Comparison of the Staphylococcal Chromosome Cassette (SCC) mec in Methicillin-Resistant Staphylococcus aureus (MRSA) and Non-aureus Staphylococci (MRNAS) from Animals and Humans

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) and non-aureus staphylococci (MRNAS) cause different infections in animals, including mastitis, in livestock and humans. This study aimed to identify and compare the staphylococcal chromosome cassette mec (SCCmec) types of MRSA or MRNAS isolated from several animal species and humans in different countries. Of 1462 S. aureus and non-aureus staphylococci, 68 grew on Chrom MRSA ID^® agar, were phenotypically resistant to cefoxitin and tested positive with the PCR for the mecA gene. These 60 MRSA and 8 MRNAS were isolated in Belgium mainly from cows (livestock-associated (LA) MRS) and humans (community-acquired (CA) MRS) and in Japan from dogs and cats. The SCCmec cassettes were identified by multiplex PCR in 52 MRSA and 7 MRNAS and by whole genome sequencing (WGS) in 8 additional MRSA. The SCCmec types IV and V were the most frequent in Belgian LA-MRS and CA-MRS, while the SCCmec type II was identified in four of the five Japanese MRSA. The remaining isolate was a bovine S. haemolyticus in which no SCCmec was identified. These results confirm the high prevalence of the SCCmec types IV and V in LA-MRS and CA-MRS in Belgium, emphasizing the possible public health hazard of the former, and the absence of SCCmec in some MRNAS.

1. Introduction

The history of methicillin-resistant Staphylococcus aureus (MRSA) began in 1961 following the development and marketing in 1959 of the methicillin antibiotic, a semisynthetic penicillin that is resistant to the activity of the β-lactamase (BlaZ) enzyme from S. aureus (SA) [1]. The mechanism of resistance of these first MRSA was not the production of any mutant Bla enzyme, but the synthesis of a β-lactam-resistant penicillin-binding protein (PBP2a), a transpeptidase involved in the bacterial cell wall formation, encoded by a newly acquired and chromosome-located mec gene [2,3]. The first MRSA were isolated from hospitalized human patients with nosocomial infections (hospital-acquired MRSA or HA-MRSA). During the 1990s, community-acquired MRSA strains (CA-MRSA) progressively emerged in humans with no history of hospitalization. HA-MRSA and CA-MRSA belong to different clonal lineages and virulotypes [4]. Though the first reported animal MRSA was isolated in 1972 from the milk of a cow with mastitis [5], they emerged in the early 2000s, not only in livestock but also in companion animals, horses and some wild animals and were generically named livestock-associated MRSA (LA-MRSA) [6].

Besides this first mec gene (renamed mecA), three other mec genes (mecB, mecC and mecD) have been identified as responsible for methicillin resistance in the Staphylococcaceae family [7,8,9]. The mecB and mecD genes were reported at first on the chromosome and/or on a plasmid of Macrococcus caseolyticus (previously named Staphylococcus caseolyticus). Recently, the mecB gene was also reported on a plasmid of one MRSA isolated from a human patient. Conversely, the mecD gene has not been reported in staphylococci so far [9,10]. Like for the mecA gene, the mecC gene was first reported in S. aureus isolates, though not from humans but from dairy cattle, and is also located on the chromosome [11]. These mecA and mecC genes are actually carried by a mobile genetic element named staphylococcal chromosome cassette (SCC) that is responsible for inter-Staphylococcus species transfer and, therefore, acquisition of methicillin resistance by non-aureus staphylococci (NAS), known as methicillin-resistant non-aureus staphylococci (MRNAS) [12,13]. Up to 14 different SCCmec have been described in MRSA, some of them being also present in MRNAS [11,14]. Nevertheless, the relative prevalence of these 14 SCCmec differs according to the host and country of origin of the MRSA or MRNAS [15,16,17]. Moreover, MRNAS can harbor additional SCCmec types that are not included in the official classification, and the mecA gene is not always located on an SCCmec in MRNAS [18,19].

