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Prevalence of extended-spectrum β-lactamases, AmpC, and carbapenemases in Proteus mirabilis clinical isolates

BMC Microbiology volume 22, Article number: 247 (2022) Cite this article

Abstract

Background

Proteus mirabilis is an opportunistic pathogen, causing a variety of community-acquired and nosocomial illnesses. It poses a potential threat to patients via the production of β-lactamases, which decrease the efficacy of antimicrobial treatment and impair the management of its pathogenicity. Hence, this study was established to determine the prevalence of extended-spectrum β-lactamases (ESBLs), AmpC, and carbapenemases of P. mirabilis isolated from various clinical specimens.

Results

Proteus mirabilis was identified in 20.7% (58/280) of specimens. ESBL producers were present at a rate of 51.7% (30/58). All AmpC-positive isolates (n = 20) produced ESBLs as well, so 66.7% of ESBL-producing isolates coproduced AmpC enzymes. The modified Hodge test confirmed carbapenemase production in six out of seven imipenem nonsusceptible isolates. Of these, only two (5.7%) isolates were also ESBL-and AmpC-positive. Antibiotic resistance reached the highest level for cotrimoxazole (62.1%, n = 36/58 isolates) and the lowest for imipenem (12.1%, n = 7/58 isolates). The levels of multidrug-resistant (MDR) was 41.4% among the tested isolates. The blaSHV (83.3%), blaAmpC (80%), and blaVIM-1 (50%) were the most detected genes in phenotypically confirmed ESBL-, AmpC-, and carbapenemase-producing isolates, respectively. Besides, more than a half of the tested P. mirabilis strains (53%) coproduced ESBLs and AmpC. Moreover, two isolates coproduced ESBLs and AmpC together with carbapenemases. Furthermore, dendrogram analysis showed great genetic divergence based on the 21 different enterobacterial repetitive intergenic consensus (ERIC) patterns (P1–P21) through the 34 β-lactamase producers. ERIC analysis distinguished clonal similarities between isolates 21 and 22 in P2 and 9 and 10 in P4, which were isolated from the same clinical source and possessed similar patterns of β-lactamase-encoding genes.

Conclusion

Hence, there is an urgent need to monitor hospitalized patients and improve healthcare in order to reduce the incidence of infection and outbreaks of infection with antibiotic-resistant Proteus.

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Background

Proteus mirabilis is an enterobacterial species that naturally colonizes the gastrointestinal lumen and is present in many environmental features, such as water, soil, and feces-contaminated material [1, 2]. It is an opportunistic pathogen responsible for serious infections of the human urinary tract, respiratory tract, wounds, otitis media, and blood. Flagella mediate its swarming mobility on the surface of solid media, so it can easily reach the kidney and invade the urinary tract. Hence, P. mirabilis is one of the most common causative agents of urinary tract infections (UTIs), particularly in catheterized patients [3]. Biofilm structures of P. mirabilis play a critical role in protecting it against antibiotics as well as host defense mechanisms and cause challenges in treatment as a result of conferring a multidrug-resistant (MDR) or extensively drug-resistant (XDR) status [4].

β-lactam resistance, mediated by the synthesis of β-lactamases, is being more and more frequently reported among P. mirabilis. Extended-spectrum β-lactamases (ESBLs), AmpC, and carbapenemases are the most common β-lactamase enzymes [5]. Infections caused by ESBL-producing isolates are a serious international problem, causing significant increases in morbidity and mortality among hospitalized patients. In addition, ESBL producers exhibit coresistance with other different antibiotic classes such as quinolones, aminoglycosides, and sulfa drugs [6]. Formerly, blaSHV and blaTEM were the predominant ESBL genotypes found in Enterobacteriaceae isolates, but recently blaCTX-M (especially blaCTX-M-15) has become the most common genotype [7].

AmpC, another variant of β-lactamases, is unlike ESBLs not affected by either cephamycins or β-lactamase inhibitors [8]. The AmpC enzyme may mask the effect of ESBLs and their recognition, so it is very complicated to treat their coexistence in the same isolate. Thus, AmpC-producing isolates act as a silent reservoir for ESBLs [9]. Carbapenems are the remaining treatment option against serious ESBL- and AmpC-related infections [10]. Unfortunately, treatment failure is observed due to the rapid propagation of carbapenem-resistant isolates [11]. Changes in the porin channel in addition to coexpression of AmpC, ESBL, or carbapenemase enzymes are the most common mechanisms of carbapenem resistance in Enterobacteriaceae [12,13,14]. The extensive resistance of Gram-negative bacteria is associated with the transfer of resistance genes via transferable genetic elements such as plasmids, which can readily pass through mutant clones and spread rapidly between countries. Most of this spread is therefore undetected as the normal human flora acquires those resistance genes and becomes a silent source of endogenous infections [15]. In view of the increasing prevalence of Proteus resistance to various antimicrobials, especially β-lactam antibiotics, the objective of this study is to detect mechanisms of resistance to β-lactams (i.e., ESBLs, AmpC, and carbapenemases) among P. mirabilis isolates collected from healthcare facilities using phenotypic and molecular testing, to support the potential therapeutic options for treating these complicated clinical infections. Then, we determined the genetic diversity of different β-lactamase-producing P. mirabilis isolates using enterobacterial repetitive intergenic consensus-polymerase chain reaction (ERIC-PCR).

Methods

Bacterial isolates and growth media

A total of 280 nonduplicate Gram-negative isolates were purified from different clinical samples such as urine, wounds, blood, sputum, and cerebrospinal fluid (CSF) from Aug to Dec 2021. The samples were collected from patients ≥ 18 years. The clinical specimens were collected from Al-Qasr Al-Aini University Hospitals with approval from the ethics committee of the Faculty of Pharmacy, Al-Azhar University (Protocol code 306 at 23/8/2021). Proteus mirabilis was provisionally identified based on characteristic growth on blood agar, non-lactose-fermenting colonies on MacConkey’s agar media (Oxoid, UK), and various biochemical reactions [16,17,18], and were confirmed using the automated Vitek 2 system (bioMérieux, Inc., Hazelwood, MO, USA). The purified isolates were preserved at − 80 °C in glycerol (25% v/v).

Antimicrobial susceptibility test

A routine antimicrobial susceptibility test was performed by the Kirby–Bauer disk diffusion method against all P. mirabilis isolates on Mueller Hinton agar (MHA; Oxoid, UK) and the results were interpreted in accordance with the Clinical and Laboratory Standards Institute [19] criteria. The antibiotics (Oxoid, UK) used were piperacillin (PRL, 100 μg), amoxicillin/clavulanic acid (AMC, 20/10 μg), aztreonam (ATM, 30 μg), imipenem (IPM, 10 μg), cefoxitin (FOX, 30 μg), ceftazidime (CAZ, 30 μg), cefotaxime (CTX, 30 μg), ciprofloxacin (CIP, 5 μg), cotrimoxazole (TS, 25 μg), gentamicin (GM, 10 μg), and amikacin (AK, 30 μg). Resistance to three or more classes of antimicrobial agents was defined as MDR [20].

The multiple antibiotic resistance index (MARI) was calculated by dividing the sum of antibiotics against which the bacterial species displayed resistance by the total number of antibiotics to which the isolates were subjected [21].

