CC BY 4.0 · Libyan International Medical University Journal 2022; 07(02): 039-044
DOI: 10.1055/s-0042-1759621
Review Article

Characteristics of Antibiotic-Resistant Bacteria in Libya Based on Different Source of Infections

Bushra Hosien
1   Department of Medical Laboratories, The University of Tripoli Alahlia, Janzur, Libya
,
Howida Belhaj
1   Department of Medical Laboratories, The University of Tripoli Alahlia, Janzur, Libya
,
2   Department of Anesthesia and Intensive Care, Faculty of Medical Technology, The University of Tripoli, Libya
› Author Affiliations
 

Abstract

In recent years and for decades, antimicrobial resistance (AMR) has expanded into a major clinical issue. Infections were no longer a life-threatening issue for clinicians after the discovery of antibiotics. The misuse or overuse of antibiotics, however, contributes to global AMR, and numerous mobile genetic elements and relevant resistant genes worsen the spread of resistance. As antibiotics lose their effectiveness, a growing number of infections such as pneumonia, tuberculosis, and gonorrhea are getting harder and sometimes impossible to treat. Infections that are resistant to antibiotics are correlated with antibiotic misuse. The majority of the antibiotic resistance in microbes is caused by improper use of antibiotics. Because there are a few antibiotics available to treat multidrug-resistant bacterial infections, there is a high rate of morbidity and mortality. Libya has a high burden of antibiotic resistance, and antimicrobial malpractice has frequently been reported. Providing information on the current state of antimicrobial resistance in Libya may assist the health authorities in addressing the problem more effectively in the future. Therefore, this review highlights the current situation of bacterial profile and their antimicrobial resistance in Libya based on the source of infection. Articles related to the topic were searched using databases and search engines such as PubMed, Google Scholar, and ResearchGate websites. These articles were selected if they were conducted in Libya and provided information on bacterial pathogens and AMR. Required data were extracted for the purpose of this review report, and then further verified for identifying the prevalence and number of susceptible and resistant pathogens in each source of infection.


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Introduction

Antimicrobial resistance (AMR), is the potency of microbes to become resistant to famous antibiotics.[1] AMR is an emerging global threat; it increases mortality and morbidity and strains healthcare systems.[2] The current antimicrobial profile studies have proved that bacteria can cause infections to become resistant to different groups of antibiotics, world health leaders have described antibiotic-resistant microorganisms as “nightmare bacteria” that “pose a catastrophic threat” to people.[3]

In the United States, according to the Center for Disease Control (CDC) in 2013, there are about 23000 deaths a year as a result of infection with bacteria that are resistant to known antibiotics, while about 2 million others develop an infection that is resistant to antibiotics.[3] While, the CDC newly report in 2022 found that infections and deaths from drug-resistant, hospital-acquired bacteria rose by 15% from 2019 to 2020, with alarming increases in some of the most highly resistant bacterial pathogens.[4] The costs of introducing a new pharmaceutical product into clinical use are very high, estimated at 1.7 billion $, according to the US department of health, which is the highest estimate based on the 2020 data.[5]

In 2017, the World Health Organization (WHO) released a list of bacteria for which new studies and medications were urgently required. High priority pathogens included methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE), while critical priority pathogens included Acinetobacter baumannii, Pseudomonas aeruginosa, carbapenem-resistant Enterobacteriaceae, and Enterobacteriaceae that produce extended spectrum beta-lactamases (ESBL).[6]

Gram-negative bacteria are more resistant than gram-positive bacteria because of their unique structure, which also contributes to their widespread global burden of morbidity and mortality.[7] The development of antimicrobial auxiliary agents, structural modification of existing antibiotics, and research into and study of chemical structures with new mechanisms of action and novel targets that resistant bacteria are sensitive to a few methods that have been reported to combat and control resistant gram-negative bacteria.[7]

