Detection of a streptomycin-resistant Mycobacterium bovis strain through antitubercular drug susceptibility testing of Tunisian Mycobacterium tuberculosis complex isolates from cattle.

BACKGROUND: A rising isolation trend of drug-resistant M. bovis from human clinical cases is documented in the literature. Here we assessed Mycobacterium tuberculosis complex isolates from cattle for drug susceptibility by the gold standard agar proportion method and a simplified resazurin microtitre assay (d-REMA). A total of 38 M. tuberculosis complex strains, including M. bovis (n = 36) and M. caprae (n = 2) isolates, from cattle in Tunisia were tested against isoniazid, rifampin, streptomycin, ethambutol, kanamycin and pyrazinamide.
RESULTS: M. caprae isolates were found to be susceptible to all test drugs. All M. bovis strains were resistant to pyrazinamide, as expected. In addition, one M. bovis isolate showed high-level resistance to streptomycin (MIC > 500.0 μg/ml). Concordant results with the two methods were found. The most common target genes associated with streptomycin resistance, namely the rrs, rpsL and gidB genes, were DNA sequenced. A non-synonymous mutation at codon 43 (K43R) was found in the rpsL gene. To the best of our knowledge, this is the first report describing the isolation of a streptomycin-resistant M. bovis isolate from animal origin.
CONCLUSIONS: Antitubercular drug susceptibility testing of M. bovis isolates from animals should be performed in settings where bTB is endemic in order to estimate the magnitude of the risk of drug-resistant tuberculosis transmission to humans.

Background

The World Organization for Animal Health (OIE) has recognized bovine tuberculosis (bTB) as an important animal disease and zoonosis [1]. bTB causes significant economic losses to farmers due to livestock deaths, reduced productivity and restrictions for trading animals.

The main causal agents of bTB are Mycobacterium bovis and, to a lesser extent, Mycobacterium caprae, both members of the Mycobacterium tuberculosis complex. These pathogens may also cause tuberculosis in humans (hereafter referred to as zoonotic tuberculosis, zTB) although the true incidence of this disease in human beings is unknown [2-4]. An extensive meta-analysis found the proportion of zTB to be ≤1.4% in countries outside Africa and 2.8% on average in African countries [3]. The vast majority of cases were due to M. bovis and the contribution of cases due to M. caprae was not quantified. Substantial evidence suggests that zTB might be underestimated because of two major issues hindering understanding of the true burden of this disease: first, the absence of systematic surveillance for M. bovis and M. caprae as cause of tuberculosis in humans in all low-income and high tuberculosis burden countries where bTB is endemic; and second, the inability of laboratory procedures most commonly used to diagnose human tuberculosis to identify and differentiate these pathogens from M. tuberculosis, with the result that all cases may be assumed to be caused by M. tuberculosis [5].

Animal test-and-slaughter schemes have successfully reduced the prevalence of bTB in most industrialized countries. The situation is profoundly different in unindustrialized countries where the WHO, in conjunction with FAO and OIE, has classified bTB as a neglected zoonosis. In South Africa, as in other regions in Africa, the lack of bTB control programmes [6] makes communities with high HIV/AIDS infection rates and those living in close contact with infected animals or animal products more vulnerable to zTB [7, 8].

M. bovis has one of the broadest host ranges of any known zoonotic pathogen and is globally distributed [9]. The phylogenomic analysis of M. bovis genomes has recently revealed large-scale polymorphisms, which may contribute to the differential adaptability of the pathogen [10]. M. bovis is naturally resistant to pyrazinamide (PZA) [11], which is one of the first-line antibiotics used to treat tuberculosis in humans. The lack of prompt identification of M. bovis human cases may result in improper treatments and have lethal consequences [12]. Several studies have documented additional drug resistances in human M. bovis isolates over the last two decades, such as toward isoniazid (INH) [13, 14], streptomycin (STR) [15] or multiple drugs [16-19].

M. caprae, on the other hand, is evolutionarily older than M. bovis and accounts for a smaller burden of zTB. Moreover, it is not globally distributed but primarily restricted to European countries [3, 20, 21]. Its resistance against first-line drugs is rarely documented [22]. Nevertheless, M. caprae has received more attention in recent years, particularly due to the increasing number of M. caprae outbreaks in wild or domestic animals which pose a threat to human health [21].

