Canadian Journal of Infectious Diseases and Medical Microbiology
Volume 2021 (2021), Article ID 6634684, 6 pages
https://doi.org/10.1155/2021/6634684

Research Article

Colistin Resistance among Enterobacteriaceae Isolated from Clinical Samples in Gaza Strip

Mohammad Qadi,¹ Safaa Alhato,² Rasha Khayyat,¹ and Abdelraouf A. Elmanama²

¹Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, An-Najah National University, P.O.Box. 7, Nablus, Palestine, State of Palestine
²Department of Medical Laboratory Sciences Faculty of Health Sciences Islamic University of Gaza, Gaza Strip, Gaza, Palestine, State of Palestine

Correspondence should be addressed to Mohammad Qadi; m.qadi@najah.edu

Received 9 December 2020; Accepted 13 April 2021; Published 20 April 2021

Academic Editor: Louis Detolla

Copyright © 2021 Mohammad Qadi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Bacterial infections, especially drug-resistant infections, are a major global health issue. The emergence of multidrug-resistant (MDR) strains of Enterobacteriaceae and the lack of new antibiotics have worrisome prospects for all of humanity. Colistin is considered the last-line drug for MDR Gram-negative bacteria (GNB), and it is often used for treatment of respiratory infections caused by MDR-GNB. In recent years, there has been a marked increase in the incidence of colistin-resistant infections. The main objective of this study was to investigate the presence of colistin resistance among clinical GNB isolated from Gaza Strip hospitals. Clinical Enterobacteriaceae isolates (100) were obtained from microbiology laboratories of the hospitals of different geographical locations in Gaza Strip Governorate over a period of six months. Samples were cultured, and bacterial identification was performed by standard microbiological procedures. Enterobacteriaceae isolates were tested for their antimicrobial susceptibility by the disk diffusion method and the MIC method for colistin. Varying degrees of susceptibility were observed for the isolates against the tested antimicrobials even within members of the same antimicrobial class. Amikacin was the most effective drug (74%), followed by chloramphenicol (48%), fosfomycin, and gentamicin (45%). High resistance was recorded against trimethoprim (85%) and tetracycline (83%). Only 59% of the tested isolates were interpreted as susceptible, while 41% was classified as resistant. The highest resistance to colistin was found to be among the Proteus spp. (63.2%), followed by Serratia spp. (57.1%). The lowest resistance was observed among Klebsiella isolates (31.6%). Only 39.0% of meropenem-resistant Enterobacteriaceae was susceptible to colistin, while 45.8% of imipenem-resistant Enterobacteriaceae was susceptible to colistin. The overall resistance to colistin was high (41%) among tested clinical isolates. Furthermore, 89% was MDR. These limit and complicate treatment options for the infections caused by Enterobacteriaceae in Gaza Strip. This calls for immediate actions to control and monitor the use of antimicrobials in general and colistin in particular.

1. Introduction

The global rise in the phenomenon of antimicrobial resistance in the fight against bacterial infections is very disturbing, and concerns regarding this issue are increasing, as it complicates infectious disease treatment and increases the financial burden on healthcare systems [1].

Bacterial infections, especially drug-resistant infections, are a major global health issue. The emergence of multidrug-resistant (MDR) strains of bacteria and the lack of new antibiotics have worrisome prospects for all of humanity. A recent report suggests failing to control drug-resistant infections that may cause an excess of 10 million deaths per year and may cost up to US$ 100 trillion by 2050 [2].

Colistin is considered the last-line drug for MDR Gram-negative bacteria (GNB) [3], and it is often used for treatment of respiratory infections caused by MDR-GNB. In recent years, there has been a marked increase in the incidence of colistin-resistant infections [4].

Colistin resistance is caused by decreases in the net negative charge of the outer membrane, loss of lipid A, or efflux pumps, and the most common resistance mechanism in Enterobacteriaceae is the covalent modification of the lipid A moiety of lipopolysaccharide (LPS) via cationic substitution; these modifications neutralize the negative charge of LPS and subsequently reduce the binding affinity of colistin for its target [5].

Increasing the use of colistin for treatment of infections caused by GNB has led to the emergence of colistin resistance in several countries worldwide. Although resistance to polymyxins is generally less than 10%, it is higher in the Mediterranean and Southeast Asia (Korea and Singapore), where colistin resistance rates are continually increasing [6].

Antimicrobial susceptibility data for 178 carbapenemase-producing Klebsiella pneumoniae (KPC-Kp) isolates revealed that 76 (43%) were resistant to colistin [7].