Phenotypic detection of β-lactamases

Detection of extended-spectrum β-lactamases (ESBLs)

A double-disk synergy test (DDST) was performed to examine the release of ESBL enzymes. The surface of MHA plates was dried and streaked with overnight cultures of the tested isolates diluted to 0.5 MacFarland. Ceftazidime (30 μg) and cefotaxime (30 μg) disks were applied on the agar surface 15 mm away from the centered amoxicillin–clavulanic acid (20/10 μg) disk and the plates were incubated at 37 °C for 24 h. Positive production of ESBL enzymes was detected by clear enhancement in the inhibitory zones around any of the expanded-spectrum cephalosporin disks toward amoxicillin–clavulanic acid, and denoted as “champagne-cork” or “keyhole” [22]. In a DDST with AmpC-positive isolates, cloxacillin (200 µg/ml) was added to the sterilized melted agar medium, at 45 °C, to act as an AmpC-type β-lactamase inhibitor [23].

Screening for AmpC β-lactamase-producing isolates by inhibitor-based test

Cefoxitin-cloxacillin DDST (CC-DDS) was conducted based on the inhibitory effect of cloxacillin on AmpC enzyme production. A disk of cefoxitin (30 μg) only and another supplemented with 20 mg of cloxacillin were placed on MHA plate inoculated with a bacterial suspension of 0.5 McFarland standards and incubated overnight at 37 °C. Any increase in the size of the inhibitory zone by ≥ 4 mm for cefoxitin/cloxacillin compared with that for the unsupplemented cefoxitin disk was considered to indicate AmpC production [24].

Detection of carbapenemase enzyme

A modified Hodge test (MHT) was performed to confirm the release of carbapenemases from P. mirabilis isolates in accordance with CLSI guidelines [25]. Escherichia coli ATCC 25922 was cultured overnight in peptone water to 0.5 McFarland opacity standards and swabbed onto MHA plate. A meropenem disk (10 µg) was placed at the center of the plate and the test isolates were streaked as a thin straight line from the edge of the disk to the plate edge. The plates were incubated in an inverted position at 37 °C overnight. The presence of a distorted inhibitory zone (clover-leaf shape) of E. coli ATCC 25922 growth toward the meropenem disk was considered to indicate a positive test result [26].

Genetic detection of β-lactamases

Phenotypically confirmed ESBL-, AmpC, and carbapenemase-positive Proteus isolates were subjected to PCR using specific primers for ESBL genes (blaTEM,blaSHV, blaCTX-2, blaCTX-M), AmpC-encoding genes (blaAmpC,blaACT, blaACC, blaFOX), and carbapenemase genes (blaKPC, blaIMP, blaNDM, blaVIM-1, blaVIM-2, and blaOXA) (Supplementary Table 1). The amplification cycles included initial denaturation at 94 °C for 3 min, followed by 35 cycles of denaturation at 94 °C for 30 s, annealing according to the temperature specified in Supplementary Table 1 for 30 s, and extension at 72 °C for 60 s; the reaction was then ended by a final extension step at 72 °C for 10 min. A negative control (molecular grade RNase free water) was included in all PCR assays.

Molecular typing of P. mirabilis isolates by enterobacterial repetitive intergenic consensus-PCR (ERIC-PCR)

P. mirabilis isolates harboring one or more β-lactamase-encoding genes as determined by PCR were fingerprinted by ERIC-PCR using the following primer pair: ERIC 1 (5′-ATGTAAGCTCCTGGGGATTCAC-3′) and ERIC 2 (5′-AAGTAAGTGACTGGGGTGAGCG-3′). The DNA amplification process was performed in a volume of 50 μL, including 2 U Go Taq DNA polymerase (Fermatas), 2.5 mM MgCl2 (Invitrogen), 0.25 mM each deoxynucleotide triphosphate, 100 ng of DNA template, and 0.5 μM primers, while the remaining volume was filled up with PCR-grade water. The PCR program used was as follows: denaturation at 95 °C for 5 min, followed by 35 cycles of denaturation at 94 °C for 30 s, annealing at 42 °C for 40 s, and extension at 72 °C for 5 min, and then a single final stage at 72 °C for 10 min [27].

Dendrogram and phylogenetic relationships

The banding pattern of PCR product was analyzed on a 1.5% agarose gel along with a negative control (without DNA template). The dendrogram was created by the unweighted pair group method with arithmetic mean (UPGMA) using the DendroUPGMA server (http://genomes.urv.cat/UPGMA) [28]. It was constructed using the Dice coefficient with a 1% tolerance limit and 1% optimization. Cluster relatedness of collected isolates with ≥ 70% similarity was considered to indicate an identical pattern type [29].

Statistical analysis

Comparison of proportions and graphic were performed with GraphPad Prism software (version 5.01) and Microsoft Excel (Microsoft Cooperation, 2010). Fisher’s exact and chi-square tests were used to determine the difference in resistance between β-lactamase positive and β-lactamase negative isolates. Moreover, the correlation between β-lactamase encoding genes was carried out using R statistical platform (https:// www.r- project. org) in R-studio version 1.4.1106, using the Spearman’s rank correlation and strength of the association was expressed as Spearman’s correlation coefficient (rs) between − 1 and + 1. For all statistical analyses, P values < 0.05 were considered to indicate a statistically significant difference.

Results

Identification of clinical isolates

Out of 280 clinical Gram-negative isolates processed, 58 P. mirabilis isolates were identified. The majority of the isolates were obtained from urine (69%, 40/58) followed by wounds (13.8%, 8/58), blood (6.9%, 4/58), sputum (6.9%, 4/58), and CSF (3.4%, 2/58).

Antimicrobial resistance pattern

The resistance pattern of the tested 4 antimicrobial categories including 11 antimicrobial agents against all P. mirabilis was clarified in Table 1. The resistance to cotrimoxazole, gentamicin, cefoxitin and ceftazidime was highly prevalent (60.3%, 37.9%, 36.2% and 32.8%, respectively). Whereas the resistance rate to piperacillin, amoxicillin-clavulanic acid, cefotaxime, ciprofloxacin and amikacin were lower than 30%. The highest sensitivity was observed for imipenem and aztreonam as 87.9% and 84.5%, respectively.

Table 1 Antibiogram results of all Proteus mirabilis isolates
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A total of 17 isolates were considered as MDR, from which 4 (23.5%) and 13 (76.5%) isolates belonged to 4 and 3 classes of antibiotics, respectively (Table 2). Among MDR isolates, 52.9% were isolated from urinary tract, 23.5% were from blood and 11.8% were from each wound and sputum. The MDR isolates showed 12 antibiotic resistance patterns to 3–9 antibiotics and including 8 unique patterns. The MARI ranged from 0.27 to 0.82 amongst all MDR Proteus isolates that are presented in Table 2.

Table 2 Different antibiotic resistance phenotypes and indices in 17 MDR P. mirabilis isolates
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Phenotypic detection of ESBLs, AmpC, and carbapenemases

Among the 58 isolates included in this study, 34 (58.6%) were β-lactamase producers. Twenty isolates (34.5%) were ESBL producers, as determined by DDST test (Fig. 1a, and Supplementary Figure S1). Twenty isolates (34.5%) were positive for AmpC β-lactamase, showing an increase in the inhibitory zone on the cefoxitin/cloxacillin disk by ≥ 4 mm relative to the inhibitory zone on the disk with cefoxitin alone (Fig. 1a, and Supplementary Figure S2).

