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Communication

Antimicrobial Resistance and Extended-Spectrum Beta-Lactamase Genes in Enterobacterales, Pseudomonas and Acinetobacter Isolates from the Uterus of Healthy Mares

by
Pamela Thomson
1,*,
Patricia García
2,
Camila del Río
1,
Rodrigo Castro
3,
Andrea Núñez
4,5 and
Carolina Miranda
6
1
Laboratorio de Microbiología Clínica y Microbioma, Escuela de Medicina Veterinaria, Facultad de Ciencias de la Vida, Universidad Andrés Bello, Santiago 8370134, Chile
2
Departamento de Laboratorios Clínicos, Escuela de Medicina, Pontificia Universidad Católica, Santiago 8940000, Chile
3
Escuela de Medicina Veterinaria, Facultad de Recursos Naturales y Medicina Veterinaria, Universidad Santo Tomás, Talca 3473620, Chile
4
Escuela de Medicina Veterinaria, Facultad de Ciencias Agrarias y Forestales, Universidad Católica del Maule, Curicó 3340000, Chile
5
Facultad de Medicina Veterinaria y Agronomía, Universidad de las Américas, Santiago 7500975, Chile
6
Laboratorio de Microbiología Red de Salud UC-CHRISTUS, Pontificia Universidad Católica, Santiago 8940000, Chile
*
Author to whom correspondence should be addressed.
Pathogens 2023, 12(9), 1145; https://doi.org/10.3390/pathogens12091145
Submission received: 14 June 2023 / Revised: 31 August 2023 / Accepted: 5 September 2023 / Published: 8 September 2023
(This article belongs to the Special Issue Detection and Epidemiology of Drug-Resistant Bacteria)
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Abstract

:
Antibiotic-resistant bacteria are a growing concern for human and animal health. The objective of this study was to determine the antimicrobial resistance and extended-spectrum beta-lactamase genes in Enterobacterales, Pseudomonas spp. and Acinetobacter spp. isolates from the uterus of healthy mares. For this purpose, 21 mares were swabbed for samples, which were later seeded on blood agar and MacConkey agar. The isolates were identified using MALDI-TOF and the antimicrobial susceptibility test was performed using the Kirby–Bauer technique. To characterize the resistance genes, a polymerase chain reaction (PCR) scheme was performed. Of the isolates identified as Gram-negative, 68.8% were Enterobacterales, represented by E. coli, Enterobacter cloacae, Citrobacter spp., and Klebsiella pneumoniae; 28.1% belonged to the genus Acinetobacter spp.; and 3.1% to Pseudomonas aeruginosa. A 9.3% of the isolates were multidrug-resistant (MDR), presenting resistance to antibiotics from three different classes, while 18.8% presented resistance to two or more classes of different antibiotics. The diversity of three genes that code for ESBL (blaTEM, blaCTX-M and blaSHV) was detected in 12.5% of the strains. The most frequent was blaSHV, while blaTEM and blaCTX-M were present in Citrobacter spp. and Klebsiella pneumoniae. These results are an alarm call for veterinarians and their environment and suggest taking measures to prevent the spread of these microorganisms.

1. Introduction

The presence of microorganisms in the uterus of mares without reproductive pathologies has shown the existence of a uterine microbiota, of which nearly 200 microorganisms have been identified by molecular techniques [1,2,3,4,5]. These microorganisms play fundamental roles [6] in processes such as embryo implantation, prevention of the growth of pathogenic microorganisms, and protection of the epithelium [7,8,9]. It has been described that alteration or dysbiosis is related to the direct entry of bacteria through mating, artificial insemination, gynecological examination [1,6,10,11], malformation of the vulva or perineal region [12,13], and lesions of the cervix or vagina. These situations have been positively associated with bacterial endometritis [9,14], where Streptococcus equi, Escherichia coli, Klebsiella spp., and Pseudomonas spp. are the most frequently isolated microorganisms in this pathology [15,16,17,18,19].
In some countries in Europe, India, and the United States, bacteria such as Enterobacterales, Pseudomonas spp., and Acinetobacter spp. isolated from the uterus and vagina of healthy mares [11,16,18,20,21,22,23] show resistance or multidrug resistance (MDR) to antibiotics [24,25,26,27,28,29,30,31]. Extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae and carbapenem-resistant Acinetobacter baumannii and Pseudomonas aeruginosa were classified by the World Health Organization (WHO) as critically important pathogens [32] and are among the main antimicrobial resistance (RAM) threats in humans [33,34] and animals [35,36,37,38,39]. These situations are a cause of concern for the medical environment due to the probable dissemination of microorganisms and the limitation of therapeutic options [40]. The objective of this study was to determine the antimicrobial resistance and extended-spectrum beta-lactamase genes in Enterobacterales, Pseudomonas spp., and Acinetobacter spp. isolates from the uterus of healthy mares.