An unpublished report in Gaza showed high resistance percentages among Escherichia coli isolated from poultry farms. Colistin use in the poultry industry in Gaza strip is indiscriminate, and farmers use it without prescription. This may contribute to resistance to colistin among animals’ bacteria which finds its way to humans through food and other means.

This study aims at investigating the resistance of Enterobacteriaceae bacteria to antimicrobials in general and particularly to colistin.

2. Materials and Methods

2.1. Bacterial Isolate Sources

One hundred clinical isolates (Enterobacteriaceae) were obtained from microbiology laboratories belonging to the Ministry of Health hospitals (20 isolates from each hospital: Al-Shifa, European Gaza Hospital (EGH), Al-Aqsa, Nasser, and Indonesian hospitals) during the period from December 2018 to May 2019. The isolates were presumptively identified by the microbiology laboratory of the corresponding hospitals and were reidentified at the Islamic University of Gaza microbiology laboratories.

2.2. Inclusion and Exclusion Criteria

All Enterobacteriaceae isolated during the study period in the mentioned hospitals were included, and no Enterobacteriaceae isolates were excluded.

2.3. Isolate Collection and Transportation

Clinical isolates were collected on a weekly basis from the five laboratories. Each lab was supplied with freshly prepared triple sugar iron agar slants (TSIA). Technicians streaked each isolate into a separate TSIA slant, incubated overnight, and placed in a refrigerator for temporary storage. Within one week of isolation, the isolates were transported to the microbiology laboratory at the Islamic university of Gaza for identity confirmation and antimicrobial testing.

2.4. Isolate Identification

After purification streak, each isolate was subjected to conventional biochemical tests such as TSIA, Simmons citrate, urease, methyl red, sulfide-indole-motility, and oxidase in addition to Gram staining.

2.5. Antimicrobial Susceptibility Testing

Each isolate was subjected to antimicrobial susceptibility testing using the disk diffusion method in accordance to the procedures and guidance of clinical laboratory sciences institute [8]. Commercial antimicrobial disks (Liofilchem, Italy) were placed onto the surface of preswabbed Muller–Hinton agar plates with a 0.5 McFarland calibrated inoculum of the test organism. Plates were placed in a refrigerator for 15 minutes to allow proper diffusion of antimicrobials and then incubated overnight at 37°C. Interpretation of the results was performed according to antimicrobial disk manufacturer tables.

2.6. Colistin Minimum Inhibitory Concentration (MIC)

The microbroth dilution method using the 96-microtiter plate was employed. Serial dilutions of pure colistin (Sigma-Aldrich Inc.) were tested against a standardized bacterial inoculum. After 16–20 hours of incubation, 20 ul of tetrazolium chloride was added to each well and incubated for 15 minutes. MIC was calculated based on colour development.

Because CLSI does not provide breakpoints for Enterobacteriaceae when testing colistin, we used the European Committee on Antimicrobial Susceptibility Testing (EUCAST) MIC breakpoints for colistin for the purpose of interpretation: ≤2 mg/l susceptible and >2 mg/l resistant [9].

3. Results

The Enterobacteriaceae isolates used in this study were obtained from clinical samples, collected from different sources as shown in Figure 1. The pus group includes pus from different sources such as wound and ear charge samples.

Figure 1: Isolates investigated in this study were obtained from sample groups (Others, 2 from blood culture and 1 each from cerebrospinal fluid and high vaginal swab). The collected Enterobacteriaceae consisted of E. coli (51%), Klebsiella spp. (19%), Proteus group (19%), Serratia spp. (7%), and Enterobacter spp. (4%).

The distribution of E. coli, Klebsiella spp., Proteus group, Serratia spp., and Enterobacter spp. isolates according to their source is given in Table 1.

Table 1: Enterobacteriaceae recovered from clinical specimen distribution by hospitals.

Enterobacteriaceae
Hospital name
Total

Indonesian hospital
Al-Shifa hospital
Al-Aqsa hospital
Nasser medical complex
European gaza hospital

E. coli
8
15
11
7
10
51

15.7%
29.4%
21.6%
13.7%
19.6%
100.0%

Enterobacter spp.
2
0
1
0
1
4

50.0%
0.0%
25.0%
0.0%
25.0%
100.0%

Proteus group
2
1
1
11
4
19

10.5%
5.3%
5.3%
57.9%
21.1%
100.0%

Serratia spp.
2
2
0
0
3
7

28.6%
28.6%
0.0%
0.0%
42.9%
100.0%

Klebsiella spp.
6
2
7
2
2
19

31.6%
10.5%
36.8%
10.5%
10.5%
100.0%

Total
20
20
20
20
20
100

20.0%
20.0%
20.0%
20.0%
20.0%
100.0%

value = 0.002.