The antimicrobial resistance crisis in Libya has reached a point where the authorities should work with other stakeholders to address it. The present review is highlighting the situation of antimicrobial resistance and bacterial pathogenic profile in Libya. Free-text web searches using PubMed, Google Scholar, and ResearchGate were searched for articles on AMR published in English using the following keywords and MeSH terms were used: “Antimicrobial Resistance and Libya,” “Antimicrobial Susceptibility and Libya,” “Bacteria Diagnostic Libya,” “AMR/antibiotic and Libya,” and “AMR/antibiotic prevalence and Libya.” These search keywords were entered in the above-mentioned searching engine. Articles were retrieved if they were conducted in Libya and reported the proportion of bacterial pathogens and AMR. Required data were extracted for the purpose of this review report, and then further verified for identifying the prevalence and number of susceptible and resistant pathogens in each source of infection.

Bacteria Resistance Pattern in Urinary Tract Infections.

Urinary tract infection (UTI) is one of the most common infections in routine clinical practice, resulting in high rates of morbidity and high economic costs associated with its treatment. It is the most common UTI and is responsible for 95% of all symptomatic urinary tract infection. The risk of UTI in the female population is higher than that in the male population although bacteria isolated from females were less resistant than those isolated from males.[8]

Ghenghesh et al, 2003, reported that Escherichia coli was detected in 538 (24%) urine samples. Other bacteria detected were Staphylococcus in 8%, Proteus in 4%, Klebsiella spp., in 2%, Pseudomonas in 1%, and beta-hemolytic streptococci in 0.3%.[9] In the same study, antimicrobial susceptibility testing of 538 E. coli strains found 74% were resistant to ampicillin, 49% to cephaloridine, 25% to nitrofurantoin, 49% to tetracycline, and 45% to trimethoprim-sulphamethoxazole.[9]

When comparing these findings to the results of a study carried out in Tripoli, Libya in 2017, shown that Staphylococci (64.5%), E. coli (29.0%), and Klebsiella pneumonia (6.5%) were the most often isolated bacteria from urine samples that had positive culture results. Staphylococci spp. (26.29%), K. pneumonia and E. coli were much more resistant (38.11% and 34.13%, respectively) and showed resistance to a wide variety of tested antibiotics. Gentamycin (17.6% resistance), erythromycin (19.0% resistance), and ciprofloxacin were the three most potent antibiotics tested that affected 87.7%, 82.4%, and 81.0% of the bacteria that cause urinary tract infections, respectively.[10] Similarly, a study conducted in Sabha, Libya in 2007 reported that 178 (68.5%) of urine samples were contaminated by E. coli with other micro-organisms. About 170 (65.4%) strains of E. coli were susceptible to nitrofurantoin, 157 (60.4%) to gentamicin, and 116 (44.6%) to cephalexin. In contrast, only 6 (2.3%) of E. coli strains were sensitive to erythromycin and 14 (5.4%) to tetracycline.[11]

Another study investigated the resistance patterns of E. coli, Klebsiella spp., and S. aureus isolated from diabetic (DM) and non-diabetic patients to antimicrobial agents, revealed that Klebsiella species from the non-DM group were significantly more resistant than isolates from the DM group to co-amoxiclav acid [p = 0.002].[12] Moreover, S. aureus isolates from the non-DM group were resistant to methicillin. Additionally, E. coli, Klebsiella spp., and S. aureus exhibited 40%, 65%, and 29% multiple drug resistance profiles, respectively.[12]

Wareg et al, in 2014, revealed that vancomycin resistance was not found in in-patient-MRSA strains while 5% of out-patient-MRSA strains were resistant by disc-diffusion assay. This result suggests that vancomycin can be used to treat MRSA infections.[13] Another study on the detection of inducible clindamycin resistance to MRSA from Libya reported 128 (24.2%) MRSA isolates collected were resistant to clindamycin, 63.2% of isolates were resistant to erythromycin.[14] The authors also emphasized that clindamycin could still be used to treat MRSA infection in Libyan hospitals.[14]

