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Journal of Clinical Microbiology, March 1999, p. 788-791, Vol. 37, No. 3
Pathobiology Institute
CICV/INTA1 and
Biotechnology Institute
CICV/INTA,
Received 22 June 1998/Returned for modification 18 August
1998/Accepted 3 November 1998
To study possible nosocomial transmission of multidrug-resistant
(MDR) Mycobacterium tuberculosis, strain types and other information on 24, mostly human immunodeficiency virus-positive patients, were collected. Isolates from 11 patients had identical IS6110 restriction fragment length polymorphism (RFLP)
patterns as well as spoligotype patterns and resistance profiles.
Noticeably, nine other isolates from related cases also exhibited
identical spoligotypes but slightly different RFLP patterns. These
results indicate that for some MDR strains, the evolutionary clock of IS6110 RFLP may run too fast for reliable interpretation of
strain typing results over a period of a few years.
The high tuberculosis (TB) morbidity
and mortality due to multidrug-resistant (MDR) TB have caused major
concern regarding the clinical management and prevention of
dissemination of the disease (10, 21). In several countries,
hospital outbreaks due to MDR TB were reported in association with
human immunodeficiency virus (HIV)-positive patients (6, 15,
16). The short intervals of only 4 to 16 weeks for HIV-positive
patients from diagnosis to death and the high transmission rates from
patients to health care providers (4) have posed an
important public health problem.
From 1989 on, the number of HIV-positive patients admitted for medical
treatment at the Dr. Cetrángolo Hospital (CH), located in the
northern suburbs of Buenos Aires, Argentina, began to increase (13). About 29% of the HIV-positive patients between 1992 and 1997 had one or more TB episodes. In this period, 19% of the TB cases were caused by MDR Mycobacterium tuberculosis strains.
The number of HIV-negative or noninvestigated patients with MDR TB remained steady and amounted to about 2% of the total number of TB
cases recorded in the hospital. Both HIV-positive and HIV-negative patients, with or without TB, received medical treatment as in- or
outpatients. However, all of them shared the same hospital facilities,
and most of the time, no effective containment was implemented to
prevent transmission of TB (13).
Restriction fragment length polymorphism (RFLP) typing of M. tuberculosis isolates has proven to be a useful tool to
investigate nosocomial outbreaks (4, 12, 15, 16).
Spoligotyping is a new method for typing M. tuberculosis
complex isolates. This method is based on the polymorphic nature of
short sequences which are interspersed among the conserved direct
repeats in the genomic direct repeat region (8, 9, 11). In
this study, the spoligotyping method, with a lower level of
discrimination than that of IS6110 RFLP typing
(5), was used as an additional tool to validate the
IS6110 RFLP typing results. In order to examine the
transmission of TB in our hospital, both methodologies were applied.
A total of 74 M. tuberculosis isolates were obtained from 58 patients. Thirty-six of these patients were coinfected with HIV. The
isolates were identified by AccuProbe tests for M. tuberculosis complex (GenProbe, San Diego, Calif.) and by standard
biochemical procedures (3). The susceptibility to
antituberculostatics was determined by the proportion method
(2) on Löwenstein-Jensen medium.
The 18 MDR TB patients among the HIV-negative patients had undergone
several episodes of anti-TB treatment while receiving medical treatment
in the hospital during an average period of 3 years (range, 2 to 5 years). In contrast, all HIV-positive patients infected with MDR TB had
a single episode of the disease, and they had an average survival
period of 5.8 months (range, 4 to 18 months) from the onset of the disease.
Seventy-four M. tuberculosis strains, isolated from 58 patients, were analyzed by RFLP typing and spoligotyping (11, 17, 18, 20). A group of 24 MDR TB patients, formed by 20 clustered patients and 4 nonclustered patients, was selected for further investigation. During alternate periods from 1992 to 1997, all of these
patients were hospitalized or received medical treatment as
outpatients, and they sometimes shared the same rooms. Figure 1 shows the RFLP and the spoligotyping
patterns as well as the drug resistance profiles of the MDR isolates
retrieved from the 20 patients, epidemiologically linked on the basis
of the strain typing results. In this figure, the data on
hospitalization period and HIV status of the patients also are
indicated.
The MDR strains from HIV-positive patients 1 to 11 (group 1) exhibited
identical RFLP patterns (type II) and spoligotype patterns (type B), as
well as the same resistance profiles. Since the patients concerned had
overlapping dates of admission to and/or release from the hospital and
they did not receive anti-TB treatment previously, it was highly likely
that a person-to-person transmission of MDR TB occurred among these patients.
The second group comprised nine MDR-TB strains isolated from patients
12 to 20. Although five highly similar RFLP patterns (type VIII) were
found in this group of nine strains, all had identical spoligotype
patterns (type C). The spoligotype patterns of the two described
outbreak strains were not found in the database comprising 285 spoligotype patterns of M. tuberculosis isolates from
Argentina. The five RFLP patterns distinguished among the nine isolates
related to the second outbreak were pattern VIII (five instances) and
the patterns VIIIa to VIIId (once each). RFLP pattern VIII was found in
five MDR TB isolates recovered from five HIV-positive patients
(patients 14, 15, and 18 to 20). Patient 20 was a health care worker at
the CH. The diagnosis of patients 14 and 15 occurred during 1993 to
1994 in a different hospital in Buenos Aires (H1). The RFLP pattern
VIIIa was found in an isolate from an HIV-negative person (patient 12)
who had a disease progression of 6 years, 1991 to 1997, and received
medical assistance in several hospitals including CH and H1 (1992 to
present). RFLP pattern type VIIIb (patient 13) was exhibited by two
isolates from one HIV-negative patient. These isolates were obtained at an interval of 1 year. All nine of these strains were resistant to
isoniazid, streptomycin, and rifampin, and some of the strains were
resistant also to pyrazinamide (patients 12 and 16 to 20) and
ethambutol (patients 12 and 17 to 20).
