PREVALENCE OF STAPHYLOCOCCUS AUREUS IN DENTAL INFECTIONS AND THE OCCURRENCE OF MRSA IN ISOLATES

Ameen Abdullah Yahya Al-Akwa1, Abdul Qader Mohammed Qasem Zabara1, Hassan Abdulwahab Al-Shamahy2image, Mohammed A Al-labani1, Khaled M Al-Ghaffari3, Ammar M Al-Mortada4

Ahmed M. Al-Haddad5, Amani Abdulhakeem Al-Sharani6 

1Orthodontics, Pedodontics and Prevention Department Faculty of Dentistry, Sana'a University, Yemen

2Departement of Basic Sciences, Faculty of Dentistry, Sana’a University, Republic of Yemen

3Department of Conservative Dentistry and Oral Health, Sana’a University, Republic of Yemen

4Department of Maxillo-Facial, Faculty of Dentistry, Sana’a University, Republic of Yemen

5Department of Medical Laboratories, College of Medicine and Health Sciences, Hadhramout University, Al-Mukalla, Yemen

6Oral Medicine and Periodontology Department, College of Dentistry, University of Sciences and Technology, Yemen

ABSTRACT 

Objectives:  Staphylococcus aureus is an opportunist that causes systemic infections and dental infections in the human being body. This organism increases its resistance to many categories of antibiotics all day and turn out to be more resistant, and this led to a growing feeling of concern in this era. Given this fact, the aims of this study were to determine the frequency of S. aureus in oral infections and to determine the prevalence of MRSA strains and the sensitivity of isolated S. aureus to antibiotics, in patients who attended dental clinics in major public hospitals and private clinics in the city of Sana'a-Yemen.

Subjects and methods:  The study was conducted for a year, early in December 2018 and ending in November 2019. The study included 296 patients, 153 male and 143 female, ages 5 to 65, with an average age of 36.2 years. Demographic and clinical data were collected in questionnaire, then pus or oral swabs were collected from patients, cultivated, isolated and identified by standard laboratory techniques. MRSA was ascertained by means of the method of disc diffusion to 1µg of oxicillin disc and 5 µg of methacillin disc; an antimicrobial sensitivity test was carried out by disc diffusion method of selected antibiotics.The oral  infections include  dental abscesses,  periodontal abscesses, gingivitis, periodentitis, dental caries,  pulpitis and oral thrush. 

Results:  Of a total of 296 cultured pus and swabs, only 217 produced a positive culture (73.3%). Gram-positive bacteria formed 67.4% of the total isolates where S. aureus was the predominant pathogen (43.1%).  The prevalence of MRSA was 23.5%. There was a higher rate of antibiotic resistance tested in MRSA isolates compared to a lower rate of resistance in MSSA as well as 22.2% of MRSA isolates were vancomycin resistant, while only 11.4% of MSSA were vancomycin resistant.

Conclusion:  It can be concluded, S. aureus was the most widespread isolate in dental infections, high rate of  MRSA,  the appearance of S. aureus isolates resistant to vancomycin and other broad choice of antibiotics have raised MRSA in oral infections into a multi-drug-resistant, making it more and more hazardous in oral infections. Consistent assessment of oral associated infections and observing the pattern of antibiotic sensitivity and strict drug policy for antibiotics are recommended.

Keywords: Antibiotic resistance, dental  infection, MRSA,  Staphylococcus  aureus,  Sana'a, Yemen.