In 2011, a study by Buzaid et al reported that of 200 S. aureus examined, 62 (31%) were MRSA. MRSA was found in 31.8% (28/88) and 30.4% (34/112) of S. aureus in female and male patients. Based on the disc diffusion results, the pattern of antibiotic resistance in 62 MRSA patients was as follows: 11 (17.7%) to vancomycin, 21 (33.9%) to ciprofloxacin, 24 (38.7%) to chloramphenicol, 26 (41.9%) to fusidic acid, and 29 (46.8%) to erythromycin.[15]

Overall, E. coli accounted for most of UTI, and exhibited resistance to the common first-line regimes such as nitrofurantoin and cotrimoxazole.


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Bacterial Resistance Pattern in Respiratory Tract Infection.

Respiratory infections are one of the most common infectious diseases of various groups that continue to emerge as major causes of clinical morbidity and mortality.[16] Upper respiratory tract infections (URTIs) involve the common cold, tonsillitis, laryngitis, pharyngitis, rhinitis, and otitis media. Lower respiratory tract infections (LRTIs) include acute bronchitis, and pneumonia.[17]

Previous study conducted by Elkammoshi in 2020 in Tripoli, Libya, in which 100 specimens divided equally between ventilator circuits and lower respiratory tract patients were analyzed. They found that the most common organism isolated was gram-negative from the ventilators (26, 68.4%) and mechanically ventilated patients' LRT was 14 (70%). Other isolates were gram-positive from patient's LRT were 6 (30%) and from ventilator circuits were 12 (31.6%), and most of the isolates were resistant to the known antibiotics.[18] In the same study, A. baumannii showed a full resistance to amoxicillin, gentamycin, and the first generation of cephalosporins, and it was intermediated to the third-generation cephalosporins. In contrast, K. pneumoniae was also a fully resistant to gentamycin and most other types of antibiotics. Pseudomonas aeruginosa was also resistant to all types of antibiotics except gentamycin, to which it was slightly sensitive. E. coli and Serratia marcescens were sensitive to most antibiotic disks except co-amoxiclav.[18]

Another study conducted by Atia in 2020 in Tripoli, showed the dominant bacterial pathogens in respiratory infection being S. pneumonia 43.3%, followed by P. aeruginosa 22.8%, S. aureus 13.8%, E. coli 6.9%, Enterobacter spp. 6.2%, Citrobacter 4.5%, and Klebsiella 2.2%.[19]

It was observed that S. pneumonia was highly resistant to gentamycin and ciprofloxacin, whereas it was least resistant to cefotaxime and doxycycline. Pseudomonas aeruginosa was resistant to β-lactam antibiotics such as co-amoxiclav, amoxicillin, ceftriaxone as well as macrolide antibiotics such as clarithromycin with percent resistance of 71%, 44%, 29%, and 37%, respectively. P. aeruginosa was also resistant to ciprofloxacin, gentamicin, and amikacin with percentages of 24%, 24%. and 23%, respectively.[19]

Another study done by El-Deeb in 2006 in Libya showed that S. aureus was the most common organism, followed by Streptococcus pyogenes and K. pneumonia. Pseudomonas aeruginosa were represented, with S. marcescens and Morganella morganii being the least isolated organisms.[18] Levofloxacin and gatifloxacin, in the same study, showed the highest activity (100%), followed by ofloxacin and ciprofloxacin (96.44% and 93.39%, respectively). Amoxicillin and tetracycline were the least active (36.64% and 32.06%, respectively).[20]

The spectrum of pathogenic bacterium causing upper respiratory infection in Libya is considerably wide, with S. pneumoniae and P. aeruginosa being the major causative bacteria.