The aims of this study were therefore: (i) to identify MRSA and MRNAS within collections from different hosts in European, African, Asian and North American countries using phenotypic and genetic assays; and (ii) to compare by multiplex PCR (mPCR) and whole genome sequencing (WGS) the SCCmec present in MRSA and MRNAS, focusing on bovine mastitis-associated staphylococci.

2. Results

2.1. Screening and Identification

A total of 78 presumptive MRS(A) was obtained after screening 1462 SA and NAS isolates on Chrom MRSA ID^® agar: 61 SA and 8 NAS from Belgium, 3 SA from Niger, 1 SA from Canada and 5 SA from Japan. The 70 SA were confirmed by MALDI-TOF while the 8 NAS were identified to three species: S. capitis (one isolate), S. epidermidis (six isolates) and S. haemolyticus (one isolate). Of these 78 presumptive MRS(A), 60 SA and the 8 NAS were resistant to cefoxitin by the disk diffusion assay and the MIC (Minimal Inhibitory Concentration) test strips and mecA PCR-positive. These 68 mecA-positive staphylococci were isolated from cows, boar, horses, humans, fomites, dogs and cats in Belgium and Japan (Table 1). Conversely, seven SA were phenotypically sensitive to cefoxitin and mecA, mecB and mecC PCR-negative. The remaining three SA growing on Chrom MRSA ID^® were resistant to cefoxitin either by the disk diffusion assay or by the MIC test strips, but all three were PCR-negative for the three mec genes.

Table 1.

Cefoxitin susceptibility test vs. mecA PCR on the 78 staphylococci growing on Chrom MRSA ID^® agar.

Country	Host Species	Staphylococcus Species	Cefoxitin R 1		Cefoxitin S 2		Total
			mecA+	mecA−	mecA+	mecA−
Belgium	Cow	aureus	26	2 3		3	31
		epidermidis	1				1
		haemolyticus	1				1
	Boar	aureus	1				1
	Horse	aureus	1				1
	Human	aureus	25	1 4			26
		capitis	1				1
		epidermidis	5				5
	Fomites	aureus	2				2
Canada	Cow	aureus				1	1
Japan	Dog	aureus	1				1
	Cat	aureus	4				4
Niger	Cow	aureus				3	3
Total			68	3	0	7	78

¹ R = resistant, ² S = sensitive, ³ one isolate was sensitive in the disk diffusion assay (diameter = 25 mm), but resistant in the MIC (Minimal Inhibitory Concentration) test strip (MIC = 6 μg/mL) and the second isolate was resistant in the disk diffusion assay (diameter = 18 mm), but sensitive in the MIC test (MIC = 4 μg/mL), ⁴ this isolate was resistant in the disk diffusion assay (diameter = 9 mm), but sensitive in the MIC test (MIC = 4 μg/mL).

2.2. SCCmec PCR

The multiplex PCR (mPCR) performed on the 68 mecA positive MRS(A) identified the SCCmec in 59 isolates: 9 isolates harbored the SCCmec type II, 2 isolates the type III, 34 isolates the type IV, 11 isolates the type V and 3 isolates the type VII (Table 2, Supplementary Table S1). The remaining nine MRS(A) were not typable (NT) by PCR including eight SA with a profile close but not identical to the SCCmec types II and IV, and one S. haemolyticus with a profile close to the SCCmec types VII and X.

Table 2.

Identification by multiplex PCR (mPCR) and whole genome sequencing (WGS) of the staphylococcal chromosome cassette mec (SCCmec) present in the 68 mecA PCR-positive staphylococci.

