Leroy Magali, Cabral Howard, Figueira Marisol, Bouchet Valérie, Huot Heather, Ram Sanjay, Pelton Stephen I, Goldstein Richard
Section of Molecular Genetics, Division of Pediatric Infectious Diseases, The Maxwell Finland Laboratory for Infectious Diseases, Boston University School of Medicine, Boston Medical Center, 774 Albany Street, Boston, MA 02118, USA.
Infect Immun. 2007 Aug;75(8):4158-72. doi: 10.1128/IAI.00318-07. Epub 2007 May 21.
The typically recovered quantity of nontypeable Haemophilus influenzae (NTHi) bacteria in an ex vivo middle ear (ME) aspirate from the chinchilla model of experimental otitis media is insufficient for direct analysis of gene expression by microarray or of lipopolysaccharide glycoforms by mass spectrometry. This prompted us to investigate a strategy of multiple consecutive lavage samplings to increase ex vivo bacterial recovery. As multiple consecutive lavage samples significantly increased the total number of bacterial CFU collected during nasopharyngeal colonization or ME infection, this led us to evaluate whether bacteria sequentially acquired from consecutive lavages were similar. Comparative observation of complete ex vivo sample series by microscopy initially revealed ME inflammatory fluid consisting solely of planktonic-phase NTHi. In contrast, subsequent lavage samplings of the same infected ear revealed the existence of bacteria in two additional growth states, filamentous and biofilm encased. Gene expression analysis of such ex vivo samples was in accord with different bacterial growth phases in sequential lavage specimens. The existence of morphologically distinct NTHi subpopulations with varying levels of gene expression indicates that the pooling of specimens requires caution until methods for their separation are developed. This study based on multiple consecutive lavages is consistent with prior reports that NTHi forms a biofilm in vivo, describes the means to directly acquire ex vivo biofilm samples without sacrificing the animal, and has broad applicability for a study of mucosal infections. Moreover, this approach revealed that the actual burden of bacteria in experimental otitis media is significantly greater than was previously reported. Such findings may have direct implications for antibiotic treatment and vaccine development against NTHi.
在实验性中耳炎的栗鼠模型中,从离体中耳(ME)吸出物中通常回收的不可分型流感嗜血杆菌(NTHi)细菌数量不足以直接通过微阵列分析基因表达或通过质谱分析脂多糖糖型。这促使我们研究一种多次连续灌洗采样的策略,以增加离体细菌回收率。由于多次连续灌洗样本显著增加了在鼻咽定植或ME感染期间收集的细菌CFU总数,这促使我们评估从连续灌洗中依次获取的细菌是否相似。通过显微镜对完整的离体样本系列进行比较观察,最初发现ME炎性液仅由浮游相NTHi组成。相比之下,对同一感染耳朵的后续灌洗采样显示,还存在另外两种生长状态的细菌,即丝状和被生物膜包裹的细菌。对此类离体样本的基因表达分析与连续灌洗标本中不同的细菌生长阶段一致。存在形态不同、基因表达水平各异的NTHi亚群,这表明在开发出分离方法之前,样本合并需要谨慎。这项基于多次连续灌洗的研究与之前关于NTHi在体内形成生物膜的报道一致,描述了在不牺牲动物的情况下直接获取离体生物膜样本的方法,并且对黏膜感染研究具有广泛的适用性。此外,这种方法表明,实验性中耳炎中细菌的实际负荷明显大于先前报道的负荷。这些发现可能对抗NTHi的抗生素治疗和疫苗开发有直接影响。