E. coli was isolated mainly from urine samples (74.5%), followed by pus (21.6), while the Proteus group was isolated mainly from pus (47.4%), followed by urine samples (36.8%). In general, urine culture constituted the major source of the isolates (58%), followed by pus (31%) as given in Table 2.

Table 2: Distribution of the isolates according to clinical sample type.

Isolate
Sample type
Total

Urine
Pus
Sputum
H.V.S
CSF
Blood

E. coli
38
11
1
1
0
0
51

74.5%
21.6%
2.0%
2.0%
0.0%
0.0%
100.0%

Enterobacter spp.
1
2
1
0
0
0
4

25.0%
50.0%
25.0%
0.0%
0.0%
0.0%
100.0%

Proteus group
7
9
1
0
0
2
19

36.8%
47.4%
5.3%
0.0%
0.0%
10.5%
100.0%

Serratia spp.
0
5
2
0
0
0
7

0.0%
71.4%
28.6%
0.0%
0.0%
0.0%
100.0%

Klebsiella spp.
12
4
2
0
1
0
19

63.2%
21.1%
10.5%
0.0%
5.3%
0.0%
100.0%

Total
58
31
7
1
1
2
100

58.0%
31.0%
7.0%
1.0%
1.0%
2.0%
100.0%

 = 0.006.

3.1. Antimicrobial Resistance of Clinical Enterobacteriaceae Isolates

Varying degrees of susceptibilities were observed for the isolates against the tested antimicrobials even within members of the same antimicrobial class. Amikacin was the most effective drug with 74%, followed by chloramphenicol (48%) and fosfomycin and gentamicin (45%). High resistance was recorded against trimethoprim (85%) and tetracycline (83%). 89 isolates (89%) were MDR, as given in Table 3.

Table 3: Percentage of antimicrobial resistance of Enterobacteriaceae tested against 15 antimicrobials.

Antimicrobial
S
I
R

Amikacin
74
7
19

Chloramphenicol
48
11
41

Fosfomycin
45
8
47

Gentamicin
45
6
49

Ciprofloxacin
43
5
52

Meropenem
39
10
51

Imipenem
33
22
45

Ceftriaxone
23
14
63

Ceftazidime
16
7
77

Trimethoprim
14
1
85

Tetracycline
13
4
83

Cefotaxime
12
9
79

Cefuroxime
12
6
82

Ampicillin
11
0
89

Trimethoprim-sulfamethoxazole
8
8
84

3.2. Colistin MIC

Bacterial isolates that showed resistance at a concentration higher than 2 mg/l were classified as resistant. Only 59% of the tested isolated were interpreted as susceptible, while 41% was classified as resistant. Table 4 provides the MIC value obtained for 100 isolates tested against colistin sulfate.

Table 4: MIC values for various Enterobacteriaceae.

MIC in mg/l
E. coli
Enterobacter
Proteus group
Serratia
Klebsiella
Total

16
6
1
8
1
2
18

33.3%
5.6%
44.4%
5.6%
11.1%
100%

8
6
1
4
1
3
15

40.0%
6.7%
26.7%
6.7%
20.0%
100%

4
5
0
0
2
1
8

62.5%
0.0%
0.0%
25.0%
12.5%
100%

2
3
1
0
1
1
6

50.0%
16.7%
0.0%
16.7%
16.7%
100%

1
9
0
3
0
2
14

64.3%
0.0%
21.4%
0.0%
14.3%
100%

0.5
22
1
4
2
10
39

56.4%
2.6%
10.3%
5.1%
25.6%
100%

Total
51
4
19
7
19
100

51.0%
4.0%
19.0%
7.0%
19.0%
100%

The highest resistance to colistin was found to be among the Proteus group (63.2%), followed by Serratia (57.1%). The lowest resistance was observed among Klebsiella isolates (31.6%) as given in Table 5. Despite variations in resistance among the different genera, no statistical difference was detected (P = 0.154).

Table 5: MIC values for various Enterobacteriaceae.

Enterobacteriaceae
Colistin MIC
Total

Susceptible
Resistant

E. coli
34
17
51

66.7%
33.3%
100%

Enterobacter
2
2
4

50.0%
50.0%
100%

Proteus group
7
12
19

36.8%
63.2%
100%

Serratia
3
4
7

42.9%
57.1%
100%

Klebsiella
13
6
19

68.4%
31.6%
100%

Total
59
41
100

59.0%
41.0%
100%

 = 0.154.