Country	Host Species	Staphylococcus Species	SCCmec Type					Not Typeable	TOTAL mecA+ Isolates
			II	III	IV	V	VII
Belgium	Cow	aureus	6		13 (2 1)	4	3		26
		epidermidis				1			1
		haemolyticus						1 2	1
	Boar	aureus		1					1
	Horse	aureus				1			1
	Human	aureus		1	22 (4)	2			25
		capitis			1				1
		epidermidis			2	3			5
	Fomites	aureus			2				2
Japan	Dog	aureus	1						1
	Cat	aureus	3 (1)		1 (1)				4
Total			10 (1)	2	41 (7)	11	3	1	68

¹ Numbers of isolates whose SCCmec could not be identified by multiplex PCR, but well by WGS; ² no SCCmec could be identified in this S. haemolyticus by either multiplex PCR or by WGS.

2.3. Whole Genomic Analysis

All genomic data related to this project, including raw reads, are available via the NCBI BioProject PRJNA607920. The genomic analysis of the eight SA and of the S. haemolyticus whose SCCmec could not be identified with the mPCR revealed that seven of the SA actually harbored one SCCmec type IV, and another one the SCCmec type II. Conversely, the S. haemolyticus harbored only a 100% sequence similarity mecA gene and a 99.68% sequence similarity IS1272 gene, but no ccr complex nor any other mec complex elements (mecR1/mec I) (Table 2, Supplementary Tables S2 and S3).

3. Discussion

The purpose of this study was to characterize and compare the SCCmec in MRSA and MRNAS from different hosts and countries isolated between 2005 and 2014 (see Materials and Methods Section 5.1). Unfortunately, only isolates from bovine mastitis and humans in Belgium—and from dogs and cats in Japan, to a lesser extent—tested positive phenotypically and genetically. Two methods were used for the identification of the SCCmec in the 68 MRSA and MRNAS studied. The mPCR results gave a perfect match with expected amplification results (Table 2) for 52 MRSA and 7 MRNAS, while the results were equivocal for 8 MRSA and 1 MRNAS. A final identification of the SCCmec in these eight MRSA was obtained by Whole Genome Sequencing (WGS) but not in the MRNAS (Table 2). Both the mPCR and the WGS indeed can present limits in the identification of the SCCmec not only in MRNAS, but even in MRSA. The limits of the mPCR are classically based on primer sequence mismatches, as consequence either of a point mutation or of the presence of a still untyped SCCmec [20]. WGS can also present some limits depending on the database used to identify the SCCmec [21].

According to the mPCR and to the WGS results, half of the SCCmec in the 26 MRSA from cattle (50%) belong to the type IV and the other ones to types II, V and VII (Table 2). An even higher percentage of human MRSA (88%) harbor one SCCmec belonging to type IV. Moreover, the SCCmec in seven of the eight bovine and human MRNAS also belong to types IV or V (Table 2). These results are similar to the published literature [22,23] with a high prevalence of type IV in CA-MRSA (like the human SA isolates of this study) and of both types IV and V in bovine LA-MRSA, with the other types present at lower prevalences. As far as MRSA from other sources are concerned, the SCCmec of three of the four Belgian isolates from boar, horses and fomites also belong to type IV and V (Table 2). Conversely, the SCCmec type II is predominant among Japanese isolates from dogs and cats (four out of five). As already published by others, the SCCmec type II is indeed the most prevalent in Japan [24]. It is also common in clinical samples from HA-MRSA and CA-MRSA in Asia and its presence in dogs and cats may be related to the proximity of these animal species with humans [25].

The only MRS in which neither mPCR nor WGS could identify the SCCmec type was one bovine S. haemolyticus. Indeed, genomic analysis did not confirm the presence of any SCCmec in this MRNAS, since no ccr complex could be identified and since SCCmec types are defined based on the ccr and mec complex elements [11,26]. Moreover, the detection of the IS1272 in the genomic structure of this strain makes it different from the ancestral mec structure of S. fleuretti, S. sciuri or S. vitulinus. This strain is nevertheless of interest, not only in livestock where NAS are also responsible for subclinical bovine mastitis cases [27,28], but also potentially in public health in general, since mastitis-causing NAS could potentially also be responsible for different infections in other animal species and in humans [13,29].