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Bacterial Resistance Pattern in Skin infections

Skin infections are a worldwide significant clinical concern characterized by microbial attack of the skin layers and underlying soft tissues. Earlier study conducted in Tripoli, Libya, showed that the dominated species of pathogenic bacteria were identified as gram-positive bacteria S. aureus (n = 272, 97.14%) and Proteus (n = 8, 2.85%). Meanwhile, gram-negative bacteria were E. coli (n = 164, 93.71%), Pseudomonas (n = 8, 4.57%), Klebsiella (n = 2, 1.14%), and Shigella (n = 1, 0.57%). Of the gram-positive bacteria, S. aureus and Proteus were highly resistant to penicillin (34.3%, 75% respectively) and ampicillin (28.6%, 62.5%, respectively). Moreover, Proteus had lower resistance rate to sulfamethoxazole and nalidixic acid (12.5%). Concerning gram-negative bacteria, E. coli was highly resistant to ampicillin (45.12%) and penicillin (35.96%), whereas the lowest resistant was against imipenem (3.05%).[21]

Similarly, a study conducted in 2015 in Sabha showed that 90.5% of S. aureus strains were resistant to vancomycin, 61.9% to tetracycline, 57.1% to amoxicillin, 52.4% to methicillin, 42.9% to erythromycin, and 23.8% streptomycin. In addition, 87.5% of Staphylococcus epidermidis isolated was resistant to vancomycin, 75% to methicillin, 62.5% to tetracycline, 50% to streptomycin 37.5% to amoxicillin, and erythromycin.[22]

In another study conducted by Dou in a different area in Libya in 2011 showed that Acinetobacter spp. was the most resistant pathogen. Most isolated gram-negative bacteria showed great resistance to third-generation cephalosporins and aminoglycosides. However, P. aeruginosa was quite susceptible to commonly used antipseudomonal therapy particularly carbapenems. Coagulase-negative staphylococci were found to be sensitive to all the antibiotics tested particularly gentamicin and vancomycin.[23]

Overall, S. aureus is stated to be among the most causative agent for skin infection, and shows high resistance to penicillin groups of antibiotics.


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Bacterial Resistance Pattern in Gynecological Infections

Bacterial vaginosis is a worldwide issue due to the raised risk of acquisition of sexually transmitted infections. Bacterial vaginosis is a state that occurs when the overgrowth of anaerobic bacteria. In some studies, however, other bacteria (E. coli, Klebsiella spp., Acinetobacter spp., Staphylococcus spp., enterococci, and S. agalactiae (group B streptococci) have been named “intermediate flora” or have been included in other studies of bacterial vaginosis.[24] Previous study conducted in Tripoli, showed that E. coli was the most frequently isolated bacterium from vaginal swab, and showed resistance to penicillin (62.5%), while the S. aureus and Streptococcus agalactiae were the dominant gram-positive bacteria showed high resistance to co-amoxiclav (40%).[24]


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Bacterial Resistance Pattern in Other Infections

Methicillin-resistant staph (MRSA) and methicillin-susceptible staph (MSSA) are important causes of infections in burn patients. A study conducted by Zorgani in Tripoli in 2012 showed that Tigecycline exhibited an excellent in vitro activity against MSSA and MRSA isolates (96.8% and 95.8%, respectively).[25]

Another study conducted by Al-awkally et al, in Tripoli 2020, aimed to assess the antibiotic susceptibility of pseudomonas aeruginosa recovered from infected swabs, abscess, burn, medical tips and blood, reported that P. aeruginosa was highly susceptible to Colistin and ciprofloxacin with some of the isolates shown resistance to septrin, tetracycline, and levofloxacin.[26]

In a study conducted by Musa et al, in Misurata, Libya, found that the most common bacteria isolated from anterior blepharitis were S. aureus 14 (25%) and S. epidermidis 14 (25%), and were resistant to vancomycin, gentamycin, ciprofloxacin, and amikacin. In contrast, they were highly resistant to ampicillin and moderately resistant to chloramphenicol, erythromycin, and cephalexin.[27]

