BioMed Research International

BioMed Research International / 2018 / Article
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Advances in Emerging and Neglected Infectious Diseases 2018

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Research Article | Open Access

Volume 2018 |Article ID 7314054 |

D. Kosova-Maali, E. Bergeron, Y. Maali, T. Durand, J. Gonzalez, D. Mouniée, H. Sandoval Trujillo, P. Boiron, M.-C. Salinas-Carmona, V. Rodriguez-Nava, "High Intraspecific Genetic Diversity of Nocardia brasiliensis, a Pathogen Responsible for Cutaneous Nocardiosis Found in France: Phylogenetic Relationships by Using sod and hsp65 Genes", BioMed Research International, vol. 2018, Article ID 7314054, 10 pages, 2018.

High Intraspecific Genetic Diversity of Nocardia brasiliensis, a Pathogen Responsible for Cutaneous Nocardiosis Found in France: Phylogenetic Relationships by Using sod and hsp65 Genes

Academic Editor: Charles Spencer
Received09 Feb 2018
Accepted31 Mar 2018
Published20 May 2018


This study aims at genetic characterization and phylogenetic relationships of Nocardia brasiliensis focusing by using housekeeping rrs, hsp65, and sodA genes. N. brasiliensis is the species responsible for 80% of cases of actinomycetoma, one form of cutaneous nocardiosis which occurs mainly in tropical regions reaching immunocompetent patients in which the disease can lead to amputation. We analyze 36 indigenous cases of N. brasiliensis that happened in France. Phylogenetic analysis targeting rrs gene showed no robustness at phylogenetic nodes level. However, the use of a concatenation of hsp65 and sodA genes showed that the tested strains surprisingly ranked in 3 well-defined genotypes. Genotypes 2 and 3 were phylogenetically closer to each other and both diverged from genotype 1 sustained by a high bootstrap of 81%. This last genotype hosts all the cases of pulmonary forms (3), the sole cerebral form, and almost all the cases of immunocompromised patients (3 out of 4). Moreover, excepting one of them, all the strains belonging to this group present a susceptibility to imipenem which is not the case in the other genotypes that rarely count among them strains being susceptible to this drug. The haplotype diversity (Hd) of hsp65 (0.927) and sodA (0.885) genes was higher than that of rrs (0.824). For this gene, we obtained 16 polymorphic sites whereas, for hsp65 and sodA genes, up to 27 and 29 were identified, respectively. This study reveals that these two genes have an important genetic discriminatory power for the evaluation of the intraspecies genetic variability of N. brasiliensis and they may be useful for identification purposes at species level. This study also reveals the possible existence of a new species harbored by genotype 1.

1. Introduction

Nocardia is a genus belonging to the aerobic actinomycetes group of bacteria which are Gram-positive bacilli and showing branching filamentous forms [1]. They are saprophytic ubiquitous bacteria which can be found in several environments such as fresh water and saltwater, soil, dust, decaying vegetation, and decaying fecal deposits from animals [1]. Nevertheless, these environmental bacteria can be opportunistic pathogens and lead to human infectious diseases called “nocardiosis” [2]. Nocardiosis can be discriminated into two groups: invasive infection, mainly caused by N. asteroides, presenting commonly as pneumonia in patients who are immunocompromised, have underlying chronic lung disease, and are with a possible dissemination to other organs [3], and cutaneous infection via a cut or abraded skin, which can be manifest clinically as (i) abscess and cellulitis, (ii) lymphangitis, (iii) skin infection secondary to dissemination, and (iv) actinomycetoma. This latter group is the most amazing infection due to their severity characterized by the presence of tumefaction, subcutaneous nodules, destructive granulomata, fistulas, and pus [2, 4].