2. Materials and Methods

2.1. Ethical Approval

This research was approved by the Scientific Committee of Ethics of the Central-South macrozone of the Santo Tomás University, Chile (Approval number 60-21) and was carried out in the Maule region (35°25′ S, 71°39′ W) during October 2021.

2.2. Subjects and Criteria Selection

The group consisted of 21 purebred Chilean mares, between 4 and 15 years old, who were fed in a mixed meadow of ryegrass and white clover with free access to water. All participants were off antibiotic treatment for at least one month before being sampled
Clinically healthy mares in the ovulatory phase were included; this was determined by a gynecological clinical examination, transrectal ultrasound (Chison Eco 6 ultrasound, 5 MHz linear transducer), and cytology [13]. No mare presented a record of abortion, embryonic losses, endometritis, dystocia, or any reproductive pathology.

2.3. Uterine Samples, Collection, Isolation, and Identification

To avoid contamination, the tail was covered with sterile gauze and the fecal material was removed from the rectum. Subsequently, the perineum, clitoral fossa, and vulva were washed with soap and lukewarm water. The vulva was dried with bleached paper and the procedure was repeated until the area was visibly clean. Sample contamination was minimized using a sterile rectal glove, and a double-guarded occluded swab (IMV, Legler, Limoges, France) [18].
The uterine swabs were introduced directly in Amies transport medium (Linsan, Santiago, Chile) and were immediately transferred to the Clinic Microbiology and Microbiome laboratory, where they were seeded within 24 h on blood agar and MacConkey agar (Merk, Darmstadt, Germany). All plates were incubated at 37 °C for 18 to 24 h. Semi-quantitative evaluation of the different morphotypes was carried out, so that those that showed abundant growth in the second quadrant of the clock were selected with the help of a magnifying glass, observing standard patterns such as colony shape, borders, topography, color, and texture [41]. Later, each morphotype was isolated on blood agar (Linsan, Santiago, Chile) and was identified using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry analysis (MALDI Biotyper, Bruker, Singapore) following the manufacturer’s instructions and as described previously [42,43]. Importantly, Citrobacter spp. were analyzed as members of the C. freundii complex due to the impossibility of identification down to the species level using the MALDI-TOF technique [44].

