A study was conducted to investigate the pathogenicity and the median lethal dose (LD50) of Aeromonas hydrophila isolated from clinically diseased catfish against apparently healthy homologous fish to evaluate the lethality of extra-cellular products (ECPs) of the isolated strain in vivo. For pathogenicity experiment, five different concentrations of Aeromonas hydrophila strain BNS 01614 including 3× 108, 1.5 × 108, 1.5 × 107, 1.5 × 106 and 1.5 × 105 CFU/fish used via intra peritoneal. The results revealed that pathogenicity of BNS 01614 was confirmed by the mortality of 30 % to 100 % of all tested fish within 4 to 12 days with LD50 1.5 × 107 CFU/fish. The Concentrated extracellular products (ECPs) of the selected bacterium were prepared and confirmed to be toxic in Clarias garipineus with LC50 of 20µg.

Aeromonas hydrophila and Campylobacter jejuni are bacteria of emerging importance in public health. However, little has been published about fish contaminated by these pathogens. The present study aimed to verify the presence of Aeromonas hydrophila and Campylobacter jejuni in fresh tuna samples (Thunnus spp.) caught off the coast of Santa Catarina State and distributed in the wholesale market of São Paulo/SP. A total of 85 tuna fillet samples were collected and examined by PCR and bacteriological analyses. Aeromonas spp. was detected in 11/85 (13%) samples, with 10/11 (90.9 %) being confirmed as Aeromonas hydrophila by PCR. Campylobacter spp. was found in 10/85 (11.7%) samples, 10/10 (100%) identified as Campylobacter jejuni by PCR and conventional biochemical analyses. Both pathogens were found in 2/85 (2.3%) samples. This is the first report on the contamination of fresh tuna by Campylobacter jejuni and Aeromonas hydrophila in Brazil. In addition to show that tuna can be a vehicle for transmission of pathogens when consumed raw, it emphasizes the importance of further studies to support the control these pathogens in fish.

This study was undertaken for isolation, identification and determination of antibiogram profile of Aeromonas hydrophila in farm raised fresh water prawn (Macrobrachium rosenbergii) on five commercial ghers. Fresh water prawns (n=25) were collected from five ghers located at Satkhira, Bagerhat and Khulna districts of Bangladesh. Brain (n=25), muscle (n=25) and intestine (n=25) samples were collected aseptically from fresh water prawn and inoculated into alkaline peptone (APW) water for enrichment at 37℃ for 8 h. Enriched cultured was streaked into Thiosulfate Citrate Bile Salt Sucrose (TCBS) agar to isolate bacteria. Bacteria were identified by cultural, Gram staining, biochemical properties and polymerase chain reaction (PCR) assay. The antibiogram profiles of bacteria were investigated against 5 commonly used antibiotics (Gentamicin, Cefalexin, Ampicillin, Azithromycin and Ciprofloxacin) by disc diffusion method. Thirteen A. hydrophila isolates were identified and the prevalence of the A. hydrophila in fresh water prawn was 17.33%. All 13 (100%) isolates were sensitive to Ciprofloxacin, Gentamicin, Azithromycin and resistant to Ampicillin and Cefalexin. The results of this study indicate that farm raised fresh water prawn harbor multidrug resistant A. hydrophila which might causes public health problem if enter into human food chain.

Nile tilapia aquaculture is a fast-growing industrial sector in Egypt. However, the progress of this industry is hindered by many challenges as poor water quality and associated bacterial infections. Aeromonas hydrophila is an important zoonotic waterborne aquatic pathogen responsible for severe outbreaks in tilapia culture so the current study aimed to investigate the prevalence of Aeromonas hydrophila in tilapia fish and their aquaculture water, the fish and water samples were collected from three farms located in Assiut and Minia Governorates, Egypt. Aeromonas hydrophila was isolated from tilapia five organs including liver, kidney, intestine, spleen and gills with a percentage of 7.1%, 6.5%, 9.1%, 5.1%, 11.7%, receptively, and from water samples with 59.7%. The isolates were molecularly confirmed as Aeromonas hydrophila in 70.9% and 82.4% of the tested isolates using 16s RNA and gyr-β primers, respectively. Aeromonas hydrophila isolates revealed a marked resistance for the tested antibiotics; amoxicillin and novobiocin (100%), streptomycin (71.4 %), chloramphenicol (57%), doxycycline and trimethoprim/Sulphamethoxazole (50%), colistin (43%), ciprofloxacin and norfloxacin (14%). The isolates showed multiple antibiotic resistance indexes ranging from 0.3 to 1. The present study highlights the Aeromonas hydrophila resistance and virulence, tilapia aquaculture health hazard to the human population, so adequate control measures should be applied. Furthermore, there is an essential need to promote an alternative non-antibiotic control in farmed fish.

