Search for


search for

CrossRef (0)
Distribution of Coagulase-Negative Staphylococci and Antibiotic Resistance
Biomed Sci Letters 2021;27:45-50
Published online June 30, 2021;
© 2021 The Korean Society For Biomedical Laboratory Sciences.

Heechul Park1,2,§,* , Sung-Bae Park1,2,§,* , Junseong Kim1,2,* and Sunghyun Kim1,2,†,**

1Department of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Korea
2Clinical Trial Specialist Program for in Vitro Diagnostics, Brain Busan 21 Plus Program, the Graduate School, Catholic University of Pusan, Busan 46252, Korea
Correspondence to: Sunghyun Kim. Department of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Korea.
Tel: +82-51-510-0560, Fax: +82-51-510-0568, e-mail:
*Graduate student, **Professor.
§The first authors contributed equally to this work.
Received May 31, 2021; Revised June 28, 2021; Accepted June 28, 2021.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Coagulase-negative staphylococci (CoNS) are a typical group of microorganisms, and the recent advances in laboratory technology and medicine has dramatically modified their significance in medical practice. CoNS, which were previously classified as normal bacterial flora, have recently been reported to be associated with serious infectious diseases, such as surgical wound infection or periprosthetic joint infection. Representative CoNS include Staphylococcus epidermidis, S. haemolyticus, and S. saprophyticus, which are known to cause serious problems in biomaterial-based and prosthetic device infections, as well as to cause simple urinary tract infections in sexually active women. Over the last decade, the clinical isolation rate of CoNS has been increasing, and antibiotic resistance has also been occurring. This review aimed to investigate the incidence of CoNS infection and to use the results as basic data for the management of CoNS, with a focus on the isolation rate and antibiotic resistance in clinical surgery.
Keywords : Coagulase-negative staphylococci (CoNS), Sepsis, Identification, Antibiotic resistance

Microorganisms are closely associated with humans. Humans have co-evolved with the trillions of microbes inhabiting the human body and creating complex, body-habitat-specific, adaptive ecosystems that are finely attuned to the constantly changing host physiology (Lloyd-Price et al., 2016). Among the numerous microorganisms, representative bacteria are the main taxa of living things. Bacteria, are commonly considered as normal flora, as they have a symbiotic relationship with humans under normal circumstances; however, they can become dangerous pathogens when the immune function is not in its normal state, such as during surgery and treatment (Marples et al., 1990).

Coagulase-negative staphylococci (CoNS) are a group of staph bacteria, which generally exist as normal flora, although several of these bacteria are potential pathogens under reduced immunity in humans (Al Tayyar et al., 2015; Argemi et al., 2019). CoNS bacteria have long been regarded as culture contaminants. However, their infective role as pathogens has become important in recent years (Natsis and Cohen, 2018). There are about 45 types of known CoNS, and the representative strains are Staphylococcus epidermidis, S. haemolyticus, and S. saprophyticus (Grace et al., 2019). CoNS strains are frequently isolated in hospital environments; the representative CoNS strains include S. cohnii, S. warneri, S. sciuri, S. homonis, S. simulans, S. pasteuri, S. arlettae, and S. xilosus (Table 1) (Al Tayyar et al., 2015; Houssaini et al., 2019; Dziri et al., 2016; Keim et al., 2011; Begum and Anbumani, 2011). Among the CoNS species associated with clinical disease, S. epidermidis is identified in infection associated with biomaterial-based and prosthetic devices. Meanwhile, S. saprophyticus causes simple urinary tract infection in sexually active women, and S. haemolyticus causes variable infection such as periprosthetic joint infections (PJI) and bacteremia (Eltwisy et al., 2020). In addition, identification of CoNS is of increasing importance in infection, as the isolation rate of CoNS from the blood of patients with risk factors has been increasing (Nickel and Costerton, 1992; Houssaini et al., 2019).

