Rakic Martinez Mira, Wiedmann Martin, Ferguson Martine, Datta Atin R
Center for Food Safety and Applied Nutrition, Food and Drug Administration, Laurel, Maryland, United States of America.
Department of Food Science, Cornell University, Ithaca, New York, United States of America.
PLoS One. 2017 Sep 12;12(9):e0184557. doi: 10.1371/journal.pone.0184557. eCollection 2017.
Several animal models have been used to understand the molecular basis of the pathogenicity, infectious dose and strain to strain variation of Listeria monocytogenes. The greater wax worm Galleria mellonella, as an alternative model, provides some useful advantages not available with other models and has already been described as suitable for the virulence assessment of various pathogens including L. monocytogenes. The objectives of this study are: 1) confirming the usefulness of this model with a wide panel of Listeria spp. including non-pathogenic L. innocua, L. seeligeri, L. welshimeri and animal pathogen L. ivanovii; 2) assessment of virulence of several isogenic in-frame deletion mutants in virulence and stress related genes of L. monocytogenes and 3) virulence assessment of paired food and clinical isolates of L. monocytogenes from 14 major listeriosis outbreaks occurred worldwide between 1980 and 2015. Larvae injected with different concentrations of Listeria were incubated at 37°C and monitored over seven days for time needed to kill 50% of larvae (LT50) and to determine change of bacterial population in G. mellonella, 2 and 24 hours post-inoculation. Non-pathogenic members of Listeria and L. ivanovii showed significantly (P < 0.05) higher LT50 (lower virulence) than the wild type L. monocytogenes strains. Isogenic mutants of L. monocytogenes with the deletions in prfA, plcA, hly, actA and virR genes, also showed significantly (P < 0.05) higher LT50 than the wild type strain at the inoculum of 106CFU/larva. Food isolates had significantly (P < 0.05) lower virulence than the paired clinical isolates, at all three inoculum concentrations. L. monocytogenes strains related to non-invasive (gastroenteritis) outbreaks of listeriosis showed significantly (P < 0.05) lower virulence than isolates of the same serotype obtained from outbreaks with invasive symptoms. The difference, however, was dose and strain- dependent. No significant differences in virulence were observed among the serotype tested in this study.
已经使用了几种动物模型来了解单核细胞增生李斯特菌致病性、感染剂量和菌株间差异的分子基础。大蜡螟(Galleria mellonella)作为一种替代模型,具有一些其他模型所没有的有用优势,并且已经被描述为适用于包括单核细胞增生李斯特菌在内的各种病原体的毒力评估。本研究的目的是:1)用包括非致病性无害李斯特菌、斯氏李斯特菌、威氏李斯特菌和动物病原体伊氏李斯特菌在内的多种李斯特菌属菌株,确认该模型的有效性;2)评估单核细胞增生李斯特菌毒力和应激相关基因的几个同框缺失突变体的毒力;3)对1980年至2015年间全球发生的14起主要李斯特菌病暴发中分离出的单核细胞增生李斯特菌的成对食品和临床分离株进行毒力评估。将注射了不同浓度李斯特菌的幼虫在37°C下培养,并在7天内进行监测,以确定杀死50%幼虫所需的时间(LT50),并在接种后2小时和24小时测定大蜡螟体内细菌数量的变化。李斯特菌的非致病成员和伊氏李斯特菌的LT50(毒力较低)显著高于野生型单核细胞增生李斯特菌菌株(P<0.05)。在接种量为106CFU/幼虫时,prfA、plcA、hly、actA和virR基因缺失的单核细胞增生李斯特菌同框突变体的LT50也显著高于野生型菌株(P<0.05)。在所有三种接种浓度下,食品分离株的毒力均显著低于成对的临床分离株(P<0.05)。与非侵袭性(胃肠炎)李斯特菌病暴发相关的单核细胞增生李斯特菌菌株的毒力显著低于从有侵袭性症状的暴发中获得的相同血清型的分离株(P<0.05)。然而,这种差异取决于剂量和菌株。在本研究中测试的血清型之间未观察到毒力的显著差异。