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Antibiotic Susceptibility Patterns of Neisseria Meningitides Isolates from Asymptomatic Carriers in Gurage Zone, Southern Ethiopia

Received: 13 March 2019     Accepted: 13 April 2019     Published: 30 May 2019
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Abstract

Neisseria meningitides represents a pathogen of great public health importance in both developed and developing countries. Resistance to some antimicrobial agents used either for therapy of invasive infections or for prophylaxis of case contacts has long been recognized. However, there is no data in relation with the circulating serotypes and antimicrobial resistance patterns of Neisseria meningitides in Ethiopia. Therefore; the aim of this study was to assess drug susceptibility patterns of Neisseria meningitides from asymptomatic carrier for all age group at Meskan and Mareko Districts, Gurage Zone, in the Southern Nations, Nationalities and Peoples Regional State Ethiopia. A Cross-sectional survey of an age-stratified population in Meskan and Mareko Districts, Gurage Zone, in the Southern Nations, Nationalities and Peoples Regional State in Ethiopia was conducted at AHRI as part of the MenAfricar project. A total of 4110 subjects were screened and from these 187 Neisseria meningitides positive isolates was selected for Antimicrobial susceptibility testing (AST). Antimicrobial susceptibility test was done on stored Neisseria meningitides isolates. The activities of ten antimicrobial agents used for treatment and prophylaxis of meningococcal disease were investigated. The AST was performed for Neisseria meningitides isolates according to the criteria of the CLSI guide line by disk diffusion method. Data were analysed by using SPSS version 20.0 software. From 187 isolates 8(4.28%) were serogroup X, 24(12.83%) were serogroup Y, 1(0.53%) were serogroup W135, and 154(82.35%) were non determinant (ND). Cotrimoxazol resistant were the highest accounting116(62%), Ciprofloxacine resistant were 112(60%), Cefotaxime resistant were 26(14%), Ceftriaxone resistant were 24(13%), Meropenenem resistantwere 21(11%), Minocycline resistant were 15(8%), Rifampine resistant were 149(7%), 10(5%) were resistant to Azithromycine, 7(4%) were resistant to Chloramphenicol and 6(3%) were resistant to Levofloxacin and 102(54.5%) isolates were resistance for more than one drug. So, it has beenconcluded that an antimicrobial susceptibility pattern of Neisseria meningitides among asymptomatic carriers is high and continued surveillance of meningococci for antimicrobial resistance is necessary to monitor early detection of changes in susceptibility patterns that might affect recommendations for chemoprophylaxis and treatment.

Published in American Journal of Health Research (Volume 7, Issue 1)
DOI 10.11648/j.ajhr.20190701.13
Page(s) 12-18
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2019. Published by Science Publishing Group

Keywords

Neisseria Meningitides, Serogroups, Sensitivity Pattern, Drug Resista

References
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[2] Stephens David S., Brian Greenwood, and Petter Brandtzaeg. "Epidemic meningitis, meningococcaemia, and Neisseria meningitides." The Lancet. 2007; 369.9580: 2196-2210.
[3] Caugant DA, Maiden MC. Meningococcal carriage and disease—population biology and evolution. Vaccine. 2009;27: B64-70.
[4] Harcourt BH, Anderson RD, Wu HM, Cohn AC, Mac Neil JR, Taylor TH, Wang X, Clark TA, Messonnier NE, Mayer LW. Population-based surveillance of Neisseria meningitidis antimicrobial resistance in the United States. In Open forum infectious diseases. Oxford University Press.2015;2(3):117.
[5] Hedberg S. T., Fredlund H., Nicolas P., Caugant D. A., Olcén P., &Unemo M. "Antibiotic susceptibility and characteristics of Neisseria meningitides isolates from the African meningitis belt, 2000 to 2006: phenotypic and genotypic perspectives." Antimicrobial agents and chemotherapy. 2009; 53(4): 1561-1566.
[6] Arreaza L., de La Fuente L., & Vázquez J. A."Antibiotic Susceptibility Patterns of Neisseria meningitides Isolates from Patients and Asymptomatic Carriers." Antimicrobial agents and chemotherapy. 2000; 44(6): 1705-1707.
[7] CLSI: Performance standards for antimicrobial susceptibility testing; twenty-fourth information supplement. CLSI document M100-S24. Wayne, PA: Clinical and Laboratory Standards Institute. 2016.
[8] Jorgensen, James H., Sharon A. Crawford, and Kristin R. Fiebelkorn. "Susceptibility of Neisseria meningitides to 16 antimicrobial agents and characterization of resistance mechanisms affecting some agents." Journal of clinical microbiology. 2005; 43(7): 3162-3171.
[9] Thulin Hedberg S. "Antibiotic susceptibility and resistance in Neisseria meningitides: phenotypic and genotypic characteristics." 2009.
[10] Bårnes GK, Kristiansen PA, Beyene D, Workalemahu B, Fissiha P, Merdekios B, Bohlin J, Préziosi MP, Aseffa A, Caugant DA. Prevalence and epidemiology of meningococcal carriage in Southern Ethiopia prior to implementation of MenAfriVac, a conjugate vaccine. BMC infectious diseases. 2016; 16(1):639.
[11] Kristiansen PA, Ba AK, Ouédraogo AS, Sanou I, Ouédraogo R, Sangaré L, Diomandé F, Kandolo D, Saga IM, Misegades L, Clark TA. Persistent low carriage of serogroup A Neisseria meningitides two years after mass vaccination with the meningococcal conjugate vaccine, MenAfriVac. BMC infectious diseases. 2014; 14(1):663.
[12] Stephens DS. Conquering the meningococcus. FEMS microbiology reviews. 2007; 31 (1): 3-14.
[13] Ercis S, Köseoğlu O, Salmanzadeh-Ahrabi S, Ercis M, Akin L, Hasçelik C. The prevalence of nasopharyngeal Neisseria meningitidis carriage, serogroup distribution, and antibiotic resistance among healthy children in Cankaya municipality schools of Ankara province. Mikrobiyolojibulteni. 2005; 39(4):411-20.
[14] Pavlopoulou ID, Daikos GL, Alexandrou H, Petridou E, Pangalis A, Theodoridou M, Syriopoulou VP. Carriage of Neisseria meningitidis by Greek children: risk factors and strain characteristics. Clinical microbiology and infection. 2004; 10 (2):137-42.
[15] Assefa A., Gelaw B., Shiferaw Y., &Tigabu Z. "Nasopharyngeal Carriage Rate and Antimicrobial Susceptibility Pattern of Potential Pathogenic Bacteria among Paediatrics Outpatients at Gondar University Teaching Hospital, Ethiopia." J Infect Dis Ther. 2013; 1.109: 2332-0877.
[16] Tentera, A. Serogroups and antibiotic susceptibility patterns of Neisseria meningitides isolated from army recruits in a training camp. Malaysian J Pathol. 2007; 29(2): 91 – 94.
[17] Manchanda V, Gupta S, Bhalla P. Meningococcal disease: history, epidemiology, pathogenesis, clinical manifestations, diagnosis, antimicrobial susceptibility and prevention. Indian journal of medical microbiology. 2006; 24(1):7.
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  • APA Style