INTRODUCTION

The human oral cavity acts as a growth medium for pathogens as a result of its moisture, temperature, and nutritional content such as fats, carbohydrates, and protein1. There are numerous categories of dental infections that happen in the patient's oral cavity such as periodontal disease, tooth decay, dental ache, dental plaque, dental abscess, dental calculus, dentin hypersensitivity, hyperdontia, acid erosion, malocclusion, ulcerative  gingivitis, dental  fluorosis, tooth impaction, acute necrotizing, etc. S. aureus is a presumed pathogen for many oral diseases, such as oral mucositis, periodontitis, peri-implantitis,  endodontic  infections and even  dental caries2-5. S. aureus is  a  Gram-positive,  non-spore forming,  non-motile, grape   like   clusters and the most   important coagulase  positive  pathogen  from  staphylococci  due  to mixture  of  invasiveness, toxic  mediated  virulence and antibiotic resistance6. Some S. aureus strains have developed drug-resistant7. Methicillin-resistant Staph.aureus (MRSA)8 are the strains of S. aureus that have been resistant to beta-lactam antibiotics, which include penicillins, amoxicillin, ampicillin, methicillin, oxacillin, cephalosporins, etc9. The tendency of S. aureus to acquire antibiotic resistance led to a global dissemination of clone expressing various anti-microbial resistances. Many bacterial diseases occur in hospitals and in community due to MRSA strains and sometimes   lead   to death10-12. S. aureus infection, including MRSA strains, has long been common in Yemen13. Because the arbitrary use of antibiotics is a typical practice, hospital environments are not clean enough and crowding of patients and health workers supports the spread of infectious germs including S. aureus13. The potential presence of S. aureus is especially important in dental infections due to its increased resistance13,14. Therefore it is very logical to check the status of the microbial resistance against the commonly used antibiotics for the treatment of dental infections that occur by S. aureus. Considering this, the aims of this study were to determine the frequency of of S. aureus in oral infections and to identify the prevalence of MRSA strains and antibiotic sensitivity of isolated S. aureus, in patients attended the dental clinics at the main general hospitals and private clinics in Sana’a city-Yemen.

 

PATIENTS, MATERIALS AND METHODS

PatientsThe study was carried out for a year, from December 2018 to November 2019. The study comprised 296 patients, 153 male and 143 female, ages 5 to 65, with an average age of 36.2 years. The selected cases were defined as all patients who had a major complaint of various oral infections and entered the dental clinics previously mentioned. The technique of sampling in the study was case– finding. As for determining the size of the sample, it was relied on taking all patients who attended dental clinics during the study period and estimated one year in which the study materials were collected, which included clinical and demographic data, etc. Demographic and clinical data were collected in a questionnaire. After that pus or oral swabs were collected from patients, cultivated, isolated and identified using standard laboratory methods. The oral infections include dental abscesses, periodontal abscesses, gingivitis, periodentitis, dental caries, pulpitis and oral thrush.

Cases definition: All patients enrolled in this study, who had a major complaint of various oral infections and entered dental clinics in the city of Sana'a. 

Data collection and processingA questionnaire was filled out for each patient with the patient's personal and clinical data. This included age, gender, profession and relevant clinical information regarding bacterial and fungal oral infections. Upon initial hospitalization, cultures were obtained from the oral infection sites in order to isolate the causative agents of various bacteria and fungi.

Antimicrobial susceptibility test:  Antibiotic resistance phenotypes (Methicillin/Oxacillin sensitivity test): All isolates of S. aureus were checked for the sensitivity to 1 μg Oxacillin disc and 5 μg Methicillin disc (Difco) by the disk diffusion method  that  instructed by NCCLS. The resistance breakpoints were ≥ 12 mm to ≤ 10 mm for 1 μg Oxacillin  and ≥14 mm to ≤ 10 mm for 5 μg Methicillin. The capacity of extra antibiotic discs to inhibit MRSA or MSSA was estimated according to the instructions provided by NCCLS using commercially available discs that include: Augmenitin (AC 30 µg), tetracycline (T,30 µg), erythromycin(E,15 µg), ceftizoxime (CEF 20 µg ), ciprofloxacin(Ci 5 µg), clindamycin(CC, 2 µg), clarithromycin (Cl 15 µg)  and vancomycin(V, 30 µg).  The zone of inhibition produced by S. aureus against each antibiotic was  measured  and  interpreted  as  resistant and  susceptible  according  to  standards  of  Clinical  Laboratory  and Standards Institute15

 

RESULTS

The positive culture rate was 73.3% and 26.7% of the specimens were negative (Table 1). A hundred and eighty 180 (67.4%) were Gram positive bacteria, 71 (26.6%) were Gram negative bacteria and 16 (6.0%) were C.albicans. The most frequent microorganism isolated was S. aureus (115 isolates), followed by Bacteroides spp (71 isolates) and Strept. pyogens (38 isolates) with percentages of 43.1%, 26.6% and 14.2% respectively.  

Table 1: Cultural results of the 296 patients with bacterial and fungal oral infections.


Table 3 shows the susceptibility patterns of S. aureus isolates towards the different commonly used antibiotics. The resistant results for MRSA of antibiotics represented in number and percentages are shown in the following order: vancomycin (22.2%), clindamycin (26%), ciprofloxacin (29.7%), ceftizoxime (40.7%), calrithromycin (37%), augmentin (55.6%), tetracycline (74%), and erythromycin (23.3%). 