Fig. 1
figure 1

The percent of P. mirabilis isolates producing β-lactamase enzymes (a): phenotypic detection of β-lactamases enzymes among isolates from different clinical sources (b): the prevalence rate of various β-lactamases enzymes among β-lactamases producing isolates. DDST: double disc synergism test, CC-DDS: cefoxitin-cloxacillin double disk synergy test and MHT: Modified Hodge Test

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Among AmpC producing isolates, ten isolates (17.2%) ((urine (n = 7, 1.1%), wound (n = 1, 1.7%) and sputum (n = 2, 3.4%)), showed positivity for ESBLs. Hence, the total number of ESBL producers was 30 isolates (51.7%) (Fig. 1b, and Supplementary Figure S3).

Seven isolates (4, 5, 8, 15, 16, 18, and 49) were not susceptible to imipenem, so were considered as putative carbapenemase producers and thus were subjected to confirmatory MHT. MHT showed that 10.3% (6/ 58 isolates) revealed clover leaf-like growth around the meropenem disk and were assigned as positive carbapenemase-producing isolates (Fig. 1a, Supplementary Figure S4). The majority of β-lactamase producers were isolated from urine (23/34 isolates, 67.6%), while P. mirabilis isolated from CSF was negative for all detected β-lactamase enzymes.

Among 34 β-lactamase producers, 14 isolates produced only single type of β-lactamases; among those 10 isolates (29.4%) were pure ESBL producers and the remaining 11.8% of isolates were pure carbapenemase producers. On the other hand, 20 isolates produced more than one type of β-lactamases as most of them (18 isolates, 52.9%) coproduced ESBLs and AmpC, whereas only two isolates (5.9%) coproduced ESBLs and AmpC together with carbapenemases (Fig. 1b).

Antimicrobial susceptibility profile and β-lactamases production

The relation of antibiotic resistance pattern between β-lactamase-producing positive and negative P. mirabilis isolates was clarified in Fig. 2. All ESBL producing isolates had high rates of resistance toward cotrimoxazole, while being susceptible to imipenem. Significantly, the rates of resistance to piperacillin (33.3% vs. 10.7%), cefotaxime (36.7% vs. 21.4%) and ciprofloxacin (33.3% vs. 17.9%) were higher in ESBL + isolates than in ESBL- isolates (Fig. 2a).

Fig. 2
figure 2

Resistance percentages among β-lacatmase negative (solid columns) and β-lacatmase positive (dashed columns) of P. mirabilis to 11 antibiotics for (a): ESBL, (b): AmpC and (c): carbapenemase enzymes. (* significant: p < 0.05, ** significant: p < 0.01 and ** *significant: p < 0.001). Statistical analysis was performed by Fisher Exact method

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Regarding AmpC production (Fig. 2b), the resistance rate in AmpC + was the highest toward cefoxitin and was the lowest toward imipenem than AmpC – isolates. With the exception of piperacillin, aztronam, imipenem, ciprofloxacin and cotrimoxazole, AmpC production had a significant effect on P. mirabilis resistance to other antibiotics tested.

Concerning carbapenemases, resistance to cotrimoxazole (83.3%) gentamicin (66.7%) and imipenem (16.7%) was significantly higher in carbapenemase-positive isolates than carbapenemase-negative ones (Fig. 2c).

Molecular detection of β-lactamases

Thirty isolates positive for ESBLs as determined using the DDST method, with or without cloxacillin, were assessed for genes encoding ESBLs (blaTEM, blaSHV, blaCTX-2, blaCTX-M) by PCR. All of those isolates, except isolate (No. 41), contained at least one of these ESBL encoding gene. Among ESBL-encoding genes, the blaSHV gene was the most common (n = 25, 83.3%), followed by blaCTX-M (n = 24, 80%) and blaTEM (n = 22, 73.3%), whereas blaCTX-2 was the least common (n = 4, 13.3%) (Supplementary Table 2).

The majority of ESBL-producing isolates (n = 26/30, 86.7%) co-harbored more than one ESBL-encoding gene versus only 10% of isolates expressed only a single gene. The highest co-existence patterns were blaTEM + blaSHV + blaCTX-M-15 and blaSHV + blaCTX-M-15, represented by 14 and 5 isolates out of 30 ESBL producers, respectively (Fig. 3a).

Fig. 3
figure 3

A bar graph illustrating the number of isolates-producing (a): ESBL, harboring ESBL-encoding genes, (b): AmpC, harboring AmpC-encoding genes and (c): carbapenemase, harboring carbapenemase-encoding genes either in combination (dashed bars) or as single genes (black bars)

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A correlation matrix between the tested ESBL genes indicated a significant and strongest correlation between blaSHV and blaCTX-M-15 (rs = 0.45) (Supplementary Figure S5a).

Among the 20 isolates phenotypically identified as AmpC producers, 19 (95%) were identified as carrying at least one of the detected AmpC genes, in the following order of prevalence: blaAmpC (n = 16, 80%), blaACT (n = 11, 55%), blaACC (n = 5, 25%), and blaFOX (n = 5, 25%). Only one isolate (No. 57) was negative for all tested AmpC genes (Supplementary Table 2).

Molecular evaluation of AmpC-producing isolates indicated that 60% of isolates co-harbored at least two AmpC-encoding genes, showing 4, 3 and 2 gene patterns (5%, 20% and 35%, respectively) (Fig. 3b). A correlation matrix between the AmpC-tested genes don not show any statistically significant correlations between each gene pair (Supplementary Figure S5b).

MHT-positive P. mirabilis isolates (n = 6) were tested for carbapenemase-encoding genes (blaOXA, blaKPC, blaNDM, blaVIM-1, and blaVIM-2). The resistance gene determinants clarified that; 2, 2 and 1 isolates harbored either blaOXA or blaVIM-1 or blaVIM-2, respectively. While only one isolate (No. 49) co-harbored blaVIM-1 and blaVIM-2. On the other hand, blaKPC and blaNDM were not detected in any of the tested isolates (Supplementary Table 2, Fig. 3c).

DNA fingerprinting analysis by ERIC-PCR

Thirty-four (58.6%) Proteus isolates were positive for at least one of the tested β-lactamase-encoding genes. The fingerprints obtained from a PCR assay with ERIC primers of these isolates showed a DNA banding profile consisting of amplified bands from 100 to 3000 bp in size (Fig. 4). Based on the binary data of these isolates, a dendrogram (Fig. 4) was constructed. Twenty-one different patterns (P1–P21) were identified among the tested isolates. Isolates were considered to have the same pattern upon a similarity level of ≥ 70%.