N. brasiliensis is the species isolated from the majority (approximately 80%) of cases of cutaneous nocardiosis, especially in actinomycetoma [2]. This species is more commonly isolated in areas with tropical or subtropical climates such as South America, Asia, and Africa. Due to false diagnosis, rural lifestyles, and poor access to care in these countries, N. brasiliensis nocardiosis constitutes a real public health problem that can lead, in the absence of treatment, to amputations and death in young populations. On the basis of epidemiological surveys conducted in France, the number of cases of nocardiosis between 2000 and 2007 according to the French Nocardiosis Observatory (OFN) was 607 with N. farcinica and N. nova being the most frequent species [5]. However, no data currently exists on the phylogenetic relationships between the indigenous N. brasiliensis strains of tropical origin and native strains isolated in France. Routine genus/species identification of Nocardia was based on macroscopic, microscopic, and biochemical characteristics. The methods described by Boiron et al. [6] were used to determine the decomposition of adenine, casein, hypoxanthine, tyrosine, and xanthine. In addition to the phenotype-based methods, species-level identification is mainly genetically based, nowadays. Classically, 16S rRNA (rrs) gene sequencing is generally used for the species-level identification [7, 8], but it fails to discriminate among some species of Nocardia because it does not have enough polymorphism to differentiate them at the species level. Multilocus sequence analysis (MLSA) using concatenated sequences of several housekeeping genes such as superoxide dismutase A (sodA) and heat shock protein 65 (hsp65) has been increasingly used to provide higher accuracy and discriminatory power in the molecular identification of Nocardia spp. [9, 10]. Indeed, a recent study seeking to identify new molecular targets shows that the polymorphism observed in the sodA gene sequence contains variable regions that allow the discrimination of closely related Nocardia species [9].

The aim of the present study was to perform a genetic characterization and assess the phylogenetic relationships of Nocardia brasiliensis focusing on using housekeeping rrs, hsp65, and sodA genes, for 36 autochthonous N. brasiliensis strains isolated in France and analyzed by the OFN between 2002 and 2012. Phenotypic characterization was also conducted by assessing antimicrobial resistance profiles, metabolic profiles, and culture condition.

2. Materials and Methods

2.1. Bacterial Strains and Culture Media

A collection of 36 human clinical strains of N. brasiliensis was studied (Table 1). All strains were identified as such, at species level by the French Nocardiosis Observatory (OFN) by genetic approach. Moreover, six Nocardia reference strains belonging to N. brasiliensis clade [9] were also used: N. brasiliensis ATCC 19296 (unknown), N. altamirensis DSM 44997 (karstic cave), N. boironii DSM 101696 (pus sample), N. iowensis DSM 45197 (garden soil), N. tenerifensis DSM 44704 (rhizosphere), and N. vulneris DSM 45737 (human leg wound). Prior to the assays, strains were cultured 72 hours in Bennett medium (made in the laboratory) aerobically at 37°C.

Sample dateNature of samplingPatient recordImmunosuppressedGenotype  
TropismPristinamycinImipenemAmikacinTrimethoprim + sulfamethoxazole

04/2002Intraoperative tissue02.56NoG3CutaneousRRSS
12/2003Pus from cutaneous thigh abscess04.21YesG1CutaneousRSSS
2004Pus from cutaneous abscess04.101NoG3CutaneousRRSS
07/2005Expectoration then LBA05.64YesG1LungRSSS
01/2005Skin biopsy05.12NoG1CutaneousRSSS
07/2005Phalanx biopsy05.63NoG3CutaneousRRSS
2007Cutaneous abscess07.168NoG3CutaneousRRSS
10/2008Wound of forehead08.178NoG3CutaneousRSSS
11/2008Subcutaneous abscess08.188NoG3SubcutaneousRRSS
10/2008Elbow abscess2985NoG3CutaneousRRSS
03/2009Pus of leg abscess09.71NoG2CutaneousRSSS
04/2009Bronchial aspiration09.106NoG1LungRSSS
10/2009Bronchial aspiration09.244YesG1LungRSSS
12/2009Finger skin09.280NoG3CutaneousRRSS
10/2009Pus from the lip10.16NoG3CutaneousRRSS
02/2010Finger abscess10.35NoG2CutaneousRRSS
05/2010Hand abscess10.82NoG3CutaneousRRSS
05/2010Toe abscess10.93YesG3CutaneousRRSS
09/2010Leg wound10.146NoG3CutaneousRRSS
11/2010Pus finger10.180NoG3CutaneousRRSS
11/2010Leg wound12786NoG2CutaneousRRSS
07/2010Sepsis hand45762NoG3CutaneousRRSS
05/2011Cutaneous abscess11.73NoG1CutaneousRSSS
05/2011Hand wound11.80NoG1CutaneousRSSS
2011Thigh abscess11.140NoG2CutaneousRRSS
09/2011Knee wound11.151NoG3CutaneousRRSS
2011Hand wound11.172NoG3CutaneousRRSS
12/2011Cutaneous abscess11.189NoG3CutaneousRRSS
02/2012Cutaneous abscess12.28NoG3CutaneousRRSS

2.2. Growth Test on Culture Media

From 0.5 McF bacterial suspension, bacterial growth was evaluated on three culture media: (i) bromocresol purple (BCP) (Biomérieux, Marcy l’étoile), (ii) Bennett (made in the laboratory), and (iii) Middlebrook (Biomérieux, Marcy l’étoile). One hundred microliters from bacterial suspension standardized was inoculated on the different plate of culture media. The plates were incubated at 37°C and the observations were performed at 48, 72, and 96 hours.