Table 2: Distribution of the 217 positive culture isolates according to their group and genus.


 

The resistant results for MSSA of antibiotics represented in number and percentages are shown in the following order: vancomycin (11.4%), clindamycin (30.3%), ciprofloxacin (22.7%), ceftizoxime (30.3%), calrithromycin (26.3%), augmentin (30.7%), tetracycline (72.7%), and erythromycin (60.2%).

 

DISCUSSION

Dental patients typically take antibiotics primarily to treat postoperative and secondary infections. In the current study all 115 coagulase positive isolates of S. aureus were subjected to disc diffusion method to 5 μg Methicillin disc and 1 μg Oxacillin disc to determine MRSA; the test results  discovered that  23.5% of isolated S. aureus were MRSA strain. The current rate of 23.5% of MRSA in all isolates of S. aureus is lower than the rate reported from Yemen in previous reports in which MRSA was isolated from 55% of health workers in Taiz, Yemen16, also it is very lower than that reported by al-Baidani and others17,  among health care workers in Al Hodeida City, Yemen where the MRSA rate was 86%. On the other hand, it was almost similar to that mentioned by Al-Safani et al.,13 (19.3%) among patients attending Military Hospital, Sana'a City; and  Alyahawi, and others among patients of some private hospitals in Sana’a City (17.6%),18.

Table 3: The antibiotic sensitivity for 115 isolated  MRSA and MSSA for tested antibiotics.


HA-MRSA occurred at a higher rate than CA-MRSA in the world, but in Yemen the rates were similar for the HA-MRSA and CA-MRSA (19.4% and 17%, respectively), as mentioned by Al-Safani et al.,13 and Alyahawi et al.,18. This result can be explained by long hospitalization, random use of antibiotics, lack of awareness, and receiving antibiotics before coming to hospital, which are some of the potential predisposing factors for the appearance of MRSA in the hospital and community. Results of current study differs from that reported in the United States of America where a high incidence of MRSA occurred in a hospital-acquired S. aureus infection (HA-MRSA) (59%), compared to a community-acquired infection of  S. aureus (17%)19 . This difference can be explained by the CA-MRSA biology appearing to be different from the HA-MRSA and the MSSA, which may allow CA-MRSA to cause diseases other than those expected from MSSA20,21.   

With the advent of HA-MRSA, it is likely that it not only replaced HA-MSSA, but also led to a comprehensive increase in Staph. aureus infection in healthcare settings22,23. In addition, almost all researchers say the same thing that inpatients and outpatients suffer from S. aureus/MRSA infection higher than S. aureus/MSSA due to the widespread prevalence of MRSA in a community environment and hospitals23-25. When comparing MRSA rate with the MRSA rate in S. aureus dental infections, current study result (23.5%) was almost lower than the 30% MRSA reported by Das Manisha et al.,26.   Also ,the prevalence of MRSA (23.5%) was higher than the results of Ayepola et al.,27 who reported 2.4%, as well as Smith et al.,28 6% of MRSA positive isolates were reported in oral infection. Another study by Renvert et al.,29 in Sweden, observed similar results associated with periodontitis patients.

According to Kurita   et al.,30 dental patients are not the only ones responsible for spreading MRSA bacteria, but a health professional may transfer this pathogen through their tools, so there are consistent guidelines for controlling MRSA as the CDC some standard precautions may be recommended which may help reduce the prevalence of MRSA among dental patients31.  The reason for conducting the current study was to know the prevalence of MRSA and the current antimicrobial profile of S. aureus in order to choose the appropriate empirical treatment for these oral infections.  In current study, vancomycin resistance (VRSA) was 22.2% in isolated MRSA. This result differs from that reported in Asian countries where the vancomycin resistance rate was no more than 10%32. The occurrence of VRSA in Asian countries has also been documented by Kaleem et al.,33 in Pakistan to be 3.3%, 6% in India, by Sonavane and Mathur34, 7.5% in Iran by Mehdinejad et al.,35 and 9% in Jordan are from Al-Zoubi and others36. The current study results  revealed  that  73% dental S. aureus isolates were found resistant to tetercycline followed by 53.9% to   erythromycin,   46.5%   to augmanten,   and   35.6%   to Cefotaxime where low rates of resistant occurred for ciprofloxacin (24.3%), Clarithromycin (28.7%), and  Clindamycin (29.6%) (Table 3).  Kim  and  Lee37  and Das Manisha  et al.,26 reported  more sensitive strains of S. aureus isolated   from   the periodontal patients   showed sensitivity  95% to ciprofloxacin (vs 75.7%) and 90% to tetracycline (vs 31%), 90% to  erythromycin (vs 46.1%), and to 3rd generation cephalosporins 95% (vs 62.4%)   that  is  comparatively higher  than the current  study.  Similar  antimicrobial  susceptibility  results were reported by previous authors8,38-40. The  higher  resistant  rates in Yemen  to  commonly  used  antibiotics indicates  indiscriminate or  haphazard  use that may have effect  on  treatment cost,  poor   prognosis as   well  as enhance  the   bacterial   infection   and   growth   virulent  pathogens. 