    Fikerte Mulatu, Zelalem Mekonnen, Biruk Yeshitela, Hiwot Tilahun, Melaku Yidnekachew, et al. (2019). Antibiotic Susceptibility Patterns of Neisseria Meningitides Isolates from Asymptomatic Carriers in Gurage Zone, Southern Ethiopia. American Journal of Health Research, 7(1), 12-18. https://doi.org/10.11648/j.ajhr.20190701.13

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    ACS Style

    Fikerte Mulatu; Zelalem Mekonnen; Biruk Yeshitela; Hiwot Tilahun; Melaku Yidnekachew, et al. Antibiotic Susceptibility Patterns of Neisseria Meningitides Isolates from Asymptomatic Carriers in Gurage Zone, Southern Ethiopia. Am. J. Health Res. 2019, 7(1), 12-18. doi: 10.11648/j.ajhr.20190701.13

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    AMA Style

    Fikerte Mulatu, Zelalem Mekonnen, Biruk Yeshitela, Hiwot Tilahun, Melaku Yidnekachew, et al. Antibiotic Susceptibility Patterns of Neisseria Meningitides Isolates from Asymptomatic Carriers in Gurage Zone, Southern Ethiopia. Am J Health Res. 2019;7(1):12-18. doi: 10.11648/j.ajhr.20190701.13

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  • @article{10.11648/j.ajhr.20190701.13,
      author = {Fikerte Mulatu and Zelalem Mekonnen and Biruk Yeshitela and Hiwot Tilahun and Melaku Yidnekachew and Marechign Yimer and Tsehaynesh Lema and Wude Mhiret and Kassu Desta and Oumer Ali and Adane Mihret},
      title = {Antibiotic Susceptibility Patterns of Neisseria Meningitides Isolates from Asymptomatic Carriers in Gurage Zone, Southern Ethiopia},
      journal = {American Journal of Health Research},
      volume = {7},
      number = {1},
      pages = {12-18},
      doi = {10.11648/j.ajhr.20190701.13},
      url = {https://doi.org/10.11648/j.ajhr.20190701.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajhr.20190701.13},
      abstract = {Neisseria meningitides represents a pathogen of great public health importance in both developed and developing countries. Resistance to some antimicrobial agents used either for therapy of invasive infections or for prophylaxis of case contacts has long been recognized. However, there is no data in relation with the circulating serotypes and antimicrobial resistance patterns of Neisseria meningitides in Ethiopia. Therefore; the aim of this study was to assess drug susceptibility patterns of Neisseria meningitides from asymptomatic carrier for all age group at Meskan and Mareko Districts, Gurage Zone, in the Southern Nations, Nationalities and Peoples Regional State Ethiopia. A Cross-sectional survey of an age-stratified population in Meskan and Mareko Districts, Gurage Zone, in the Southern Nations, Nationalities and Peoples Regional State in Ethiopia was conducted at AHRI as part of the MenAfricar project. A total of 4110 subjects were screened and from these 187 Neisseria meningitides positive isolates was selected for Antimicrobial susceptibility testing (AST). Antimicrobial susceptibility test was done on stored Neisseria meningitides isolates. The activities of ten antimicrobial agents used for treatment and prophylaxis of meningococcal disease were investigated. The AST was performed for Neisseria meningitides isolates according to the criteria of the CLSI guide line by disk diffusion method. Data were analysed by using SPSS version 20.0 software. From 187 isolates 8(4.28%) were serogroup X, 24(12.83%) were serogroup Y, 1(0.53%) were serogroup W135, and 154(82.35%) were non determinant (ND). Cotrimoxazol resistant were the highest accounting116(62%), Ciprofloxacine resistant were 112(60%), Cefotaxime resistant were 26(14%), Ceftriaxone resistant were 24(13%), Meropenenem resistantwere 21(11%), Minocycline resistant were 15(8%), Rifampine resistant were 149(7%), 10(5%) were resistant to Azithromycine, 7(4%) were resistant to Chloramphenicol and 6(3%) were resistant to Levofloxacin and 102(54.5%) isolates were resistance for more than one drug. So, it has beenconcluded that an antimicrobial susceptibility pattern of Neisseria meningitides among asymptomatic carriers is high and continued surveillance of meningococci for antimicrobial resistance is necessary to monitor early detection of changes in susceptibility patterns that might affect recommendations for chemoprophylaxis and treatment.},
     year = {2019}
    }
    