Prevalence of CoNS in hospital environments

Previous studies (publication year) Dziri et al. (2016) Al Tayyar et al. (2015) Azih and Enabulele (2013) Keim et al. (2011) Begum and Anbumani (2011)
Species n (%) n (%) n (%) n (%) n (%) Total, n (%)
Staphylococcus epidermidis 2 (2.4) 122 (54.7) 16 (26.7) 70 (36.6) 49 (43.4) 259 (38.7)
Staphylococcus haemolyticus 38 (45.8) 52 (23.4) 17 (28.3) 33 (17.3) 19 (16.8) 159 (23.7)
Staphylococcus saprophyticus 30 (36.1) 7 (3.1) 11 (18.3) 5 (2.6) 4 (3.5) 57 (8.5)
Staphylococcus warneri 2 (2.4) 4 (1.8) ND* 35 (18.3) 7 (6.2) 48 (7.2)
Staphylococcus simulans 1 (1.2) 2 (0.9) 6 (10.0) 21 (11.0) 5 (4.4) 35 (5.2)
Staphylococcus hominis ND* 13 (5.8) ND* 4 (2.1) 11 (9.7) 28 (4.2)
Staphylococcus capitis ND* 8 (3.6) ND* 4 (2.1) 7 (6.2) 19 (2.8)
Staphylococcus sciuri 2 (2.4) ND* ND* 15 (7.9) ND* 17 (2.5)
Staphylococcus xylosus 4 (4.8) 2 (0.9) 6 (10.0) 3 (1.6) 1 (0.9) 16 (2.4)
Staphylococcus cohni 2 (2.4) ND* ND* ND* 9 (8.0) 11 (1.6)
Staphylococcus lugdunensis ND* 9 (4.0) ND* ND* 1 (0.9) 10 (1.5)
Staphylococcus auricularis ND* 4 (1.8) ND* 1 (0.5) ND* 5 (0.7)
Staphylococcus chromogenes ND* ND* 3 (5.0) ND* ND* 3 (0.4)
Staphylococcus pasteuri 1 (1.2) ND* ND* ND* ND* 1 (0.1)
Staphylococcus arlettae 1 (1.2) ND* ND* ND* ND* 1 (0.1)
Staphylococcus schleiferi ND* ND* 1 (1.7) ND* ND* 1 (0.1)
Total, n (%) 83 (12.4) 223 (33.3) 60 (9.0) 191 (28.5) 113 (16.9) 670 (100.0)

*ND: not detected

1. Importance of CoNS

In recent years, the use of devices such as intravascular catheters as well as the increase in invasive manipulation in immunosuppressed patients, have been recognized as one of the important factors associated with nosocomial infections caused by bacteria (Supré et al., 2011). The frequency of CoNS infection has been increasing mainly due to bacteremia, catheter-related infections, endocarditis, and urinary tract infections; moreover, resistance to antibiotics, especially vancomycin, is a serious problem, as bacteria demonstrating severe resistance have been identified (Koksal et al., 2009; De Vecchi et al., 2018). A 2013 study for Azih et al., has reported that 105 CoNS were isolated from 79 clinical specimens, such as discharge from wounds, urine, and male genital infections, which could cause secondary infections, such as sepsis (Azih and Enabulele, 2013). These CoNS infections are usually internal or implanted foreign bodies that cause immune damage and are emerging as the cause of infectious diseases in both the community and hospital environment (Chu et al., 2008; Piette and Verschraegen, 2009).

