Pusterla Nicola, Mapes Samantha, Rejmanek Daniel, Gebhart Connie
Department of Medicine and Epidemiology, University of California, Davis, California 95616, USA.
J Wildl Dis. 2008 Oct;44(4):992-8. doi: 10.7589/0090-3558-44.4.992.
The objective of this study was to determine whether Lawsonia intracellularis was present in the feces of free-living animals collected on two equine premises with documented occurrence of equine proliferative enteropathy (EPE). Fresh feces from black-tailed jackrabbits (Lepus californicus, n=100), striped skunks (Mephitis mephitis, n=22), feral cats (Felis catus, n=14), Brewer's Blackbirds (Euphagus cyanocephalus, n=10), Virginian opossums (Didelphis virginiana, n=9), raccoons (Procyon lotor, n=4), California ground squirrels (Spermophilus beecheyi, n=3), and coyotes (Canis latrans, n=2) were collected from August 2006 to January 2007 either from the ground while walking the premises or after trapping the animals using live traps. Nucleic acid purified from feces was directly processed for polymerase chain reaction (PCR) analysis using a real-time PCR assay targeting the aspartate ammonia lyase gene of L. intracellularis. Purified DNA samples were also precipitated, preamplified for L. intracellularis, and analyzed using the same real-time PCR assay, to increase the detection limit to one L. intracellularis organism per extracted sample. Feces from jackrabbits, striped skunks, Virginian opossums, and coyotes tested PCR positive for L. intracellularis, whereas all feces from feral cats, Brewer's Blackbirds, raccoons, and ground squirrels tested PCR negative for L. intracellularis. PCR testing on DNA extracted directly from feces was positive for L. intracellularis in six of 164 fecal samples. When DNA purification from feces was followed by a precipitation and preamplification step, five additional fecal samples tested PCR positive for L. intracellularis (11/164). The largest number of PCR positive L. intracellularis fecal samples was observed in striped skunks, followed by Virginian opossums, jackrabbits, and coyotes. This is the first description of L. intracellularis in these four species. Because the fecal samples were collected at equine farms with confirmed cases of EPE, striped skunks, Virginian opossums, jackrabbits, and coyotes may act as potential sources of infection to susceptible weanlings.
本研究的目的是确定在两个有记录发生马增生性肠炎(EPE)的马场采集的自由生活动物粪便中是否存在胞内劳森菌。2006年8月至2007年1月,从黑尾长耳大野兔(Lepus californicus,n = 100)、条纹臭鼬(Mephitis mephitis,n = 22)、野猫(Felis catus,n = 14)、棕头燕八哥(Euphagus cyanocephalus,n = 10)、弗吉尼亚负鼠(Didelphis virginiana,n = 9)、浣熊(Procyon lotor,n = 4)、加利福尼亚地松鼠(Spermophilus beecheyi,n = 3)和郊狼(Canis latrans,n = 2)收集新鲜粪便,要么在巡视场地时从地面收集,要么使用活捉陷阱捕获动物后收集。从粪便中纯化的核酸直接用于聚合酶链反应(PCR)分析,使用针对胞内劳森菌天冬氨酸氨裂解酶基因的实时PCR检测方法。纯化的DNA样本也进行沉淀,对胞内劳森菌进行预扩增,并使用相同的实时PCR检测方法进行分析,以将检测限提高到每个提取样本中一个胞内劳森菌生物体。黑尾长耳大野兔、条纹臭鼬、弗吉尼亚负鼠和郊狼的粪便经PCR检测胞内劳森菌呈阳性,而野猫、棕头燕八哥、浣熊和地松鼠的所有粪便经PCR检测胞内劳森菌呈阴性。对直接从粪便中提取的DNA进行PCR检测,164份粪便样本中有6份胞内劳森菌呈阳性。当从粪便中纯化DNA后进行沉淀和预扩增步骤时,又有5份粪便样本经PCR检测胞内劳森菌呈阳性(11/164)。在条纹臭鼬中观察到PCR阳性的胞内劳森菌粪便样本数量最多,其次是弗吉尼亚负鼠、黑尾长耳大野兔和郊狼。这是这四个物种中胞内劳森菌的首次描述。由于粪便样本是在确诊有EPE病例的马场收集的,条纹臭鼬、弗吉尼亚负鼠、黑尾长耳大野兔和郊狼可能是易感断奶幼驹的潜在感染源。