2.3. Antimicrobial Susceptibility

The susceptibility of the isolates to different antimicrobials was determined by disk diffusion method with a panel of 31 antibiotics (Biorad, Marnes-la-Coquette France) on Muller Hinton E medium (Biomérieux, Marcy l’étoile, France). Susceptibility testing was done with amikacin 30 μg, gentamycin 15 μg, tobramycin 10 μg, ciprofloxacin 5 μg, levofloxacin 5 μg, moxifloxacin 5 μg, minocycline 30 μg, doxycycline 30 μg, tigecycline 15 μg, cefotaxime 30 μg, ceftriaxone 30 μg, cefepime 30 μg, cefuroxime 30 μg, amoxicillin 25 μg, amoxicillin + clavulanic acid 20/10 μg, ampicillin 10 μg, ertapenem 10 μg, meropenem 10 μg, imipenem 10 μg, vancomycin 30 μg, pristinamycin 15 μg, erythromycin 15 μg, trimethoprim + sulfamethoxazole 1.25/23.75 μg, rifampicin 30 μg, and linezolid 30 μg.

From visible colonies, bacterial suspension was done in sterile water, using a cotton swab to obtain a concentration of 0.5 McFarland according to the Clinical and Laboratory Standards Institute standard M24-A2 [11]. Seeding was done according to the swab method. In this latter, the bacterial inoculum was spread on the agar using a sterile cotton swab in three different directions. The disks were dispensed with a dispenser and the plates were incubated at 37°C for 72 hours and read manually according to the thresholds defined in the recommendations of the SFM 2013 [12].

2.4. Substrate Degradation

The methods of Boiron et al. [6], Goodfellow et al. [13, 14], and Goodfellow and Lechevalier [15] were used to determine the decomposition of adenine, casein, and uric acid [9]. Clinical strains of N. brasiliensis and the strains of species belonging to the N. brasiliensis clade (N. brasiliensis, N. altamirensis, N. iowensis, N. tenerifensis, N. boironii, and N. vulneris) were tested [9]. Strains N. boironii DSM 101696, N. brasiliensis ATCC 19296, and N. vulneris DSM 45737 were incubated at 37°C, and N. altamirensis DSM 44997, N. tenerifensis DSM 44704, and N. iowensis DSM 45197 were incubated at 28°C [9]. The readings were performed at 3, 7, 10, 14, 17, and 21 days.

2.5. Methods of DNA Extraction

DNA extraction from Nocardia strains was performed with achromopeptidase according to the method reported by Rodríguez-Nava et al. [10]. Colonies were picked off with a loop, and one loopful was suspended in 200 μL of sterile water containing a dozen glass beads and vortexed for 5 minutes. The mixture was then incubated for 15 minutes at 70°C. The suspension supplemented with 3.4 μL of achromopeptidase (Sigma, Steinheim, Germany) at 10 U/mL was incubated at 55°C for 15 minutes. The suspensions were then centrifuged for 5 minutes at 13,000 rpm. The supernatants were stored at −20°C until use.

2.6. Amplification and Sequencing

Gene rrs. A 606-bp fragment of the rrs gene was amplified with primers Noc1, 5′-GCTTAACACATGCAAGTCG-3′, and Noc2, 5′-GAATTCCAGTCTCCCCTG-3′, and PCR program and reaction mixture were carried out according the recommendations of Rodríguez-Nava et al. [10].

Gene hsp65. A 441-bp fragment of the hsp65 gene encoding the 65-kDa heat shock protein was amplified with primers described by Telenti et al. (TB11: 5′-ACCAACGATGGTGTGTCCAT-3′ and TB12: 5′-CTTGTCGAACCGCATACCCT-3′) [16]. PCR program and reaction mixture were carried out according to the recommendations of Sánchez-Herrera et al. [17].

Gene sodA. A 440-bp fragment of the sodA gene was amplified and sequenced with primers SodV1 (5′-CAC CAY WSC AAG CAC CA-3′) and SodV2 (5′-CCT TAG CGT TCT GGT ACT G-3′) where Y = C or T, W = A or T, and S = C or G. The amplification was also done according to the recommendations of Sánchez-Herrera et al. [17].

All resulting PCR products were sequenced and verified (Biofidal, Lyon, France).