2. Distribution of CoNS in sepsis, surgical wound infection (SWI), and periprosthetic joint infection (PJI)

2.1. CoNS in Sepsis

Sepsis is one of the most common causes of death among hospitalized patients, and it can be caused by bacteria, fungi, or viruses (Rello et al., 2017). The causative agent of sepsis varies, but 11 pathogens are known as the major causative organisms (Liu et al., 2018). S. aureus and Escherichia coli are the most common causes; CoNS is also frequently isolated from blood, which in turn is considered contaminated, although no symptoms have been reported in such cases (Biedenbach et al., 2004). However, in developed countries, CoNS, such as S. epidermidis and S. haemolyticus, are indicated as the major pathogens involved in late-onset sepsis (Goli흦ska et al., 2020) and are among the pathogenic bacteria implicated in catheter-related blood stream infection (CRBSI) (Osaki et al., 2020). According to one report, approximately 10% of the causative pathogens of sepsis are CoNS (Chun et al., 2015), and the most detected CoNS was S. epidermidis (20%), followed by S. hominis; S. aureus was detected at a rate of approximately 9% (Osaki et al., 2020). In Korea, in 13,519 blood cultures obtained from pediatric patients, 750 bacteria were identified, 560 (74.67%) of which were CoNS (Table 2). Indeed, the degree of contamination is high, and this finding is significant because contaminations are highly associated with diseases (Chun et al., 2019).

Prevalence of potential pathogens isolated from the blood culture in the Republic of Korea

Microorganism No. True pathogen (%) Contaminated (%) Reference
Coagulase-negative staphylococci 560 133 (23.8) 427 (76.2) Chun et al., 2019
Viridans group Streptococcus 93 43 (46.2) 50 (53.8)
Bacillus species 54 15 (27.7) 39 (72.3)
Corynebacterium species 21 4 (19.0) 17 (81.0)
Micrococcus species 14 0 (0.0) 14 (100.0)
Propionibacterium acnes 8 0 (0.0) 8 (100.0)
Total 750 195 555

2.2. CoNS in surgical wound infection (SWI)

SWI is one of the complications in variable surgery, and the risk of SWI is 1.9 per 100 interventions (Hijas-Gómez et al., 2017). Also, SWI remains as the most common and expensive hospital-acquired infection, accounting for 20% of cases (Campwala et al., 2019). During infection, pain, swelling, erythema, warmth, and impairment of function are consistently seen (Peel and Taylor, 1991).

In one study involving SWI patients, 82 samples were analyzed; CoNS were identified in 54.9% of the samples, especially methicillin-resistant CoNS (MR-CoNS) (13.4%) (Ahmed et al., 2021). In another study, S. aureus (53.2%) and CoNS (23.4%) were identified in 74 SWI patients (Liang et al., 2019). In yet another study, 31 of the 52 patients were confirmed to have bacterial growth, and 20 of them were infected with S. epidermidis (65%). These results suggest that in SWI patients, the proportion of CoNS is quite high, and this phenomenon remains a serious healthcare-associated infection (HAI) problem.

2.3. CoNS in periprosthetic joint infection (PJI)

PJI carries both a higher economic burden and greater morbidity and mortality compared with other aseptic complications (Gross et al., 2021). A PJI infection requires extended periods of hospitalization and re-operations and thus poses a significant financial burden (Li et al., 2020). Therefore, management of established PJI requires a combination of pathogen-specific antibiotics and surgical intervention (De Vecchi et al., 2018).

These PJIs are frequently caused by CoNS; importantly, antibiotic resistance among causative pathogens of PJI has been increasing (Veltman et al., 2019). A study involving 50 CoNS and 39 S. aureus infection cases has found that the CoNS were significantly more resistant to daptomycin and gentamicin and were more susceptible to rifampicin than S. aureus (De Vecchi et al., 2018). Another study reported that in 106 PJI cases, 43 cases involved S. aureus and 32 involved streptococci infections; only 8 cases involved CoNS infections (Rakow et al., 2019). Another study involving 74 patients showed that PJI was caused by methicillin-resistant S. aureus (MRSA) (20.3%), methicillin-resistant S. epidermidis (MRSE) (32.4%), methicillin-susceptible S. aureus (MSSA) (18.9%), and methicillin-susceptible S. epidermidis (MSSE) (28.4%) (Hischebeth et al., 2019). These results suggested that in PJI, the major causative agents are gram-positive bacteria, especially S. aureus and CoNS. Moreover, the incidence of MRSE has been increasing; thus, MRSE must be diagnosed and treated promptly.

