Pasteurellaceae members with similar morphological patterns associated with respiratory manifestations in ducks

Aim: A total of 112 freshly dead ducks aged from 2 to 20 weeks old with a history of respiratory manifestations were investigated for the implication of Pasteurellaceae family members.. Materials and Methods: Isolation and identification to the family level were conducted by conventional bacteriological methods, including microscopic examination and biochemical characterization. Identification to the species level was conducted by polymerase chain reaction (PCR) and analytical profile index (API) 20E kits. Results: Conventional bacteriological isolation and biochemical characterization revealed the infection of 16/112 examined birds with a prevalence rate of 14.3%. PCR confirmed the detection of Pasteurellaceae family conserved genes RpoB and Bootz in 16/16 (100%) isolates. PCR was also used for genus and species identification of the isolated Pasteurellaceae members; the results revealed that 5/16 (31.3%) of isolates were Gallibacterium anatis and 2/16 of isolates (12.5%) were Pasteurella multocida. Riemerella anatipestifer, Mannheimia haemolytica, and Avibacterium paragallinarum were not detected by PCR. Biotyping by API 20E successfully identified 5/16 (31.3%) isolates that could not be typed by PCR and confirmed their belonging to Pasteurella pneumotropica. Neither the available PCR primer sets nor API 20E succeeded for species identification of 4/16 (25%) isolates. Antibiotic susceptibility profiling of isolates revealed that 16/16 (100%) of isolates demonstrated multidrug resistance (MDR) phenotypes. Moreover, 16/16 (100%) of isolates demonstrated a phenotypic resistance pattern to neomycin. Conclusion: Combined genotypic, phenotypic, biotyping, and virulence characterizations are required for laboratory identification of pathogenic Pasteurellaceae. Moreover, P. multocida was not the prevailed member implicated in respiratory problems in ducks as P. pneumotropica, G. anatis, and unidentified strains were involved with higher prevalence. Chloramphenicol and ampicillin demonstrated the highest in vivo effects on the studied Pasteurellaceae. Furthermore, the prevalence of multidrug-resistant isolates signified the demand to implement targeted surveillance in the ducks' production sector, and MDR survey in poultry sectors in Egypt to apply effective control measures

Detection of Antibiotic and Disinfectant Resistant Genes in E. coli Isolated from Broilers Chickens

Avian colibacillosis is one of the most serious diseases that affect poultry and causes substantial morbidity and mortality rates as well as high economic losses. E. coli, are capable of acquiring resistance genes via gene transfer. The development of extended spectrum lactamases, or broad-spectrum lactamases, in E. coli is the most serious resistance mechanism. The goal of the current study was to detect the resistance associated genes of multi drug resistant E. coli isolated from broiler chicken by using PCR technique. In the current study PCR applied on 10 multidrug resistant E. coli isolates for detecting β-lactamases resistance genes (blaTEM, blaSHV), integron resistance gene (Int1, Int3), PCR was also used to detect disinfectant resistance genes as Quaternary ammonium compounds resistance genes (QacCD, QacA/B and QacED1). PCR results for antibiotic resistance associated gene showed that (10/10) of tested isolates had blaTEM and int1(10/10), blaSHV (6/10) and int3 (2/10) also PCR results for disinfectant resistance associated genes showed that (8/10) of E. coli isolates had QacED1, QacCD (2/10), and QacA/B (2/10). The (10) broilers flocks investigated in the study were infected with multi drug resistant, strains of E. coli, that haboured β-lactamases, integron resistance associated gene and quaternary ammonium compounds resistance genes

Mobile Colistin Resistance Determinants among Enterobacteriaceae Isolated from Different Poultry Species

Antimicrobial resistance (AMR) is a global threat that requires serious attention, particularly when it is developed against colistin, which is considered one of the ‘last resort’ antibiotics in the poultry industry. This study aimed to investigate the AMR profile of Enterobacteriaceae isolates from different poultry species, detect colistin resistance and investigate the existence of mcr genes in multi and extreme-resistant isolates. A total of 233 birds, chickens, ducks, turkeys, and quails, of various ages and breeds were collected from several localities of the Sharkia governorate and analyzed bacteriologically. The disc diffusion and E-test assays scrutinized the patterns of antibiotic, multidrug-resistant (MDR), and colistin resistance. The PCR assay was carried out to detect the mcr variants. Bacteriological examination revealed the incidence of 42.3% (99/233) of different Enterobacteriaceae members with a high predominance of E. coli, Salmonella, and Klebsiella species. Disc diffusion findings disclosed that 78.78% of isolates were resistant to colistin but E-test detected 19.19% only. Observed colistin resistance was strongly linked to the distribution of plasmid mcr-operons. The mcr 1, 2, 3, 4, and 7.1 genes were detected in 42.1, 63.15, 57.89, 52.63, and 47.36% of the phenotypic resistant isolates, and about 36.84% harbored at least four mcr clusters. However, the mcr5 gene was not discovered. The statistical assessment revealed a significant association between colistin resistance and MDR (p≤0.05). Moreover, there was a strong correlation between MCR-abundance and doxycycline, fosfomycin, beta-lactams, imipenem, and tobramycin resistances. In conclusion, this study highlights the alarming occurrence of colistin-resistant Enterobacteriaceae in various poultry aspects. An urgent strategy must be adopted to avert the spread of this phenomenon