The breakpoints for identification based in sodA and hsp65 genes are 99% for each one [17, 18]. For the rrs gene, a higher breakpoint of 99.6% is used, according to CLSI [19].

2.7. Phylogenetic Analysis

The rrs gene sequences which we obtained for the 36 clinical isolates of N. brasiliensis and the reference strains were aligned manually for the comparative phylogenetic analysis using the Seaview program.

MLSA was performed using hsp65 and sodA sequences of the strains collection. The trimmed aligned sequences were concatenated in the order sodA-hsp65 to generate an 846 bp sequence using the Seaview program. The Seaview program was also used to infer the evolutionary trees according to the neighbour-joining method [20] and Kimura’s two-parameter model [21]. The robustness of the tree was performed with a bootstrap of 1000 replicates.

Taking into account the breakpoints for identification at species level of sodA and hsp65 genes individually, the breakpoint for concatenated sequence has been also fixed at 99%.

2.8. DNA Polymorphism of rrs, hsp65, and sodA Genes

The number of haplotypes, the haplotype diversity (Hd), the number of polymorphic sites, and other variables were obtained with DnaSP software [22].

3. Results

3.1. Growth on Culture Medium

The three culture media allowed the growth of clinical strains of N. brasiliensis. The Bennett medium showed abundant and rapid growth (48 hours). Middlebrook medium showed strong growth but also it was slightly slower (72 hours). The BCP medium presented interesting results with good rapid growth at 48 hours. N. brasiliensis clade tested type strains showed similar patterns to the clinical strains, except that N. boironii had a difficult growth on BCP and no growth on Middlebrook; this seems a peculiarity of this species.

3.2. Antimicrobial Susceptibilities

Eight out of 31 antibiotic molecules tested were active on all the strains’ collection: linezolid, tigecycline, trimethoprim + sulfamethoxazole, moxifloxacin, amikacin, amoxicillin + clavulanic acid, tobramycin, and gentamycin. Regarding the imipenem and pristinamycin molecules, resistance was observed on the majority of clinical isolates of N. brasiliensis (Table 1).

3.3. Degradation of Substrate

The assimilation test of adenine and uric acid proved negative for all the strains tested of the N. brasiliensis clade including clinical and reference ones. The casein degradation test showed that all clinical strains are able to metabolize casein except the clinical strain 12.28. In addition our result showed that some types of strains such as N. vulneris, N. tenerifensis, N. boironii, and N. iowensis are also able to degrade casein in the same way as N. brasiliensis except N. altamirensis. Casein is ultimately a marker that can be used for the phenotypic identification of the N. brasiliensis clade and not the N. brasiliensis species as it has been believed for many years.

3.4. Phylogeny

Primers Noc1 and Noc2 amplified the expected 606-bp fragment of the rrs gene for all the collection strains. Phylogenetic trees (Figure 1) based upon rrs showed homogeneity within clinical strains of N. brasiliensis. For this, the rrs gene is not relevant to show intraspecies diversity.

In addition, based upon the concatenation of sodA and hsp65 housekeeping genes, the phylogenetic tree generated (Figure 2) had several distinct genotypes: (i) genotype 1 containing clinical strains, (ii) genotype 2 harboring some clinical strains, and (iii) genotype 3 harboring some clinical strains and N. brasiliensis ATCC 19296. For the tropical N. brasiliensis HUJEG01 strain, it is observed that it does not belong to any of the 3 genotypes and is positioned alone in the tree between genotypes 1 and 2. This distribution of clinical strains of N. brasiliensis in 3 different genotypes shows an intraspecies diversity rather important. To better understand the polymorphism showed by phylogenetic trees, we studied the percentages of the similarities between the sequences. The average percentages of similarities based on the rrs gene (Table 2) range from 99.39% to 99.57% between the clinical strains and the 2 reference strains of N. brasiliensis (type and tropical strains). According to the CLSI, the similarity percentage needed for identification at species level must be greater than or equal to a threshold of 99.6% [19]. The clinical strains that showed a similarity percentage lower than this threshold for both reference strains of N. brasiliensis were anyway considered as belonging to this species because no higher similarity percentage was obtained for any other species. In the same way, the N. vulneris type strain was also revealed to be close to clinical strains according to the average of percentage of similarity (98.77%). Between the 2 reference strains of N. brasiliensis the percentage of similarity is higher, up to 99.82%. The percentages of similarities based on the concatenation of the sodA-hsp65 genes (Table 2) decrease and range now from 97.99% to 99.19% between the clinical strains and the 2 reference strains of N. brasiliensis. Between the type and reference strains of N. brasiliensis the percentage of similarity does not reach 99% this time. The comparison of the 3 genotypes between them (based on the representation of each genotype by 3 clinical strains) by using sodA-hsp65 genes shows that genotypes 2 and 3 are closer to each other (98.97% of similarity). The average of the percentages of similarity between genotypes 1 and 2 were 97.97%. and 98.28% between genotypes 1 and 3. Finally this value goes up to 98.97% between genotypes 2 and 3. This means that the more distant genotypes between them are 1 and 2 and the closer ones are 2 and 3.

