Guard Jean, Gast Richard K, Guraya Rupa
U.S. Department of Agriculture, Athens, GA 30677, USA.
Avian Dis. 2010 Jun;54(2):857-61. doi: 10.1637/9069-091109-Reg.1.
Leghorn hens were infected with Salmonella Enteritidis cultures of known genomic content and subpopulation characteristics to determine comparative abilities to colonize the avian reproductive tract. Group 1 received phage-type (PT)4 22079, which is a dimorphic subpopulation that can both contaminate eggs and form biofilm. Group 2 received a 90:10 mixture of monomorphic PT13a strains 21027 and 21046, which produce biofilm or contaminate eggs, respectively. Group 3 received a 10:90 mixture of the same two PT13a strains, respectively. Trials were repeated three times and a total of 30 hens per treatment group were infected. Dosage was by oral gavage and was calculated as 8.6 +/- 2.01 X 10(7) colony-forming units per hen. Liver, spleen, and three different sections of oviduct (ovary, upper oviduct, and lower oviduct) were cultured per bird. Results were that all three groups had livers and spleens that were mostly positive (90.0% and 94.4% of 270 hens cultured, respectively). Reproductive-tract organs yielded 75 positives from 270 hens (27.8%), and treatment groups ranged from a low of 6.7% to a high of 76.7% positive cultures in any one trial. There was no significant difference between the numbers of positive reproductive-tract samples between treatment groups due to variance. These results suggest that the status of the reproductive tract at the time of infection may impact recovery of culture-positive tissue and contribute to variance. It is suggested that Salmonella Enteritidis cultures that vary in subpopulation composition have subtle differences in colonization of reproductive tissue that contribute to variance in egg contamination. Culture of non-reproductive-tract organs such as the liver and spleen was overall more reliable for detection of infected hens. The spleen was especially useful for detection because of its small size. Further research is needed to determine how sex hormones influence the infection pathway that results in egg contamination.
将来航鸡感染已知基因组内容和亚群特征的肠炎沙门氏菌培养物,以确定其在禽类生殖道定殖的相对能力。第1组接受噬菌体分型(PT)4 22079,它是一种双态亚群,既能污染鸡蛋又能形成生物膜。第2组接受单态PT13a菌株21027和21046的90:10混合物,它们分别产生生物膜或污染鸡蛋。第3组分别接受相同两种PT13a菌株的10:90混合物。试验重复进行三次,每个处理组共感染30只母鸡。给药方式为口服灌胃,计算剂量为每只母鸡8.6 +/- 2.01 X 10(7)个菌落形成单位。对每只鸡的肝脏、脾脏和输卵管的三个不同部位(卵巢、输卵管上段和输卵管下段)进行培养。结果是,所有三组的肝脏和脾脏大多呈阳性(分别为培养的270只母鸡中的90.0%和94.4%)。生殖道器官在270只母鸡中产生了75个阳性样本(27.8%),在任何一次试验中,处理组的阳性培养物比例从低至6.7%到高至76.7%不等。由于方差,处理组之间生殖道阳性样本数量没有显著差异。这些结果表明,感染时生殖道的状态可能会影响培养阳性组织的恢复,并导致方差。有人认为,亚群组成不同的肠炎沙门氏菌培养物在生殖组织定殖方面存在细微差异,这导致了鸡蛋污染的差异。对肝脏和脾脏等非生殖道器官进行培养,总体上对检测感染母鸡更可靠。脾脏因其体积小而特别有助于检测。需要进一步研究以确定性激素如何影响导致鸡蛋污染的感染途径。