3. Distribution of antibiotic-resistant CoNS

As mentioned previously, the distribution of CoNS in various diseases as well as the incidence of antibiotic-resistant CoNS have been increasing. In addition, biofilm formation has been observed among CoNS, making them more difficult to treat because of their antibiotic resistance compared with non-biofilm bacteria (Saber et al., 2017). Methicillin resistance in staphylococci is caused by the expression of PBP2a (PBP') encoded by the mecA gene (Hanssen et al., 2004). According to one study, S. epidermidis is the most frequent isolate among methicillin-resistant CoNS (Schuster et al., 2018). Oxacillin resistance is often mediated by the mecA gene, which encodes a supplemental penicillin binding protein (PBP2a) with low affinity to semisynthetic penicillins (Archer and Niemeyer, 1994). The mecA gene is located on a mobile genetic element known as the staphylococcal cassette chromosome mec (SCCmec) that comprises the mec complex consisting of the mecA gene and its regulator genes mecI and mecRI, along with the ccr complex, which is responsible for integration (Pereira et al., 2020). Among the several MR-CoNS, S. epidermidis and S. haemolyticus were the most common species identified (Venugopal et al., 2019). Also, according to one study, S. haemolyticus isolates demonstrated the overall highest resistance rates (Tekeli et al., 2020). Another study investigated the antibiotic resistance and virulence factors of CoNS isolated from blood cultures. Among the 93 CoNS species, 86 were resistant to cefoxitin, and 49 displayed multi-antibiotic resistance (Al-Haqan et al., 2020). Also, vancomycin-resistant CoNS is a recent health concern, especially in serious infections, such as bloodstream infections, as it may lead to failure of therapy (Mashaly and El-Mahdy, 2017). Therefore, early detection of antibiotic-resistant CoNS is important in order to effectively eliminate the bacteria that causes bloodstream infection.


The management of the CoNS plays an important role in controlling S. aureus-related infectious diseases in recent years. CoNS has a symbiotic relationship with humans in a normal environment, but it can become a dangerous pathogen when immune function is not normal, such as surgery or treatment. Besides, if CoNS are identified in blood cultures, it remains a serious healthcare problem whether infection or a contaminant (Muñoz-Gamito et al., 2020). Recently, it was confirmed that the treatment for surgical wound infection and the separation rate of CoNS from the joint around the prosthesis were increased, and the infection rate was also increased in septic patients. Also, the abuse and misuse of antibiotics, and antibiotic-resistant CoNS, which is caused when appropriate treatment was not conducted, are also becoming a problem in the community. After all, CoNS has been regarded as a contaminant, however its importance has increased in relation to various clinical diseases. Therefore, a research of CoNS on the distribution in variable diseases and antibiotic-resistant patterns are important to dissolve these situations. In addition, it is necessary to characterize the role of virulence factor and pathogenesis of CoNS in the host to identify the etiology in human.


This paper was supported by RESEARCH FUND from Catholic University of Pusan.


The authors declare that they have no conflict of interest.