Ermalli in 2017, collected 94 gram-negative bacteria isolates from different sources at a single hospital in Tripoli, and reported different antimicrobial resistance phenotypes including to the carbapenem classes. About 48% of the collection was identified as A. baumannii, 50% K. pneumoniae, and 2% E. coli. Resistance to the carbapenem classes was reported in 96% of the A. baumannii strains and 94% of the K. pneumoniae strains. Approximately 78% of the isolates showed different multidrug-resistant (MDR) phenotypes, of which K. pneumoniae expressing the highest rates of MDRs (i.e., 91%).[28]


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Conclusion

This review reported the current state of antimicrobial resistance in Libya. Drug resistance to frequently administered antibiotics is very widespread in Libya. Microbiological identification and susceptibility testing methods must be improved for national and international organizations to assess the scope of the AMR problem.


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Conflict of Interest

None declared.

Note

The article has not been previously presented or published, and is not part of a thesis project.


  • Reference

  • 1 Chiș AA, Rus LL, Morgovan C. et al. Microbial resistance to antibiotics and effective antibiotherapy. Biomedicines 2022; 10 (05) 1121 DOI: 10.3390/biomedicines10051121.
  • 2 Prestinaci F, Pezzotti P, Pantosti A. Antimicrobial resistance: a global multifaceted phenomenon. Pathog Glob Health 2015; 109 (07) 309-318
  • 3 Health Udo and H. Services. Antibiotic Resistance Threats in The United States, 2013, Centers for Disease Control and Prevention. Georgia, GA, USA: 2013
  • 4 CDC report shows rise in resistant infections, deaths in first COVID-19 year. Accessed October 1, 2022, at: https://www.cidrap.umn.edu/news-perspective/2022/07/cdc-report-shows-rise-resistant-infections-deaths-first-covid-19-year
  • 5 Schlander M, Hernandez-Villafuerte K, Cheng CY, Mestre-Ferrandiz J, Baumann M. How much does it cost to research and develop a new drug? A systematic review and assessment. PharmacoEconomics 2021; 39 (11) 1243-1269
  • 6 World Health Organization. WHO publishes list of bacteria for which now antibiotics are urgently needed. Accessed October 1, 2022, at: https://www.who.int/news/item/27-02-2017-who-publishes-list-of-bacteria-for-which-new-antibiotics-are-urgently-needed
  • 7 Breijyeh Z, Jubeh B, Karaman R. Resistance of gram-negative bacteria to current antibacterial agents and approaches to resolve it. Molecules 2020; 25 (06) 1340 DOI: 10.3390/molecules25061340.
  • 8 Gu J, Chen X, Yang Z, Bai Y, Zhang X. Gender differences in the microbial spectrum and antibiotic sensitivity of uropathogens isolated from patients with urinary stones. J Clin Lab Anal 2022; 36 (01) e24155 DOI: 10.1002/jcla.24155.
  • 9 Ghenghesh K, Altomi A, Gashout S, Abouhagar B. High antimicrobial-resistance rates of Escherichia coli from urine specimens in Tripoli-Libya. Garyounis Med J 2003; 20: 89-93
  • 10 Elsayah K, Atia A, Bkhait N. Antimicrobial resistance pattern of bacteria isolated from patients with urinary tract infection in Tripoli City, Libya. Asian J Pharm Health Sci 2017; 7 (04) 1751-1755
  • 11 Ahmed M, Orwa J. Antimicrobial susceptibility of Escherichia coli urine isolates in South Libya. Sebha Med J. 2007; 6 (01) 46-50
  • 12 Ghenghesh KS, Elkateb E, Berbash N. et al. Uropathogens from diabetic patients in Libya: virulence factors and phylogenetic groups of Escherichia coli isolates. J Med Microbiol 2009; 58 (Pt 8): 1006-1014 DOI: 10.1099/jmm.0.007146-0.