Fig. 4
figure 4

DNA fingerprinting by ERIC-PCR. a) Dendrogram analysis of 34 P. mirabilis isolates at ≥ 70% similarity using UPGMA based on Dice coefficients method derived from analysis of the ERIC-PCR profiles. Each isolate clinical source and β-lactamase encoding genes pattern are also shown. b) Agarose gel electrophoresis of ERIC-PCR for P. mirabilis isolates which exhibited Extended Spectrum β-lactamases, AmpC and Carbapenemases using primers ERIC 1 and ERIC 2

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All patterns were associated with a low number of isolates, varying from 1 to 4. The predominant pattern was P2 (4 isolates), followed by P1, P4, P9 (3 isolates each), and P7, P8, P10, P11 (2 isolates each). All patterns of isolates were from the same source, with the exceptions of P2 and P9, which were from different sources. Isolates in P1 and P11 were pure carbapenemase and ESBL producers, respectively. Meanwhile, other repetitive patterns (P2, P4, P7, P8, P9, and P10) contained ESBL- and AmpC-producing isolates. Finally, 100% ERIC typing similarities were found between isolates 21 and 22 (in P2), and 9 and 10 (in P4).

Discussion

The genus Proteus is one of the resident microbiota in the human gastrointestinal tract. It is an inherent cause of community-acquired infections and ranks third as a cause of hospital-associated cases [30, 31]. Proteus mirabilis is one of the species most commonly isolated from the urine since it is a common causative agent of catheter-associated UTIs [3, 32].

In the present study, 58 P. mirabilis isolates were isolated from various clinical samples: urine, wound, blood, sputum, and CSF. The highest percentage of isolates was from urine (69%), followed by wound specimens (13.8%). The ability of P. mirabilis to produce urease and accumulate ammonia leads to the creation of an environment where it can survive, colonize the urinary tract, and increase the risk of pyelonephritis and upper UTIs [33].

In the past, the majority of P. mirabilis isolates were susceptible to common classes of antibiotics, but recently the emergence of antibiotic resistance has been increasingly reported [34]. In this study, the highest rate of resistance was to cotrimoxazole (60.3%), which is similar to the rate in a study conducted in Iran [34, 35] and China [36]. On the other hand, imipenem showed the lowest rate of resistance (1.7%) among the tested antibiotics, as also previously detected in India [37]. Moreover, slightly low resistance was detected against aztreonam (13.8%) compared with the level previously detected in Egypt [2], suggesting that these antibiotics can be used in the treatment of P. mirabilis infections (Table 1).

The coexistence of resistance to different antibiotics indicates a simultaneous and continuous transfer of resistance traits among bacterial pathogens and highlights the propensity for MDR to emerge in P. mirabilis [4]. This study showed a lower MDR level (29.3%) than in studies performed in Gondar (87.4%) [38] and Bahir Dar (93.1%) [39] in Ethiopia. However, the magnitude of MDR found here was both very close to Pandey and coauthors [40] and higher than results reported by others [34].

Most of MDR isolates were from urine source (52.9%), indicating that P. mirabilis has a higher propensity for colonizing the urinary tract and expressing resistance to different antibiotic classes, especially cephalosporins, fluoroquinolones, and aminoglycosides [41]. The emergence of MDR is a cause of concern that requires the establishment of strong infection control strategies to reduce this burden [42]. The MARI value obtained ranged from 0.27 to 0.82 (Table 2), which significantly exceeds the maximum MARI value calculated at 0.2 [43]. This high MARI values suggest that the tested antibiotics are being used intensively in the area of sample collection and implies an environment with a high risk of antimicrobial resistance proliferation [44].

AmpC β-lactamase-producing isolates are the major cause of nosocomial outbreaks and treatment failure [45]. In this study, 28 isolates were not susceptible to cefoxitin; however, confirmation by a cloxacillin inhibitor-based test showed that 20 (34.5%) isolates were positive for AmpC production (Fig. 1a, Supplementary Figure S2). A study performed in India (37%) [46] showed equivalent levels; however, studies performed in Iran (1.5%) [47] and Spain (14.2%) [48] showed a low incidence of AmpC production. Eight P. mirabilis isolates were not susceptible to cefoxitin and did not produce AmpC. This may be attributable to other resistance mechanisms, such as porin channel mutation [49]. On the other hand, some of the AmpC-producing isolates (7 isolates) showed in vitro sensitivity to amoxicillin/clavulanic acid, but the therapeutic use of this antibiotic is doubtful due to AmpC not being inhibited by β-lactamase inhibitors [50].

The current study also demonstrated the coexistence of AmpC with ESBL enzymes since all of the 20 AmpC-producing isolates were also ESBL-positive (Fig. 1b), as reported at low levels in India and Ghana [37, 51, 52]. The effect of ESBLs can be blocked by the overproduction of plasmid-mediated AmpC β-lactamase enzymes [53]. Therefore, simultaneous detection of ESBLs, in the presence of AmpC inhibitor, is important to prevent the possibility of false-negative results.

The overall rate of ESBL-producing P. mirabilis in the present study was 51.7% (30 isolates) (Fig. 1a, Supplementary Figure S3), which is in line with other studies [39, 54,55,56]. In contrast, our prevalence rate was higher than that reported in earlier Egyptian studies, namely, 17% by [57] and 38.8% by [58]. Therefore, an increase in the ESBL production rate has emerged over time in Egypt due to the uncontrolled use of antimicrobials, mostly third-generation cephalosporins, as routine therapy against UTIs [59, 60].

Concerning the relation between in vitro antimicrobial resistance profiles and β-lactamase production (Fig. 2), this study showed that β-lactamase-producing isolates had significantly higher resistance to most of antibiotics tested compared to non-β-lactamase producers. Furthermore, the rate of MDR in β-lactamase producers (88.2%) was significantly higher than that in non-β-lactamase producers (11.8%, p < 0.0001). These results are quite concerning that implies the undermining of existing antibiotics’ efficacy and could also hinder the development of new ones [44].

At the genotypic level, out of 30 ESBL-producing isolates, 29 (96.7%) isolates were positive for ESBL genes, with blaSHV type being the most predominant (Supplementary Table 1). BlaSHV- and blaTEM-positive strains are usually reported as hospital-related pathogens [61]; both genes were abundant among our isolates (n = 25, 83.3%; and n = 22, 73.3%, respectively). In addition, higher frequencies of both genes in our work and in a recent report from our area may indicate that blaSHV and blaTEM are endemic in our locality [62]. Co-carriage of multiple ESBL genes was detected in 86.7% of our isolates (Fig. 3a). Similar prevalence rates have also been reported in E. coli, K. pneumonia, and Enterobacteriaceae [62,63,64,65].

The molecular detection of bla genes conferring resistance to AmpC β-lactamase revealed that blaAmpC was the most amplified gene (80%), however, blaACC and blaFOX were the least observed genes among our isolates (each 25%) (Supplementary Table 2). Meanwhile, CIT [66] and DHA [67] and FOX genes [68, 69] were commonly detected in previous studies. Seven isolates had only one type of AmpC β-lactamase and there were 12 isolates with the co-occurrence of more than one AmpC gene, whereas the majority of the shared genotypes occurred uniquely (Fig. 3b).

Seven P. mirabilis isolates were not susceptible to imipenem (Table 1). MHT was performed on these isolates to clarify their mechanism of resistance, showing that 85.7% (6/7 isolates) were able to produce carbapenemases. PCR analysis showed that blaOXA,blaVIM-1, and blaVIM-2 were the only positive genes (Supplementary Table 2, Fig. 3c). Co-harboring of carbapenemase genes was seen in only one isolate (No. 49), which is also an isolate coproducing ESBLs and AmpC. Generally, KPC and VIM-1 are the most common carbapenemase-encoding genes in P. mirabilis isolates [70]. Few studies have revealed the presence of OXA-23 [71] and NDM [72, 73] in P. mirabilis isolates. However, the study by Bontron and colleagues revealed that blaVIM-1 mediated elevated resistance to carbapenems in P. mirabilis [74].

