Eid Samah, Marouf Sherif, Hefny Hefny Y, Al-Atfeehy Nayera M
Department of Bacteriology, Reference Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Agricultural Research Centre, Nadi El-Seid St., P.O. Box 246, Dokki, Giza 12618, Egypt.
Department of Microbiology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Vet World. 2019 Dec;12(12):2061-2069. doi: 10.14202/vetworld.2019.2061-2069. Epub 2019 Dec 26.
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 family members.
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.
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 family conserved genes B and z in 16/16 (100%) isolates. PCR was also used for genus and species identification of the isolated members; the results revealed that 5/16 (31.3%) of isolates were and 2/16 of isolates (12.5%) were . , , and 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 . 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.
Combined genotypic, phenotypic, biotyping, and virulence characterizations are required for laboratory identification of pathogenic . Moreover, was not the prevailed member implicated in respiratory problems in ducks as , , and unidentified strains were involved with higher prevalence. Chloramphenicol and ampicillin demonstrated the highest effects on the studied . 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.
对112只2至20周龄有呼吸道症状病史的刚死亡鸭子进行调查,以研究其家族成员的影响。
采用常规细菌学方法进行到家族水平的分离和鉴定,包括显微镜检查和生化特性分析。采用聚合酶链反应(PCR)和分析谱指数(API)20E试剂盒进行到种水平的鉴定。
常规细菌学分离和生化特性分析显示,112只受检禽类中有16只感染,感染率为14.3%。PCR证实16株分离株(100%)中均检测到家族保守基因B和z。PCR还用于分离的家族成员的属和种鉴定;结果显示,16株分离株中有5株(31.3%)为某属,2株(12.5%)为某属。PCR未检测到另外几种属。通过API 20E进行的生物分型成功鉴定出16株分离株中5株(31.3%)无法通过PCR分型,并确认它们属于某属。对于16株分离株中的4株(25%),现有的PCR引物组和API 20E均未成功进行种鉴定。分离株的抗生素敏感性分析显示,16株分离株(100%)均表现出多重耐药(MDR)表型。此外,16株分离株(100%)均表现出对新霉素的表型耐药模式。
实验室鉴定致病性家族成员需要结合基因型、表型、生物分型和毒力特征。此外,某属并非鸭子呼吸道问题中占主导的家族成员,因为另外几种属和未鉴定菌株的感染率更高。氯霉素和氨苄西林对所研究的家族成员显示出最高的抗菌效果。此外,多重耐药分离株的流行表明需要在鸭子生产部门实施有针对性的监测,并在埃及家禽部门进行MDR调查,以采取有效的控制措施。