Genus Aeromonas Research Articles

Aeromonas and mcr–3: A Critical Juncture for Transferable Polymyxin Resistance in Gram-Negative Bacteria

Polymyxin antibiotics B and colistin are considered drugs of last resort for the treatment of multi-drug and carbapenem-resistant Gram-negative bacteria. With the emergence and dissemination of multi-drug resistance, monitoring the use and resistance to polymyxins imparted by mobilised colistin resistance genes (mcr) is becoming increasingly important. The Aeromonas genus is widely disseminated throughout the environment and serves as a reservoir of mcr–3, posing a significant risk for the spread of resistance to polymyxins. Recent phylogenetic studies and the identification of insertion elements associated with mcr–3 support the notion that Aeromonas spp. may be the evolutionary origin of the resistance gene. Furthermore, mcr–3-related genes have been shown to impart resistance in naïve E. coli and can increase the polymyxin MIC by up to 64-fold (with an MIC of 64 mg/L) in members of Aeromonas spp. This review will describe the genetic background of the mcr gene, the epidemiology of mcr-positive isolates, and the relationship between intrinsic and transferable mcr resistance genes, focusing on mcr–3 and mcr–3-related genes.

Impact of Arthrospira maxima Feed Supplementation on Gut Microbiota and Growth Performance of Tilapia Fry (Oreochromis niloticus)

Microalgae are promising as prebiotics in aquaculture. Arthrospira maxima has potential nutritional value but is poorly studied. We assessed A. maxima feed supplementation in tilapia fry and evaluated its effect on growth performance and gut microbiota. Fish were cultivated in ponds under 0%, 5%, 10%, and 15% A. maxima inclusion treatments. Growth parameters and biomass proximate analysis were assessed. A meta-amplicon analysis was performed on the gut microbiota using DADA2 and PICRUST2 for functional prediction. Among treatments, the 5% supplementation group seemed to present no negative effect on growth parameters and did not compromise the nutritional quality of tilapia fry biomass. Microbial composition was characterized by Cetobacterium, Pseudomonas and Aeromonas genera, and a predominance of beneficial metabolic pathways. Microbiota of tilapia fry fed with A. maxima showed unique genera with reported beneficial functions in tilapia. The abundance of potential pathogenic taxa was significantly decreased in supplementation treatments, possibly related to valuable compounds of A. maxima. The inclusion of the microalgae supported the stability of the microbiota, favoring the growth of commensal species. This seems to have an effect on decreasing the presence of pathogenic genera in the gastrointestinal tract. Overall, our work proposes 5% feed inclusion of A. maxima to be the most suitable for tilapia fry aquaculture to maintain production rates while improving general health.

Biological analysis of phage vB_AhaP_PT2 and treatment rescued crucian carp infected with Aeromonas hydrophila

Phage therapy is an alternative approach to overcoming the problem of multidrug resistance in bacteria. In this study, we isolated and purified a virulent phage named vB_AhaP_PT2 from A. hydrophila-TPS. We examined the biological characteristics and genome sequences of vB_AhaP_PT2. After intraperitoneal injection of bacteriophage (8 × 107 PFU/mL) into crucian carp, most of the phage distributed in the liver, spleen, kidney, intestine, and peripheral blood, and disappeared within 72 h. No substantial adverse symptoms were found in major organs after receiving phage injections continuously for 14 days. Vitro and Vivo results indicated that phage can effectively eliminate A. hydrophila-TPS. The phage vB_AhaP_PT2 (8 × 107 PFU/mL, 100 μL) can effectively protect the fish that exhibited a double median lethal dose of bacteria (2 × 106 CFU/fish). Although phage vB_AhaP_PT2 triggered the generation of phage-specific antibodies in carp, when the antibody titer was maximum, 8 × 107 PFU doses of bacteriophage could still protect crucian carp with lethal bacterial infections, the survival rate could reach 80 %. We also found that members of the genus Aeromonas could enter and colonize the intestine. The phage vB_AhaP_PT2 reduced the number of colonies of the genus Aeromonas. However, no significant changes were observed in α-diversity and β-diversity parameters, which suggested that the consumed phage had little effect on the intestine microflora. All the above results suggested that vB_AhaP_PT2 was a safe and effective therapeutic that can be considered as a potential tool to treat the infection caused by A. hydrophila-TPS in aquaculture.