2.4. Antimicrobial Susceptibility Testing

All isolates corresponding to Enterobacterales, Pseudomonas spp., and Acinetobacter spp. were tested against a panel of 13 antibiotics using the disk diffusion Kirby–Bauer method following CLSI guidelines in the M100 and VET01S [45,46]. Antibiotics tested included amikacin (AMK, 30 μg); ampicillin (AMP, 10 μg); amoxicillin/clavulanic acid (AUG 20/10 μg); ceftazidime (CAZ, 30 μg); ciprofloxacin (CIP, 5 μg); ceftriaxone (CRO, 30 μg); doxycycline (DXT, 30 μg); enrofloxacin (ENR, 5 μg); ertapenem (ETP, 10 μg); gentamicin (GEN, 10 μg); imipenem (IPM, 10 μg); ampicillin/sulbactam (SAM, 10/10 μg); and trimethoprim/sulfamethoxazole (SXT, 1.25/23.75 μg). All of these were supplied by OXOID (Hampshire, UK). The AMP disc was not used for Pseudomonas spp., Enterobacter spp., Citrobacter spp., and Klebsiella spp. In addition, for Acinetobacter spp. we only tested carbapenems, within the group of beta-lactams [46].
The screening of organisms producing extended-spectrum b-lactamases (ESBLs) and/or AmpC was performed using Cefotaxime 30 μg (CTX), CTX + clavulanic acid, and CTX + cloxacillin disc (Liofilchem, Teramo, Italy). For Acinetobacter spp. and P. aeruginosa, CTX + clavulanic acid + cloxacillin disc (Liofilchem, Teramo, Italy) were used to inhibit the chromosomal AmpC b-lactamase, which can antagonize the synergistic effect with clavulanate [46].
In all experiments, Klebsiella quasipneumoniae ATCC 700603 and E. coli ATCC 25922 were used as resistant and susceptible controls, respectively. Bacterial isolates resistant to ≥1 agent in >3 antimicrobial different classes were cataloged as multidrug-resistant (MDR) following previously standardized criteria [47].
The genes encoding ESBLs (blaCTX-M, blaSHV, blaTEM, blaPER and blaGES) were detected by a conventional PCR scheme, as previously reported [30,48,49]. Briefly, PCR was performed in a volume of 25 µL in a Veriti® thermal cycler (Applied Biosystems). The reaction mix contained 1× Green GoTaq®Flexi Buffer (Promega, Madison, WI, USA), PCR buffer, 800 nM of each primer (Table 1), 200 nM of dNTPs, 1.5 nM of MgCl2, 5 µL of DNA, and 1 U of Taq polymerase. The amplification program was an initial denaturation of 5 min at 94 °C, then 35 equal cycles of 40 s at 94 °C, 40 s at 52/57 °C, and 60 s at 72 °C. Finally, a final extension of 7 min at 72 °C occurred (Table 1). Tubes were stored at 4 °C until detection of the PCR product on 1.5% agarose gel. In cases where there was doubt that the size obtained in the PCR product was a non-specific amplification, it was decided to sequence them to confirm that they corresponded. For this, they were sequenced by the Sanger method using the BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Waltham, MA, USA) in the SeqStudio Genetic Analyzer (Applied Biosystems). The obtained sequences were compared with the GenBank database using the BLAST program. The sequences were deposited in the NCBI GenBank database (accession numbers OR242737, OR242738, OR242739, OR242740, and OR242741).

2.5. Data Analysis

Data analysis was performed using Excel (Microsoft 365), open-source statistical computing package release 1.3.4; upset plots [50] were made employing the UpSetPlot package (https://github.com/jnothman/UpSetPlot, access on 25 April 2022), release 0.6.0.

3. Results

The group of 21 mares studied were composed of purebred Chilean females, with more than two births, between 4 and 15 years old, with an average age of 8 years.
As a result, each mare had a mixed bacterial growth in 100% of the cases, isolating at least two or three different bacteria, corresponding to 42.8% and 52.4%, respectively. In contrast, the largest bacterial population with four isolates was present in only one mare, representing 4.8%.
Of the 55 bacterial isolates, 39 (70.9%) were Gram-negative bacteria of which 22 (56.4%) belonged to Enterobacterales, represented by 17 Escherichia coli, 3 Enterobacter cloacae, 1 Citrobacter spp., and 1 Klebsiella pneumoniae; and 17 were Gram-negative non-fermenting rod bacteria, represented by 9 Acinetobacter spp. (2 A. lwoffii, 1 A. johnsonii, and 6 Acinetobacter spp.), 3 Brevundimonas diminuta, 3 Sphingobacterium spp., 1 Pseudomonas aeruginosa, and 1 Ochrobactrum anthropi. In contrast, 16 (29.1%) of the isolates were Gram-positive bacteria: 10 Enterococcus spp. (6 E. casseliflavus, 2 E. faecalis, and 2 E. faecium), 4 Streptococcus equi, and 1 Corynebaterium sp. (Figure 1).
Of all antibiotics tested against the Enterobacterales and Pseudomonas spp. (n = 23), the third generation cephalosporins were shown a 26.1% resistance, followed by GM. In the strains of the Acinetobacter spp. tested, AMP was shown the greatest resistance with 44.4% (Figure 2). Only 9.3% (n = 32) of isolates showed MDR, corresponding to Escherichia coli, Enterobacter cloacae, and Klebsiella pneumoniae; also, 18.8% of isolates presented resistance to two or more classes of antibiotics. On the contrary, the carbapenems IPM and ETP were sensitive to all isolates (Table 2).
These results revealed the diversity of three ESBL genes (Table 3), blaTEM, blaCTX-M and blaSHV, in four isolates found (Escherichia coli, Acinetobacter spp., Klebsiella pneumoniae and Citrobacter spp.). The most frequent was blaSHV, being detected in all four isolates, while blaTEM and blaCTX-M were only present in Klebsiella pneumoniae and Citrobacter spp., which also exhibited coexistence of the three genes (blaCTX-M, blaSHV and blaTEM).