 

CONCLUSION

The prevalence of S. aureus in dental patients is very high and showed resistance to commonly used antibiotics in addition to a high rate of MRSA. Despite these results, the sample size of this study was insufficient and the study period was too short to reveal the actual picture of MRSA involved in dental infection in Sana'a, Yemen. We recommend extensive studies to determine the prevalence of MRSA, genome analysis, identification of toxin gene and other antibiotic resistant gene. Teeth should be brushed regularly, maintain oral hygiene, and  consulting with  dental  doctors  to  check up the teeth once in a month should be taken to maintain a distance from dental infections. 

 

AUTHOR'S CONTRIBUTION

 This research work is part of a research work under the supervision of Hassan Al-Shamahy. The field, clinical and laboratory works of the research was done by the corresponding author, the fifth author, the sixth author and the eighth author. The first, second, fourth, and seventh author supervised the work and edited the manuscript.

 

ACKNOWLEDGMENTS 

The authors thank the University of Sana’a for financial support.

 

CONFLICT OF INTEREST 

No conflict of interest associated with this work. 

 

REFERENCES

1. Mohapatra SB,  Pattnaik  M,  Ray  P.  Microbial  association  of dental  caries.  Asian  J Exp  Biol Sci 2012; 3(2):360-367. 

2. Gibson J, Wray D, Bagg J. Oral staphylococcal mucositis: A new clinical entity in orofacial granulomatosis and Crohn’s disease. Oral Surgery,   Oral   Medicine,   Oral   Pathology,   Oral   Radiology,   and Endodontology  2000; 89(2):171-176. 

3. Heitz-Mayfield LJ, Lang NP. Comparative biology of chronic and aggressive periodontitis vs. peri implantitis. Periodontology 2010; 53(1):167-181.

https://doi.org/10.1111/j.1600-0757.2010.00348.x

4. Poeschl PW, Crepaz V, Russmueller G, et al.  Endodontic pathogens causing deep neck space infections: clinical   impact   of   different   sampling   techniques   and   antibiotic susceptibility. J Endodontics 2011; 37(9):1201-1205.

https://doi.org/10.1016/j.joen.2011.05.029

5. Passariello C, Puttini M, Iebba V, et al.  Influence of oral  conditions  on  colonization  by  highly  toxigenic Staphylococcus aureus strains. Oral Diseases  2012;18(4):402-409. 

https://doi.org/10.1111/j.1601-0825.2011.01889.x

6. Loir  LY,  Baron  F,  Gautier  M. Staphylococcus  aureus and  food poisoning. Genetics and Molecular Research J  2003; 2(1):63-76.  PMID:12917803

7. Faden  A.  Methicillin-resistant Staphylococcus  aureus (MRSA) screening   of   hospital   dental   clinic   surfaces. Saudi   J Biol Sci 2019; 26(7):1795-1798.

https://doi.org/10.1016/j.sjbs.2018.03.006

8. Rajaduraipandi    K,  Mani  KR,  Panneerselvam  K,  et al.  Prevalence  and  antimicrobial  susceptibility pattern  of  methicillin  resistant Staphylococcus  aureus:  A  multicentre study. Indian J Med Microbiol 2006; 24(1):34-38. https://doi.org/10.4103/0255-0857.19892

9. David MZ, Daum RS. Community-associated methicillin-resistant Staphylococcus aureus: epidemiology and  clinical  consequences  of an emerging epidemic. Clin Microbiol Rev 2010; 23(3):616-687. https://doi.org/10.1128/CMR.00081-09

10. Bannerman T, Peacock  S.  Staphylococcus,  Micrococcus,  and other catalase positive cocci. In: Murray, P., Baron, E., Jorgensen, J., Landry, M., Pfaller, M. (Eds.), Manual of Clinical Microbiology 9th ed. ASM Press, Washington, DC, 2007; 390-411.  