Effects of Aeromonas infection on the immune system, physical barriers and microflora structure in the intestine of juvenile grass carp (Ctenopharyngodon idella)

Grass carp (Ctenopharyngodon idella) is an intensively cultured and economically important herbivorous fish species in China, but its culture is often impacted by Aeromonas pathogens such as Aeromonas hydrophila and Aeromonas veronii. In this study, healthy grass carp were separately infected with A. hydrophila or A. veronii for 12, 24, 48 or 72 h. The results showed that the mRNA expression levels of intestinal inflammatory factors (tnf-α, il-1β and il-8), complement factors (c3 and c4), antimicrobial peptides (hepcidin, nk-lysin and β-defensin-1), immunoglobulins (igm and igt), and immune pathway-related signaling molecules (tlr1, tlr2, tlr4, myd88, irak4, irak1, traf6, nf-κb p65 and ap-1) were differentially upregulated in response to A. hydrophila and A. veronii challenge. Additionally, the expression levels of the intestinal pro-apoptotic genes tnfr1, tnfr2, tradd, caspase-8, caspase-3 and bax were significantly increased, whereas the expression of the inhibitory factor bcl-2 was significantly downregulated, indicating that Aeromonas infection significantly induced apoptosis in the intestine of grass carp. Moreover, the expression of intestinal tight junction proteins (occludin, zo-1, claudin b and claudin c) was significantly decreased after infection with Aeromonas. Histopathological analysis indicated the Aeromonas challenge caused severe damage to the intestinal villi with adhesions and detachment of intestinal villi accompanied by severe inflammatory cell infiltration at 12 h and 72 h. The 16S rRNA sequencing results showed that Aeromonas infection significantly altered the structure of the intestinal microflora of the grass carp at the phylum (Proteobacteria, Fusobacteria, Bacteroidetes and Firmicutes) and genus (Proteus, Cetobacterium, Bacteroides, and Aeromonas) levels. Take together, the findings of this study revealed that Aeromonas infection induces an intestinal immune response, triggers cell apoptosis, destroys physical barriers and alters microflora structure in the intestine of juvenile grass carp; the results will help to reveal the pathogenesis of intestinal bacterial diseases in grass carp.

Impacts of water treatments on bacterial communities of biofilm and loose deposits in drinking water distribution systems

Treated drinking water is delivered to customers through drinking water distribution systems (DWDSs). Although studies have focused on exploring the microbial ecology of DWDSs, knowledge about the effects of different water treatments on the bacterial community of biofilm and loose deposits in DWDS is limited. This study assessed the effects of additional treatments on the bacterial communities developed in 10 months’ old pilot DWDSs. The results showed a similar bacterial community in the pipe-wall biofilm, which was dominated by Novosphingobium spp. (20–82 %) and Sphingomonas spp. (11–53 %), regardless of the treatment applied. The bacterial communities that were retained in the distribution systems (including pipe-wall biofilm and loose deposits) were similar to the particle-associated bacteria (PAB) in the corresponding supply water. The additional treatments showed clear effects of the removal and/or introduction of particles. The genera Aeromonas spp., Clostridium spp., Legionella spp., and Pseudomonas spp., which contain opportunistic pathogenic species, were only detected among the PAB in ion exchange system. Our study demonstrated that the biofilm community is consistent across treatments, and the contribution from bacteria in loose deposits is important but can be controlled by removing particles. These findings offer more insight into the origin and development of microbial ecology in DWDSs and suggest paths for further research on the possibility of managing the microbial ecology in distribution systems.

Effect of copper on fermentative hydrogen production from sewage sludge: Insights into working mechanisms

The effect of Copper (Cu) on fermentative hydrogen production from sewage sludge (SSL) was firstly explored, and glucose was chosen as typical substrate to make a comparison. Results showed that the stimulative dosages of Cu on hydrogen production from glucose and SSL were 20–60 mg/L and 20–100 mg/L, respectively. The stimulation was more significant to SSL (6.3–43.8 %) than glucose (4.8–16.1 %). 500–1000 mg/L Cu posed obvious inhibition to hydrogen production, and the inhibition was more significant to glucose (80.6–91.9 %) than SSL (25.0–37.5 %), which was due to the protective effect of SSL to hydrogen producers from adsorbing Cu. The exposure enriched the Cu-resistant microorganisms like genus Aeromonas, Comamonas, Pseudomonas and Dechloromonas. Metabolic analysis shows that low dosages of Cu stimulated hydrogen production by strengthening the formate decomposition process, and weakening the lactate formation and homoacetogenesis processes, while high dosages of Cu inhibited hydrogen production by weakening all hydrogen-producing processes including formate decomposition, ferredoxin hydrogenation and glucose decomposition processes.

