A slow decay to extinction: cold temperatures and reduced microbial complexity prolong the persistence of planktonic Francisella tularensis.

IF 4.2 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Johanna Thelaus, Dawn Birdsell, Stina Bäckman, Malin Granberg, Emelie Salomonsson, Igor Golovliov, Eva Lundmark, David Sundell, Jonas Näslund, Laila Noppa, Anna-Lena Johansson, Karin Wallgren, Joseph D Busch, Jason W Sahl, Anders Johansson, Mats Forsman, David M Wagner
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引用次数: 0

Abstract

Francisella tularensis is a zoonotic pathogen transmitted to humans through contact with infected animals, arthropod vectors, or contaminated environmental sources. Although replication occurs primarily within eukaryotic host cells, persistence outside a host is thought to be critical for long-term maintenance and transmission in natural ecosystems. To better understand persistence in aquatic habitats outside of mammalian hosts, we studied virulent strains of F. tularensis subspecies tularensis (type A) and subspecies holarctica (type B) incubated in a planktonic state (free living in water) under various axenic aquatic conditions. After 1 year in cold, nutrient-poor treatments, the type B strain (FSC200) caused disease in mice and remained culturable on laboratory media, whereas the type A strain (Schu S4) caused disease but with delayed onset and became non-responsive to laboratory growth conditions. In 1.5-year persistence experiments, type B still caused disease in mice, but with delayed onset, whereas type A no longer caused disease. The rate of bacterial decline depended on subspecies, temperature, and the initial inoculum size. We further explored the persistence of type A and type B populations in natural pond water, which corroborated findings from axenic conditions and revealed that both strains perpetuated disease from a non-replicative inactive persistent state. This study provides timeframes for the persistence of virulent planktonic F. tularensis subspecies tularensis and holarctica populations in various aquatic conditions, contributing to increased understanding of host-independent survival as a component of the perpetuation of tularemia.

Importance: Long-term persistence of planktonic (free living in water) Francisella tularensis subspecies tularensis (type A) and subspecies holarctica (type B) requires low temperatures and reduced microbial complexity. These conditions are typical of water wells, supporting the epidemiological observations that drinking water reservoirs may serve as sources of human F. tularensis infections (specifically type B). Importantly, persistence of types A and B did not correlate with molecular viability assays and culturability. This suggests that risk assessment of contagious bacteria based on these methods may not be appropriate. This is the first study to perform side-by-side comparisons of fully virulent strains of type A (Schu S4) and type B (FSC200), to evaluate persistence (defined by the capability to cause tularemia in mice) outside the host-restricted niche under stress conditions in water. The results contribute to the understanding of long-term persistence of F. tularensis between tularemia outbreaks in humans and other mammals.

缓慢的腐烂直至灭绝:低温和微生物复杂性的降低延长了浮游土拉菌的持久性。
土拉弗朗西斯菌是一种人畜共患病原体,通过接触受感染的动物、节肢动物媒介或受污染的环境源传播给人类。虽然复制主要发生在真核宿主细胞内,但宿主外的持久性被认为是自然生态系统中长期维持和传播的关键。为了更好地了解在哺乳动物宿主以外的水生栖息地的持久性,我们研究了在各种无菌水生条件下浮游状态(自由生活在水中)培养的土拉菌亚种土拉菌(A型)和亚种holarctica (B型)的毒力菌株。在寒冷、营养不良的条件下处理1年后,B型菌株(FSC200)在小鼠中引起疾病,并在实验室培养基上保持可培养性,而A型菌株(Schu S4)引起疾病,但发病延迟,对实验室生长条件无反应。在1.5年的持续性实验中,B型小鼠仍然致病,但发病延迟,而A型小鼠不再致病。细菌减少的速度取决于亚种、温度和初始接种量。我们进一步探索了A型和B型种群在天然池塘水中的持久性,这证实了无菌条件下的发现,并揭示了这两种菌株从非复制的无活性持久性状态延续疾病。本研究提供了在各种水生条件下,毒力强的浮游土拉菌亚种土拉菌和全北极菌种群持续存在的时间框架,有助于增加对土拉菌病长期存在的一个组成部分——不依赖宿主生存的理解。重要性:浮游生物(水中自由生活)的长期持续生存需要低温和降低微生物复杂性。土拉菌弗朗西斯菌亚种(A型)和holarctica亚种(B型)。这些情况是水井的典型情况,支持流行病学观察,即饮用水水库可能是人类土拉菌感染(特别是B型)的来源。重要的是,A型和B型的持久性与分子活力测定和培养能力无关。这表明基于这些方法的传染性细菌风险评估可能不合适。这是首次对A型(Schu S4)和B型(FSC200)的全毒力菌株进行并排比较的研究,以评估在水中应激条件下宿主限制生态位外的持久性(由引起小鼠兔热病的能力定义)。这些结果有助于理解人类和其他哺乳动物中土拉菌病暴发之间土拉菌病的长期持久性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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