  • 13 Wareg S, Foster H, Daw M. Antimicrobial susceptibility patterns of methicillin-resistant Staphylococcus aureus isolates collected from healthcare and community facilities in Libya show a high level of resistance to fusidic acid. J Infect Dis Ther 2014; 2: 189 DOI: 10.4172/2332-0877.1000189.
  • 14 Ahmed MO, Alghazali MH, Abuzweda AR, Amri SG. Detection of inducible clindamycin resistance (MLSB(i)) among methicillin-resistant Staphylococcus aureus (MRSA) from Libya. Libyan J Med 2010; 5 (01) DOI: 10.3402/ljm.v5i0.4636.
  • 15 Buzaid N, Elzouki AN, Taher I, Ghenghesh KS. Methicillin-resistant Staphylococcus aureus (MRSA) in a tertiary surgical and trauma hospital in Benghazi, Libya. J Infect Dev Ctries 2011; 5 (10) 723-726
  • 16 Atia A, Abired A, Ammar A, Elyounsi N, Ashour A. Prevalence and types of bacterial infections of the upper respiratory tract at a tertiary care hospital in the City of Tripoli. Libyan Int Med Univ J 2018; 3: 54-58
  • 17 Wang L, Qiao X, Ai L, Zhai J, Wang X. Isolation of antimicrobial resistant bacteria in upper respiratory tract infections of patients. 3 Biotech 2016; 6 (02) 166 DOI: 10.1007/s13205-016-0473-z.
  • 18 Elkammoshi A, Ben Ashur A, El Magrahi H, Abdulatif A, Almarouq M. The role of bacterial colonization of ventilator circuit in development of ventilator associated pneumonia in ICU of Medical Center Hospital in Tripoli, Libya. Iberoam J Med 2021; 3 (02) 109-114
  • 19 Atia A, Elyounsi N, Abired A, Wanis A, Ashour A. Antibiotic resistance pattern of bacteria isolated from patients with upper respiratory tract infections; a four year study in Tripoli city. Iberoam J Med. 2020; 2 (03) 155-160
  • 20 Eldeeb A, Khashan E. Microbiological study on respiratory tract infections in Libya. Egypt J Hosp Med 2006; 24 (01) 442-459
  • 21 Atia A, Ashour A, Shaban N, Omar F. Incidence of bacterial skin infections in Libya: a retrospective population-based study. Estudos Ibero-Americanos 2021; 3: 3-6 DOI: 10.5281/zenodo.4252549.
  • 22 Abdalla A, Elzen A, Alshahed ASh. et al. Identification and determination of antibiotic resistance of pathogenic bacteria isolated from septic wounds. J Adv Lab Res Bio 2015; 6 (04) 97-101
  • 23 Dau AA, Tloba S, Daw MA. Characterization of wound infections among patients injured during the 2011 Libyan conflict. East Mediterr Health J 2013; 19 (04) 356-361
  • 24 Atia A. Prevalence of bacterial vaginosis and their antibiotic susceptibility among women attending different private clinics in Tripoli, Libya. Libyan J Med Sci 2021; 5: 79-82
  • 25 Zorgani A, Elahmer O, Ziglam H, Ghenghesh K. In-vitro activity of tigecycline against methicillin-resistant Staphylococcus aureus isolated from wounds of burn patients in Tripoli-Libya. J Micr Infec Dise 2012; 2 (03) 109-112
  • 26 Al-awkally N, Ali M, Al-awkally R, AL-awkally A, Ali F, Abouserwel A. Antibiotic susceptibility and resistant pattern of isolates of Pseudomonas aeruginosa recovered from infected swabs, abscess, burn, medical tips and blood from patients at 4 geographical locations in Libya (Al- Bayda, Shahat, Derna and Benghazi). Int J Curr Microbiol Appl Sci 2019; 8 (10) 143-149 DOI: 10.20546/ijcmas.2019.810.015.
  • 27 Musa A, Nazeerullah R, Sarite S. Bacterial profile and antimicrobial susceptibility pattern of anterior blepharitis in Misurata region, Libya. Dent Med Res 2014; 2: 8-13
  • 28 Elramalli A, Almshawt N, Ahmed MO. Current problematic and emergence of carbapenemase-producing bacteria: a brief report from a Libyan hospital. Pan Afr Med J 2017; 26: 180 DOI: 10.11604/pamj.2017.26.180.9637.