N. brasiliensis HUJEG01N. brasiliensis ATCC 19296N. vulneris DSM 45737

N. brasiliensis ATCC 19296Similarity average (%)98.5199.82----
N. vulneris DSM 4573798.3898.7398.5198.55--
N. altamirensis DSM 4499795.9198.2495.4198.0795.9197.47
N. boironii DSM 10169696.5398.0796.2897.8996.1597.29
N. iowensis DSM 4519794.9197.8995.2997.7194.5497.64
N. tenerifensis DSM 4470496.2896.6796.0396.4995.9196.03

Genotype 1Similarity range (%)(97.77–98.38)-(97.77–98.26)-(97.52–98.14)-
Similarity average (%)98.01-97.99-97.67-

Genotype 2Similarity range (%)(98.39–98.88)-(98.88–99.38)-(98.63–98.88)-
Similarity average (%)98.73-99.19-98.80-

Genotype 3Similarity range (%)(98.14–98.88)-(98.26–99.00)-(98.01–98.76)-
Similarity average (%)98.63-98.76-98.50-

All clinical strainsSimilarity range (%)-(98.57–100)-(98.38–99.82)-(98.01–99.09)
Similarity average (%)-99.57-99.39-98.77

In parallel, an epidemiological study based on the clinical files was carried out, and the data were presented in Table 1. In order to know the link between the genetic diversity and the tropism of the clinical strains, a superposition of data was made between the phylogenetic tree obtained by the concatenation of sodA and hsp65 and the tropism of the clinical strains (Figure 2). Thus, we can see that in genotypes 2 and 3 we have almost all the clinical strains that have a cutaneous tropism except the 08.188 strain which has a subcutaneous tropism. Regarding genotype 1 it is more heterogeneous with various tropism: (i) pulmonary, (ii) cerebral, and (iii) cutaneous. Regarding the immunocompetence of patients, we have only 4 patients who have immunodepression factors, whose strains are in genotype 1 except the 10.93 strain which is in genotype 3.

3.5. Analysis of rrs, hsp65, and sodA Genes Polymorphism

The 36 clinical strains and 2 reference strains of N. brasiliensis studied showed (i) for rrs gene 16 polymorphic sites sharing 16 haplotypes and showing a Hd of 0.824; (ii) for hsp65 gene, 27 polymorphic sites and up to 22 different haplotypes with a Hd of 0.927; and, (iii) for sodA gene, up to 29 polymorphic sites sharing 14 haplotypes having a Hd of 0.885 (Table 3).

Nocardia speciesGenes Number of haplotypes
(Hd, S2, SD)
Number of of polymorphic sites

N. brasiliensis
(: 36 clinical strains and 2 reference strains)
rrs (569)16 (0.824, 0.00300, 0.055)16
hsp65 (401)22 (0.927, 0.00087, 0.029)27
sodA (406)14 (0.885, 0.00080, 0.028)29

Resulting fragment size without the primers sequences; Hd: haplotype (gene) diversity, S2: variance of haplotype diversity, and SD: standard deviation of haplotype diversity.

4. Discussion

Nocardia spp. are common soil-inhabiting bacteria that frequently infect humans through traumatic injuries or inhalation routes and cause infections, such as actinomycetoma and nocardiosis, respectively. N. brasiliensis is the main aetiological agent of actinomycetoma in various countries [23]. The input data used in this study highlight the existence of indigenous cases of cutaneous and subcutaneous (such as actinomycetoma) nocardiosis caused by N. brasiliensis in France. Moreover, we can observe that N. brasiliensis is also responsible for severe cases of disseminated nocardiosis in immunocompromised patients (pulmonary and cerebral cases).

To determine whether there is an association between clinical tropism of strains and their genetic profile we performed genetic characterization of 36 indigenous cases of N. brasiliensis that happened in France.