Analysis of the genetic diversity of 34 non-repeated positive β-lactamase-producing Proteus isolates was carried out by the ERIC-PCR fingerprint method, although wide ranges of other molecular typing techniques are currently available. ERIC-PCR is a recommended technique because it is fast, cheap, easy to use, and provides acceptable data, but it has low reproducibility [75, 76]. Based on ERIC-PCR typing, a dendrogram was created, showing genotypic heterogeneity among the 34 P. mirabilis isolates. Twenty-one patterns were detected, including eight patterns repeated among analogous isolates at a rate of ≥ 70%. On the other hand, isolates number 21 and 22 from P2 and isolates number 9 and 10 from P4 had the same gel banding patterns, giving 100% homogeneity (Fig. 4). Regarding the ERIC profile, this indicated clonal similarities among these isolates. Clonally similar isolates were in a relationship with the pattern of β-lactamase-encoding genes that they exhibited. Accordingly, outbreaks of antibiotic resistance may be due to the spread of different β-lactamase genes [77].

Conclusion

The data obtained in this study revealed a high prevalence of ESBL and AmpC production among P. mirabilis clinical isolates, especially urinary isolates, with the co-occurrence of their respective genes in the same isolates. β-lactamase production is an important cause of multiple and extensive drug resistance. Although, most of isolates were resistance to the tested antimicrobials, imipenem and aztreonam are considered the remaining options for controlling and managing Proteus pathogenicity. ERIC-PCR-based genotyping indicated that some isolates had a 100% identical banding profile, which proved the rapid dissemination of β-lactamase-encoding genes. The occurrence of multiple β-lactamases in bacterial isolates reinforces the importance of an antimicrobial resistance surveillance system and an effective antibiotic policy. In addition, the need for sanitary procedures is crucial to prevent the increased rate of antibiotic resistance among the isolates in the future.

Availability of data and materials

Datasets generated and analyzed during this study are included in this published article and its supplementary information files. Also, the datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

P . mirabilis :

Proteus mirabilis

UTIs:

Urinary tract infections

MDR:

Multi-drug resistant

XDR:

Extensively drug-resistant

ESBLs:

Extended-Spectrum β-lactamases

CSF:

Cerebrospinal fluid

PRL:

Piperacillin

AMC:

Amoxicillin/clavulanic acid

ATM:

Aztreonam

IPM:

Imipenem

FOX:

Cefoxitin

CAZ:

Ceftazidime

CTX:

Cefotaxime

CIP:

Ciprofloxacin

TS:

Cotrimoxazole

GM:

Gentamicin

AK:

Amikacin

MHA:

Muller Hinton Aga

DDST:

Double-disk synergy test

CC:

Cefoxitin-cloxacillin

MHT:

Modified Hodge test

ERIC-PCR:

Enterobacterial Repetitive Intergenic Consensus-Polymerase Chain Reaction

UPGMA:

Unweighted pair group method with arithmetic mean

References

  1. Kishore J. Isolation, identification & characterization of Proteus penneri–a missed rare pathogen. Indian J Med Res. 2012;135:341–5.

    PubMed  PubMed Central  Google Scholar 

  2. Serry F, Gomaa S, Abbas H. Antimicrobial resistance of clinical Proteus mirabilis isolated from different sources. Zagazig J Pharm Sci. 2018;27(1):57–63.

    Article  CAS  Google Scholar 

  3. Schaffer JN, Pearson MM. Proteus mirabilis and Urinary Tract Infections. Microbiology spectrum. 2015;3(5):383-433.

  4. Al-Shamarti M, Alhassani A, Al-Luhaiby A. The Relationship Between the Type of Infection and Antibiotic Resistance. J Pure Appl Microbiology. 2018;12:845–54.

    Article  CAS  Google Scholar 

  5. Doddaiah V, Anjaneya D. Prevalence of ESBL, AmpC and Carbapenemase among Gram Negative Bacilli Isolated from Clinical Specimens. Am J Life Sci. 2014;2:76–81.

    Google Scholar 

  6. Pitout JD, Nordmann P, Laupland KB, Poirel L. Emergence of Enterobacteriaceae producing extended-spectrum beta-lactamases (ESBLs) in the community. J Antimicrob Chemother. 2005;56(1):52–9.

    Article  CAS  PubMed  Google Scholar 

  7. Sengodan T, Kannaiyan DM, Sureshkumar B, Mickymaray S. Antibiotic Resistance Mechanism of ESBL Producing Enterobacteriaceae in Clinical Field: A Review. 2018.

    Google Scholar 

  8. Bush K, Jacoby GA. Updated functional classification of beta-lactamases. Antimicrob Agents Chemother. 2010;54(3):969–76.

    Article  CAS  PubMed  Google Scholar 

  9. Rao M, Harle S. M P: prevalence of extended spectrum beta-lactamases and amp-c beta-lactamases in clinical isolates of gram-negative bacilli at a tertiary care hospital. J Evol Med Dent Sci. 2018;7:4272–6.

    Article  CAS  Google Scholar 

  10. Carvalhaes CG, Picão RC, Nicoletti AG, Xavier DE, Gales AC. Cloverleaf test (modified Hodge test) for detecting carbapenemase production in Klebsiella pneumoniae: be aware of false positive results. J Antimicrob Chemother. 2010;65(2):249–51.

    Article  CAS  PubMed  Google Scholar 

  11. Horner CS, Abberley N, Denton M, Wilcox MH. Surveillance of antibiotic susceptibility of Enterobacteriaceae isolated from urine samples collected from community patients in a large metropolitan area, 2010–2012. Epidemiol Infect. 2014;142(2):399–403.

    Article  CAS  PubMed  Google Scholar 

  12. Hung KH, Yan JJ, Lu JJ, Chen HM, Wu JJ. Characterization of the modified Hodge test-positive isolates of Enterobacteriaceae in Taiwan. J Microbiol Immunol Infect. 2013;46(1):35–40.

    Article  CAS  PubMed  Google Scholar 

  13. Barwa R, Shaaban M. Molecular Characterization of Klebsiella pneumoniae Clinical Isolates with Elevated Resistance to Carbapenems. Open Microbiol J. 2017;11:152–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Mona S, Ahmed A-Q, Mohammed A-A, Rasha B. Molecular characterization of resistance mechanisms in Pseudomonas aeruginosa isolates resistant to carbapenems. J Infect Dev Ctries. 2018;11(12):935-43.

  15. Hawkey PM, Jones AM. The changing epidemiology of resistance. J Antimicrob Chemother. 2009;64(Suppl 1):i3-10.

    Article  CAS  PubMed  Google Scholar 

  16. Holt JG, Krieg NR, Sneath PHA, Stanley JTa, William ST: Bergeys manual of determinative bacteriology. 9th ed., Baltimore; Wiliams and Wilkins, USA. QMJ VOL.9 No.16 158 Dec 1994.

  17. Collee JG, Mackie TJ, McCartney JE. Mackie & McCartney practical medical microbiology. New York: Churchill Livingstone; 1996.