Replacement of fishmeal with a microbial single-cell protein induced enteropathy and poor growth outcomes in barramundi (Lates calcarifer) fry.

Fish meal (FM) replacement is essential for the sustainable expansion of aquaculture. This study focussed on the feasibility of replacing FM with a single-cell protein (SCP) derived from methanotrophic bacteria (Methylococcus capsulatus, Bath) in barramundi fry (Lates calcarifer). Three isonitrogenous and isoenergetic diets were formulated with 0%, 6.4% and 12.9% inclusion of the SCP, replacing FM by 0%, 25% and 50%. Barramundi fry (initial body weight 2.5 ± 0.1 g) were fed experimental diets for 21 days to assess growth performance, gut microbiome composition and gut histopathology. Our findings revealed that both levels of SCP inclusion induced detrimental effects in barramundi fry, including impaired growth and reduced survival compared with the control group (66.7% and 71.7% survival in diets replacing FM with SCP by 25% and 50%, respectively; p < .05). Both dietary treatments presented mild necrotizing enteritis with subepithelial oedema and accumulation of PAS positive, diastase resistant droplets within hepatocytes (ceroid hepatopathy) and pancreatic atrophy. Microbiome analysis revealed a marked shift in the gut microbial community with the expansion of potential opportunistic bacteria in the genus Aeromonas. Reduced overall performance in the highest inclusion level (50% SCP) was primarily associated with reduced feed intake, likely related to palatability issues, albeit pathological changes observed in gut and liver may also play a role. Our study highlights the importance of meticulous optimization of SCP inclusion levels in aquafeed formulations, and the need for species and life-stage specific assessments to ensure the health and welfare of fish in sustainable aquaculture practices.

Rapid discrimination methods for clinical and environmental strains of Aeromonas hydrophila and A. veronii biovar sobria using the N-terminal sequence of the flaA gene and investigation of antimicrobial resistance.

Although the genus Aeromonas inhabits the natural environment, it has also been isolated from hospital patient specimens as a causative agent of Aeromonas infections. However, it is not known whether clinical strains live in the natural environment, and if these strains have acquired antimicrobial resistance. In this study, we performed the typing of flagellin A gene (flaA) of clinical and environmental strains of Aeromonas hydrophila and A. veronii biovar sobria using Polymerase Chain Reaction (PCR) assay with newly designed primers. Detection rates of the clinical and environmental flaA types of A. hydrophila were 66.7% and 88.2%, and the corresponding rates for A. veronii biovar sobria were 66.7% and 90.9%. The PCR assays could significantly discriminate between clinical and environmental strains of both species in approximately 4 h. Also, among the 63 clinical Aeromonas strains used, only one extended-spectrum β-lactamase-producing bacteria, no plasmid-mediated quinolone resistance bacteria, and only four multidrug-resistant bacteria were detected. Therefore, the PCR assays could be useful for the rapid diagnosis of these Aeromonas infections and the monitoring of clinical strain invasion into water-related facilities and environments. Also, the frequency of drug-resistant Aeromonas in clinical isolates from Okinawa Prefecture, Japan, appeared to be low.

Use of Matrix-Assisted and Laser Desorption/Ionization Time-of-Flight Technology in the Identification of Aeromonas Strains Isolated from Retail Sushi and Sashimi.