While mycobacteria isolated from human cases are generally assessed for drug susceptibility, studies on antitubercular drug susceptibility testing of M. bovis and M. caprae isolated from animals are limited [23-29]. So far, M. bovis isolates from cattle resistant to INH and rifampin (RIF) have been documented in Italy [23] and Brazil [29], to the best of our knowledge. Monitoring of antitubercular drug resistance of M. bovis isolated from animals may thus contribute to reducing the risk of drug-resistant M. bovis transmission from animals to humans and among human beings.

In Tunisia, bTB is enzootic and the consumption of raw milk and unpasteurized dairy products is common. A previous study demonstrated that raw milk consumers are at high risk of being infected with M. bovis [30]. Numerous clinical cases of human extrapulmonary tuberculosis due to M. bovis have been recently documented in Tunisia [31, 32] and the consumption of unpasteurized dairy products has been indicated as the most likely source of transmission [33]. Implementation of effective and comprehensive strategies to control bTB and to prevent zTB are therefore of primary importance in the country.

In this study we assessed drug susceptibility of M. bovis and M. caprae isolates from cattle in Tunisia towards six antitubercular drugs – PZA, INH, RIF, ethambutol (EMB), STR and kanamycin (KAN) – by both the gold standard agar proportion method and the simplified resazurin microtitre assay (REMA), the dichotomous REMA (d-REMA) recently proposed by Marianelli and colleagues [27].

Methods

All experimental procedures here described were carried out at the Department of Food Safety, Nutrition and Public Animal Health of the Istituto Superiore di Sanità (ISS), (Italy).

M. tuberculosis complex strains

A total of 38 M. tuberculosis complex strains, including M. bovis (n = 36) and M. caprae (n = 2) previously isolated in Tunisia and molecular typed by spoligotyping and MIRU-VNTR analysis [34], were provided by the University of Sfax (Tunisia). The isolates were analysed for susceptibility to INH, RIF, STR, EMB, KAN and PZA at ISS.

Isolates were subcultured in Middlebrook 7H9 medium (Biolife, Italy) with 10% oleic acid-albumin-dextrose-catalase (OADC) enrichment (Becton Dickinson and Company) before being tested. To aid the dispersion of bacterial clumps, 3-mm glass beads were added to the tubes and bacterial suspensions were vigorous vortexed for 15 s. Any remaining large bacterial clumps were allowed to settle. Bacterial suspensions were then adjusted to match a 1.0 McFarland turbidity standard.

All M. bovis and M. caprae strains were isolated from lymph node and tissue samples showing tuberculosis-compatible lesions. Samples were collected at the abattoir during the postmortem inspection, in accordance with national laws.

d-REMA testing

The d-REMA test, based on Palomino and colleagues [35] and slightly modified by Marianelli and colleagues [27] by testing only two concentrations per drug – the cut-off value for drug resistance, R, and the cut-off value of REMA drug susceptibility, S – was used. The R values were determined in studies where REMA was validated against the gold standard method [35-40]. The test was carried out in triplicate in 96-well plates, as previously described [27]. Briefly, drug solutions were prepared at concentrations of 20 mg/ml (PZA; Sigma-Aldrich, UK) and 2 mg/ml in distilled water (INH, STR, EMB, and KAN; Sigma-Aldrich, UK) or methanol (RIF; Sigma-Aldrich, UK), filter sterilised, and frozen until used.

One hundred microliters of Middlebrook 7H9 medium supplemented with OADC was inoculated into each well. One hundred microliters of each bacterial suspension – previously adjusted to a 1.0 McFarland standard and then diluted 1:20 in the same medium – was then inoculated. The antitubercular drugs were subsequently added at two final concentrations, R and S: 0.1 (S) and 0.25 (R) μg/ml for INH, 0.25 (S) and 0.5 (R) μg/ml for RIF, 0.5 (S) and 1.0 (R) μg/ml for STR, 2.5 (S) and 3.125 μg/ml for EMB, 2.5 (S) and 3.125 (R) μg/ml for KAN and 100.0 (S) and 800.0 (R) μg/ml for PZA.

Plates were covered with lids, placed in a plastic bag and incubated at 37 °C for 7 days. Finally, 30 μl of freshly prepared 0.01% resazurin solution (Acros Organics, USA) was added to each well. The plates were incubated overnight at 37 °C and assessed for colour development. The d-REMA testing was repeated twice for those isolates showing either resistance or ambiguous chromatic change.

