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Antibiotic Resistance Profiles and MLST Typing of Staphylococcus Aureus Clone Associated with Skin and Soft Tissue Infections in a Hospital of China
Authors Ji X, Zhu W, Lu H, Wu Z, Chen H, Lin C, Zeng Z , You C , Li L
Received 9 April 2024
Accepted for publication 14 June 2024
Published 21 June 2024 Volume 2024:17 Pages 2555—2566
DOI https://doi.org/10.2147/IDR.S465951
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Prof. Dr. Héctor Mora-Montes
Xiaojuan Ji,1,* Wenjie Zhu,1,* Hongfei Lu,2 Zhiwei Wu,1 Huaqing Chen,1 Chunli Lin,1 Zhaolin Zeng,1 Cong You,1 Longnian Li1
1Department of Dermatology, First Affiliated Hospital of Gannan Medical University, Joint Organization of Jiangxi Clinical Medicine Research Center for Dermatology, Ganzhou, People’s Republic of China; 2Clinical Laboratory, First Affiliated Hospital of Gannan Medical University, Ganzhou, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Cong You; Longnian Li, Department of Dermatology, First Affiliated Hospital of Gannan Medical University, Ganzhou, People’s Republic of China, Email [email protected]; [email protected]
Objective: To analyze the antibiotic resistance profile, virulence genes, and molecular typing of Staphylococcus aureus (S. aureus) strains isolated in skin and soft tissue infections at the First Affiliated Hospital, Gannan Medical University, to better understand the molecular epidemiological characteristics of S. aureus.
Methods: In 2023, 65 S. aureus strains were isolated from patients with skin and soft tissue infections. Strain identification and susceptibility tests were performed using VITEK 2 and gram-positive bacteria identification cards. DNA was extracted using a DNA extraction kit, and all genes were amplified using polymerase chain reaction. Multilocus sequence typing (MLST) was used for molecular typing.
Results: In this study, of the 65 S. aureus strains were tested for their susceptibility to 16 antibiotics, the highest resistance rate to penicillin G was 95.4%. None of the staphylococcal isolates showed resistance to ceftaroline, daptomycin, linezolid, tigecycline, teicoplanin, or vancomycin. fnbA was the most prevalent virulence gene (100%) in S. aureus strains isolated in skin and soft tissue infections, followed by arcA (98.5%). Statistical analyses showed that the resistance rates of methicillin-resistant S. aureus isolates to various antibiotics were significantly higher than those of methicillin-susceptible S. aureus isolates. Fifty sequence types (STs), including 44 new ones, were identified by MLST.
Conclusion: In this study, the high resistance rate to penicillin G and the high carrying rate of virulence gene fnbA and arcA of S.aureus were determine, and 44 new STs were identified, which may be associated with the geographical location of southern Jiangxi and local trends in antibiotic use. The study of the clonal lineage and evolutionary relationships of S. aureus in these regions may help in understanding the molecular epidemiology and provide the experimental basis for pathogenic bacteria prevention and treatment.
Keywords: Staphylococcus aureus, skin and soft tissue infections, antibiotic resistance, multilocus sequence typing, virulence gene
Introduction
Staphylococcus aureus (S. aureus) is a common pathogen that causes nosocomial and community infections and various infectious diseases. The pan-genome of this bacterium encodes several toxins, including three families of toxins: pore-forming toxins, exfoliating toxins, and superantigens. Most genes encoding toxins are located on mobile genetic elements,1 including the following representative genes.2 Encoding mupirocin-acquired resistance (mupA; accession: NG_048008.1), the gene associated with a high-level resistance (minimum inhibitory concentration ≥512 μg/mL) to mupirocin;3 erythromycin resistance methylase (erm)A and ermC;4 Panton-Valentine leukocidin (PVL), the leukocidin toxin gene;5,6 fibronectin binding protein A (fnbA);7,8 arginine catabolism mobile element (arcA),9,10 which has the advantage of selective skin colonization); toxic shock syndrome toxin (TSST)-1 gene-encoding TSST,11 and mecA, related to β-lactam antibiotic resistance. The distribution of toxin genes in the clonal lineages of S. aureus is not random, but phylogenetically characteristic.