3.3. Colistin Resistance among Carbapenem-Resistant Enterobacteriaceae

Colistin is being used as last choice for carbapenem-resistant Enterobacteriaceae, and therefore, resistance against colistin was compared to that of imipenem and meropenem. Only 39.0% of meropenem-resistant Enterobacteriaceae was susceptible to colistin, while 45.8% of imipenem-resistant Enterobacteriaceae was susceptible to colistin as given in Table 6.

Table 6: Colistin resistance among carbapenem-resistant Enterobacteriaceae.

Colistin
Susceptible
Intermediate
Resistant
Total (%)
value

Meropenem

    Susceptible
28
47.5%
8
13.5%
23
39.0%
59
59.0
0.014

    Resistant
11
26.8%
2
4.9%
28
68.3%
41
41.0

Imipenem

    Susceptible
16
27.1%
16
27.1%
27
45.8%
59
59.0
0.192

    Resistant
17
41.5%
6
14.6%
18
43.9%
41
41.0

4. Discussion

One hundred clinical isolates of Enterobacteriaceae were tested against 16 antimicrobials. The lowest antimicrobial resistance was for amikacin (19%); this percent is higher than the percent reported years ago, where the percent of amikacin resistance among GNB responsible for nosocomial bacteremia was 3.9%, while among community-acquired isolates, it was 1.8% [10]. On the other hand, it is lower than amikacin resistance among ESBL-producing isolates of Enterobacteriaceae in a study performed by Tayh et al. in 2019 [11] which was 33.3%

The highest antimicrobial resistance was against ampicillin (89%); this percent is higher than the percent reported in 2003 [12], which was 71.6%. This means that ampicillin resistance increases with the rise of its use over time. Another study [11] conducted on ESBL-producing Enterobacteriaceae in urinary tract infections showed that the percent of ampicillin resistance in ESBL-producing isolates was 100%, and in non-ESBL-producing isolates, it was 58.2%. Moreover, in a study conducted on E.coli isolated from chicken droppings in Gaza strip [13], the percent of ampicillin resistance was 100%.

Our results showed that the percent of colistin resistance was 41%. Interestingly, this percent is lower than the percent reported in [14], a study which revealed a percent of 63.4% of colistin resistance and higher than the percent of colistin resistance in the study conducted on E. coli isolates [13] which was 14.5%.

Percent of E. coli resistance to colistin was 33.3%, and for Klebsiella, it was 31.6%.

It is obvious that we are reporting a higher percent of colistin resistance in comparison to the published data in Kuwait in 2018 by Alfoiuzan et al. [15] where the team reported resistance of 4.3% for E. coli and 7.7% for Klebsiella.

Carbapenem-resistant Gram-negative pathogens have become a major healthcare burden in the 21st century, and treatment options had been limited to agents such as colistin and tigecycline in combination with other antibiotics [16]. In this study, only 39% of meropenem-resistant Enterobacteriaceae was susceptible to colistin, while 45.8% of imipenem-resistant Enterobacteriaceae was susceptible to colistin. Our findings highlight how much resistance to colistin has increased within the last ten years. For example, in England, ten years ago, the activity of colistin was evaluated against 81 carbapenem-resistant Enterobacteriaceae isolates, and colistin was active against 75/81 isolates (92.6%) [17].

In [18] a study of colistin resistance in Klebsiella pneumoniae and E.coli strains isolated from cancer patients, 45% of colistin-resistant isolates were meropenem resistant.

In [19] a study, the percent of imipenem and meropenem resistant GNB was 8.1% and 0.8% respectively, and in the [11] study, the percentage of imipenem resistance in ESBL-producing isolates of Enterobacteriaceae was 20%. Those reported percentages are much less than the percent determined by our study, which was 43.9% for imipenem and 68.3% for meropenem. This calls for setting policies to (1) prevent misuse and overuse of antibiotics in general and carbapenems, and colistin in particular, especially with the high rate of MDR detected in our study, and (2) applying procedures for infection control and screening policies for antibiotic resistance on a routine basis.

5. Conclusion

In conclusion, overall resistance to colistin was high (41%), and in the same context, MDR percentage was 89% among tested clinical isolates. These limit and complicate treatment options of infection caused by Enterobacteriaceae in Gaza Strip, which in turn calls for immediate actions to control and monitor the use of antimicrobials in general and colistin in particular.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Acknowledgments

This research was funded in part by Al Maqdisi Program 2018-2020 (French Consulate Jerusalem). The authors would like to acknowledge Faculty of Health Sciences at Islamic University of Gaza, Gaza Strip, Palestine, and Faculty of Medicine and Health Sciences at An-Najah National University, West Bank, Palestine, for facilitating the accomplishment of the current study. The authors are also thankful for the Palestinian Ministry of Health.

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