11. Moussa IM, Al-Qahtani AA, Gassem MA, et al.  Pulsed-field  gel  electrophoresis  (PFGE)  as  an epidemiological marker for typing of methicillin-resistant Staphylococcus  aureus recovered  from  King  Saudi  Arabia  (KSA). African J Microbiol Res 2011; 5(12):1492-1499. 

12. Peters PJ, Brooks JT, McAllister SK, et al. Methicillin-resistant Staphylococcus aureus colonization  of  the  groin  and  risk  for  clinical  infection  among HIV-infected adults. Emerging Infectious Diseases 2013; 19(4):623-629.

http://dx.doi.org/10.3201/eid1904.121353

13. Al-Safani AMA, Al-Shamahy HA, Al-Moyed KA. Prevalence, antimicrobial susceptibility pattern and risk factors of MRSA isolated from clinical specimens among military patients at 48 medical compound in Sana'a city-Yemen. Universal J Pharm Res2018; 3(3): 40-44. 

https://doi.org/10.22270/ujpr.v3i3.165

14. Vellappally S, Divakar DD, Al Kheraif AA, et al. Occurrence of vancomycin-resistant Staphylococcus  aureus in  the  oral  cavity  of patients  with  dental  caries. Acta Microbiologica  et  Immunologica Hungarica  2017; 64(3):343-351.

https://doi.org/10.1556/030.64.2017.033

15. Clinical and Laboratory Standards Institute [CLSI). Performance Standards for Antimicrobial Disc Susceptibility Tests. (11th edn.), Approved standard M02-A11– Publication of Clinical and Laboratory Standards Institute [CLSI), 2012; USA, 32.

16. Abdel Monem, MO. Nasal Carriage of Staphylococcus aureus among Healthcare Workers in Althawra Hospital, Taiz City, Republic of Yemen. Australian J Basic App Sci 2012; 6(7): 417-424. 

17. Al-Baidani AR, El-Shouny WA, Shawa TM. Antibiotic susceptibility of MRSA in three hospitals at Hodeida city Yemen. Globle J Pharma 2011; 5(2):106-111.

18. Alyahawi A, Alkaf A, Alhomidi A. Prevalence of methicillin resistant Staphylococcus aureus (MRSA) and antimicrobial susceptibility patterns at a private hospital in Sana’a, Yemen. Universal J Pharm Res 2018; 3(3): 4-9. https://doi.org/10.22270/ujpr.v3i3.159

19. Fridkin SK, Hageman JC, Morrison M, et al. Methicillin-resistant Staphylococcus aureus disease in three communities. N Engl J Med 2005; 352:1436–44.

https://doi.org/10.1056/NEJMoa043252

20. Askarian M, Zeinazadeh A, Japoni A, et al. Prevalence of nasal carriage o Methicillin resistance Staphylococcus aureus and its antibiotic susceptibility pattern in healthcare workers at Namazi Hospital, Shiraz, Iran. Int J Infect Dis 2009; 13:e241–e247. 

https://doi.org/10.1016/j.ijid.2008.11.026

21. Mahalingam U, Thirunvukarasu T, Murugananthan K. Methicillin resistant Staphylococcus aureus among nurses in a tertiary care hospital in Sri Lanka. Ceylon Medical J 2014; S9:63–65.

https://doi.org/10.4038/cmj.v59i2.7067

22. Elie-Turenne MC, et al. Prevalence and characteristics of Staphylococcus aureus colonization among healthcare professionals in an urban teaching hospital. Infection Control Hosp Epidemiol 2010; 31:S74–S80. 

https://doi.org/10.1086/652525

23. Radhakrishna M, D'Souza M, Kotigadde S, et al.  Prevalence of methicillin resistant Staphylococcus aureus carriage amongst health care workers of critical care units in Kasturba Medical College Hospital, Mangalore, India. J Clin Diagnostic Research 2013; 7(12):2697–2700. https://doi.org/10.7860/JCDR/2013/5160.3735

24. Shibabaw A, Abebe T, Mihret A. Nasal carriage rate of methicillin-resistant Staphylococcus aureus among Dessie Referral hospital health care workers; Dessie Northeast, Ethiopia. Antimicrobial Resistance and Infection Control 2013; 2:25.