The genus Aeromonas includes well-known pathogenic species for fishes and humans that are widely distributed in the aquatic environment and foods. Nowadays, one of the main issues related to wild Aeromonas isolates is their identification at the species level, which is challenging using classical microbiological and biomolecular methods. This study aims to test MALDI-TOF MS technology in the identification of Aeromonas strains isolated from n. 60 retail sushi and sashimi boxes using an implemented version of the SARAMIS software V4.12. A total of 43 certified Aeromonas strains were used to implement the SARAMIS database by importing the spectra obtained from their identification. The original SARAMIS version (V4.12) failed to recognize 62.79% of the certified strains, while the herein-implemented version (V4.12plus) allowed the identification of all the certified strains at least to the genus level with a match of no less than 85%. Regarding the sushi and sashimi samples, Aeromonas spp. was detected in n. 18 (30%) boxes. A total of 127 colonies were identified at the species level, with A. salmonicida detected as the most prevalent species, followed by A. bestiarum and A. caviae. Based on the results of the present study, we could speculate that MALDI-TOF technology could be a useful tool both for the food industry to monitor product contamination and for clinical purposes to make diagnoses effectively and quickly.

Description of a pathogenic strain of Aeromonas dhakensis isolated from Ancherythroculter nigrocauda in an inland region of China.

Aeromonas dhakensis is reported as an emerging pathogenic species within the genus Aeromonas and is widely distributed in tropical coastal areas. This study provided a detailed description and characterization of a strain of A. dhakensis (202108B1) isolated from diseased Ancherythroculter nigrocauda in an inland region of China. Biochemical tests identified the isolate at the genus level, and the further molecular analysis of concatenated housekeeping gene sequences revealed that the strain belonged to the species A. dhakensis. The isolated A. dhakensis strain was resistant to five antibiotics, namely, penicillin, ampicillin, clindamycin, cephalexin and imipenem, while it was susceptible or showed intermediate resistance to most of the other fifteen tested antibiotics. The isolated strain of A. dhakensis caused acute haemorrhagic septicaemia and tissue damage in artificially infected A. nigrocauda, with a median lethal dose of 7.76×104 CFU/fish. The genome size of strain 202108B1 was 5043286 bp, including one chromosome and four plasmids. This is the first detailed report of the occurrence of infection caused by an A. dhakensis strain causing infection in an aquaculture system in inland China, providing important epidemiological data on this potential pathogenic species.

Characterisation, prevalence and antibiogram of Aeromonas hydrophila in turtles: insights into virulence factors, antimicrobial resistance genes and innate immunity

ABSTRACT Bacterial infection poses a significant threat to the health and survival of turtles, both in their natural habitats and in captivity. Notably, the presence and interactions of bacteria, such as those belonging to the Aeromonas genus, have been identified for their adverse impact on turtle health and ecosystem dynamics. This study investigated the prevalence, antibiotic susceptibility, virulence factors, and antimicrobial resistance genes of Aeromonas hydrophila in Trachemys scripta elegans (Red-eared Slider) and Chelonia mydas (Green Turtle). The study also examined the innate immunity of T. scripta elegans and C. mydas. Buccal and cloacal swabs from 39 turtles were collected and examined alongside 45 water samples to try to isolate and amplify A. hydrophila. Polymerase chain reaction (PCR) amplifications were then sequenced to identify the presence of specific genes associated with virulence, and antimicrobial resistance. The findings revealed that A. hydrophila had a prevalence rate of 35.9% in all examined turtle species, with 14 water samples accounting for 31% of the total samples. Buccal samples from Green and Red-eared turtles showed a higher rate of A. hydrophila isolates than cloacal samples. Sensitivity to norfloxacin (85.71%), gentamycin (71.42%), and ceftriaxone (64.28%) was observed, whereas resistance to amoxicillin (64.28%), ampicillin (57.14%), and rifamycin (57.14%) was apparent. Antibiotic resistance genes, including blaTEM and blaSHV, in A. hydrophila isolates, were present in 42.86% and 28.5% of the samples, respectively. PCR analysis confirmed the genetic identity of A. hydrophila, and five virulence genes were detected: AHCYTOEN (100%), followed by aerolysin (92.8%), alt and act (85.7%), and lipase (78.5%). Genetic sequences of the isolates had a 99% identity with the reference strains in GenBank. Furthermore, the study found the innate immunity of turtles to be robust due to serum lysozyme activity, bactericidal killing assay (BKA), total leukocyte count, heterophil/lymphocyte ratio, and packed cell volume (PCV%), all of which help to protect them from infections. Overall, this research highlights the need for continued monitoring and management of antibiotic resistance in aquatic ecosystems.