Before the identification procedure of the types of SCCmec, MRS had to be identified and the different tests used showed some limits related to different factors. Of the 78 presumptive MRS(A) obtained after screening on Chrom MRSA ID^®, only 68 MRS(A) were confirmed by disc diffusion assay and MIC test strips with cefoxitin (Table 1). As described by Van Griethuysen and collaborators, the mecA gene is lost in 14.4% of MRS(A) after 2 years of storage at −80 °C [30]. The isolates used in this study were screened on Chrom MRSA ID^® in 2014 and then confirmed with a cefoxitin susceptibility test in 2016 after storage at −80 °C. This may explain the loss of the cefoxitin resistance by these 10 presumptive MRS(A), if this resistance was due to the presence of a mec gene. Moreover, false positive or negative results can occur with the use of the cefoxitin disc diffusion assay for the detection of methicillin resistance [31]. The three SA isolates that were cefoxitin-resistant at either disc diffusion assay or MIC test strips, but mecA/B/C PCR negative could be explained by different hypotheses. At first, small interpretation errors of the results could have occurred since the results, at least for the two bovine SA are borderline (Table 1). Conversely, the disk diffusion assay of the human SA is not borderline and was similar after retesting. Secondly, staphylococci can use other resistance mechanisms, such as β-lactamase hyper-production, mutations at PBP-encoding or other genes (f.i., mutations at gdpP or yjbH genes induce PBP4 overproduction), the presence of other mec genes like mecD that was not looked for or still undescribed, or cell wall defective forms with intrinsic β-lactam resistance [32]. Further genomic analysis of these three isolates may bring answers to these questions. Meanwhile, the results suggest that the Chrom MRSA ID^® should be used as a first-line screening test, while the phenotypic resistance tests to cefoxitin and the mec gene PCR as second-line confirmatory tests.

4. Conclusions

In conclusion, the results of this study confirm: (i) the presence of a majority of SCCmec types IV and V in bovine mastitis-associated MRSA and MRNAS, like in human CA-MRSA [22,23]; (ii) the strengths and limits of phenotypic and genetic tests for the identification of MRS and for SCCmec typing; and (iii) the need of more studies on MRNAS considering the potential of SCCmec interspecies transferability and the increasing impact of NAS in public health [13,29].

5. Materials and Methods

5.1. Isolate Collections and MRS Phenotypic Identification

A total of 1462 staphylococci isolated between 2005 and 2014 from human (n = 51), bovine milk (n = 1160), dog (n = 185), cat (n = 50), wild boar (n = 6), horse (n = 1), deer (n = 1), hare (n = 1), roe (n = 3) and fomites from an equine clinic (n = 4) were included in this study. Of these 1462 staphylococci, 723 originated from Belgium [23,33,34], 45 from Italy, 25 from Switzerland, 90 from Canada [35], 233 from Japan [36], 256 from Niger [37] and 90 from Senegal [38].

Although several of these staphylococci had already been studied for MR, all the 1462 isolates were screened for methicillin resistance with the Chrom MRSA ID^® agar (BioMérieux, Craponne, France). To confirm the resistance to methicillin, disc diffusion assays were performed on the growing isolates with the cefoxitin discs (Neo-sensitabs, Rosco Diagnostica, Taastrup, Denmark) (30 µg/mL) and the minimal inhibitory concentrations (MIC) were assessed by MIC test strips (Liofilchem Diagnostic, Roseto degli Abruzzi, Italy) (0.16–256 µg/mL) on Mueller–Hinton agar (Oxoid, Cambridge, UK) with a 0.5 McFarland bacterial suspension. After overnight incubation at 37 °C, inhibition zones were measured using the SIRSCAN micro device (i2a, Montpellier, France) for cefoxitin discs and manually for the MIC test strips, and interpreted according to the Clinical and Laboratory Standards Institute recommendations [39]: the inhibition zone for resistant SA is ≤21 mm and ≥22 mm for sensitive SA while the diameter is ≤24 mm for resistant NAS and ≥25 mm for sensitive NAS; the MIC for resistant SA is >4 µg/mL and ≤4 µg/mL for sensitive SA, while they are >0.25 µg/mL for resistant NAS and ≤0.25 µg/mL for sensitive NAS. The quality control strains where the ATCC 29,213 methicillin-sensitive Staphylococcus aureus, the ATCC 4330 MRSA for the mecA gene and the ATCCBAA-2312 MRSA for the mecC gene.