    Google Scholar 

  18. MacFaddin JF. Biochemical Tests for Identification of Medical Bacteria. 3rd ed. Philadelphia: Lippincott Williams & Wilkins; 2000.

    Google Scholar 

  19. CLSI: Clinical and Laboratory Standards Institute, Performance standards for antimicrobial susceptibility testing. CLSI Document M100. Wayne: Clinical and Laboratory Standards Institute; 2017.

  20. Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, Harbarth S, Hindler JF, Kahlmeter G, Olsson-Liljequist B, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268–81.

    Article  CAS  PubMed  Google Scholar 

  21. Krumperman PH. Multiple antibiotic resistance indexing of Escherichia coli to identify high-risk sources of fecal contamination of foods. Appl Environ Microbiol. 1983;46(1):165-70.

  22. Maravić A, Skočibušić M, Svjetlana C, Fredotović Ž, Puizina J. Prevalence and diversity of extended-spectrum-β-lactamase-producing Enterobacteriaceae from marine beach waters. Mar Pollut Bull. 2014;90:60-7.

  23. Aubert D, Girlich D, Naas T, Nagarajan S, Nordmann P. Functional and structural characterization of the genetic environment of an extended-spectrum beta-lactamase blaVEB gene from a Pseudomonas aeruginosa isolate obtained in India. Antimicrob Agents Chemother. 2004;48(9):3284–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Polsfuss S, Bloemberg GV, Giger J, Meyer V, Bottger EC, Hombach M. Practical approach for reliable detection of AmpC beta-lactamase-producing Enterobacteriaceae. J Clin Microbiol. 2011;49(8):2798–803.

    Article  PubMed  PubMed Central  Google Scholar 

  25. CLSI: Clinical and Laboratory Standards Institute. Methods for dilution of antimicrobial susceptibility tests for bacteria that grow aerobically. Approved Standard—10th Edition. CLSI Document M07-A10. Wayne: Clinical and Laboratory Standards Institute; 2015.

  26. Bakour S, Olaitan AO, Ammari H, Touati A, Saoudi S, Saoudi K, Rolain JM. Emergence of Colistin- and Carbapenem-Resistant Acinetobacter baumannii ST2 Clinical Isolate in Algeria: First Case Report. Microb Drug Resist. 2015;21(3):279–85.

    Article  CAS  PubMed  Google Scholar 

  27. Ramazanzadeh R, Zamani S, Zamani S. Genetic diversity in clinical isolates of Escherichia coli by enterobacterial repetitive intergenic consensus (ERIC)-PCR technique in Sanandaj hospitals. Iran J Microbiol. 2013;5(2):126–31.

    PubMed  PubMed Central  Google Scholar 

  28. Garcia-Vallve S, Palau J, Romeu A. Horizontal gene transfer in glycosyl hydrolases inferred from codon usage in Escherichia coli and Bacillus subtilis. Mol Biol Evol. 1999;16(9):1125–34.

    Article  CAS  PubMed  Google Scholar 

  29. Khakabimamaghani S, Najafi A, Ranjbar R, Raam M. GelClust: a software tool for gel electrophoresis images analysis and dendrogram generation. Comput Methods Programs Biomed. 2013;111(2):512–8.

    Article  PubMed  Google Scholar 

  30. Pal N, Hooja S, Sharma R, Maheshwari RK. Phenotypic Detection and Antibiogram of beta-lactamase-producing Proteus Species in a Tertiary Care Hospital, India. Ann Med Health Sci Res. 2016;6(5):267–73.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Zafar U, Taj MK, Nawaz I, Zafar A, Taj I. Characterization of Proteus mirabilis Isolated from Patient Wounds at Bolan Medical Complex Hospital, Quetta. Jundishapur J Microbiol. 2019;12(7): e87963.

    Article  CAS  Google Scholar 

  32. Fallah F, Parhiz S, Azimi L. Rashidan M Distribution and Antibiotic Resistance Pattern of Bacteria Isolated from Patients with Community-acquired Urinary Tract Infections in Iran A Cross-sectional Study. 2019.

    Google Scholar 

  33. Jamil R, Foris A, Snowden J. Proteus mirabilis infections. In StatPearls. Treasure Island: StatPearls Publishing; 2021.

  34. Mirzaei A, Habibi M, Bouzari S, Asadi Karam MR. Characterization of Antibiotic-Susceptibility Patterns, Virulence Factor Profiles and Clonal Relatedness in Proteus mirabilis Isolates from Patients with Urinary Tract Infection in Iran. Infect Drug Resist. 2019;12:3967–79.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Jafari E, Mostaan S, Bouzari S. Characterization of antimicrobial susceptibility, extended-spectrum β-lactamase genes and phylogenetic groups of enteropathogenic Escherichia coli isolated from patients with diarrhea. Osong Public Health and Research Perspectives. 2020;11(5):327.

  36. Li Z, Peng C, Zhang G, Shen Y, Zhang Y, Liu C, Liu M, Wang FJPS. Prevalence and characteristics of multidrug-resistant Proteus mirabilis from broiler farms in Shandong Province. China. 2022;101(4): 101710.

    CAS  Google Scholar 

  37. Datta P, Gupta V, Arora S, Garg S, Chander J. Epidemiology of extended-spectrum beta-lactamase, AmpC, and carbapenemase production in Proteus mirabilis. Jpn J Infect Dis. 2014;67(1):44–6.

    Article  PubMed  Google Scholar 

  38. Eshetie S, Unakal C, Gelaw A, Ayelign B, Endris M, Moges F. Multidrug resistant and carbapenemase producing Enterobacteriaceae among patients with urinary tract infection at referral Hospital, Northwest Ethiopia. Antimicrob Resist Infect Control. 2015;4:12.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Abera B, Kibret M, Mulu W. Extended-Spectrum beta (beta)-Lactamases and Antibiogram in Enterobacteriaceae from Clinical and Drinking Water Sources from Bahir Dar City, Ethiopia. PLoS One. 2016;11(11): e0166519.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Pandey JK, Tyagi AK. Prevalence of Proteus species in clinical samples, antibiotic sensitivity pattern and ESBL production. Int J Curr Microbiol Appl Sci. 2013;2:253–61.

    Google Scholar 

  41. Khan AU. Musharraf A Plasmid-mediated multiple antibiotic resistance in Proteus mirabilis isolated from patients with urinary tract infection. Med Sci Monit. 2004;10(11):CR598-602.

    CAS  PubMed  Google Scholar 

  42. Tekele SG, Teklu DS, Tullu KD, Birru SK, Legese MH. Extended-spectrum Beta-lactamase and AmpC beta-lactamases producing gram negative bacilli isolated from clinical specimens at International Clinical Laboratories, Addis Ababa, Ethiopia. PLoS One. 2020;15(11): e0241984.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Osundiya O, Oladele R. Oduyebo OJAJoC, Microbiology E: Multiple antibiotic resistance (MAR) indices of Pseudomonas and Klebsiella species isolates in Lagos University Teaching. Hospital. 2013;14(3):164–8.

    Google Scholar 

  44. Fadare FT. Okoh AIJPo: Distribution and molecular characterization of ESBL, pAmpC β-lactamases, and non-β-lactam encoding genes in Enterobacteriaceae isolated from hospital wastewater in Eastern Cape Province. S Afr. 2021;16(7):e0254753.