It is important to understand the genetic background and pathogenesis of the different clonal lineages of S. aureus. Owing to the continuous application of new antibiotics in clinical practice and the widespread abuse of antibiotics in recent years, drug resistance by S. aureus has been increasing annually. Particularly, the rise in methicillin-resistant S. aureus (MRSA) worldwide has brought greater challenges to the treatment of S. aureus infections. Therefore, it is particularly important to further study the resistance of S. aureus and its relationship with resistance genes to strengthen the understanding of molecular epidemiology of S. aureus in human populations. To date, we have successfully reported primers for the representative genes, mupA, ermA, ermC, PVL, fnbA, mecA, arcA, and TSST-1 in a toxin profile.12 We also intend to use polymerase chain reaction (PCR) assay to detect gene fragments in pathogenic S. aureus toxin profile. In 2023, in this study, 65 S. aureus isolates from pus secretions and other samples from the First Affiliated Hospital of Gannan Medical University were included. Drug resistance and virulence gene analyses and molecular typing were performed to analyze the drug resistance and virulence gene-carrying rates of S. aureus in patients with skin and soft tissue infections. Differences in the molecular characteristics between MRSA and methicillin-sensitive S. aureus (MSSA) isolates were compared.
Materials and Methods
Source, Identification, and Drug Sensitivity Profile of S. Aureus Strains
In 2023, 65 strains of S. aureus were isolated from pus and secretion samples of 65 patients with skin and soft tissue infections in our hospital. The distribution of departments were as follows: dermatology (23.15%), orthopedic (21.5%), endocrinology (12.3%), burn (10.8%) and so on. (Figure 1). Automated matrix-assisted laser desorption ionization–time-of-flight mass spectrometry was used to identify the strains, AST-P639 Chinese customized card in VITEK 2 compact (French biomerieux Ltd.) was used for drug susceptibility testing and drug susceptibility results were determined according to the Clinical and Laboratory Standards Institute (CLSI) M100 31st edition.13 S. aureus American Type Culture Collection (ATCC) 27,696 and 27,697 were used as quality control strains. This study was approved by the Ethics Committee of the First Affiliated Hospital of Gannan Medical University (process number: LLSC-2023175). All patients provided written informed consent for their data to be published in the article.
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Figure 1 Distribution constituent ratio of Staphylococcus aureus infection departments in 2023. |
DNA Extraction and Detection and MRSA Identification
Bacterial DNA was extracted by using a centrifugal column bacterial genomic DNA extraction kit (Tianlong Technology Co., Ltd. Xi’an, China), according to the manufacturer’s manual. After preliminary screening based on drug sensitivity results and mecA amplification by PCR, the drug sensitivity results for S. aureus indicated resistance to oxacillin and the virulence gene mecA test was positive. On the basis of these results, the strain was judged to be MRSA; otherwise, it was judged to be MSSA. Representative samples with successful amplification were selected for gene sequencing by General Biology (Anhui) Co., LTD, to verify the success of eight-primer amplification of target genes. After the results were returned, the peak map was observed by SeqMan software to confirm the sequence quality. The sequencing results were compared and analyzed using the GenBank database.12
Virulence Genes and Resistance Genes Detection
Eight types of toxin genes were detected by PCR, including TSST, PVL, and mupA. These promote the invasion, colonization, and growth of S. aureus in the host by enhancing the bacterial growth microenvironment and inhibiting immune response. Others included genes associated with resistance to oxacillin, erythromycin, levofloxacin, and gentamicin (arcA); promoting the adhesion of S. aureus to host tissues (fnbA); associated with resistance to macrolides, lincosamide, and streptogramin B (MLSB) (ermA and ermC); and associated with resistance to erythromycin, levofloxacin, and gentamicin (arcA); genes for β-lactam resistance (mecA). The primer sequences and product sizes of the eight toxin genes are detailed in Table 1, and the PCR electrophoresis patterns in Figure 2.
