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布鲁氏菌属omp25/omp31家族中的DNA多态性:在鲸布鲁氏菌中鉴定出一个1.7 kb的倒位以及一个15.1 kb的基因组岛,该基因组岛在绵羊布鲁氏菌中不存在,与光滑型脂多糖的合成有关。

DNA polymorphism in the omp25/omp31 family of Brucella spp.: identification of a 1.7-kb inversion in Brucella cetaceae and of a 15.1-kb genomic island, absent from Brucella ovis, related to the synthesis of smooth lipopolysaccharide.

作者信息

Vizcaíno Nieves, Caro-Hernández Paola, Cloeckaert Axel, Fernández-Lago Luis

机构信息

Departamento de Microbiología y Genética, Edificio Departamental, Universidad de Salamanca, Plaza Doctores de la Reina s/n, 37007 Salamanca, Spain.

出版信息

Microbes Infect. 2004 Jul;6(9):821-34. doi: 10.1016/j.micinf.2004.04.009.

Abstract

Five genes homologous to the well-known omp25 and omp31 genes, that code for two major Brucella spp. outer membrane proteins (OMPs), have been detected in the genome of Brucella melitensis 16M and Brucella suis 1330. In this work we have determined the nucleotide sequence of these five genes, named omp31b, omp25b, omp25c, omp25d and omp22, in the six classical Brucella species reference strains and in representative strains of the recently proposed species Brucella cetaceae and Brucella pinnipediae that classify the Brucella strains isolated in the last years from marine mammals. Although these genes are quite conserved in the genus Brucella, several important differences have been found between species (i) omp31b contains a premature stop codon in B. canis and B. ovis truncating the encoded protein; (ii) the 5' end of omp31b is deleted in the three biovars of B. melitensis which probably prevents synthesis of Omp31b in this species; (iii) only B. melitensis, B. suis and B. neotomae would be able to synthesize the Omp25b protein with the characteristics shared by the Omp25/Omp31 group of proteins (characteristic signal sequence and C-terminal phenylalanine); (iv) a DNA inversion of 1747 bp including omp25b was detected in B. cetaceae strains; (v) a DNA deletion of about 15 kb was detected in all the six B. ovis strains tested. This deletion in B. ovis includes, among other genes, omp25b and wboA, a gene that has been shown to be required for the synthesis of the O-polysaccharide chain of the Brucella spp. smooth lipopolysaccharide. Several features of the DNA region absent from B. ovis suggest that this DNA fragment is a genomic island acquired by the Brucella ancestor by horizontal transfer and later deleted from B. ovis. The DNA polymorphism we have found in this work within the genus Brucella might be involved in the differences in pathogenicity and host preference displayed by the Brucella species.

摘要

在布鲁氏菌16M和布鲁氏菌猪种1330的基因组中,已检测到与著名的omp25和omp31基因同源的五个基因,这两个基因编码布鲁氏菌属的两种主要外膜蛋白(OMPs)。在这项研究中,我们测定了这五个基因(命名为omp31b、omp25b、omp25c、omp25d和omp22)在六种经典布鲁氏菌参考菌株以及最近提议的布鲁氏菌鲸种和布鲁氏菌海豹种的代表性菌株中的核苷酸序列,这些菌株对近年来从海洋哺乳动物中分离出的布鲁氏菌菌株进行了分类。尽管这些基因在布鲁氏菌属中相当保守,但在不同物种之间发现了一些重要差异:(i)omp31b在犬布鲁氏菌和绵羊布鲁氏菌中含有一个提前终止密码子,导致编码的蛋白质截短;(ii)布鲁氏菌羊种三个生物变种中omp31b的5'端缺失,这可能阻止了该物种中Omp31b的合成;(iii)只有布鲁氏菌羊种、布鲁氏菌猪种和布鲁氏菌新墨西哥种能够合成具有Omp25/Omp31蛋白组共同特征(特征性信号序列和C端苯丙氨酸)的Omp25b蛋白;(iv)在布鲁氏菌鲸种菌株中检测到一个包含omp25b的1747 bp的DNA倒位;(v)在所有测试的六种绵羊布鲁氏菌菌株中检测到约15 kb的DNA缺失。绵羊布鲁氏菌中的这种缺失包括omp25b和wboA等基因,wboA基因已被证明是布鲁氏菌属光滑脂多糖O-多糖链合成所必需的。绵羊布鲁氏菌中缺失的DNA区域的几个特征表明,这个DNA片段是布鲁氏菌祖先通过水平转移获得并随后从绵羊布鲁氏菌中删除的基因组岛。我们在这项研究中发现的布鲁氏菌属内的DNA多态性可能与布鲁氏菌物种所表现出的致病性和宿主偏好差异有关。

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