Trypan blue dye decolorization by Aeromonas caviae isolated from water sewage in Jakarta, Indonesia

Abstract. Pinontoan R, Susanto TSR, Lucy J, Angelina C, Soentoro SE, Purnomo JS, Cornelia M. 2024. Trypan blue dye decolorization by Aeromonas caviae isolated from water sewage in Jakarta, Indonesia. Biodiversitas 25: 1631-1637. The textile industry generates a substantial amount of hazardous chemical waste, which requires proper treatment to mitigate negative environmental and health consequences if left untreated. Studies on the removal of Trypan Blue (TB), a widely used commercial diazo textile dye, by indigenous bacteria are limited. Therefore, this study aimed to isolate, identify, and characterize microorganisms capable of decolorizing TB in textile dye-contaminated wastewater from Jakarta. Microorganisms were initially screened for decolorization activity in solid media containing TB. Among the isolated strains, TB2 isolate exhibited the highest decolorizing potential and was selected for further analysis. The morphological, biochemical, molecular, and phylogenetic characteristics of the TB2 isolate revealed that it belonged to the species Aeromonas caviae. To examine the ability of the isolate to remove TB, various culture conditions, such as pH, temperature, and agitation, were tested. The results demonstrated that the A. caviae TB2 strain could reduce up to 77.10% of TB (0.0025% (w/v)) under static conditions, pH 7.0, and 27°C over six days. To our knowledge, this is the first study to report the ability of the Aeromonas genus to decolorize TB. These results imply the potential use of A. caviae for decolorizing dye-bearing industrial wastewater.

Effects on growth performance and immunity of Monopterus albus after high temperature stress.

To investigate the impact of the effect of high temperature stimulation on Monopterus albus larvae after a certain period of time, five experimental groups were established at different temperatures. Then, the M. albus under high temperature stress was fed at 30°C for 70days. After that, the growth index of the M. albus was counted and analyzed. In terms of growth index, high temperature stress had significant effects on FCR, FBW, WGR, and SGR of M. albus (p < 0.05). The SR increased after being stimulated by temperature (p < 0.1). The study revealed that liver cells of M. albus were harmed by elevated temperatures of 36°C and 38°C. In the experimental group, the activities of digestive enzymes changed in the same trend, reaching the highest point in the 32°C group and then decreasing, and the AMS activity in the 38°C group was significantly different from that in the 30°C group (p < 0.05). The activities of antioxidase in liver reached the highest at 34°C, which was significantly different from those at 30°C (p < 0.05). In addition, the expression levels of TLR1, C3, TNF-α, and other genes increased in the experimental group, reaching the highest point at 34°C, and the expression level of the IL-1β gene reached the highest point at 32°C, which was significantly different from that at 30°C (p < 0.05). However, the expression level of the IRAK3 gene decreased in the experimental group and reached its lowest point at 34°C (p < 0.05). The expression level of the HSP90α gene increased with the highest temperature stimulus and reached its highest point at 38°C (p < 0.05). In the α diversity index of intestinal microorganisms in the experimental group, the observed species, Shannon, and Chao1 indexes in the 34°C group were the highest (p < 0.05), and β diversity analysis revealed that the intestinal microbial community in the experimental group was separated after high temperature stimulation. At the phylum level, the three dominant flora are Proteus, Firmicutes, and Bacteroides. Bacteroides and Macrococcus abundance increased at the genus level, but Vibrio and Aeromonas abundance decreased. To sum up, appropriate high-temperature stress can enhance the immunity and adaptability of M. albus. These results show that the high temperature stimulation of 32°C-34°C is beneficial to the industrial culture of M. albus.

Isolation and complete genome sequence of Aeromonas bacteriophage Gekk3-15.

Bacteria of the genus Aeromonas, especially A. hydrophila and A. veronii are recognized as important fish pathogens that cause significant economic losses in aquaculture. Environmentally friendly bacteriophage-based solutions for the treatment of fish and for the reduction of colonization by pathogenic bacteria in production facilities are currently in high demand. The bacteriophage Gekk3-15 was isolated during a search for novel phage strains potentially suitable for Aeromonas biocontrol applications. Genome sequencing revealed that this virus is a relatively small myovirus with a 64847 bp long dsDNA genome, which is consistent with virion electron microscopy data. Bacteriophage Gekk3-15 is distinct in its nucleotide and encoded aa sequences from all other sequenced bacteriophage genomes, and may represent a new viral taxon at the genus or subfamily level.