    CAS  Google Scholar 

  45. Ogefere HO, Osikobia JG, Omoregie R. Prevalence of AmpC beta-lactamase among gram negative bacteria recovered from clinical specimens in Benin City, Nigeria. Trop J Pharm Res. 2016;15(9):1947.

    Article  CAS  Google Scholar 

  46. Shivanna V, Rao A. Detection of co-existence of β-lactamases in Gram negative bacteria using disc potentiation tests. Indian J Microbiol Res. 2017;4:64-7.

  47. Farrokhnazar E, Bidhendi SM, Karimi S. Prevalence of AmpC type Extended spectrum beta-lactamases genes in clinical Samples of E. coli isolated from Poultry and Humans. Int J Med Res Health Sci. 2016;5(7):83–93.

    Google Scholar 

  48. Gomara M, Lopez-Calleja AI, Iglesia B, Ceron IF, Lopez AR, Pinilla MJR. Detection of carbapenemases and other mechanisms of enzymatic resistance to beta-lactams in Enterobacteriaceae with diminished susceptibility to carbapenems in a tertiary care hospital. Enferm Infecc Microbiol Clin. 2018;36(5):296–301.

    Article  Google Scholar 

  49. Peter-Getzlaff S, Polsfuss S, Poledica M, Hombach M, Giger J, Bottger EC, Zbinden R, Bloemberg GV. Detection of AmpC beta-lactamase in Escherichia coli: comparison of three phenotypic confirmation assays and genetic analysis. J Clin Microbiol. 2011;49(8):2924–32.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Jacoby GA. AmpC beta-lactamases. Clin Microbiol Rev. 2009;22(1):161–82 Table of Contents.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Shenoy SM, Sinha R. Antibiotic Sensitivity pattern of clinical isolates of Proteus species with special reference to ESBL and Amp C production. IJAR. 2013;3(3):293–4.

    Article  Google Scholar 

  52. Feglo P, Opoku S. AmpC beta-lactamase production among Pseudomonas aeruginosa and Proteus mirabilis isolates at the Komfo Anokye Teaching Hospital, Kumasi, Ghana. Journal of Microbiology and Antimicrobials. 2014;6(1):13-20.

  53. Shahandeh Z, Sadighian F, Rekabpou K. Phenotypic study of Extended-spectrum beta-lactamase, AmpC and Carbapenemase among <i>E.coli</i> clinical isolates in affiliated hospitals of Babol University of Medical Sciences. Int J Health Syst Disaster Manag. 2015;3(2):74–8.

    Google Scholar 

  54. Mansouri S, Abbasi S: Prevalence of Multiple Drug Resistant Clinical Isolates of Extended-Spectrum Beta-Lactamase Producing Enterobacteriaceae in Southeast Iran. Iran J Med Sci 2010, 35.

  55. Ibrahim Y, Sani Y, Saleh Q, Saleh A, Hakeem G. Phenotypic Detection of Extended Spectrum Beta lactamase and Carbapenemase Co-producing Clinical Isolates from Two Tertiary Hospitals in Kano, North West Nigeria. Ethiop J Health Sci. 2017;27(1):3–10.

    Article  PubMed  PubMed Central  Google Scholar 

  56. Teklu DS, Negeri AA, Legese MH, Bedada TL, Woldemariam HK, Tullu KD. Extended-spectrum beta-lactamase production and multi-drug resistance among Enterobacteriaceae isolated in Addis Ababa, Ethiopia. Antimicrob Resist Infect Control. 2019;8(1):39.

    Article  PubMed  PubMed Central  Google Scholar 

  57. Fam N, Leflon-Guibout V, Fouad S, Aboul-Fadl L, Marcon E, Desouky D, El-Defrawy I, Abou-Aitta A, Klena J, Nicolas-Chanoine MH. CTX-M-15-producing Escherichia coli clinical isolates in Cairo (Egypt), including isolates of clonal complex ST10 and clones ST131, ST73, and ST405 in both community and hospital settings. Microb Drug Resist. 2011;17(1):67–73.

    Article  CAS  PubMed  Google Scholar 

  58. Shash RY, Elshimy AA, Soliman MY, Mosharafa AA. Molecular Characterization of Extended-Spectrum β-Lactamase Enterobacteriaceae Isolated from Egyptian Patients with Community- and Hospital-Acquired Urinary Tract Infection. Am J Trop Med Hyg. 2019;100(3):522–8.

    Article  CAS  PubMed  Google Scholar 

  59. Canton R, Novais A, Valverde A, Machado E, Peixe L, Baquero F, Coque TM. Prevalence and spread of extended-spectrum beta-lactamase-producing Enterobacteriaceae in Europe. Clin Microbiol Infect. 2008;14(Suppl 1):144–53.

    Article  CAS  PubMed  Google Scholar 

  60. Pandit R, Awal B, Shrestha SS, Joshi G, Rijal BP, Parajuli NP. Extended-Spectrum beta-Lactamase (ESBL) Genotypes among Multidrug-Resistant Uropathogenic Escherichia coli Clinical Isolates from a Teaching Hospital of Nepal. Interdiscip Perspect Infect Dis. 2020;2020:6525826.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Chong Y, Ito Y, Kamimura T. Genetic evolution and clinical impact in extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella pneumoniae. Infect Genet Evol. 2011;11(7):1499–504.

    Article  CAS  PubMed  Google Scholar 

  62. Hassuna NA, Khairalla AS, Farahat EM, Hammad AM, Abdel-Fattah M. Molecular characterization of Extended-spectrum β lactamase- producing E. coli recovered from community-acquired urinary tract infections in Upper Egypt. Sci Rep. 2020;10(1):2772.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Abdel-Moaty MM, Mohamed WS, Abdel-All SM, El-Hendawy HH. Prevalence and molecular epidemiology of extended spectrum Î2-lactamase producing Escherichia coli from hospital and community settings in Egypt. J App Pharm Sci. 2016;6(1):042–7.

    Article  CAS  Google Scholar 

  64. Eltai NO, Al Thani AA, Al-Ansari K, Deshmukh AS, Wehedy E, Al-Hadidi SH, Yassine HM. Molecular characterization of extended spectrum beta -lactamases enterobacteriaceae causing lower urinary tract infection among pediatric population. Antimicrob Resist Infect Control. 2018;7:90.

    Article  PubMed  PubMed Central  Google Scholar 

  65. Maleki N, Tahanasab Z, Mobasherizadeh S, Rezaei A, Faghri J. Prevalence of CTX-M and TEM beta-lactamases in Klebsiella pneumoniae Isolates from Patients with Urinary Tract Infection, Al-Zahra Hospital, Isfahan. Iran Advanced biomedical research. 2018;7:10.

    Article  PubMed  Google Scholar 

  66. Rensing KL, Abdallah HM, Koek A, Elmowalid GA, Vandenbroucke-Grauls CMJE, Al Naiemi N, van Dijk K. Prevalence of plasmid-mediated AmpC in Enterobacteriaceae isolated from humans and from retail meat in Zagazig Egypt. Antimicrob Resis Infect Control. 2019;8:45.