The three culture media allow the growth of clinical strains of N. brasiliensis. However, on Bennett’s medium more abundant and fast growth (48 hours) was observed. But the downside of this medium is its inaccessibility in the hospital because it is not marketable. Middlebrook medium shows strong growth but also it was slightly slower (72 hours). This medium is very expensive and not accessible to all budgets. However, it is an interesting alternative in isolating Nocardia from a complex sample. It is a selective medium of Mycobacteria, which promotes the growth of some Nocardia to the detriment of other external bacteria or commensal flora that may be in the biological sample analyzed. The BCP medium, used routinely in hospitals for Gram-negative bacteria, has interesting results with good fast growth (48 hours). It would therefore be advisable to use it as isolation medium for urgent cases, by the speed of growth.

Antibiograms results show resistance of most of the clinical strains to imipenem. This can pose therapeutic problems since it is part of molecules proposed during a phase of a general treatment for nocardiosis [24]. However, all clinical strains of N. brasiliensis were sensible to SXT and would be an effective molecule during treatments. The sensibility of N. brasiliensis type strain to this antibiotic has already been observed by Gilquin et al. [9].

Our study confirms that all clinical strains of N. brasiliensis are capable of degrading casein except 12.28 clinical strain. As shown by Seol et al. the N. brasiliensis type strain is able to degrade casein as well [25]. However, the test on the reference strains reveals that N. vulneris, N. tenerifensis, N. boironii, and N. iowensis are also capable of degrading casein in the same way as N. brasiliensis, as also shown by Gilquin et al. [9]. This type of test is used in some countries without the necessary molecular biology tools to identify N. brasiliensis. But, now, they must be aware that with this test we target several species of clade N. brasiliensis. So, it is no longer a criterion of identification proper to N. brasiliensis.

Phylogenetic tree based on the rrs gene sequence of our collection showed a low genetic diversity resulting in low polymorphism sequence. In addition, we can note that N. vulneris DSM 45737, identified as a new species by Lasker et al., present a genetic sequence very close to N. brasiliensis strains [26] with percentages of similarities on average greater than 98%.

Analysis of the phylogenetic tree (Figure 2) based on the MLSA by the concatenation of sodA and hsp65 housekeeping genes showed that the isolates are surprisingly classified according to 3 genotypes. These groups were formed upon similarity percentages and existing phylogenetic distances between the sequences of the strains studied. Genotype 1 concerns a well-defined cluster containing 9 clinical strains only which is sustained by a bootstrap of 81%. This genotype hosts all the cases of pulmonary forms (3), the sole cerebral form, and almost all the cases of immunocompromised patients (3 out of 4). Moreover, eight out of twelve strains susceptible to imipenem can be found in this group. There is just one remaining strain in this group not presenting this kind of susceptibility. The reason may be an acquired resistance to this drug due to a previous treatment. This well-defined genotype evokes the possible existence of another species or a strong variability in this case. This may have been caused by environmental pressures in the ecosystem of these isolates which may have resulted in the selection of strains that may have acquired, by mutations or genetic transfer with other microorganisms, new virulence characters different from that of the strain type N. brasiliensis. Regarding genotypes 2 and 3, they include clinical strains and N. brasiliensis ATCC 19296 type strain. However, the discrimination between these 2 genotypes is less clear than that with genotype 1 because of being in weak bootstrap that is less than 50. The genetic differences do not allow distinguishing them properly and their phenotypic behavior remains similar. Then, it would be interesting to study on another gene capable of generating more divergences, for example, gyrB and rpoB genes, which have already successfully been used for studying the polymorphism of some other Nocardia species [27, 28].

Concerning the percentage of similarity between the type and tropical strain of N. brasiliensis, it is 99.82% according to the rrs and goes down to 98.51% with the concatenation of sodA and hsp65. The fact of highlighting a greater dissimilarity with the concatenation between the type and tropical N. brasiliensis strain shows the advantage of the use of 2 markers like sodA and hsp65 vis-à-vis the rrs. The discriminatory power of these two genes may be explained by the presence of more polymorphic sites (hsp65: 27; sodA: 29) than in the case of rrs gene (16) and also by having Hd values higher than that of rrs gene (hsp65: 0.927; sodA: 0.885; rrs: 0.824).

It would be interesting to identify the genes involved in the virulence of different genotypes, including those of actinomycetoma. Interesting leads can be considered: (i) as identification of virulence genes expressed using the RNAseq method or (ii) to identify noncoding RNAs [23]. In addition, to genomically distinguish N. brasiliensis and N. vulneris a specific PCR to N. vulneris, using a specific gene of the species, should be developed.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


The authors thank Audrey Dubost for her technical support in bioinformatics analysis.