5.2. MRS Species Identification

The species identity of the isolates growing on Chrom MRSA ID^® agar was confirmed with an Autoflex Biotyper Mass Spectrometer (MALDI-TOF MS^®, Bruker Daltonics, Bremen, Germany) using the direct transfer method and α-cyano-4-hydroxycinnamic acid as matrix, according to the manufacturer’s instructions. In case of no peak detection, the samples were retested with the extended direct transfer method, using either on-target formic acid treatment or full ethanol-formic acid extraction. The spectra were analyzed with the MBT (MALDI BioTyper) Compass software version 4.1. (Bruker Daltonics, Bremen, Germany), which includes reference databases of 8252 bacterial and fungal species, expanded with 13 MSP covering 8 species of coagulase-negative staphylococci as previously described [40]. Only the identifications with a score value between 2.00 and 3.00 (green color) were considered.

5.3. PCR for mec Gene and SCCmec Identification

The DNA of the MRS(A) isolates were extracted following a protocol adapted from Unal and collaborators [41]. One colony was suspended into 50 µL of lysostaphin (0.1 mg/mL) (Sigma-Aldrich, Overijse, Belgium) and incubated at 37 °C for 10 min. Then, a mix of 45 µL of sterile water, 5 µL of proteinase K (2 mg/mL) (Sigma–Aldrich, Overijse, Belgium) and 150 µL of TRIS-HCL (0.1 M, pH 8) was added to the suspension and incubated at 56 °C for 10 min then at 95 °C for 5 min and centrifuged at 13,000× g for 5 min. Supernatants were recovered and stored at −20 °C until further use.

Two duplex PCR (mecA/nuc and mecC/16S rDNA staph) and one uniplex PCR (mecB) were performed with the multiplex PCR (mPCR) kit^® (QIAGEN, Venlo, The Netherlands) using 1.5 µL of DNA suspension. For each PCR, the MIX contained 7.5 µL of PCR reaction mix 2x, 3 µL of Q solution and 0.375 µL of each primer (10 µM) in a total volume of 13.5 µL. The targeted genes, primer sequences and PCR product lengths are reported in Table 3 [41,42,43]. The PCR amplification conditions were the same for the two duplex PCR: an initial denaturation step at 95 °C for 15 min; 35 cycles at 95 °C for 30 s (denaturation), 57 °C for 90 s (annealing) and 72 °C for 90 s (extension); and a final extension step at 72 °C for 10 min. Only the annealing temperature was different for the mecB PCR, at 59.7 °C instead of 57 °C.

Table 3.

Primers used for the mecA/nuc, mecC/16S rDNA staph and mecB gene detection by PCR.

Genes	Primers	Primer Sequence 5′-3′	PCR Product Length (bp 1)	References
mecA	mecA1	AAAATCGATGGTAAAGGTTGGC	533	[43]
	mecA2	AGTTCTGCAGTACCGGATTTGC
nuc	nuc1	GCGATTGATGGTGATACGGTT	279	[43]
	nuc2	AGCCAAGCCTTGACGAACTAAAGC
mecC	mecC454-F	GTCCCTAACAAAACACCCAAAGA	454	This study
	mecC454-R	GAAGATCTTTTCCGTTTTCAGC		[42]
16S rDNA staph	16S RNA1	GTTATTAGGGAAGAACATATGTG	750	[43]
	16S RNA2	CCACCTTCCTCCGGTTTGTCACC
mecB	mecB-for	TTAACATATACACCCGCTTG	279	[9]
	mecB-rev	TAAAGTTCATTAGGCACCTCC

¹ bp = base pair.

