Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164-7040, USA.
BMC Genomics. 2010 Oct 4;11:535. doi: 10.1186/1471-2164-11-535.
Mannhemia haemolytica is a Gram-negative bacterium and the principal etiological agent associated with bovine respiratory disease complex. They transform from a benign commensal to a deadly pathogen, during stress such as viral infection and transportation to feedlots and cause acute pleuropneumonia commonly known as shipping fever. The U.S beef industry alone loses more than one billion dollars annually due to shipping fever. Despite its enormous economic importance there are no specific and accurate genetic markers, which will aid in understanding the pathogenesis and epidemiology of M. haemolytica at molecular level and assist in devising an effective control strategy.
During our comparative genomic sequence analysis of three Mannheimia haemolytica isolates, we identified a number of genes that are unique to each strain. These genes are "high value targets" for future studies that attempt to correlate the variable gene pool with phenotype. We also identified a number of high confidence single nucleotide polymorphisms (hcSNPs) spread throughout the genome and focused on non-synonymous SNPs in known virulence genes. These SNPs will be used to design new hcSNP arrays to study variation across strains, and will potentially aid in understanding gene regulation and the mode of action of various virulence factors.
During our analysis we identified previously unknown possible type III secretion effector proteins, clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated sequences (Cas). The presence of CRISPR regions is indicative of likely co-evolution with an associated phage. If proven functional, the presence of a type III secretion system in M. haemolytica will help us re-evaluate our approach to study host-pathogen interactions. We also identified various adhesins containing immuno-dominant domains, which may interfere with host-innate immunity and which could potentially serve as effective vaccine candidates.
曼海姆菌是一种革兰氏阴性菌,也是牛呼吸道疾病复合症的主要病原体。在病毒感染和运输到牛群等应激条件下,它们会从良性共生菌转变为致命病原体,并导致急性胸膜肺炎,通常称为运输热。仅美国牛肉产业每年因运输热损失超过 10 亿美元。尽管其具有巨大的经济重要性,但目前还没有特定和准确的遗传标记,这些标记将有助于在分子水平上了解曼海姆菌的发病机制和流行病学,并有助于制定有效的控制策略。
在对三种曼海姆菌分离株的比较基因组序列分析中,我们鉴定出了一些菌株特有的基因。这些基因是未来研究的“高价值目标”,旨在尝试将可变基因库与表型相关联。我们还鉴定出了许多散布在整个基因组中的高可信度单核苷酸多态性(hcSNP),并集中研究了已知毒力基因中的非同义 SNPs。这些 SNPs 将用于设计新的 hcSNP 阵列来研究菌株间的变异,并可能有助于了解基因调控和各种毒力因子的作用模式。
在分析过程中,我们鉴定出了以前未知的可能的 III 型分泌效应蛋白、规律成簇间隔短回文重复序列(CRISPR)和 CRISPR 相关序列(Cas)。CRISPR 区域的存在表明与相关噬菌体存在共同进化。如果证明其具有功能,那么曼海姆菌中 III 型分泌系统的存在将有助于我们重新评估研究宿主-病原体相互作用的方法。我们还鉴定出了含有免疫显性结构域的各种黏附素,这些结构域可能干扰宿主固有免疫,并且可能潜在地作为有效的疫苗候选物。