  1. V. Kandi, “Human Nocardia Infections: A Review of Pulmonary Nocardiosis., Human Nocardia Infections: A Review of Pulmonary Nocardiosis,” Cureus Cureus, vol. 7, no. 8, pp. e304–e304, 2015. View at: Google Scholar
  2. S. Maraki, S. Chochlidakis, E. Nioti, and Y. Tselentis, “Primary lymphocutaneous nocardiosis in an immunocompetent patient,” Annals of Clinical Microbiology and Antimicrobials, vol. 3, article no. 24, 2004. View at: Publisher Site | Google Scholar
  3. M. A. Saubolle and D. Sussland, “Nocardiosis: review of clinical and laboratory experience,” Journal of Clinical Microbiology, vol. 41, no. 10, pp. 4497–4501, 2003. View at: Publisher Site | Google Scholar
  4. B. A. Brown-Elliott, J. M. Brown, P. S. Conville, and R. J. Wallace Jr., “Clinical and laboratory features of the Nocardia spp. based on current molecular taxonomy,” Clinical Microbiology Reviews, vol. 19, no. 2, pp. 259–282, 2006. View at: Publisher Site | Google Scholar
  5. V. Rodriguez-Nava, D. Lebeaux, O. Lortholary, P. Boiron, and Nocardia., “Nocardia. Précis de Bactériologie Clinique,” Nocardia, no. 2, 2007. View at: Google Scholar
  6. P. Boiron, F. Provost, and B. Dupont, “Technical protocols,” In Methodes de laboratoire pour le diagnostic de la nocardiose, Institut Pasteur, Paris, France, 1993, 107-126. View at: Google Scholar
  7. A. Betrán, M. C. Villuendas, A. Rezusta, J. Pereira, M. J. Revillo, and V. Rodríguez-Nava, “Clinical significance, antimicrobial susceptibility and molecular identification of Nocardia species isolated from children with cystic fibrosis,” Brazilian Journal of Microbiology, vol. 47, no. 3, pp. 531–535, 2016. View at: Publisher Site | Google Scholar
  8. A. Ramírez-Radilla, V. Rodríguez-Nava, H. V. Silva-Rojas, M. Hernández-Tellez, H. Sandoval, and N. Ramírez-Durán, “Phylogenetic identification of Nocardia brasiliensis strains isolated from actinomycetoma in Mexico State using species-specific primers,” Journal de Mycologie Médicale, vol. 21, no. 2, pp. 113–117, 2011. View at: Publisher Site | Google Scholar
  9. J. M. Gilquin, B. Riviere, V. Jurado et al., “First Case of Actinomycetoma in France Due to a Novel,” mSphere, vol. 1, no. 6, p. e00309-16, 2016. View at: Publisher Site | Google Scholar
  10. V. Rodríguez-Nava, A. Couble, G. Devulder, J.-P. Flandrois, P. Boiron, and F. Laurent, “Use of PCR-restriction enzyme pattern analysis and sequencing database for hsp65 gene-based identification of Nocardia species,” Journal of Clinical Microbiology, vol. 44, no. 2, pp. 536–546, 2006. View at: Publisher Site | Google Scholar
  11. Susceptibility testing of Mycobacteria, Nocardiae, and other aerobic actinomycetes, Approved Standard, vol. 56, Clinical and Laboratory Standards Institute, Wayne, PA, USA, 2011, M24-A2. View at: Publisher Site
  12. “CA-SFM, “Les recommandations du Comité de l’Antibiogramme de la Société Française de Microbiologie,” Paris: Société Française de Microbiologie, 2013. View at: Publisher Site | Google Scholar
  13. M. Goodfellow, “The genus Nocardia Trevisan,” in Topley and Wilson’s microbiology and microbial infections, A. Balows and B. I. Duerden, Eds., pp. 464–489, Edward Arnold, London, UK, 2 edition, 1998. View at: Google Scholar
  14. M. Goodfellow, The family Nocardiaceae, The prokaryotes, Springer, New York, NY, USA, 2 edition, 1992, 1188–1213. View at: Publisher Site
  15. M. Goodfellow and M. P. Lechevalier, “Genus Nocardia Trevisan,” in Bergey’s manual of systematic bacteriology, S. T. Williams, M. E. Sharpe, and J. G. Holt, Eds., vol. 4, pp. 2350–2361, Lippincott Williams & Wilkins, Baltimore, MD, USA, 1989. View at: Google Scholar
  16. A. Telenti, F. Marchesi, M. Balz, F. Bally, E. C. Böttger, and T. Bodmer, “Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis,” Journal of Clinical Microbiology, vol. 31, no. 2, pp. 175–178, 1993. View at: Google Scholar