The third group of isolates comprised nonclustered patients 21 to 24. The RFLP patterns V, XIII, and XIV and the spoligotypes D, G, and E
were obtained from different MDR TB isolates from three HIV-negative
patients (patients 21, 22, and 24, respectively [data not shown]).
The patients had a disease progression of 3 years; they remained
positive by smear examination during this period although they were
receiving appropriate therapy. From the remaining HIV-negative patient
of the third group, patient 23, we obtained two isolates, at an
interval of 1 year (Fig. 2). The RFLP
patterns of these isolates differed in a single band of 1.5 kb, present
in the first isolate and absent in the second. Both strains had the
same spoligotype, F.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
The IS6110 Restriction Fragment Length
Polymorphism in Particular Multidrug-Resistant Mycobacterium
tuberculosis Strains May Evolve Too Fast for Reliable Use in
Outbreak Investigation
ABSTRACT
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FIG. 1.
Patient information, drug resistance profiles, and DNA
fingerprints of M. tuberculosis isolates related to the two
described TB outbreaks. (A) First outbreak; (B) second outbreak. The
column "Drug susc." indicates resistance to the drugs abbreviated
as follows: H, isoniazid; S, streptomycin; R, rifampin; E, ethambutol;
Z, pyrazinamide. ND, not determined. Dates are given as month/year.
*, period of patient's attendance at hospital H1; **, period of
patient's attendance at hospital H2.
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FIG. 2.
IS6110 RFLP patterns of two M. tuberculosis strains isolated from an HIV-negative patient
(patient 23) at an interval of 1 year. The RFLP pattern of the first
isolate, shown in lane A, contains one additional band at the 1.5-kb
position. Both strains exhibited the unique spoligotype F.
All isolates from the first group of patients (patients 1 to 11) had identical RFLP and spoligotype patterns as well as resistance profiles. In contrast, the isolates from the second group of patients (patients 12 to 20) had identical spoligotype patterns and highly similar, but not identical, RFLP patterns. The second outbreak strain provoked an outbreak in hospital H1 which also extended to other hospitals (15). Since we are quite sure that all of the isolates from the second group of patients are derived from a common ancestor within a period of 4 years, it is tempting to speculate on the instability of IS6110 RFLP in these strains with regard to bacterial factors and host-dependent influences. Also, the serial isolates recovered from MDR TB patient 23 showed a change in the RFLP pattern. Many reports have proved the stability of IS6110 RFLP during in vivo and in vitro (7, 19) incubation of M. tuberculosis strains. In contrast, this study indicates that particular strains, such as those causing the second outbreak, may have a higher mutation frequency. In a recent study by Yeh et al. (22), it was found that serial isolates from 14 (29%) of 49 patients showed changes in their DNA genotypes between isolates (12 in IS6110 RFLPs and 2 in polymorphic GC-rich sequence RFLPs). However, the changed IS6110 RFLPs were not related to the bacterial drug susceptibility or to the patient's HIV serum status or adherence to therapy. In contrast, in this study the instability of IS6110 RFLP found in the second outbreak strain may be somehow related to the selective pressure of a combination of drugs, as these drug-resistant patients were difficult to treat. On the other hand, the patient population in the first outbreak did not differ significantly from the patient group in the second microepidemic; however, we did not observe any alteration in the IS6110 RFLP of this strain. Therefore, the factor influencing the transposition frequency may be strain dependent. For instance, IS6110 elements in the second outbreak strain may be inserted in particular genomic promoter regions, resulting in a higher transposition pressure.
Spoligotyping, in addition to IS6110 RFLP, can be useful in determining more distant relationships among isolates. This has been proven for the first time in the disclosure of the Beijing genotype family of M. tuberculosis strains (20). One representative of this type of M. tuberculosis strain, the W variant, has been transmitted in New York hospitals since the early 1990s (14). In the study by Moss et al. (14), 8 of 128 (6.5%) W-type MDR TB strains isolated in New York City hospitals in 1992 also exhibited IS6110 RFLP patterns slightly different from those of the predominant type. Within a relatively short period (a few years), this W-type strain developed several lineages with slightly different, but recognizable, IS6110 RFLPs (1). In our current study, the relative instability of IS6110 RFLP was found in one of two MDR outbreak strains; however, not fewer than four of nine of the IS6110 RFLP patterns showed a minor and different alteration. Therefore, the transposition rate may be strongly related to the M. tuberculosis genotype represented.
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ACKNOWLEDGMENTS |
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The work in Argentina was supported by the Centro Argentino-Brasileño de Biotecnología (CABBIO), AC and MIR, and fellowships of CONICET, Argentina.
We acknowledge the help of Simone van de Pas and Kristin Kremer in preparing the manuscript.
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FOOTNOTES |
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* Corresponding author. Mailing address: National Institute of Public Health and the Environment, P.O. Box 1, 3720 BA Bilthoven, The Netherlands. Phone: 31-30-2742363. Fax: 31-30-2744414. E-mail: d.van.soolingen{at}rivm.nl.
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Journal of Clinical Microbiology, March 1999, p. 788-791, Vol. 37, No. 3
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Copyright © 1999, American Society for Microbiology. All rights reserved.
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