4. Discussion

It is currently recognized that mares and their reproductive environment are a source of origin of different microorganisms, which can be disseminated to other animals and to humans through direct and indirect contact [40,51].
Of the group of mares sampled, all presented between two and four different bacterial isolates, information which is consistent with previous articles [4,11,12,13,14,15,16,17,18,19,20,21,22,23,52,53]. According to these results, the Enterobacterales group was the most predominant, with Escherichia coli being the most frequent bacterium [17,54,55,56]. Some studies indicate that the source of origin of this agent would be fecal matter that contaminates the vulva and perineum, associated with a bad anatomical conformation [12,13,15]. Likewise, Enterococcus spp., Acinetobacter spp., Streptococcus equi spp. and to a lesser extent Klebsiella pneumoniae and Pseudomonas aeruginosa [4,53,56,57,58,59,60,61].
A retrospective study carried out with bacteria isolated from the reproductive tract of 4122 mares with endometritis identified Escherichia coli and Streptococcus equi more frequently, adding that over the years the antimicrobial efficacy of cefquinome against E. coli decreased significantly, and the same is true of ampicillin, cefquinome, and penicillin against S. equi [22]. Previously, Pseudomonas spp. were reported in mares with fertility problems [62] in chronic endometritis and in those without response to antibiotic treatments [63,64]. On the other hand, Klebsiella pneumoniae has been frequently found in respiratory and digestive conditions in horses [65,66]. Enterococcus spp. are rare to find in the uterus of healthy mares; however, E. faecalis has been isolated from mares with chronic endometritis and infertility [67]. Acinetobacter baumannii has been found in the uterus of healthy mares, and in equine patients with wounds, septicemia, eye infections, bronchopneumonia, neonatal encephalopathy, and venous catheter [36,37,68,69]. Therefore, Lupo et al. indicate that A. baumannii has become a nosocomial pathogen in veterinary hospitals [70]. Finally, Citrobacter freundi, along with other species, has been detected in a case of uterine infection with purulent discharge [71] and another of endocarditis in a foal [72].
Although antimicrobial resistance (RAM) has been previously reported in bacteria from the equine reproductive tract [11,22,62,73], it is unknown whether its origin is related to local or systemic treatments. Similarly, it is considered that exposure to low levels of antibiotics through semen diluents would be a probable cause of antibiotic resistance in mares [62,73]. RAM has been identified as one of the major problems facing human and animal health [74,75,76]; in this regard, the British Equine Veterinary Association has indicated that the use of fluoroquinolones and third generation cephalosporins should be regulated in empirical or prophylactic therapies [77,78]. In addition, Benko et al., point out that microorganisms such as Pseudomonas, Klebsiella, and Escherichia coli are considered highly resistant to β-lactam class antibiotics and ampicillin [16].
These results exhibited high resistance to the third generation cephalosporins and ampicillin, which coincides with what was mentioned in other studies [79,80,81,82] and could be attributed to the empirical use of ceftiofur in equine Gram-negative bacterial infections [78,83,84,85,86]. Likewise, the use of broad-spectrum cephalosporins could be a selection factor for bacteria with ESBL. Generally, the resistance genes that code for the expression of this ESBL phenotype, such as blaCTX-M, blaSHV, blaTEM, and blaCTX-M, are in plasmids or integron-type structures, which would facilitate horizontal gene transfer [30,40,66,87,88,89,90].
In 1998, the first ESBL strain was detected in bacteria of animal origin, an E. coli carrier of the SHV-12 gene [91]. Currently, there are several authors who report the presence of these bacteria in different animal species, emphasizing transmission to humans [26,28,29,87,92,93,94,95,96,97]. A study carried out from rectal swab samples in pairs of healthy mares and newborn foals reported the presence of ESBL in Escherichia coli strains in 25% and 29%, respectively, noting that during hospitalization this number increased significantly [98], the same as previously reported [99], suggesting an association with high use of antimicrobials, even in untreated animals [26], and nosocomial acquisition of ESBL in a hospital setting [100,101]. On the other hand, Klebsiella spp. have become a major health problem, leading to treatment failure in humans and animals. A previous report, carried out in healthy horses, reported only one K. pneumoniae isolate confirmed as a producer of ESBL (blaCTX-M) [92]. Another study carried out in the USA recovered E. coli isolates from clinical samples of equine patients over a period of five years, finding resistance to ceftiofur in 13 out of 48 of them, while the CTX-M and SHV genes were detected in 7 of them, which code for ESBL [84].
Interestingly, the literature reports that bacteria such as Acinetobacter spp., E. coli, Klebsiella spp., and Pseudomonas spp. can survive on inanimate surfaces for months [102,103]. The persistence of these bacteria ranges from 3 days to 5 months for Acinetobacter spp. [104], 1.5 h to 16 months for E. coli, 2 h to 30 months for Klebsiella spp., and 6 h to 16 months for Pseudomonas spp. [84,105,106]. The emergence of ESBL-producing bacteria is alarming, necessitating surveillance studies to understand the transmission and epidemiology of such microorganisms [30,84]. It is necessary to consider reinforcing measures such as hygiene, hand washing, identification of infected patients, cleaning, and disinfection of environmental sources of contamination.
ESBL-producing Enterobacteriaceae are a global public health alert, and so antimicrobial efficacy monitoring programs are crucial to consciously use antibiotics and preserve their effectiveness for both human and veterinary medicine.
The contribution of this study is its focus on antimicrobial resistance. So far, there is no evidence related to the presence of ESBL in isolates of Enterobacterales, Pseudomonas, and Acinetobacter obtained from a population of reproductively active mares in Chile. Although the group of animals studied was limited, the results revealed the diversity of three ESBL genes, blaTEM, blaCTX-M and blaSHV, which co-existed in Klebsiella pneumoniae and Citrobacter spp. It would be interesting to continue with these studies and apply them to a larger population to include other molecular techniques for the detection of resistance genes, such as the sequencing of the complete genome, to better understand the situation at the national level. This communication alerts us to the presence of multi-resistant bacteria in the uterus of healthy mares and urges us to emphasize cleaning and disinfection protocols to prevent dissemination at the animal–human–environment interface.