Address for correspondence

Ahmed Atia, PhD
Department of Anesthesia and Intensive Care, Faculty of Medical Technology, The University of Tripoli
Libya   

Publication History

Article published online:
19 December 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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  • Reference

  • 1 Chiș AA, Rus LL, Morgovan C. et al. Microbial resistance to antibiotics and effective antibiotherapy. Biomedicines 2022; 10 (05) 1121 DOI: 10.3390/biomedicines10051121.
  • 2 Prestinaci F, Pezzotti P, Pantosti A. Antimicrobial resistance: a global multifaceted phenomenon. Pathog Glob Health 2015; 109 (07) 309-318
  • 3 Health Udo and H. Services. Antibiotic Resistance Threats in The United States, 2013, Centers for Disease Control and Prevention. Georgia, GA, USA: 2013
  • 4 CDC report shows rise in resistant infections, deaths in first COVID-19 year. Accessed October 1, 2022, at: https://www.cidrap.umn.edu/news-perspective/2022/07/cdc-report-shows-rise-resistant-infections-deaths-first-covid-19-year
  • 5 Schlander M, Hernandez-Villafuerte K, Cheng CY, Mestre-Ferrandiz J, Baumann M. How much does it cost to research and develop a new drug? A systematic review and assessment. PharmacoEconomics 2021; 39 (11) 1243-1269
  • 6 World Health Organization. WHO publishes list of bacteria for which now antibiotics are urgently needed. Accessed October 1, 2022, at: https://www.who.int/news/item/27-02-2017-who-publishes-list-of-bacteria-for-which-new-antibiotics-are-urgently-needed
  • 7 Breijyeh Z, Jubeh B, Karaman R. Resistance of gram-negative bacteria to current antibacterial agents and approaches to resolve it. Molecules 2020; 25 (06) 1340 DOI: 10.3390/molecules25061340.
  • 8 Gu J, Chen X, Yang Z, Bai Y, Zhang X. Gender differences in the microbial spectrum and antibiotic sensitivity of uropathogens isolated from patients with urinary stones. J Clin Lab Anal 2022; 36 (01) e24155 DOI: 10.1002/jcla.24155.
  • 9 Ghenghesh K, Altomi A, Gashout S, Abouhagar B. High antimicrobial-resistance rates of Escherichia coli from urine specimens in Tripoli-Libya. Garyounis Med J 2003; 20: 89-93
  • 10 Elsayah K, Atia A, Bkhait N. Antimicrobial resistance pattern of bacteria isolated from patients with urinary tract infection in Tripoli City, Libya. Asian J Pharm Health Sci 2017; 7 (04) 1751-1755
  • 11 Ahmed M, Orwa J. Antimicrobial susceptibility of Escherichia coli urine isolates in South Libya. Sebha Med J. 2007; 6 (01) 46-50
  • 12 Ghenghesh KS, Elkateb E, Berbash N. et al. Uropathogens from diabetic patients in Libya: virulence factors and phylogenetic groups of Escherichia coli isolates. J Med Microbiol 2009; 58 (Pt 8): 1006-1014 DOI: 10.1099/jmm.0.007146-0.
  • 13 Wareg S, Foster H, Daw M. Antimicrobial susceptibility patterns of methicillin-resistant Staphylococcus aureus isolates collected from healthcare and community facilities in Libya show a high level of resistance to fusidic acid. J Infect Dis Ther 2014; 2: 189 DOI: 10.4172/2332-0877.1000189.
  • 14 Ahmed MO, Alghazali MH, Abuzweda AR, Amri SG. Detection of inducible clindamycin resistance (MLSB(i)) among methicillin-resistant Staphylococcus aureus (MRSA) from Libya. Libyan J Med 2010; 5 (01) DOI: 10.3402/ljm.v5i0.4636.