The SCCmec typing was based on a set of 5 multiplex PCR (mPCR) targeting the ccr and mec gene complexes and performed following an adapted protocol from Argudín and collaborators [42] using the multiplex PCR kit^® (QIAGEN, Venlo, The Netherlands). For each mPCR, 2 µL of DNA obtained by boiling was used and the mix was constituted of 7.5 µL of PCR reaction mix 2x, 3 µL of Q solution, 5µL of primer mix (10 µM). The targeted genes, primer sequences and the PCR product lengths (bp) are reported in the Table 4 [43,44,45,46]. The PCR amplification conditions for PCR1a and PCR1b were an initial denaturation at 95 °C for 15 min, 40 cycles of 95 °C for 30 s (denaturation), 57 °C for 90 s (annealing), and 72 °C for 2 min (extension), and a final extension at 72 °C for 10 min. For PCRs 2, 3 and 4 the conditions were different, with 35 cycles of 94 °C for 2 min (denaturation), 60 °C of 90 s (annealing) and 72 °C for 3 min (extension). All PCR amplified fragments were visualized by electrophoresis in 1.5% (w/v) agarose gel after staining with Midori green Advance DNA Stain (Nippon Genetics, Düren, Germany).

Table 4.

Primers used for the SCCmec typing by multiplex PCR.

mPCR 1	Genes	Primers	Primer Sequence 5′-3′ 3	PCR Product Lengths (bp 4)	References
PCR1a	Type 1 ccr 2	α1-dege	AACCTATATCATYAATCAGTRCGT	695	[44]
		βc	ATTGCCTTGATAATAGCCITCT
	Type 2 ccr	α2	TAAAGGCATCAATGCACAAACACT	937	[44]
		βc	ATTGCCTTGATAATAGCCITCT
	Type 3 ccr	α3	AGCTCAAAAGCAAGCAATAGAAT	1791	[44]
		βc	ATTGCCTTGATAATAGCCITCT
	Type 7 ccr	α1-dege	AACCTATATCATYAATCAGTRCGT	417	[44]
		ccr7.4-rev	ACATGCGCTGTAGTGCAGGG
PCR1b	mecA	mA1	TGCTATCCACCCTCAAACAGG	286	[44]
		mA2	AACGTTGTAACCACCCCAAGA
	Type 4 ccr	α4.2	GTATCAATGCACCAGAACTT	1287	[44]
		β4.2 dege	TTGCGACTCTCTTGRCGTTT
	Type 5 ccr	γR	CCTTTATAGACTGGATTATTCAAAATAT	518	[44]
		γF	CGTCTATTACAAGATGTTAAGGATAAT
PCR2	class A mec	mI6	CATAACTTCCCATTCTGCAGATG	1963	[44]
		mA7	ATATACCAAACCCGACAACTACA
	class B mec	IS7	ATGCTTAATGATAGCATCCGAATG	2827	[44]
		mA7	ATATACCAAACCCGACAACTACA
	class C2 mec	IS2	TGAGGTTATTCAGATATTTCGATGT	804	[44]
		mA7	ATATACCAAACCCGACAACTACA
PCR3	mecA	mecA 1	AAAATCGATGGTAAAGGTTGGC	533	[43]
		mecA 2	AGTTCTGCAGTACCGGATTTGC
	class C1a/C1b mec	ISF4	CGGATTTTCGCCATGCCACGA	1232/286	[46]
		mA7	ATATACCAAACCCGACAACTACA
PCR4	Type 8 ccr	ccr8.4-fw	CTCAAGCGATACGGTCACAA	1388	[42]
		ccr8.3-rev	TCAGGCCTTTACGACGTTTT
	class E mec	mecC-fw	TTTTGCCTCGCTCTGATTTT	1083	[42]
		mecR1-rv	GCCAAAAGACCATTGGATTC
	mec C	mecALGA251MultiFP	GAAAAAAAGGCTTAGAACGCCTC	138	[45]
		mecALGA251MultiRP	GAAGATCTTTTCCGTTTTCAGC

¹ mPCR = multiplex PCR, ² ccr = cassette chromosome recombinase-encoding gene, ³ R = A or G; I = Inosine; Y = C or T, ⁴ bp = base pair.

