Prevalence of Multi-Drug Resistant Bacterial Isolates in Healthcare Environments
Abstract:
To
evaluate and measure the frequency of multi-drug resistance bacterial isolates
in various healthcare environments. This study employed the disc diffusion
susceptibility test to assess the antibiotic resistance of Acinetobacter, E.
coli, Klebsiella sp., and Pseudomonas sp. to carbapenem, extended-spectrum
β-lactamase (ESBL), and colistin. In the present study, Acinetobacter was
generally found resistant to carbapenem at 72% and 71% at 75 µg/ml and minimum
for Carbapenem + Colistin at 11% at 150 µg/ml. E. coli counts of the
antibiotic-resistant carbapenem samples were 85% and 71% at 150 µg/ml and the
lowest in colistin 12% at 225 µg/ml. The Klebsiella isolates obtained were
highly sensitive to carbapenem (98%) at 150 µg/ml, followed by 75 µg/ml (96%)
and 225 µg/ml (92%). Low colistin resistance was also observed (7%). The
evaluation presented in Pseudomonas sp. of the antibiotic-resistant carbapenem
samples was high at 47 at 225 µg/ml, and minimum in ESBL + Colistin at 5% at
150 µg/ml. Klebsiella (92%), Acinetobacter (71%), E. coli (64%), and
Pseudomonas sp. (47%) were highly sensitive to 75 µg/ml carbapenem. The MICs of
carbapenem-resistant Acinetobacter were shown in the 6.45 (OD values) at 75
µg/mL. Carbapenem and ESBL antibiotic-resistant Klebsiella were found at OD
values of 9.14, 9.74, 9.61, and 3.45, 3.21 3.67, (OD values) at 75, 150, and
225 µg/mL, respectively, and the highest susceptibility was observed with
Carbapenem 9.74 at 150 µg/mL. The ternary colour frequency of the graph indicates
that Klebsiella sp. showed good susceptibility to carbapenem, carbapenem +
ESBL, carbapenem, and colistin. Carbapenem is a highly effective therapy
against infections caused by antibiotic-resistant Klebsiella sp.
References:
[1].
Prestinaci,
F., Pezzotti, P., Pantosti, A., 2015, Antimicrobial resistance: a global
multifaceted phenomenon. Pathogens and Global Health, 109(7), 309-318.
[2]. Das, B., Sarma, M., Kumar, R., Borah, P., Sinha, S.,
Gupta, P., Durlabhji, P., 2020, Isolation, identification and antibiotic
sensitivity pattern of Escherichia coli
isolated from various clinical sample in a tertiary care hospital, Jaipur,
Rajasthan, India. International Journal of Research in Medical
Sciences, 8(5), 1774-1778.
[3]. Kamala, K., Sivaperumal, P., 2023,
Predominance of multi-drug resistant extended spectrum β lactamase producing
bacteria from marine fishes. Environmental Pollution, 323, 121314.
[4]. Khan, D., Zeb, M., Khattak, S.K., Shah, A.A., Abdullah,
M., Bilal, M., 2023, Molecular characterization and antibiotic susceptibility
pattern of bacterial strains isolated from diabetic foot ulcers. Endocrine
and Metabolic Science, 12, 100136.
[5]. Jabeen, K., Saleem, S., Jahan, S., Nizamudin, S., Arshad,
F., Huma, Z.E., Raza, S.M., Mehmood, M., Roman, M., Haq, F.U., 2023, Molecular
characterization of extensively drug-resistant Salmonella enterica Serovar Typhi clinical isolates from Lahore,
Pakistan. Infection and Drug Resistance, 2987-3001.
[6]. Sivaperumal, P., Kamala, K., Ganapathy,
D.M., Dharani, G., Sundarrajan, S., Ramakrishna, S., 2023, Fabrication of AgNPs
mediated fibrous membrane from Rhizophora
mucronata mangrove plant extract for biological properties. Journal of
Drug Delivery Science and Technology, 86, 104710.
[7]. Chaudhary, L., Pandey, A., Singh, P., Chaturvedi, P., Bisht,
A.S., 2023, Bacterial Profile and Antimicrobial Susceptibility Pattern of Gram-Negative
Bacteria Isolated from Skin and Soft Tissue Infections in a Tertiary Care
Hospital of Western Uttar Pradesh, 14(3), 135.
[8]. Vasoo, S., 2017, Susceptibility testing for the
polymyxins: two steps back, three steps forward?. Journal of Clinical
Microbiology, 55(9), 2573-2582.
[9]. Pauline, C.R., Akshita, Pavithra, T.,
Kannan, K., Sivaperumal, P., 2024, Characterization and Biological Activity of
Silver Nanoparticles from (Rhizophora mucronata)
Mangrove Extract. Nano Life, 2450018.