  • 15 Buzaid N, Elzouki AN, Taher I, Ghenghesh KS. Methicillin-resistant Staphylococcus aureus (MRSA) in a tertiary surgical and trauma hospital in Benghazi, Libya. J Infect Dev Ctries 2011; 5 (10) 723-726
  • 16 Atia A, Abired A, Ammar A, Elyounsi N, Ashour A. Prevalence and types of bacterial infections of the upper respiratory tract at a tertiary care hospital in the City of Tripoli. Libyan Int Med Univ J 2018; 3: 54-58
  • 17 Wang L, Qiao X, Ai L, Zhai J, Wang X. Isolation of antimicrobial resistant bacteria in upper respiratory tract infections of patients. 3 Biotech 2016; 6 (02) 166 DOI: 10.1007/s13205-016-0473-z.
  • 18 Elkammoshi A, Ben Ashur A, El Magrahi H, Abdulatif A, Almarouq M. The role of bacterial colonization of ventilator circuit in development of ventilator associated pneumonia in ICU of Medical Center Hospital in Tripoli, Libya. Iberoam J Med 2021; 3 (02) 109-114
  • 19 Atia A, Elyounsi N, Abired A, Wanis A, Ashour A. Antibiotic resistance pattern of bacteria isolated from patients with upper respiratory tract infections; a four year study in Tripoli city. Iberoam J Med. 2020; 2 (03) 155-160
  • 20 Eldeeb A, Khashan E. Microbiological study on respiratory tract infections in Libya. Egypt J Hosp Med 2006; 24 (01) 442-459
  • 21 Atia A, Ashour A, Shaban N, Omar F. Incidence of bacterial skin infections in Libya: a retrospective population-based study. Estudos Ibero-Americanos 2021; 3: 3-6 DOI: 10.5281/zenodo.4252549.
  • 22 Abdalla A, Elzen A, Alshahed ASh. et al. Identification and determination of antibiotic resistance of pathogenic bacteria isolated from septic wounds. J Adv Lab Res Bio 2015; 6 (04) 97-101
  • 23 Dau AA, Tloba S, Daw MA. Characterization of wound infections among patients injured during the 2011 Libyan conflict. East Mediterr Health J 2013; 19 (04) 356-361
  • 24 Atia A. Prevalence of bacterial vaginosis and their antibiotic susceptibility among women attending different private clinics in Tripoli, Libya. Libyan J Med Sci 2021; 5: 79-82
  • 25 Zorgani A, Elahmer O, Ziglam H, Ghenghesh K. In-vitro activity of tigecycline against methicillin-resistant Staphylococcus aureus isolated from wounds of burn patients in Tripoli-Libya. J Micr Infec Dise 2012; 2 (03) 109-112
  • 26 Al-awkally N, Ali M, Al-awkally R, AL-awkally A, Ali F, Abouserwel A. Antibiotic susceptibility and resistant pattern of isolates of Pseudomonas aeruginosa recovered from infected swabs, abscess, burn, medical tips and blood from patients at 4 geographical locations in Libya (Al- Bayda, Shahat, Derna and Benghazi). Int J Curr Microbiol Appl Sci 2019; 8 (10) 143-149 DOI: 10.20546/ijcmas.2019.810.015.
  • 27 Musa A, Nazeerullah R, Sarite S. Bacterial profile and antimicrobial susceptibility pattern of anterior blepharitis in Misurata region, Libya. Dent Med Res 2014; 2: 8-13
  • 28 Elramalli A, Almshawt N, Ahmed MO. Current problematic and emergence of carbapenemase-producing bacteria: a brief report from a Libyan hospital. Pan Afr Med J 2017; 26: 180 DOI: 10.11604/pamj.2017.26.180.9637.

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