The drug-sensitive M. bovis ATCC 19210 (used as negative control) and two resistant M. avium strains (used as positive controls) – one resistant to EMB and one resistant to both INH and EMB – from the Italian bacteria collection were included in the study.

Agar proportion method in Middlebrook 7H11 medium

The agar proportion method was performed in Middlebrook 7H11 agar. The test was carried out according to the approved standard (M24A) for Susceptibility Testing of Mycobacteria, Nocardiae, and Other Aerobic Actinomycetes published by the Clinical and Laboratory Standards Institute (CLSI) [41]. Briefly, the turbidity of the inoculum was adjusted to match a 1.0 McFarland standard, and diluted 1:100 and 1:10,000. One hundred microliters of these solutions was then inoculated into 35 mm plates with and without the test drug. The test was carried out in duplicate. The following final critical drug concentrations were used: 0.2 μg/ml for INH; 1.0 μg/ml for RIF; 7.5 μg/ml for EMB; 2.0 μg/ml for STR; 6.0 μg/ml for KAN; and 100 μg/ml for PZA [40, 41]. After 3 weeks of incubation at 37 °C, the number of colony forming units (CFU) growing on the drug-containing medium was compared with those growing on the drug-free medium and expressed as a percentage of the latter. The isolate was considered resistant if the number of colonies on a medium containing an antimicrobial agent, relative to the number observed on a drug-free medium was ≥1%. Negative (M. bovis ATCC 19210) and positive (M. avium strains) controls were also included in the test. The test was repeated twice for isolates showing resistance.

Streptomycin MIC determination by REMA

MIC testing was to be performed only in case of drug resistance. Since M. bovis growth was observed only in the presence of STR and the control drug PZA (as expected) in both the d-REMA assay and agar proportion method (see Results), MIC testing was carried out only for STR. The test was performed in triplicate according to Palomino and colleagues [35]. Ten dilutions were tested (2.5, 5.0, 10.0, 20.0, 50.0, 100.0, 200.0, 300.0, 400.0 and 500.0 μg/ml). The MIC was defined as the lowest drug concentration that prevented resazurin colour change from blue to pink. The M. bovis ATCC control was also tested.

DNA sequencing

Sequencing, too, was to be performed only in case of drug resistance. Since resistance was observed only in M. bovis and towards STR and the control drug PZA (see Results), the most common target genes associated with resistance to STR encoding 16S rRNA (rrs), ribosomal protein S12 (rpsL) [42] and a 7-methylguanosine methyltransferase (gidB) [43], were investigated in the resistant M. bovis isolate and in three randomly selected STR-susceptible M. bovis isolates..

DNA was extracted from cultures using a commercial kit (InstaGene Matrix; Bio-Rad Laboratories, Italy). The whole rrs, rpsL and gidB genes were PCR amplified and sequenced. The reference sequence accession number (AC) NC_002945 of M. bovis AF2122/97 available at NCBI was used to design primers for the PCR amplification and sequencing of the rrs gene. The rpsL and gidB genes were PCR amplified and sequenced according to Feuerriegel and colleagues [44].

PCR products were analysed by 2% agarose gel electrophoresis, stained with GelRed Nucleic Acid Stain (Biotium Inc., Hayward, CA), purified by ExoSAP-IT PCR Product Cleanup (Affymetrix, CA) and sequenced by using PCR and, if required, sequencing primers. Sequences were analysed using the ABI Prism SeqScape Software, version 2.0 (Applied Biosystems, Foster City, CA). All consensus sequences generated were then compared to the published, drug-sensitive M. bovis AF2122/97 reference strain, to detect genetic variation. Mutations were confirmed through resequencing. To distinguish silent from missense mutations, amino acid sequences were theoretically deduced. PCR and DNA sequencing primers used, PCR conditions followed and size of the amplicons obtained are listed in Table 1.