Author Contributions

Conceptualization, P.T. and P.G.; methodology, P.T., P.G., C.M., C.d.R., R.C. and A.N.; formal analysis, P.T. and P.G.; investigation, P.T. and C.d.R.; resources, P.T.; writing—original draft preparation, C.d.R.; writing—review and editing, P.T., P.G. and C.M.; project administration, P.T.; funding acquisition, P.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research, together with the APC, was financed by ANID, PAI project # 77190079.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Ethics Committee of the Universidad Santo Tomás, protocol code 60-21, on 7 July 2021.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors thank ANID, PAI project # 77190079, for the financial support given to this project.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Total number of isolates present in the uterus of healthy mares, represented by Escherichia coli (17), Enterobacter cloacae (3), Citrobacter spp. (1), Klebsiella pneumoniae (1), Acinetobacter spp. (9), Pseudomonas aeruginosa (1), Brevundimonas diminuta (3), Sphingobacterium spp. (3), Ochrobactrum anthropi (1), E. casseliflavus (6), E. faecalis (2), E. faecium (2), Enterococcus spp. (10), Streptococcus equi (4) and Corynebaterium spp. (2).
Figure 1. Total number of isolates present in the uterus of healthy mares, represented by Escherichia coli (17), Enterobacter cloacae (3), Citrobacter spp. (1), Klebsiella pneumoniae (1), Acinetobacter spp. (9), Pseudomonas aeruginosa (1), Brevundimonas diminuta (3), Sphingobacterium spp. (3), Ochrobactrum anthropi (1), E. casseliflavus (6), E. faecalis (2), E. faecium (2), Enterococcus spp. (10), Streptococcus equi (4) and Corynebaterium spp. (2).
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Pathogens 12 01145 g002
Figure 2. Representation of the cumulative resistance of different antibiotics against Enterobacterales, Acinetobacter spp. and Pseudomonas aeruginosa, isolated from the uterus of mares.
Figure 2. Representation of the cumulative resistance of different antibiotics against Enterobacterales, Acinetobacter spp. and Pseudomonas aeruginosa, isolated from the uterus of mares.
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Table 1. Primers used for ESBL PCRs.
Table 1. Primers used for ESBL PCRs.
β-Lactamase GenePrimer Sequence (5′ → 3′)Product
Length (bp)		T°
Annealing
blaCTX-MMA1: SCSATGTGCAGYACCAGTAA554 57 °C
MA2: CCGCRATATGRTTGGTGGTG
blaSHVSHV F: TCGGCCTTCACTCAAGGATG78557 °C
SHV R: ATGCCGCCGCCAGTCATATC
blaTEMTEM F: TTAGACGTCAGGTGGCACTT97252 °C
TEM R: GGACCGGAGTTACCAATGCT
blaPERPER F: AAAGAGCAAATTGAATCCATAGTC83557 °C
PER R: GTTAATTTGGGCTTAGGGCAG
blaGESGES F: ATGCGCTTCATTCACGCAC86457 °C
GES R: CTATTTGTCCGTGCTCAGG
