Harper Claudia G, Whary Mark T, Feng Yan, Rhinehart Howard L, Wells Randall S, Xu Shilu, Taylor Nancy S, Fox James G
Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
J Clin Microbiol. 2003 Jul;41(7):2842-8. doi: 10.1128/JCM.41.7.2842-2848.2003.
Helicobacter cetorum sp. nov. has been cultured from the stomach of Atlantic white-sided dolphins (Lagenorhynchus acutus) and the feces of Pacific white-sided (L. obliquidens) and Atlantic bottlenose (Tursiops truncatus) dolphins and a beluga whale (Delphinapterus leucas). H. cetorum has high homology to Helicobacter pylori as shown by 16S rRNA sequencing, and H. cetorum infection has been associated with gastritis and clinical signs in cetaceans. Because the prevalence of H. cetorum in wild populations is unknown, minimally invasive techniques for detecting H. cetorum were compared for 20 wild bottlenose dolphins sampled as part of a long-term health study. Fecal samples were tested for helicobacter by culture, Southern blotting, and PCR using genus-specific and H. cetorum-specific primers. An enzyme-linked immunosorbent assay (ELISA) was developed to measure H. cetorum immunoglobulin G (IgG). H. cetorum was cultured from 4 of 20 fecal samples, 7 samples were positive using Helicobacter sp. PCR, and 8 samples were positive for H. cetorum using species-specific primers. Two additional fecal samples were positive by Helicobacter sp. Southern blotting, suggesting infection with another helicobacter. All 20 sera contained high levels of IgG antibodies to H. cetorum that were significantly lowered by preabsorption of the sera with whole-cell suspensions of H. cetorum (P < 0.02). Until the specificity of the serum ELISA can be determined by testing sera from dolphins confirmed to be uninfected, PCR and Southern blot screenings of feces are the most sensitive techniques for detection of H. cetorum, and results indicate there is at least a 50% prevalence of H. cetorum infection in these dolphins.
新型鲸源幽门螺杆菌(Helicobacter cetorum sp. nov.)已从大西洋白侧海豚(Lagenorhynchus acutus)的胃以及太平洋白侧海豚(L. obliquidens)、大西洋宽吻海豚(Tursiops truncatus)的粪便和一头白鲸(Delphinapterus leucas)中培养出来。16S rRNA测序显示,鲸源幽门螺杆菌与幽门螺杆菌(Helicobacter pylori)具有高度同源性,并且鲸源幽门螺杆菌感染与鲸类动物的胃炎及临床症状有关。由于野生种群中鲸源幽门螺杆菌的流行情况未知,作为一项长期健康研究的一部分,对20头野生宽吻海豚采用了微创技术来检测鲸源幽门螺杆菌。通过培养、Southern印迹法以及使用属特异性和鲸源幽门螺杆菌特异性引物的PCR对粪便样本进行幽门螺杆菌检测。开发了一种酶联免疫吸附测定(ELISA)来检测鲸源幽门螺杆菌免疫球蛋白G(IgG)。20份粪便样本中有4份培养出了鲸源幽门螺杆菌,7份样本使用幽门螺杆菌属PCR呈阳性,8份样本使用种特异性引物对鲸源幽门螺杆菌呈阳性。另外两份粪便样本通过幽门螺杆菌属Southern印迹法呈阳性,表明感染了另一种幽门螺杆菌。所有20份血清中均含有高水平的抗鲸源幽门螺杆菌IgG抗体,用鲸源幽门螺杆菌全细胞悬液对血清进行预吸收后,抗体水平显著降低(P < 0.02)。在通过检测经确认未感染的海豚血清来确定血清ELISA的特异性之前,粪便的PCR和Southern印迹筛查是检测鲸源幽门螺杆菌最敏感的技术,结果表明这些海豚中鲸源幽门螺杆菌感染率至少为50%。