  1. Ahmed E, Gad G, Soliman W, El-Asady R, Hasaneen A, Abdelwahab SF. Prevalence of methicillin-resistant coagulase-negative staphylococci among Egyptian patients after surgical interventions. Trop Doct. 2021. 51: 40-44.
    Pubmed CrossRef
  2. Al Tayyar I, Al-Zoubi M, Hussein E, Khudairat S, Sarosiekf K. Prevalence and antimicrobial susceptibility pattern of coagulase -negative staphylococci (CoNS) isolated from clinical specimens in Northern of Jordan. Iran J Microbiol. 2015. 7: 294-301.
    Pubmed KoreaMed
  3. Al-Haqan A, Boswihi SS, Pathan S, Udo EE. Antimicrobial resistance and virulence determinants in coagulase-negative staphylococci isolated mainly from preterm neonates. Plos One. 2020. 15: e0236713.
    Pubmed KoreaMed CrossRef
  4. Archer G, Niemeyer D. Origin and evolution of DNA associated with resistance to methicillin in staphylococci. Trends Microbiol. 1994. 2: 343-347.
    Pubmed CrossRef
  5. Argemi X, Hansmann Y, Prola K, Prevost G. Coagulase-negative staphylococci pathogenomics. Int J Mol Sci. 2019. 20: 1215.
    Pubmed KoreaMed CrossRef
  6. Azih A, Enabulele I. Species distribution and virulence factors of coagulase negative staphylococci isolated from clinical samples from the University of Benin Teaching hospital, Edo State, Nigeria. J Nat Sci Res. 2013. 3: 38-43.
  7. Begum E, Anbumani N. Prevalence and antimicrobial susceptibility pattern of Coagulase-negative Staphylococcus. Int J Med Public Health. 2011. 1: doi:10.5530/ijmedph.4.2011.14.
  8. Biedenbach D, Moet G, Jones R. Occurrence and antimicrobial resistance pattern comparisons among bloodstream infection isolates from the SENTRY Antimicrobial Surveillance Program (1997-2002). Diagn Microbiol Infect Dis. 2004. 50: 59-69.
    Pubmed CrossRef
  9. Campwala I, Unsell K, Gupta S. A comparative analysis of surgical wound infection methods: predictive values of the CDC, ASEPSIS, and Southampton scoring systems in evaluating breast reconstruction surgical site infections. Plast Surg. 2019. 27: 93-99.
    Pubmed KoreaMed CrossRef
  10. Chu VH, Woods CW, Miro JM, Hoen B, Cabell CH, Pappas PAPappas PA et al. Emergence of coagulase-negative staphylococci as a cause of native valve endocarditis. Clin Infect Dis. 2008. 46: 232-242.
    Pubmed CrossRef
  11. Chun K, Syndergaard C, Damas C, Trubey R, Mukindaraj A, Qian SQian S et al. Sepsis pathogen identification. J Lab Autom. 2015. 20: 539-561.
    Pubmed CrossRef
  12. Chun S, Kang CI, Kim YJ, Lee NY. Clinical Significance of Isolates Known to Be Blood Culture Contaminants in Pediatric Patients. Medicina. 2019. 55: 696.
    Pubmed KoreaMed CrossRef
  13. De Vecchi E, George DA, Romanò CL, Pregliasco FE, Mattina R, Drago L. Antibiotic sensitivities of coagulase-negative staphylococci and Staphylococcus aureus in hip and knee periprosthetic joint infections: does this differ if patients meet the International Consensus Meeting Criteria? Infect Drug Resist. 2018. 11: 539-546.
    Pubmed KoreaMed CrossRef
  14. Dziri R, Klibi N, Lozano C, Ben Said L, Bellaaj R, Tenorio C, Boudabous ABoudabous A et al. High prevalence of Staphylococcus haemolyticus and Staphylococcus saprophyticus in environmental samples of a Tunisian hospital. Diagn Microbiol Infect Dis. 2016. 85: 136-140.
    Pubmed CrossRef
  15. Houssaini ZE, Harrar N, Zerouali K, Belabbes H, Elmdaghri N. Prevalence of Coagulase-Negative Staphylococci in Blood Cultures at the Ibn-Rochd University Hospital in Casablanca. Pan Afr Med J. 2019. 33: 193.
    Pubmed KoreaMed CrossRef