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Table 1 Pre-Amplified Nucleotide Sequences of Primers |
Multilocus Sequence Typing (MLST) of S. Aureus
According to the S. aureus MLST database (https://pubmlst.org/saureus/), there are seven housekeeping genes (arcC, aroE glpF, GMK, pta, tpi, and yqiL) for the 65 strains of S. aureus causing skin and soft tissue infections. All seven primer pairs were sent to General Biology Co., Ltd for primer synthesis. The primer sequences and product sizes are detailed in Table 2. The returned sequencing results were assembled using DNASTAR software (https://www.dnastar.com/) and uploaded to the S. aureus multilocus typing database to obtain the corresponding genotype and sequence type (STs). When the uploaded data did not match the data in the database, the website administrator was contacted to obtain new genotypes and STs after confirming the sequencing results.
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Table 2 Primer Sequences and Product Sizes of Seven Housekeeping Genes for MLST Molecular Typing |
Statistical Analysis
IBM SPSS Statistics for Windows, version 27 (IBM Corp., Armonk, NY, USA) was used for statistical analysis in this study. The χ2 test or Fisher’s exact probability method was used for count data as applicable. Results were considered statistically significant at P < 0.05.
Results
Distribution of MRSA and MSSA Strains
In this study, oxacillin was used to replace methicillin, and oxacillin-resistant S. aureus with a positive mecA gene were defined as MRSA. In total, 21 MRSA and 44 MSSA strains were detected, with an MRSA detection rate of 32.3%.
Drug Resistance Rate of Strains
In this study, 65 S. aureus strains were tested for their susceptibility to 16 antibiotics. All MRSA isolates were resistant to oxacillin and penicillin, but none were resistant to daptomycin, ceftaroline, linezolid, tigecycline, teicoplanin, or vancomycin. In general, the resistance rate of the MRSA strains to the tested antibiotics was much higher than that of the MSSA strains. In this study, the resistance rates to rifampicin, levofloxacin, gentamicin, moxifloxacin, and penicillin G were not statistically significant, whereas those to other drugs were significant (P<0.05) (Table 3 and Figure 3).
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Table 3 Comparison of the Resistance Rates of MRSA and MSSA Strains Among Staphylococcus Aureus in Skin Infections |
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Figure 3 Antibiotic resistance analysis of S. aureus, MRSA and MSSA. |
As shown in Table 4, among the eight S. aureus toxin genes, fnbA, which promotes the adhesion of S. aureus to host tissues and arcA, which promotes the invasion, colonization, and growth of S. aureus in the host had the highest detection rates (100% vs 98.5%). The detection rates of PVL, TSST, mupA (related to mupirocin resistance), mecA (oxacillin resistance), and ermA and ermC (macrolide resistance) were 12.3%; 20%; 9.2%; 56.9%; and 21.5% and 18.5%, respectively. The gene mecA, detected in both the MSSA and MRSA groups, had a higher detection rate in the MRSA group than that in the MSSA group.
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Table 4 Comparison of the Detection Rates of MRSA and MSSA Toxin Genes in Skin- Infected Staphylococcus Aureus |
MLST Typing of S. Aureus
Fifty STs were identified in the 65 S. aureus isolates, including 44 new STs. The information on the new STs was uploaded to the database, and the new STs are numbered as ST8815-8831, ST8833-8842, ST8844-8855, ST8858-8861, and ST8864. The distribution of the major STs is shown in Figure 4. All ST data were entered into the PHYLOVIZ software (http://www.phyloviz.net). for cluster analysis, and the minimum number of identical alleles required to clone the complex (CC) was set at five; the Results are shown in Figure 5. The 17 STs were grouped into the following 12 clusters: ST8854, ST8846, ST8859, ST8852, ST8825, ST8838, ST8855, ST8848, ST8365, ST8837, ST8860, and ST8861 as nodes of CC8854, CC8846, CC8859, CC8852, CC8825, CC8838, CC8855, CC8848, CC8365, CC8837, CC8860, and CC8861, respectively. Multilocus sequence typing is detailed in Table 5. The genetic distance between ST8854 and ST8846 was 1, indicating that the evolutionary difference was small and that the two types were genetically close. The evolutionary divergence between STs that are genetically distant from each other is also greater and the genetic relationships are distant.
