Hinnebusch B Joseph, Bland David M, Bosio Christopher F, Jarrett Clayton O
Laboratory of Zoonotic Pathogens, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, United States of America.
PLoS Negl Trop Dis. 2017 Jan 12;11(1):e0005276. doi: 10.1371/journal.pntd.0005276. eCollection 2017 Jan.
Transmission of Yersinia pestis by flea bite can occur by two mechanisms. After taking a blood meal from a bacteremic mammal, fleas have the potential to transmit the very next time they feed. This early-phase transmission resembles mechanical transmission in some respects, but the mechanism is unknown. Thereafter, transmission occurs after Yersinia pestis forms a biofilm in the proventricular valve in the flea foregut. The biofilm can impede and sometimes completely block the ingestion of blood, resulting in regurgitative transmission of bacteria into the bite site. In this study, we compared the relative efficiency of the two modes of transmission for Xenopsylla cheopis, a flea known to become completely blocked at a high rate, and Oropsylla montana, a flea that has been considered to rarely develop proventricular blockage.
METHODOLOGY/PRINCIPAL FINDINGS: Fleas that took an infectious blood meal containing Y. pestis were maintained and monitored for four weeks for infection and proventricular blockage. The number of Y. pestis transmitted by groups of fleas by the two modes of transmission was also determined. O. montana readily developed complete proventricular blockage, and large numbers of Y. pestis were transmitted by that mechanism both by it and by X. cheopis, a flea known to block at a high rate. In contrast, few bacteria were transmitted in the early phase by either species.
A model system incorporating standardized experimental conditions and viability controls was developed to more reliably compare the infection, proventricular blockage and transmission dynamics of different flea vectors, and was used to resolve a long-standing uncertainty concerning the vector competence of O. montana. Both X. cheopis and O. montana are fully capable of transmitting Y. pestis by the proventricular biofilm-dependent mechanism.
鼠疫耶尔森菌通过跳蚤叮咬传播有两种机制。跳蚤从菌血症哺乳动物吸食血液后,下次进食时就有可能传播病菌。这种早期传播在某些方面类似于机械传播,但其机制尚不清楚。此后,鼠疫耶尔森菌在跳蚤前肠的前胃瓣膜中形成生物膜后才会发生传播。生物膜会阻碍甚至有时完全阻断血液摄入,导致细菌反流至叮咬部位而传播。在本研究中,我们比较了两种传播模式的相对效率,这两种模式分别针对印鼠客蚤(一种已知极易完全堵塞的跳蚤)和山蚤(一种被认为很少发生前胃堵塞的跳蚤)。
方法/主要发现:让吸食含有鼠疫耶尔森菌感染性血液的跳蚤维持四周,并监测其感染情况和前胃堵塞情况。还确定了两组跳蚤通过两种传播模式传播的鼠疫耶尔森菌数量。山蚤很容易出现完全性前胃堵塞,通过这种机制,它和印鼠客蚤(一种已知堵塞率很高的跳蚤)都能传播大量鼠疫耶尔森菌。相比之下,两种跳蚤在早期传播的细菌都很少。
开发了一个包含标准化实验条件和生存能力对照的模型系统,以更可靠地比较不同跳蚤媒介的感染、前胃堵塞和传播动态,并用于解决关于山蚤媒介能力的长期不确定性问题。印鼠客蚤和山蚤都完全能够通过前胃生物膜依赖机制传播鼠疫耶尔森菌。