viggiani P, Cenci E, Nisticò S, Rognoni V, Sala E, Cichero P, Frizzera E, Monzillo V, Morini F, Scarparo C, Borroni E, Cirillo DM, Tortoli E. Multicenter evaluation of xpert MTB/RIF ultra tests reporting detection of “Trace” of Mycobacterium tuberculosis DNA. Int J Mycobacteriol 2021;10:101-3
|How to cite this URL:|
Mazzola E, Monte PD, Piersimoni C, Giudice AD, Camaggi A, Pedrotti C, Gurrieri F, Russo C, Farina C, Lombardi A, Viggiani P, Cenci E, Nisticò S, Rognoni V, Sala E, Cichero P, Frizzera E, Monzillo V, Morini F, Scarparo C, Borroni E, Cirillo DM, Tortoli E. Multicenter evaluation of xpert MTB/RIF ultra tests reporting detection of “Trace” of Mycobacterium tuberculosis DNA. Int J Mycobacteriol [serial online] 2021 [cited 2021 Apr 22];10:101-3. Available from: https://www.ijmyco.org/text.asp?2021/10/1/101/310503
The Xpert RIF/TB (Xpert) (Cepheid, Sunnyvale, CA, USA) test for the detection of Mycobacterium tuberculosis DNA in clinical specimens has been recently replaced by the new Xpert MTB/RIF Ultra (Ultra). A major difference with previous kit is the introduction of the new semi-quantitative category “trace” to report paucibacillary samples, with still detectable multicopy targets (IS6110 and/or IS1081) but without measurable amount of the single copy rpoB gene. This innovation, aiming to improve the sensitivity of the test, made the report of “trace” very frequent. uncertainty about its significance led to different interpretations of “trace” calls, including the suggestion to repeat the test.,,
Trying to make clarity on this point, we planned, in a low-prevalence high-resource setting, a multicenter study involving 21 laboratories performing routine Ultra test. The centers were requested, for each test resulting “trace,” to entry a number of microbiological and clinical information in an ad hoc questionnaire. The entries included the incidence of tuberculosis (TB) in the country of origin of the patient, the type of clinical sample, the results of microbiological tests (microscopy, culture in solid and liquid medium, identification), the presence of signs and symptoms of TB (cough, fever, night sweat, thoracic pain, and hemoptysis), and information about previous TB, contacts with TB patients, chest X-ray, anti-TB treatment, and clinical diagnosis.
The decision of repeating the tests scoring “trace” was left to single laboratories; they were requested instead to extend up to 56 days the incubation of MGIT (mycobacteria growth indicator tube) cultures still negative at 42 days. Liquid cultures become positive after 42 days were, however, less than 5%. The identification of mycobacteria grown in culture was performed by molecular tests. This study was retrospective and the patients' information was anonymized before analysis.
In a period of approximately 24 months, 32,835 tests Ultra were performed; of them, 29,882 were negative, 2,659 positive (any category including “trace”), and 305 invalid or error. Of positive tests, 317 (11.9%) scored “trace.”
Most of patients originated from high-incidence TB countries (29.5%) or from high–middle-incidence countries (27.0%), 4.9% from low–middle-incidence countries, and 38.6% from low-incidence countries. The proportion of patients with diagnosis of TB was significantly lower in patients from low-incidence countries (61.1%) in comparison with patients from other countries (89.2%–100%), P = 0.00001 (Chi-square test).
Out of the 122 tests that were repeated, a positive result, “trace” or higher, was reported in 86 (70.5%) cases such that confirming the common experience of the low repeatability of amplification results in deeply paucibacillary specimens.
Microbiological features of the samples scoring “trace” are reported in [Table 1].
To interpret the significance of tests flagged “trace” they were assigned to different categories. (a) Were regarded as true-positive (148, 46.7%) samples with growth of M. tuberculosis in culture (solid, liquid, or both). (b) Equally true positive were considered the samples without growth in culture but collected from patients (91, 28.7%) with definite or probable diagnosis, some of which were under TB treatment. (c) Were in contrast considered false-positive the samples from 25 patients (7.9%) with history of previous TB and from 53 patients (16.7%) with excluded or improbable diagnosis of TB. Our data confirm the well-known poor sensitivity of molecular diagnosis of TB in smear-negative specimens,, with 75.4% of our tests scoring “trace” being true positive and 24.6% false positive. The introduction of the semi-quantitative category “trace” allowed achieving a substantial increase of sensitivity versus a reasonable loss of specificity.
With the aim of excluding technical false-positive results, most of the cartridges detecting “trace” were frozen at − 80°C at the end of the test. Of them, the ones corresponding to samples negative in culture were retrospectively tested with a home-made PCR to detect, in the amplification cell of the cartridge, IS6110 and IS1081. At least one of the two insertion elements above was detected in all of them.
Although Ultra and Xpert as well are recommended for use with pulmonary specimens only, both revealed effective with extrapulmonary samples too., With biopsies and gastric aspirates in particular, the sensitivity of Ultra was 89% and 100%, respectively.
Several studies investigated sensitivity and specificity of Ultra, but none of them evaluated the significance of “trace.” Different approaches have been proposed to interpret the test flagged as “trace”: (a) to consider all of them negative, (b) to consider negative the tests from patients with history of TB (therefore attributing the positivity to previous disease), (c) to repeat the test on the same or a new sample, and (d) to validate the result obtained at repetition. Using rule (a), 148 tests from samples culture positive and 91 from patients with diagnosis and/or treatment of TB would be reclassified as negative. According to criterion (b), a decrease of specificity would be produced due to the grading as positive of 78 samples from patients not diagnosed to have TB. According to criterion (c), a decrease in sensitivity would be produced by the reclassification as negative of 66 tests from patients with diagnosis of TB. In any case, the cost is higher than the benefit.
In our opinion, the introduction of the semi-quantitative category “trace” represents an important improvement in comparison with the previous Xpert. The proportion of true-positive results clearly exceeds the false positives with the latter being easily avoidable by not performing the Ultra test for samples from patients with diagnosis of TB clinically excluded.
The detection of “trace” is anyway an objective finding confirmed by the presence in clinical specimen of amplicons specific for M. tuberculosis complex. This is understandable in patients with history of previous TB; in others, subclinical forms of TB are assumable. Should this be the case, an added value of the test would emerge.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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