Fish is one of the most important foods because of its high nutritional value, high palatability, and easy digestion. At the same time, it acts as a vehicle for many types of pathogenic microorganisms especially Aeromonas species, which results in public health hazards. Therefore, the present study was conducted to evaluate the prevalence of Aeromonas species in fresh fish (catfish, mullet, lizardfish, and coralfish) marketed in Zagazig city, Sharkia Governorate, Egypt. In addition, multiplex PCR was performed to detect some virulence-associated genes in A. hydrophila isolates. Furthermore, antimicrobial susceptibility testing was carried out on A. hydrophila isolates using commonly used antimicrobials in Egypt through the disc diffusion method. The achieved results indicated contamination of fish with different species of Aeromonas such as A. veronii, A. sobria, A. caviae and A. hydrophila. The results revealed that Aeromonas species isolated with an overall percentage of 55% of all examined fish. Bacteriological examinations revealed 20% A. hydrophila, 20% A. sobria, 10% A. caviae and 5% A. veronii. Antibiotic sensitivity declared high resistance of the isolates to different antimicrobial agents used in Egypt, including penicillin (100%), Ampicillin (90.0%), Streptomycin (90.9%), Cephalothin (72.7%), Tetracycline (72.7%), Cefotaxime (63.6%), and Sulfamethoxazole (54.5%). Therefore, hygienic measures should be adopted to control microbial contamination either in the aquatic environment or in fish markets.

The purpose of the study was to verify the existence and pathogenicity of Aeromonas hydrophila (A. hydrophila) in fish by validating the bactericidal effects of microwave and Gamma radiation on infected fish fillets. A total of 100 frozen Basa fish fillet samples were collected randomly from different markets in Zagazig, Sharkia Governorate, Egypt, and subjected to microbiological examination. The results revealed a 14% prevalence rate of A. hydrophila in fish fillets, which were tested for the presence of seven virulence genes: aerA, act, ast, alt, hyl, ahhR, and ahh1. All isolates exhibited traits related to virulence. The most predominated gene was ast (64.2%), followed by aerA, act, hyl, and ahhR (57.14% for each). Then, an experimental protocol for several treatments showed that Gamma radiation at a dose of 1 kGy decreased the count of A. hydrophila in fish fillets by 4.4 log10 CFU/g whereas doses of 2 and 3 kGy eradicated the pathogen. The same positive effect was recorded towards the microwave after cooking for 1, 2, and 3 minutes. Therefore, using microwave cooking and Gamma-irradiation alone and in combination with other decontamination methods may be more efficient in lowering the pathogen counts in fish meat.

Objective: The aerolysin (aerA) is a virulence indicator used to identify the pathogenicity of the Aeromonas strain. Targeting a pathogen's crucial virulence gene for detection is essential, as it determines the potential threat to the host. This study aimed to develop a gold nanoparticle (AuNP) probe for detecting the gene aerA in Aeromonas hydrophila among field samples. Materials and Methods: Kidney samples among both healthy and sick Nile tilapias in five provinces of Luzon Island were collected for bacterial analysis. Screening using specific primers targeting aerA was conducted in parallel with testing the AuNPs probe on the same sample set. The positive control provided by BFAR-NFLD, confirmed by polymerase chain reaction (PCR) assay, was used as a positive sample containing the target gene. Results: The AuNP probe demonstrated a computed accuracy of 81.32%, sensitivity of 100%, and specificity of 81.26%. Among the 257 reactions, 59 were false positives, while no false negative results were observed. The AuNP probe could detect aerA at levels as low as 30 ng/μl. The low prevalence of the target gene may be attributed to the use of general media instead of specific media like Rimler-Shotts agar. Conclusion: The established colorimetric detection method for A. hydrophila with the aerA gene offers a swift alternative to PCR, negating the requirement for advanced equipment like a thermal cycler. [J Adv Vet Anim Res 2023; 10(4.000): 593-598]