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Table 5 Multilocus Sequence Typing and Cloning Complexes of Staphylococcus Aureus |
Discussion
In this study, 16 antibiotics, penicillin, clindamycin, erythromycin, oxacillin, cefoxitin, moxifloxacin, levofloxacin, rifampicin, sulfamethoxazole, gentamicin, daptomycin, linezolid, tigecycline, teicoplanin, cephalosporin, and vancomycin, were tested against S. aureus isolates from infected patients. Genes associated with S. aureus pathogenicity and resistance (mupA, fnbA, arcA, PVL, TSST, mecA, ermC, and ermA) were targeted because of their prevalence in the invasive isolates. After PCR amplification, Sanger sequencing was used. Consistent amplified bands with the normal sequences of the eight genes was obtained. It indicate that the primer design was reasonable and amplification was successful. The results showed the detection rate of fnbA (100%) as the highest, followed by that of arcA (98.5%).
The significant susceptibility of S. aureus to vancomycin, linezolid, and chloramphenicol may be related to the limited use of these antibiotics due to market shortages, high costs, and high toxicity.15 The 100% susceptibility of S. aureus isolated from patient secretions to vancomycin confirms this observation,16,17 thereby strengthening the finding of vancomycin efficacy against this pathogen. However, large doses of vancomycin can increase the risk of nephrotoxicity. Therefore, when using vancomycin, the test for vancomycin therapeutic drug concentration monitoring, renal function and the MIC value of the causative organism to vancomycin should be conducted.18 n addition, this study revealed significant resistance to penicillin and oxacillin (84.6% vs 76.9%).16 In our study, the resistance rates of penicillin and oxacillin were 95.4% and 32.3%, respectively. The resistance rate of penicillin was higher than that of oxacillin, and the resistance rates of penicillin and oxacillin were different from the literature, which may be related to the different tendency of using antibiotics in different regions. Studies have shown that MRSA prevalence in infectious diseases is high (89.9%).19 Although our study reported a lower MRSA prevalence, the rising incidence of MRSA infection has resulted in increased treatment costs and longer hospital stays.20 Therefore, detailed molecular epidemiological studies of S. aureus are essential.
Multidrug resistance (MDR) is defined as nonsusceptibility to at least one agent in three or more antimicrobial classes. In our study, the MDR of S. aureus isolates was 63.1%, which was higher than the 52.4% rate reported in previous studies,19 indicating a high incidence in this study area. Another study reported an MDR rate as high as 94.8%,16 higher than that reported in this study; indicating a lower rate in this area than that in other areas. This MDR of S. aureus may be related to the irrational use of antibacterial drugs. The pattern of high resistance to commonly used antibiotics, such as penicillin G, clindamycin, erythromycin, and oxacillin, may be attributed to increased exposure to specific classes of antibiotics. This results in drug target mutations that cause resistance or cell wall rearrangements, leading to the disruption of drug accumulation in the cytoplasm.2
Owing to the diversity of S. aureus strains and the influence of clinical treatment, the number of STs in the MLST database continues to increase. To date, 8914 STs have been identified. Minimum spanning tree plot of the 65 MLST clinical isolate data of S. aureus in skin infections were clustered (Figure 5). All STs are represented by elliptical spheres, and each ellipsoid represents an ST. We set the elliptical sphere at the center of each branch in the evolutionary tree, the representative ST of the lineage, as the origin of the clonal complex. Other STs connected to the oval sphere, representing the ST center, were single-site or multisite mutants.
Many studies have used MLST to determine the population structure of highly clonal S. aureus.21 The MLST database contains sequence data for thousands of S. aureus strains and is an important data source for large-scale epidemiological and genetic association studies on S. aureus.22 A previous study reported that alleles with a single-nucleotide mutation should be marked as a novel ST.23 The 65 strains of S. aureus typed by MLST clearly reflected the molecular characteristics of S. aureus isolated from Jiangxi Province. In this study, 50 STs of S. aureus were identified, of which 44 were newly discovered, indicating a rich diversity of S. aureus from southern Jiangxi. Ganzhou area, located in the south of Jiangxi Province in eastern China, upstream of the Ganjiang River, in the transitional zone extending from the southeast coastal area to the central inland area, is an important channel from the mainland to the southeast coastal area. This prefecture-level city has the largest population and subordinate counties and cities in Jiangxi Province, and the resident population is approximately 20%. It is possible that this densely populated host environment led to the rich diversity of S. aureus isolates from southern Jiangxi.