[10]. Clinical
and Laboratory Standards Institute, (CLSI), 2019. Performance
Standards for antimicrobial Susceptibility Testing; 28th Informational
Supplement; CLSI Document m100-S29. Clinical and Laboratory Standards Institute.
[11]. Khalid, S., Migliaccio, A., Zarrilli, R., Khan, A.U.,
2023, Efficacy of Novel Combinations of Antibiotics against
Multidrug-Resistant—New Delhi Metallo-Beta-Lactamase-Producing Strains of
Enterobacterales. Antibiotics, 12(7), 1134.
[12]. Vasaikar, S., Obi, L., Morobe, I., Bisi-Johnson, M., 2017,
Molecular characteristics and antibiotic resistance profiles of Klebsiella
isolates in Mthatha, Eastern Cape province, South Africa. International Journal
of Microbiology, 2017(1), 8486742.
[13]. Magiorakos, A.P., Srinivasan, A., Carey, R.B., Carmeli,
Y., Falagas, M.E., Giske, C.G., Harbarth, S., Hindler, J.F., Kahlmeter, G.,
Olsson-Liljequist, B., Paterson, D.L., 2012, Multidrug-resistant, extensively
drug-resistant and pan drug-resistant bacteria: an international expert
proposal for interim standard definitions for acquired
resistance. Clinical Microbiology and Infection, 18(3), 268-281.
[14]. Onanuga, A., Mahindroo, J., Singh, S., Taneja, N., 2019,
Phenotypic and molecular characterization of antimicrobial resistant
Escherichia coli from urinary tract infections in Port-Harcourt,
Nigeria. African Medical Journal, 34(1).
[15]. Rosenthal, V.D., Maki, D.G., Jamulitrat, S., Medeiros,
E.A., Todi, S.K., Gomez, D.Y., Leblebicioglu, H., Khader, I.A., Novales,
M.G.M., Berba, R., Wong, F.M.R., 2010, International nosocomial infection
control consortium (INICC) report, data summary for 2003-2008. American Journal
of Infection Control, 38(2), 95-104.
[16]. Suma, P., Swetha, C.S.,
Sudhanthiramani., Goud, S.S., Annie Supriya., Jagadeesh Babu, A., 2016, A study
on the antibiotic resistance patterns of Staphylococcus
aureus isolated from market milk in and around Tirupati, Andhra Pradesh.
International Journal of Recent Scientific Research, 7(4), 10429-10435.
[17]. Gupta, M., Naik, A.K., Singh,
S.K., 2019, Bacteriological profile and antimicrobial resistance patterns of
burn wound infections in a tertiary care hospital. Heliyon, 5(12). e02956.
[18]. Lagha, R., Abdallah, F.B., ALKhammash, A.A., Amor, N.,
Hassan, M.M., Mabrouk, I., Alhomrani, M., Gaber, A., 2021, Molecular
characterization of multidrug-resistant Klebsiella
pneumoniae clinical isolates recovered from King Abdulaziz Specialist
Hospital at Taif City, Saudi Arabia Journal of Infection and Public
Health, 14(1), 143-151.
[19]. Apenteng, J.A., Yeboah, E.E.A., Kyere-Davies, G., 2022,
Antibiotic susceptibility of bacteria isolates from ward environment of a
hospital in Tema, Ghana. African Journal of Microbiology
Research, 16(6), 211-216.
[20]. Zhang, Y., Li, D., Yang, Y., Su, J., Xu, X., Wang, M.,
Chen, Y., Li, Y., 2021, Clinical and molecular characteristics of
Chryseobacterium indologenes isolates at a teaching hospital in Shanghai,
China. Annals of Translational Medicine, 9(8).
[21]. Zarras, C., Karampatakis, T., Pappa, S., Iosifidis, E.,
Vagdatli, E., Roilides, E., Papa, A., 2023, Genetic characterization of
carbapenem-resistant Klebsiella
pneumoniae clinical isolates in a tertiary hospital in Greece,
2018–2022. Antibiotics, 12(6), 976.
[22]. Khalid, S., Migliaccio, A., Zarrilli, R., Khan, A.U.,
2023, Efficacy of Novel Combinations of Antibiotics against
Multidrug-Resistant—New Delhi Metallo-Beta-Lactamase-Producing Strains of
Enterobacterales. Antibiotics, 12(7), 1134.
[23]. Shanahan, P.M., Jesudason, M.V., Thomson, C.J., Amyes,
S.G., 1998, Molecular analysis of and identification of antibiotic resistance
genes in clinical isolates of Salmonella
typhi from India. Journal of Clinical Microbiology, 36(6),
1595-1600.