Table 1

PCR and DNA sequencing primers

Primer	Sequence (5′ → 3′)	PCR conditionsa			Size (bp)	Reference
		D (s)	A (°C, s)	E (s)
rrs-F	CGT GGC CGT TTG TTT TGT CA	30	55, 30	90	1744	This study
rrs-R	AAG TCC GAG TGT TGC CTC AG
rrs-seq1	GAA GAA GCA CCG GCC AAC TA
rrs-seq2	TTG TAC CGG CCA TTG TAG CA
rpsL-F	ATG AGA CGA ATC GAG TTT GAG	30	55, 30	60	632	[44]
rpsL-R	GCT CAA GCG CAC CAT AAA CAA
gidB-F	CGC CGA GTC GTT GTG CT	30	55, 30	60	892	[44]
gidB-R	AGC CTG GCC CGA CCT TA

aEach PCR assay includes an initial denaturation step at 95 °C for 15 min to fully denature the template, followed by 35 cycles of denaturation, annealing and extension steps. D, denaturation time in s at 95 °C; A, annealing conditions (temperature and time in s); extension time in s

Results

Drug susceptibility

M. bovis and M. caprae isolates, as well as control strains, have been tested here against PZA, INH, RIF, EMB, STR and KAN by both the agar proportion method and d-REMA.

d-REMA results were obtained after 8 days of incubation. All M. bovis strains, including the M. bovis ATCC control, were resistant to PZA as expected. One out of 36 M. bovis isolates showed an additional drug resistance, the STR resistance as shown in Fig. 1, lines G–I. On the other hand, M. caprae isolates showed sensitivity against all drugs. The susceptibility of the M. bovis ATCC control to all test drugs (Fig. 1, lines J–L) was confirmed, as was the resistance of the two M. avium controls towards either INH or INH and ETB (Fig. 1, lines M–O). Results were confirmed through retesting the resistant isolate and controls by both drug susceptibility methods.

Fig. 1

Drug susceptibility profiles. Drug susceptibility to INH, RIF, STR, EMB and KAN by d-REMA. A–C, D–F, G–I: sample triplicates. J–L: M. bovis ATCC control in triplicates; M–O: M. avium control resistant to both INH and EMB in triplicates. 1–2: 0.1 (S) and 0.25 (R) μg/ml for INH; 3–4: 0.25 (S) and 0.5 (R) μg/ml for RIF; 5–6: 0.5 (S) and 1.0 (R) μg/ml for STR; 7–8: 2.5 (S) and 3.125 (R) μg/ml for EMB: 9–10: 2.5 (S) and 3.125 (R) μg/ml for KAN; (+) positive control containing no drug; (−) negative control containing uninoculated media

After 3 weeks of incubation, d-REMA results were confirmed by the agar proportion method.

The STR-resistant M. bovis isolate was subjected to further investigation, including STR MIC determination and DNA sequencing. The isolate showed resistance to all ten test dilutions: the blue-to-mauve colour change occurred at MIC values ranging from 2.5 to 500.0 μg/ml. We were thus unable to determine the STR MIC, as shown in Fig. 2, lines A–C. The M. bovis ATCC control, on the other hand, did not grow at any drug concentration tested (Fig. 2, lines D–F).

Fig. 2

STR MIC results. A–C STR-resistant M. bovis isolate in triplicates. D–F: M. bovis ATCC control in triplicates. 1–10: 2.5, 5.0, 10.0, 20.0, 50.0, 100.0, 200.0, 300.0, 400.0 and 500.0 μg/ml for STR; (+) positive control containing no drug; (−) negative control containing uninoculated media

DNA sequencing of drug target genes

We then PCR amplified and sequenced the most common target genes associated with resistance to STR, namely the rrs, rpsL and gidB genes, in the resistant M. bovis isolate and in three randomly selected STR-susceptible M. bovis isolates.

A consensus sequence for each gene was generated and compared to the reference strain M. bovis AF2122/97 available in GenBank to detect genetic variation. A non-synonymous mutation – nucleotide substitution AAG → AGG at codon 43 (mutation K43R) – was found only in the rpsL gene of the STR-resistant isolate. No mutations were detected in the other two target genes in either of the isolates.

Discussion

Tunisia is an endemic country for bTB. Despite the implementation of a national bTB control programme, many intensive farms belonging to the state or parastatal sector still do not meet sanitary standards for effective prophylaxis; others, belonging to private owners, also have scarce, if any, veterinary activity [45]. bTB therefore continues to be widespread in this country, mainly in the private sector, which owns more than 70% of the cattle livestock [46]. In Tunisia, the consumption of raw milk and unpasteurized dairy products is common. A previous study has shown that raw milk may spread M. bovis, putting consumers of raw milk or derivatives at high risk of being infected [30]. Although the exact contribution of M. bovis to the burden of zTB in Tunisia remains unknown, recent studies have indicated M. bovis as the main etiological agent of human extrapulmonary tuberculosis [31-33]. In consideration of the above, bTB represents a serious public health problem in Tunisia and effective disease control programmes have to be implemented urgently.