Table 2. Specific antibiotic resistance against 32 isolates: Enterobacterales, Acinetobacter spp. and Pseudomonas spp.
Table 2. Specific antibiotic resistance against 32 isolates: Enterobacterales, Acinetobacter spp. and Pseudomonas spp.
IsolateSpecific Antibiotic Resistance
Acinetobacter lwoffiiAMP
Acinetobacter lwoffii-
Acinetobacter spp.-
Acinetobacter spp.AMP
Acinetobacter spp.AMP
Acinetobacter spp.AMP
Acinetobacter spp.-
Acinetobacter spp.-
Acinetobacter johnsonii-
Citrobacter spp.CAZ-SAM-CRO
Enterobacter cloacaeCAZ-GM-CRO
Enterobacter cloacaeSAM-CIP-SXT-GM-CRO-ENR
Enterobacter spp.CAZ-GM
Escherichia coliCAZ-CIP-SXT-GM-CRO-AMP-ENR-AUG-DXT
Escherichia coliDXT
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Escherichia coli-
Klebsiella pneumoniaeCAZ-SAM-CIP-SXT-GM-CRO-ENR-AUG-DXT
Pseudomonas spp.-
Table 3. Genetic characterization of extended-spectrum beta-lactamase (ESBL)-positive bacterial isolates of equine origin.
Table 3. Genetic characterization of extended-spectrum beta-lactamase (ESBL)-positive bacterial isolates of equine origin.
SpeciesESBL bla Genes
Acinetobacter lwoffii−−
Acinetobacter spp.+blaSHV
Acinetobacter spp.+−
Acinetobacter spp.+−
Citrobacter sp.+blaCTX-M, blaTEM, blaSHV
Enterobacter cloacae−−
Enterobacter cloacae−−
Escherichia coli+blaSHV
Klebsiella pneumoniae+blaCTX-M, blaTEM, blaSHV
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MDPI and ACS Style

Thomson, P.; García, P.; Río, C.d.; Castro, R.; Núñez, A.; Miranda, C. Antimicrobial Resistance and Extended-Spectrum Beta-Lactamase Genes in Enterobacterales, Pseudomonas and Acinetobacter Isolates from the Uterus of Healthy Mares. Pathogens 2023, 12, 1145. https://doi.org/10.3390/pathogens12091145

AMA Style

Thomson P, García P, Río Cd, Castro R, Núñez A, Miranda C. Antimicrobial Resistance and Extended-Spectrum Beta-Lactamase Genes in Enterobacterales, Pseudomonas and Acinetobacter Isolates from the Uterus of Healthy Mares. Pathogens. 2023; 12(9):1145. https://doi.org/10.3390/pathogens12091145

Chicago/Turabian Style

Thomson, Pamela, Patricia García, Camila del Río, Rodrigo Castro, Andrea Núñez, and Carolina Miranda. 2023. "Antimicrobial Resistance and Extended-Spectrum Beta-Lactamase Genes in Enterobacterales, Pseudomonas and Acinetobacter Isolates from the Uterus of Healthy Mares" Pathogens 12, no. 9: 1145. https://doi.org/10.3390/pathogens12091145

APA Style

Thomson, P., García, P., Río, C. d., Castro, R., Núñez, A., & Miranda, C. (2023). Antimicrobial Resistance and Extended-Spectrum Beta-Lactamase Genes in Enterobacterales, Pseudomonas and Acinetobacter Isolates from the Uterus of Healthy Mares. Pathogens, 12(9), 1145. https://doi.org/10.3390/pathogens12091145

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