The emergence of these new STs is not accidental; the associated mutants may have emerged a long time ago and spread throughout the population. However, these new STs were only recently identified, probably because of the lack of studies on S. aureus molecular typing in Jiangxi Province. These new STs may become important molecular types of MRSA in Jiangxi Province. Surveillance of new STs using isolates obtained during epidemics should be enhanced. We speculate that isolates from different countries and regions often have different molecular subtypes. Isolates of the same molecular type may have the same or similar antibiotic-resistance profiles. Isolates obtained from different regions or sources may have different molecular types, and isolates with different molecular types may have different antibiotic resistance, which is presumed to be the result of different molecular types competing under antibiotic screening pressure in different regions.24 The prevalence of dominant molecular types promotes the spread of antibiotic-resistant bacteria.
In this study, cluster analysis of the 50 STs showed that they were co-clustered into 12 clonal complexes. These unique clonal complexes all originate from southern Jiangxi, according to the MLST analysis. Thus, MLST analysis of strains in different regions may reveal the clonal lineage and evolutionary relationships of S. aureus in those regions and help in understanding the molecular epidemiology and provide the experimental basis for pathogenic bacteria prevention and treatment.
fnbA, a cell wall-anchoring protein involved in host cell adhesion and invasion, is the main protein involved in S. aureus infection.25 This protein interacts with host-cell integrins via a fibrin bridge to induce actin rearrangement, leading to bacterial internalization.26 Among 65 strains of S. aureus isolated from skin infection secretion samples, the PCR detection rate of fnbA (100%) exceed the 45.8% reported in another study.14 However, the prevalence of fnbA in other hospitals’ burn wards was significantly lower than 2.9%.27 This difference suggests that S. aureus may adjust its virulence gene expression in response to environmental conditions in patients with burns who lack intact skin barrier. The 100% detection rate of fnbA may underscores its critical role in promoting S. aureus adherence to host tissues in infections. The S. aureus isolated in this study from secretion samples of patients with skin infections was highly invasive.
In this study, the detection rate of arcA (98.5%) was the highest, followed by that of mecA (56.9%), ermC (18.5%), TSST (20.0%), ermA (21.5%), mupA (9.2%), and PVL (12.3%). arcA is known to promote the invasion, colonization, and growth of S. aureus; enhance the bacterial growth microenvironment; and suppress immune responses. It is also associated with resistance to oxacillin, erythromycin, levofloxacin, and gentamicin.28 The high detection rate of arcA in S. aureus samples may indicates a strong invasive capacity and substantial resistance to antibiotics. These findings are consistent with our drug susceptibility test results, and further confirm the strong invasive potential and antibiotic resistance of S. aureus in hospitalized patients with skin infections at our hospital.
PVL is mainly associated with community-acquired MRSA infections, especially skin or soft tissue infections. One study reported a PVL positivity rate of 11.6%.29 This finding is consistent with the prevalence of PVL in our study. However, another study on S. aureus in skin and soft tissue infections found a significantly higher PVL-positive rate of 63.5%.30 In the same study,30 48 strains (50%) were mecA-positive, similar to those in our study, indicating that S. aureus isolates from these two studies had similar resistance patterns.
Previous studies have shown that among 197 strains,31 134 (68%) included TSST and 172 (87.3%) mecA; these values are much higher than our data. Because we included secretion samples of patients with skin infections, this may indicate that S. aureus in skin infections is less likely to express TSST. The findings may be related to the lesser role played by TSST in the invasion of the skin by S. aureus in skin infections. TSST-1, encoded by the TSST gene, is an important member of the S. aureus superantigen (sags) and may cause staphylococcal toxic shock syndrome (TSS) in susceptible hosts.32 The relatively high rate of TSST-positive S. aureus isolation coupled with the low incidence of TSS strongly suggests that adequate expression of TSST leads to disease only under appropriate environmental and/or genetic regulation.33 mecA confers resistance to β-lactam antibiotics in S. aureus. The positivity rate of mecA in our S. aureus isolates was lower than that reported in the literature, indicating that our isolates were less resistant to β-lactam antibiotics, which may facilitate the clinical use of antibiotics.