Novel Qnr Families as Conserved and Intrinsic Quinolone Resistance Determinants in Aeromonas spp.

The environment has been identified as an origin, reservoir, and transmission route of antibiotic resistance genes (ARGs). Among diverse environments, freshwater environments have been recognized as pivotal in the transmission of ARGs between opportunistic pathogens and autochthonous bacteria such as Aeromonas spp. In this study, five environmental strains of Aeromonas spp. exhibiting multidrug resistance (MDR) were selected for whole-genome sequencing to ascertain their taxonomic assignment at the species-level and to delineate their ARG repertoires. Analyses of their genomes revealed the presence of one protein almost identical to AhQnr (A. hydrophila Qnr protein) and four novel proteins similar to AhQnr. To scrutinize the classification and taxonomic distribution of these proteins, all Aeromonas genomes deposited in the NCBI RefSeq genome database (1,222 genomes) were investigated. This revealed that these Aeromonas Qnr (AQnr) proteins are conserved intrinsic resistance determinants of the genus, exhibiting species-specific diversity. Additionally, structure prediction and analysis of contribution to quinolone resistance by AQnr proteins of the isolates, confirmed their functionality as quinolone resistance determinants. Given the origin of mobile qnr genes from aquatic bacteria and the crucial role of Aeromonas spp. in ARG dissemination in aquatic environments, a thorough understanding and strict surveillance of AQnr families prior to the clinical emergence are imperative. In this study, using comparative genome analyses and functional characterization of AQnr proteins in the genus Aeromonas, novel Aeromonas ARGs requiring surveillance has suggested.

Isolation and Characterization of a Novel Aeromonas salmonicida-Infecting Studiervirinae Bacteriophage, JELG-KS1.

Representatives of the bacterial genus Aeromonas are some of the most notorious aquaculture pathogens associated with a range of diseases in different fish species. As the world forges toward the post-antibiotic era, alternative options for combating bacterial pathogens are needed. One such alternative option is phage biocontrol. In this study, a novel podophage-JELG-KS1-infecting Aeromonas salmonicida was retrieved from wastewater along with its host strain. The genome of the JELG-KS1 phage is a 40,505 bp dsDNA molecule with a GC% of 53.42% and 185 bp direct terminal repeats and encodes 53 predicted proteins. Genomic analysis indicates that JELG-KS1 might represent a novel genus within the subfamily Studiervirinae. Podophage JELG-KS1 is a strictly lytic phage without any identifiable virulence or AMR genes that quickly adsorbs onto the surface of host cells to initiate a 48 min long infectious cycle, resulting in the release of 71 ± 12 JELG-KS1 progeny virions per infected cell. JELG-KS1 effectively lyses its host population in vitro, even at very low multiplicities of infection. However, when challenged against a panel of Aeromonas spp. strains associated with diseases in aquaculture, JELG-KS1 shows host-specificity that is confined only to its isolation strain, immediately compromising its potential for Aeromonas spp. biocontrol in aquaculture.

Biodegradation of 17α-Ethinylestradiol by Strains of Aeromonas Genus Isolated from Acid Mine Drainage

17α-ethinylestradiol (EE2), a synthetically derived analogue of endogenous estrogen, is widely employed as a hormonal contraceptive and is recognized as a highly hazardous emerging pollutant, causing acute and chronic toxic effects on both aquatic and terrestrial organisms. It has been included in the initial Water Watch List. The aim of this study was to isolate bacteria from consortia recovered from mine sediments and acid mine drainage samples, both considered extreme environments, with the ability to degrade EE2. From the most promising consortia, isolates affiliated with the Aeromonas, Rhizobium, and Paraburkholderia genera were obtained, demonstrating the capability of growing at 50 mg/L EE2. Subsequently, these isolates were tested with 9 mg/L of EE2 as the sole carbon source. Among the isolated strains, Aeromonas salmonicida MLN-TP7 exhibited the best performance, efficiently degrading EE2 (95 ± 8%) and reaching concentrations of this compound below the limits of detection within 7 and 9 days. The final metabolites obtained are in accordance with those of the TCA cycle; this may indicate EE2 mineralization. As far as is known, Aeromonas salmonicida was isolated for the first time and identified in acid mine drainage, demonstrating its capacity to degrade EE2, making it a promising candidate for bioaugmentation and suggesting its possible applicability in low pH environments.