So far, no study has been conducted to estimate the risk of drug or multi-drug resistant bTB transmission to humans in Tunisia where M. bovis infection is endemic in livestock. On that account, we assessed at ISS the susceptibility of 36 M. bovis and two M. caprae isolates from Tunisia to six antibiotic drugs commonly administered to patients with tuberculosis. We detected STR resistance in one M. bovis isolate and characterized the nucleotide mutation associated with that resistance.

Drug susceptibility testing is rarely carried out on M. bovis and other Mycobacterium isolates of animal origin although bTB poses a serious threat to human health particularly in low-income and bTB endemic countries [3, 5]. Multidrug-resistant M. bovis outbreaks in humans have occurred, some with serious consequences [16, 18, 47]. M. bovis isolates from cattle with drug resistance towards either RIF or INH or towards both drugs have already been documented [23, 29]. Drug susceptibility surveillance of M. bovis from animals may therefore contribute to preventing the transmission of multidrug-resistant strains to humans and to controlling possible outbreaks.

Several techniques for testing mycobacterial drug susceptibility are available for M. tuberculosis and include the conventional assays [48] and the more rapid colorimetric [49] and molecular methods [50]. The WHO has recently recommended the use of colorimetric assays, which are highly sensitive, specific, rapid and inexpensive methods employing specific reagents to produce a change in colour [51].

Among these, REMA, an indirect method based on the reduction of the coloured dye resazurin added to liquid culture medium on a microtitre plate after exposure of mycobacterial strains to antituberculosis drugs in vitro, was successfully tested on human isolates of M. tuberculosis [35, 36, 39, 40]. The REMA plate method proposed by Palomino and colleagues [35] has recently been simplified by Marianelli and colleagues by testing only two concentrations per drug per isolate, the R and S cut-off values, the d-REMA assay [27]. Here, we used both d-REMA and the agar proportion method to assess the bovine isolates for drug susceptibility. We found agreement between the results from the two methods. M. caprae isolates were sensitive to all test drugs and M. bovis isolates were all PZA resistant, as expected. In addition, one M. bovis isolate showed high-level resistance to STR (MIC > 500.0 μg/ml). To our knowledge, this is the first study describing an STR-resistant M. bovis isolate of animal origin. We further investigated the STR resistance here observed by sequencing the most common STR target genes, namely the rrs, rpsL and gidB genes. We found a non-synonymous mutation AAG → AGG at codon 43 (K43R) in the rpsL gene.

The K43R substitution in the rpsL gene is the single most frequent mutation associated with high-level STR resistance in M. tuberculosis [42, 52]. It may explain why our M. bovis isolate still grew at the highest STR concentration tested (500.0 μg/ml), preventing us from determining the STR MIC. Although the most common target genes associated with resistance to STR have been analysed, we cannot exclude, however, that other mechanisms may be involved. The isolation from human clinical cases of highly STR-resistant M. tuberculosis strains carrying the K43R substitution is largely documented in the literature [53-55]. The isolation of STR monoresistant [15] and multidrug-resistant M. bovis isolates from humans [16-19] is also described. Drug- and multidrug-resistant tuberculosis is one of the major threats to human medicine. It leads to treatment failures and, in the worst cases, to untreatable infections that cause death.

A recent 15-year laboratory-based surveillance programme conducted in Mexico City on mycobacterial isolates from human clinical samples showed a rising trend of M. bovis isolates which caused a higher proportion of pulmonary tuberculosis than previously observed in that area [15]. Additionally, the authors described an increasing rate of primary STR monoresistance in M. bovis isolates from humans over time, perhaps as a result of STR usage in cattle [15].

Our results, coupled with the literature, suggest that overuse and misuse of antibiotics in cattle from bTB endemic areas may lead to the development of drug-resistant M. bovis strains which, consequently, put humans at risk for primary drug resistant zTB. More effective strategies to reduce antibiotic use in farm animals should therefore be implemented urgently.

Conclusions

We describe, for the first time, the detection of high-level STR resistance in M. bovis from animal origin. Our results suggest that antitubercular drug susceptibility testing of M. bovis isolates from animals should be performed in settings where bTB is endemic in order to estimate the magnitude of the risk of drug-resistant tuberculosis transmission to humans.