  16. Eltwisy HO, Abdel-Fattah M, Elsisi AM, Omar MM, Abdelmoteleb AA, El-Mokhtar MA. Pathogenesis of Staphylococcus haemolyticus on primary human skin fibroblast cells. Virulence. 2020. 11: 1142-1157.
    Pubmed KoreaMed CrossRef
  17. Goli흦ska E, Strus M, Tomusiak-Plebanek A, Wi휌cek G, Kozie흦 흟, Lauterbach R. Coagulase-Negative Staphylococci Contained in Gut Microbiota as a Primary Source of Sepsis in Low-and Very Low Birth Weight Neonates. J Clin Med. 2020. 9: 2517.
    Pubmed KoreaMed CrossRef
  18. Grace JA, Olayinka BO, Onaolapo JA, Obaro SK. Staphylococcus aureus and coagulase-negative staphylococci in bacteraemia: the epidemiology, predisposing factors, pathogenicity and antimicrobial resistance. Clin Microbiol. 2019. 8: 1-5.
  19. Gross CE, Della Valle CJ, Rex JC, Traven SA, Durante EC. Fungal Periprosthetic Joint Infection: A Review of Demographics and Management. J Arthroplasty. 2021. 36: 1758-1764.
    Pubmed CrossRef
  20. Hanssen AM, Kjeldsen G, Sollid JU. Local variants of Staphylococcal cassette chromosome mec in sporadic methicillin-resistant Staphylococcus aureus and methicillin-resistant coagulase-negative Staphylococci: evidence of horizontal gene transfer? Antimicrob Agents Chemother. 2004. 48: 285-296.
    Pubmed KoreaMed CrossRef
  21. Hijas-Gómez AI, Egea-Gámez RM, Martínez-Martín J, González-Díaz R, Losada-Viñas JI, Rodríguez-Caravaca G. Surgical Wound Infection Rates and Risk Factors in Spinal Fusion in a University Teaching Hospital in Madrid, Spain. Spine (Phila Pa 1976). 2017. 42: 748-754.
    Pubmed CrossRef
  22. Hischebeth GT, Randau TM, Ploeger MM, Friedrich MJ, Kaup E, Jacobs C, Molitor E, Hoerauf A, Gravius S, Wimmer MD. Staphylococcus aureus versus Staphylococcus epidermidis in periprosthetic joint infection-Outcome analysis of methicillin-resistant versus methicillin-susceptible strains. Diagn Microbiol Infect Dis. 2019. 93: 125-130.
    Pubmed CrossRef
  23. Keim LS, Torres-Filho SR, Silva PV, Teixeira LA. Prevalence, aetiology and antibiotic resistance profiles of coagulase negative staphylococci isolated in a teaching hospital. Braz J Microbiol. 2011. 42: 248-255.
    Pubmed KoreaMed CrossRef
  24. Koksal F, Yasar H, Samasti M. Antibiotic resistance patterns of coagulase-negative staphylococcus strains isolated from blood cultures of septicemic patients in Turkey. Microbiol Res. 2009. 164: 404-410.
    Pubmed CrossRef
  25. Li C, Renz N, Trampuz A, Ojeda-Thies C. Twenty common errors in the diagnosis and treatment of periprosthetic joint infection. Int Orthop. 2020. 44: 3-14.
    Pubmed KoreaMed CrossRef
  26. Liang Z, Rong K, Gu W, Yu X, Fang R, Deng Y, Lu L. Surgical site infection following elective orthopaedic surgeries in geriatric patients: Incidence and associated risk factors. Int Wound J. 2019. 16: 773-780.
    Pubmed KoreaMed CrossRef
  27. Liu CF, Shi XP, Chen Y, Jin Y, Zhang B. Rapid diagnosis of sepsis with TaqMan-Based multiplex real-time PCR. J Clin Lab Anal. 2018. 32: e22256.
    Pubmed KoreaMed CrossRef
  28. Lloyd-Price J, Abu-Ali G, Huttenhower C. The healthy human microbiome. Genome Med. 2016. 27. 8: 51.
    Pubmed KoreaMed CrossRef
  29. Marples RR, Richardson JF, Newton FE. Staphylococci as part of the normal flora of human skin. Soc Appl Bacteriol Symp Ser. 1990. 19: 93S-99S.
    Pubmed CrossRef
  30. Mashaly GE, El-Mahdy RH. Vancomycin heteroresistance in coagulase negative Staphylococcus blood stream infections from patients of intensive care units in Mansoura University Hospitals, Egypt. Ann Clin Microbiol Antimicrob. 2017. 19; 16: 63.
    Pubmed KoreaMed CrossRef