According to previous studies, 18.7% of isolates carry ermC, followed by 15.6% for ermA.34 These are similar to the results of the present study, indicating that the prevalence of macrolide-resistant S. aureus is similar in different regions. In contrast to our results, mupA was not detected in isolates in one study.35 In addition, a systematic review and meta-analysis reported a low proportion of mupA-positive S. aureus in Africa (0.5% and 8%), while the expression rate of mupA in our study of 9.2% differs from the data reported in the literature.36 Given that mupA is associated with acquired resistance to mupirocin,37 the higher use of mupirocin in our study area compared to other regions may account for this difference. Thus, this highlights the need to consider mupirocin dosing to reduce resistance in the future, or use mupirocin in combination with other antibiotics to reduce treatment cycles.38
S. aureus in southern Jiangxi has abundant molecular types and varying degrees of antibiotic resistance to various antibiotics. The emergence and rapid spread of antibiotic resistance genes has brought serious challenges to global public health, and also complicates the clinical treatment of infection. The results of this study will be helpful for promoting drug resistance monitoring of MRSA isolates in southern Jiangxi, China. The results of this study suggest that the use of β-lactam, macrolide, and lincosamide antimicrobial agents should be reduced. Therefore, in the medical environment, we need to use antibiotics carefully,39 strengthen the monitoring of drug resistance, and choose antibiotics rationally according to the results of drug sensitivity. The dosage of antibiotics should be strictly controlled, and the rotation of drugs and withdrawal period should be strictly implemented. In addition, it is necessary to actively research, develop, and promote use of Chinese herbal medicines, microecological agents, and other new non-antibiotic drugs.40
A limitation of this study is the inability to detect more virulence genes. The inclusion of a larger number of isolated bacterial specimens could enhance the referential values of the conclusions.
Conclusion
The increasing prevalence of bacterial resistance poses a serious challenge to the effectiveness of antibiotics, especially with the increase in MRSA. The results showed that MRSA strains were significantly associated with mecA. Resistance rates of MRSA to oxacillin, cefoxitin, clindamycin, and erythromycin were higher than those of MSSA. The high carrying rate of virulence gene fnbA and arcA of S. aureus were determine, and 44 new STs were identified. These may be associated with the geographical location of southern Jiangxi and local trends in antibiotic use. The study of the clonal lineage and evolutionary relationships of S. aureus in these regions may help in understanding the molecular epidemiology and provide the experimental basis for pathogenic bacteria prevention and treatment. Future research should explore a wider range of virulence genes and employ a wider range of genetic characterization approaches to enhance the overall understanding of S. aureus isolates, contributing to ongoing efforts to combat antibiotic resistance.
Abbreviations
MLST, multilocus sequence typing; MRSA, methicillin-resistant S. aureus; PCR, polymerase chain reaction; MSSA, methicillin-sensitive S. aureus; CLSI, Clinical and Laboratory Standards Institute; ATCC, American Type Culture Collection; STs, sequence types; CC, clone the complex.
Data Sharing Statement
This paper reports the data is stored in national genomics GenBase Beijing genomics institute, Chinese Academy of Sciences, China data center12 biological information center, Chinese Academy of Sciences, the entry numbers are C_AA042252.1, C_AA042259.1, C_AA042258.1, C_AA042257.1, C_AA042256.1, C_AA042255.1, C_AA042254.1, C_AA042253.1, publicly to https://ngdc.cncb.ac.cn/genbase.
Ethics Approval and Informed Consent
This study was approved by the Ethics Committee of the First Affiliated Hospital of Gannan Medical University (process number: LLSC-2023175). All patients provided written informed consent for their data to be published in the article.
Author Contributions
All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.
Funding
This study was supported by the National Natural Science Foundation of China (Grant No: 81960566). The study sponsor was not involved in performing the research or in writing the paper.
Disclosure
The authors report no conflicts of interest in this work.
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