Antimicrobial susceptibility profile of bacteria of the genus Aeromonas and Escherichia coli isolated from samples of yellow hake (Cynoscion acoupa).

The aim of this study was to evaluate the antimicrobial susceptibility profile of Aeromonas sp., and Escherichia coli isolated from samples of yellow hake (Cynoscion acoupa). We analyzed 53 Aeromonas spp. and four E. coli isolates. We observed increased resistance of E. coli to levofloxacin and sulfa-trimethoprim as well as resistance of Aeromonas spp. to ampicillin, amoxicillin-clavulanate, cefuroxime, and cefotaxime. The multiple antimicrobial resistance(MAR) index indicated multidrug resistance in 90.54% (n=48) of Aeromonas spp. isolates and in 50% (n=2) of E. coli isolates. One strain of Aeromonas spp. was resistant to all 11tested antimicrobials (MAR index = 1.00). In vitro,piperacillin + tazobactam was the most effective antimicrobial for E. coli,and cefepime and levofloxacin were the most effective antimicrobials for Aeromonas spp. Therefore, in case of illnesses caused by these microorganisms, these antimicrobials should be used. The multidrug resistance of Aeromonas spp. and E. coli in this study is elevated. This is worrisome considering the increase in bacteria resistant to multiple drugs, reducing the options for successful clinical antimicrobial use.

Türkiye'de Yetiştiriciliği Yapılan Levrek Balıklarında (Dicentrarchus labrax) Aeromonas veronii biovar veronii Enfeksiyonu

Fish in aquaculture systems are susceptible to infectious agents as they are kept in a densely populated and often physically restricted environment. Genus Aeromonas include well-known pathogens, and the member Aeromonas veronii has been reported to cause diseases in both humans and animals, either as primary infection or as mixed infection with other pathogens. This study describes a low mortality epizootic caused by Aeromonas veronii biovar veronii in European seabass (Dicentrarchus labrax) farmed in the Aegean Sea. The gills, kidneys and livers of moribund fish were pale. Erythema, haemorrhage and superficial ulcerative lesions were detected on the skin. In addition, petechial haemorrhage was observed on the tongue, maxilla, and operculum. The spleen was enlarged and multiple granulomas were detected in both the kidney and the spleen. Some fish had skin depigmentation, ecchymosis in the liver, and a bloody exudate in the abdominal cavity. The intestinal walls were lined with a clear yellowish fluid. Twenty-nine motile, Gram-negative bacterial isolates were obtained from the internal organs of diseased fish. According to morphology, biochemical properties and 16S rRNA gene sequencing results, all isolates were identified as Aeromonas veronii bv. veronii. All isolates were resistant to amoxicillin and ampicillin, and sensitive to oxytetracycline, enrofloxacin, ciprofloxacin, florfenicol, and flumequine.

Potential Role of microRNAs in Response to Aeromonas Infection in Fish.

The genus Aeromonas is a widespread pathogen that includes more than 30 Gram-negative species, many of which are opportunistic bacteria. Aeromonas species are naturally distributed in various aquatic sources. Infectious processes in marine animals such as fish usually develop under stressful conditions, and when their immune systems are weakened. MicroRNAs (miRNAs/miRs) are short, non-coding RNAs that post-transcriptionally regulate gene expression. Their diverse biological functions, such as influencing cell development, proliferation, differentiation, tumorigenesis, metabolism, and apoptosis have been studied in various animals. Fish is the most important source of aquatic nutrients throughout the world, and its market is constantly growing. Overpopulation in aquaculture brings infectious diseases that threaten the development of aquaculture around the world. There is extensive evidence that microRNAs are involved in modulating infectious processes and regulating the inflammatory response to major bacterial fish infections, including Aeromonas. Here, we review the current literature on the fish microRNA repertoire and outline the physiological roles assigned to microRNAs to provide a foundation for future research during Aeromonas infection. Understanding the interaction between microRNAs and Aeromonas may provide clues to a remarkable strategy for preventing Aeromonas infections in fish.