5.4. WGS

Bacterial DNA was extracted from the MRS(A) whose SCCmec could not be identified by mPCR using an overnight bacterial culture pellet suspended in 495 µL of buffer (75 Mm NaCl, 25 Mm EDTA pH 8, 20 Mm Tris HCl pH 7). After addition of 50 µL of lysostaphin (50 µg mL⁻¹) and 10 µL of RNase (10 µg mL⁻¹), the suspension was incubated for 1 h at 37 °C. Then, 50 µL of 10% SDS and 5 µL of proteinase K (100 µg mL⁻¹) were added and the suspension was incubated for 1 h at 55 °C. After adding 200 µL of NaCl 5 M, 700 µL of chloroform/isoamyalcohol (24/1) and the ethanol precipitation, the dried pellet containing DNA was suspended in 20 µL MiliQ water and stored at −20 °C until further use.

The genomic DNA libraries of MRS(A) were prepared for Illumina sequencing according to the manufacturer’s instructions using the Nextera XT kit and sequenced by the NovaSeq 6000 Sequencing System (Illumina, San Diego, CA, USA). The raw read sequences were assembled into contigs with the pipeline shovill 1.0.4 including trimmomatic 0.38 for the cleaning and annotated using Prokka 1.13.3 [47]. Nanopore MinION long-read sequencing was performed using the Rapid Barcoding Sequencing kit (Oxford Nanopore) for library preparation. After guppy_gpu base calling, assembly of nanopore reads was done using Canu 1.8. The Illumina reads were cleaned with trimmomatic 0.36 (ILLUMINACLIP:illumina_oligos_and_revcomp:2:30:5:1:true LEADING:3 TRAILING:3 MAXINFO:40:0.2 MINLEN:36 options) and aligned with Canu assembly using BWA 0.7.15-r1140. Pilon 1.23 was run on this alignment for preliminary corrections. The final result was the corrected consensus provided by Pilon.

The SCCmec identification was performed using SCCmecFinder 1.2 available from the Center for Genomic Epidemiology (https://cge.cbs.dtu.dk/, accessed on 21 February 2020) with a %ID threshold of 90% and minimum length of 60%. An SCCmec Finder confirmation was performed for the not matching sequences with a %ID threshold and a minimum length of 80% and 40% respectively [21,26,44].

Supplementary Materials

The following are available online at https://www.mdpi.com/2079-6382/10/3/256/s1, Suppl. Table S1: The different SCCmec type profiles based on the multiplex PCR; Suppl. Table S2: The different SCCmec type profiles based on genomic analysis with SCCmecFinder 1.2; Suppl. Table S3: Identification with SCCmecFinder 1.2 after WGS of the SCCmec types in the nine staphylococci untypeable with the multiplex PCR.

Author Contributions

All the authors contributed to the study conception and design. J.M. and D.T. supervised the study. C.N.T. carried out bacterial purification/isolation and MRSA ID screening. C.N.T. and J.-N.D. performed the cefoxitin susceptibility test and the MIC determination. F.B. and F.H. carried out MALDI-TOF identification. C.N.T. and M.A.A. carried out and analyzed the multiplex PCR results. P.L., Y.B., C.N.T. and D.T. performed the sequencing and the genomic analysis. C.N.T. wrote the manuscript and D.T. and J.M. reviewed the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was not supported by any external financing.

Data Availability Statement

All genomic data related to this project, including raw reads, are available via the NCBI BioProject PRJNA607920.

Conflicts of Interest

The authors declare no conflict of interest.