https://doi.org/10.1186/2047-2994-2-25

25. Iyer A, Kumosani T, Azhar E, Barbour E, Harakeh S. High incidence rate of methicillin-resistant Staphylococcus aureus among healthcare workers in Saudi Arabia. J Infect Dev Ctnes 2014; 8(3):372–378. 

https://doi.org/10.3855/jidc.3589

26. Das Manisha, Al Momen Sabuj Abdullah, Haque Zobayda Farzana et al.  Characterization of Staphylococcus aureus isolated from human dental infection.  Afr J Microbiol Res 2019; 13(14):273-278.

https://doi.org/10.5897/AJMR2019.9076

27. Ayepola  OO,  Olasupo  NA,  Egwari LO,  et al. Molecular  characterization  and  antimicrobial  susceptibility  of Staphylococcus    aureus isolates    from    clinical    infection    and asymptomatic carriers in Southwest Nigeria. Plos One 2015; 10(9):e0137531.  

https://doi.org/10.1371/journal.pone.0137531

28. Smith AJ, Robertson D, Tang  MK, et al.  S.  aureus in   the   oral   cavity:   a   three-year retrospective   analysis   of   clinical   laboratory   data. British   Dental J 2003; 195(12):701-703. 

https://doi.org/10.1038/sj.bdj.4810832

29. Renvert S,  Lindahl  C,  Renvert  H,  Persson  GR.  Clinical  and microbiological   analysis   of   subjects   treated   with   Brånemark   or AstraTech  implants:  a  7-year  follow-up  study. Clin Oral Imp Res 2008;19(4):342-347.  

https://doi.org/10.1111/j.1600-0501.2007.01476.x

30. Kurita H,  Kurashina  K,  Honda  T .  Nosocomial  transmission  of methicillin-resistant Staphylococcus  aureus via  the  surfaces  of the dental operatory. British Dental J 2006; 201(5):297-300.  

 https://doi.org/10.1038/sj.bdj.4813974

31. Harte JA.  Standard and transmission-based precautions:  an update for dentistry. The J American Dent Assoc  2010; 141(5):572-581. 

https://doi.org/10.14219/jada.archive.2010.0232

32. Mehmood A, Butt T, Usman M. A study on MRSA isolates to detect reduced susceptibility to vancomycin: A preliminary report. Infect Dis J 2007; 16:102–104. 

33. Kaleem F, Usman J, Uddin Roz. Sensitivity pattern of methicillin resistant Staphylococcus aureus isolated from patients admitted in a tertiary care hospital of Pakistan. Iran J Microbiol 2010; 2(3): 143–146. PMID: 22347563

34. Sonavane A, Mathur M. Screening for vancomycin intermediate-resistant Staphylococcus aureus among clinical isolates of MRSA. Indian J Med Microbiol 2007; 25:79–80. 

https://doi.org/10.4103/0255-0857.31078

35. Mehdinejad M, Sheikh AF, Jolodar A. Study of methicillin resistance in Staphylococcus aureus and species of coagulase negative Staphylococci isolated from various clinical specimens. Pak J Med Sci 2008; 24:719–24. 

36. Al-Zoubi, MS, Ibrahim Ali Al-Tayyar, Emad Hussein, et al. Antimicrobial susceptibility pattern of Staphylococcus aureus isolated from clinical specimens in Northern area of Jordan. Iran J Microbiol 2015; 7(5): 265–272. PMID: 26719783

37. Kim  GY,  Lee  CH.  Antimicrobial  susceptibility  and  pathogenic genes  of Staphylococcus  aureus isolated  from  the  oral  cavity  of patients   with   periodontitis. J Periodon  Implant Sci 2015;  45(6):223-228. 

https://doi.org/10.5051/jpis.2015.45.6.223

38. Khan  AH,  Shamsuzzaman  AKM,  Paul  SK, et al.  Antimicrobial  susceptibility  and  coagulase  typing of  MRSA strains   at   Mymensingh   Medical   College. Bangladesh   J Med Microbiol 2007; 1(2):56-60. 

39. Kim    Y.    Multiple    antimicrobial    resistance    patterns    of Staphylococcus  aureus isolated  from  periodontitis  patients  in  Seoul, Korea. Korean  J Oral  Maxillofacial  Pathol 2012; 36:317-339.

https://doi.org/10.5051/jpis.2015.45.6.223

40. Naeem  M,  Adil  M,  Naz  SM,  et al. Resistance and sensitivity pattern of Staphylococcus aureus; a  study  in  lady  reading  hospital  Peshawar. J Postgraduate Med Inst 2012; 27(1):42-47.