    Article  Google Scholar 

  67. Mohamed ES, Khairy RMM, Abdelrahim SS. Prevalence and molecular characteristics of ESBL and AmpC beta -lactamase producing Enterobacteriaceae strains isolated from UTIs in Egypt. Antimicrob Resist Infect Control. 2020;9(1):198.

    Article  PubMed  PubMed Central  Google Scholar 

  68. Helmy MM, Wasfi R. Phenotypic and Molecular Characterization of Plasmid Mediated AmpC <i>β</i>-Lactamases among <i> Escherichia coli </i>, <i>Klebsiella </i> spp., and <i> Proteus mirabilis </i> Isolated from Urinary Tract Infections in Egyptian Hospitals. BioMed Res Int. 2014;2014:171548.

    Article  PubMed  PubMed Central  Google Scholar 

  69. Wassef M, Behiry I, Younan M, El Guindy N, Mostafa S, Abada E. Genotypic Identification of AmpC beta-Lactamases Production in Gram-Negative Bacilli Isolates. Jundishapur J Microbiol. 2014;7(1): e8556.

    Article  PubMed  PubMed Central  Google Scholar 

  70. Hu L, Lv H, Wang S. Emergence of Proteus mirabilis Isolates Possessing the KPC-2 Carbapenem-Hydrolyzing β-lactamase in China. J Al- tern Complement Integr Med. 2017;3:028.

    Google Scholar 

  71. Bonnet R, Marchandin H, Chanal C, Sirot D, Labia R, De Champs C, Jumas-Bilak E, Sirot J. Chromosome-encoded class D beta-lactamase OXA-23 in Proteus mirabilis. Antimicrob Agents Chemother. 2002;46(6):2004–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  72. Kanzari L, Ferjani S, Saidani M, Hamzaoui Z, Jendoubi A, Harbaoui S, Ferjani A, Rehaiem A. Boutiba Ben Boubaker I, Slim A: First report of extensively-drug-resistant Proteus mirabilis isolate carrying plasmid-mediated bla(NDM-1) in a Tunisian intensive care unit. Int J Antimicrob Agents. 2018;52(6):906–9.

    Article  CAS  PubMed  Google Scholar 

  73. Bitar I, Mattioni Marchetti V, Mercato A, Nucleo E, Anesi A, Bracco S, Rognoni V, Hrabak J, Migliavacca R. Complete Genome and Plasmids Sequences of a Clinical Proteus mirabilis Isolate Producing Plasmid Mediated NDM-1 from Italy. Microorganisms. 2020;8(3):339.

  74. Bontron S, Poirel L, Kieffer N, Savov E, Trifonova A, Todorova I, Kueffer G, Nordmann P. Increased Resistance to Carbapenems in Proteus mirabilis Mediated by Amplification of the blaVIM-1-Carrying and IS26-Associated Class 1 Integron. Microb Drug Resist. 2019;25(5):663–7.

    Article  CAS  PubMed  Google Scholar 

  75. Adzitey F, Huda N, Ali GR. Molecular techniques for detecting and typing of bacteria, advantages and application to foodborne pathogens isolated from ducks. 3Biotech. 2013;3(2):97–107.

    Google Scholar 

  76. Behzadi P, Behzadi E, Ranjbar R. Basic Modern Molecular Biology. 1st ed. Tehran: Persian Science & Research Publisher; 2014.

    Google Scholar 

  77. Loncaric I, Stalder GL, Mehinagic K, Rosengarten R, Hoelzl F, Knauer F, Walzer C. Comparison of ESBL – And AmpC Producing Enterobacteriaceae and Methicillin-Resistant Staphylococcus aureus (MRSA) Isolated from Migratory and Resident Population of Rooks (Corvus frugilegus) in Austria. PLoS One. 2014;8(12):e84048.

    Article  Google Scholar 

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Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB). This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. Copyediting service funding was provided by The Egyptian Knowledge Bank (EKB).

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  1. Mona Shaaban and Soha Lotfy Elshaer contributed equally to this work.

Authors and Affiliations

  1. Department of Microbiology and Immunology, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt

    Mona Shaaban & Soha Lotfy Elshaer

  2. Department of Microbiology and Immunology, Faculty of Pharmacy (Girls), Al-Azhar University, Cairo, 11651, Egypt

    Ola A. Abd El-Rahman

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All authors contributed to the design of the work, analysis, interpretation of data, drafting the work, agreement on the work and resolved final approval of the version to be published. First, Mona Shaaban, and last authors, Ola A Abd El-Rahman, contributed equally to the research.

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Supplementary Information

Additional file 1: Supplementary Table 1.

Specific amplification primer sets for Proteus mirabilis clinical isolates. Supplementary Table 2. Genotypic detection of β-lactamases in 34 Proteus mirabilis isolates. Supplementary Figure 1. Detection of extended spectrum β-lactamase (ESBLs) by Double disc synergy test (DDST) in P. mirabilis tested isolates 10, 13, 20, 21, 22, 23, 25, 26, 27, 28, 31,32, 34, 38, 39, 44, 45, 52, 55, and 58; Positive production of ESBLs enzymes was detected by a clear cut enhancement in the inhibition zones around ceftazidime (30 μg) and cefotaxime (30 μg) disks towards amoxicillin–clavulanic acid (20/10 μg) disc, as ‘keyhole. Supplementary Figure 2. Detection of AmpC by Cefoxitin-Cloxacillin double disc synergy test (DDST) among P. mirabilis tested isolates 8, 9, 10, 13, 20, 23, 28, 29, 30, 31, 32, 34, 35, 36, 38, 39, 40, 41, 49, and 57. An increase in the size of the inhibition zone by ≥ 4 mm of the cefoxitin/cloxacillin compared to the un-supplemented cefoxitin disc is an indication of AmpC production. Supplementary Figure 3. Detection of extended spectrum β-lactamase (ESBLs) in AmpC-positive isolates by adding cloxacillin (200 µg/ml) to the sterilized melted agar medium. P. mirabilis isolates 8, 9, 29, 30, 35, 36, 40, 41, 49, and 57) were positive for ESBLs. Positive production of ESBLs enzymes was detected by enhancement in the inhibition zones around ceftazidime (30 μg) and cefotaxime (30 μg) discs towards amoxicillin–clavulanic acid (20/10 μg) disk. Supplementary Figure 4. Detection of carbapenemases by Modified Hodge test (MHT) in P. mirabilis tested isolates 4, 5, 8, 15, 16, and 49, while isolate 18 was negative. The presence of a distorted inhibition zone (clover-leaf shaped) of E. coli ATCC 25922 growth towards the meropenem disc was considered as a positive test. Supplementary Figure 5. A Correlogram representing correlation coefficients between each pair of the investigated (a) ESBL-encoding genes and (b) AmpC-encoding genes. The color intensity represents Spearman’s rank correlation coefficient (rs) value (blue circles are positive correlations and red circles are negative ones). Non-statistically significant correlations are crossed out and only statistically significant ones (p-value ≤ 0.05) were considered.

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Shaaban, M., Elshaer, S.L. & Abd El-Rahman, O.A. Prevalence of extended-spectrum β-lactamases, AmpC, and carbapenemases in Proteus mirabilis clinical isolates. BMC Microbiol 22, 247 (2022). https://doi.org/10.1186/s12866-022-02662-3

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