  31. Muñoz-Gamito G, Cuchí E, Roigé J, Gómez L, Jaén À, Pérez JPérez J et al. Higher accuracy of genotypic identification compared to phenotyping in the diagnosis of coagulase-negative staphylococcus infection in orthopedic surgery. Infect Dis (Lond). 2020. 52: 883-890.
    Pubmed CrossRef
  32. Natsis NE, Cohen PR. Coagulase-Negative Staphylococcus Skin and Soft Tissue Infections. Am J Clin Dermatol. 2018. 19: 671-677.
    Pubmed CrossRef
  33. Nickel JC, Costerton JW. Coagulase-negative staphylococcus in chronic prostatitis. J Urol. 1992. 147: 398-400.
    Pubmed CrossRef
  34. Osaki S, Kikuchi K, Moritoki Y, Motegi C, Ohyatsu S, Murakawa YMurakawa Y et al. Distinguishing coagulase-negative Staphylococcus bacteremia from contamination using blood-culture positive bottle detection pattern and time to positivity. J Infect Chemother. 2020. 26: 672-675.
    Pubmed CrossRef
  35. Peel AL, Taylor EW. Proposed definitions for the audit of postoperative infection: a discussion paper. Surgical Infection Study Group. Ann R Coll Surg Engl. 1991. 73: 385-388.
    Pubmed KoreaMed
  36. Pereira VC, Romero LC, Pinheiro-Hubinger L, Oliveira A, Martins KB, Cunha MLRSD. Coagulase-negative staphylococci: a 20-year study on the antimicrobial resistance profile of blood culture isolates from a teaching hospital. Braz J Infect Dis. 2020. 24: 160-169.
    Pubmed CrossRef
  37. Piette A, Verschraegen G. Role of coagulase-negative staphylococci in human disease. Vet Microbiol. 2009. 16. 134: 45-54.
    Pubmed CrossRef
  38. Rakow A, Perka C, Trampuz A, Renz N. Origin and characteristics of haematogenous periprosthetic joint infection. Clin Microbiol Infect. 2019. 25: 845-850.
    Pubmed CrossRef
  39. Rello J, Valenzuela-Sánchez F, Ruiz-Rodriguez M, Moyano S. Sepsis: A Review of Advances in Management. Adv Ther. 2017. 34: 2393-2411.
    Pubmed KoreaMed CrossRef
  40. Saber H, Jasni AS, Jamaluddin TZMT, Ibrahim R. A Review of Staphylococcal Cassette Chromosome mec (SCCmec) Types in Coagulase-Negative Staphylococci (CoNS) Species. Malays J Med Sci. 2017. 24: 7-18.
    Pubmed KoreaMed CrossRef
  41. Schuster D, Josten M, Janssen K, Bodenstein I, Albert C, Bierbaum GBierbaum G et al. Detection of methicillin-resistant coagulase-negative staphylococci harboring the class A mec complex by MALDI-TOF mass spectrometry. Int J Med Microbiol. 2018. 308: 522-526.
    Pubmed CrossRef
  42. Supré K, Haesebrouck F, Zadoks RN, Vaneechoutte M, Piepers S, De Vliegher S. Some coagulase-negative Staphylococcus species affect udder health more than others. J Dairy Sci. 2011. 94: 2329-2340.
    Pubmed CrossRef
  43. Tekeli A, Öcal DN, Dolapç캇 캅. Two-stage revision arthroplasty for coagulase-negative staphylococcal periprosthetic joint infection of the hip and knee. World J Orthop. 2019. 18. 10: 348-355.
    Pubmed KoreaMed CrossRef
  44. Veltman ES, Moojen DJF, van Ogtrop ML, Poolman RW. detection and typing of methicillin-resistant Staphylococcus aureus and methicillin-resistant coagulase-negative staphylococci isolated from cattle, animal handlers, and their environment from Karnataka, Southern Province of India. Vet World. 2019. 12: 1760-1768.
    Pubmed KoreaMed CrossRef
  45. Venugopal N, Mitra S, Tewari R, Ganaie F, Shome R, Shome BRShome BR et al. Molecular detection and typing of methicillin-resistant Staphylococcus aureus and methicillin-resistant coagulase-negative staphylococci isolated from cattle, animal handlers, and their environment from Karnataka, Southern Province of India. Vet World. 2019. 12: 1760-1768.
    Pubmed KoreaMed CrossRef