  17. K. Sánchez-Herrera, H. Sandoval, D. Mouniee et al., “Molecular identification of Nocardia species using the sodA gene: Identificación molecular de especies de Nocardia utilizando el gen sodA.,” New Microbes and New Infections, vol. 19, pp. 96–116, 2017. View at: Publisher Site | Google Scholar
  18. C. Y. Turenne, M. Semret, D. V. Cousins, D. M. Collins, and M. A. Behr, “Sequencing of hsp65 distinguishes among subsets of the Mycobacterium avium complex,” Journal of Clinical Microbiology, vol. 44, no. 2, pp. 433–440, 2006. View at: Publisher Site | Google Scholar
  19. CLSI, “Interpretive Criteria for Identification of Bacteria and Fungi by DNA Target Sequencing,” in Approved Guideline. CLSI document MM18- A. Wayne, PA, vol. CLSI document MM18- A, Clinical and Laboratory Standards Institute, Wayne, PA, USA, 2008. View at: Google Scholar
  20. J. A. Soddell, F. M. Stainsby, K. L. Eales, R. M. Kroppenstedt, R. J. Seviour, and M. Goodfellow, “Millisia gen. nov., sp. nov., an actinomycete isolated from activated sludge foam,” International Journal of Systematic and Evolutionary Microbiology, vol. 56, no. 4, pp. 739–744, 2006. View at: Publisher Site | Google Scholar
  21. V. A. Steingrube, R. W. Wilson, B. A. Brown et al., “Rapid identification of clinically significant species and taxa of aerobic actinomycetes, including Actinomadura, Gordona, Nocardia, Rhodococcus, Streptomyces, and Tsukamurella isolates, by DNA amplification and restriction endonuclease analysis,” Journal of Clinical Microbiology, vol. 35, no. 4, pp. 817–822, 1997. View at: Google Scholar
  22. J. Rozas, A. Ferrer-Mata, J. C. Sánchez-DelBarrio et al., “DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets,” Molecular Biology and Evolution, vol. 34, no. 12, pp. 3299–3302, 2017. View at: Publisher Site | Google Scholar
  23. J. S. Cruz-Rabadán, J. Miranda-Ríos, G. Espín-Ocampo, L. J. Méndez-Tovar, H. R. Maya-Pineda, and F. Hernández-Hernández, “Non-coding RNAs are differentially expressed by Nocardia brasiliensis in vitro and in experimental actinomycetoma,” The Open Microbiology Journal, vol. 11, pp. 112–125, 2017. View at: Publisher Site | Google Scholar
  24. S. Valdezate, N. Garrido, G. Carrasco et al., “Epidemiology and susceptibility to antimicrobial agents of the main Nocardia species in Spain,” Journal of Antimicrobial Chemotherapy, vol. 72, no. 3, pp. 754–761, 2017. View at: Publisher Site | Google Scholar
  25. C.-A. Seol, H. Sung, D.-H. Kim, M. Ji, Y.-P. Chong, and M.-N. Kim, “The first korean case of disseminated mycetoma caused by nocardia pseudobrasiliensis in a patient on long-term corticosteroid therapy for the treatment of microscopic polyangiitis,” Annals of Laboratory Medicine, vol. 33, no. 3, pp. 203–207, 2013. View at: Publisher Site | Google Scholar
  26. B. A. Lasker, M. Bell, H.-P. Klenk, C. Spröer, P. Schumann, and J. M. Brown, “Nocardia vulneris sp. nov., isolated from wounds of human patients in North America,” Antonie van Leeuwenhoek-Journal of Microbiology, vol. 106, no. 3, pp. 543–553, 2014. View at: Publisher Site | Google Scholar
  27. L. R. McTaggart, S. E. Richardson, M. Witkowska, and S. X. Zhang, “Phylogeny and identification of Nocardia species on the basis of multilocus sequence analysis,” Journal of Clinical Microbiology, vol. 48, no. 12, pp. 4525–4533, 2010. View at: Publisher Site | Google Scholar
  28. G. Carrasco, S. Valdezate, N. Garrido, P. Villalón, M. J. Medina-Pascual, and J. A. Sáez-Nieto, “Identification, typing, and phylogenetic relationships of the main clinical nocardia species in spain according to their gyrb and rpob genes,” Journal of Clinical Microbiology, vol. 51, no. 11, pp. 3602–3608, 2013. View at: Publisher Site | Google Scholar

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