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  • TY  - JOUR
    T1  - Antibiotic Susceptibility Patterns of Neisseria Meningitides Isolates from Asymptomatic Carriers in Gurage Zone, Southern Ethiopia
    AU  - Fikerte Mulatu
    AU  - Zelalem Mekonnen
    AU  - Biruk Yeshitela
    AU  - Hiwot Tilahun
    AU  - Melaku Yidnekachew
    AU  - Marechign Yimer
    AU  - Tsehaynesh Lema
    AU  - Wude Mhiret
    AU  - Kassu Desta
    AU  - Oumer Ali
    AU  - Adane Mihret
    Y1  - 2019/05/30
    PY  - 2019
    N1  - https://doi.org/10.11648/j.ajhr.20190701.13
    DO  - 10.11648/j.ajhr.20190701.13
    T2  - American Journal of Health Research
    JF  - American Journal of Health Research
    JO  - American Journal of Health Research
    SP  - 12
    EP  - 18
    PB  - Science Publishing Group
    SN  - 2330-8796
    UR  - https://doi.org/10.11648/j.ajhr.20190701.13
    AB  - Neisseria meningitides represents a pathogen of great public health importance in both developed and developing countries. Resistance to some antimicrobial agents used either for therapy of invasive infections or for prophylaxis of case contacts has long been recognized. However, there is no data in relation with the circulating serotypes and antimicrobial resistance patterns of Neisseria meningitides in Ethiopia. Therefore; the aim of this study was to assess drug susceptibility patterns of Neisseria meningitides from asymptomatic carrier for all age group at Meskan and Mareko Districts, Gurage Zone, in the Southern Nations, Nationalities and Peoples Regional State Ethiopia. A Cross-sectional survey of an age-stratified population in Meskan and Mareko Districts, Gurage Zone, in the Southern Nations, Nationalities and Peoples Regional State in Ethiopia was conducted at AHRI as part of the MenAfricar project. A total of 4110 subjects were screened and from these 187 Neisseria meningitides positive isolates was selected for Antimicrobial susceptibility testing (AST). Antimicrobial susceptibility test was done on stored Neisseria meningitides isolates. The activities of ten antimicrobial agents used for treatment and prophylaxis of meningococcal disease were investigated. The AST was performed for Neisseria meningitides isolates according to the criteria of the CLSI guide line by disk diffusion method. Data were analysed by using SPSS version 20.0 software. From 187 isolates 8(4.28%) were serogroup X, 24(12.83%) were serogroup Y, 1(0.53%) were serogroup W135, and 154(82.35%) were non determinant (ND). Cotrimoxazol resistant were the highest accounting116(62%), Ciprofloxacine resistant were 112(60%), Cefotaxime resistant were 26(14%), Ceftriaxone resistant were 24(13%), Meropenenem resistantwere 21(11%), Minocycline resistant were 15(8%), Rifampine resistant were 149(7%), 10(5%) were resistant to Azithromycine, 7(4%) were resistant to Chloramphenicol and 6(3%) were resistant to Levofloxacin and 102(54.5%) isolates were resistance for more than one drug. So, it has beenconcluded that an antimicrobial susceptibility pattern of Neisseria meningitides among asymptomatic carriers is high and continued surveillance of meningococci for antimicrobial resistance is necessary to monitor early detection of changes in susceptibility patterns that might affect recommendations for chemoprophylaxis and treatment.
    VL  - 7
    IS  - 1
    ER  - 

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Author Information
  • International Livestock Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Department of Medical Laboratory Sciences, School of Allied Health Sciences, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

  • Armauer Hansen Research Institute, Addis Ababa, Ethiopia

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