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The tick endosymbiont Candidatus Midichloria mitochondrii and selenoproteins are essential for the growth of Rickettsia parkeri in the Gulf Coast tick vector
被引:82
作者:
Budachetri, Khemraj
[1
]
Kumar, Deepak
[1
]
Crispell, Gary
[1
]
Beck, Christine
[2
]
Dasch, Gregory
[3
]
Karim, Shahid
[1
]
机构:
[1] Univ Southern Mississippi, Dept Biol Sci, Hattiesburg, MS 39406 USA
[2] Delta State Univ, Cleveland, MS 38733 USA
[3] Ctr Dis Control, Rickettsial Zoonoses Branch, Atlanta, GA 30329 USA
来源:
基金:
美国食品与农业研究所;
美国农业部;
关键词:
Rickettsia parkeri;
Endosymbionts;
Ticks;
Selenogenes;
Pathogen;
Colonization;
FRANCISELLA-LIKE ENDOSYMBIONTS;
MACULATUM ACARI IXODIDAE;
INFECTING WOOD TICKS;
AMBLYOMMA-MACULATUM;
DERMACENTOR-ANDERSONI;
ANAPLASMA-PHAGOCYTOPHILUM;
TRANSOVARIAL TRANSMISSION;
SUPEROXIDE-DISMUTASE;
NATIVE MICROBIOTA;
IXODES-RICINUS;
D O I:
10.1186/s40168-018-0524-2
中图分类号:
Q93 [微生物学];
学科分类号:
071005 [微生物学];
摘要:
Background: Pathogen colonization inside tick tissues is a significant aspect of the overall competence of a vector. Amblyomma maculatum is a competent vector of the spotted fever group rickettsiae, Rickettsia parkeri. When R. parkeri colonizes its tick host, it has the opportunity to dynamically interact with not just its host but with the endosymbionts living within it, and this enables it to modulate the tick's defenses by regulating tick gene expression. The microbiome in A. maculatum is dominated by two endosymbiont microbes: a Francisella-like endosymbiont (FLE) and Candidatus Midichloria mitochondrii (CMM). A range of selenium-containing proteins (selenoproteins) in A. maculatum ticks protects them from oxidative stress during blood feeding and pathogen infections. Here, we investigated rickettsial multiplication in the presence of tick endosymbionts and characterized the functional significance of selenoproteins during R. parkeri replication in the tick. Results: FLE and CMM were quantified throughout the tick life stages by quantitative PCR in R. parkeri-infected and uninfected ticks. R. parkeri infection was found to decrease the FLE numbers but CMM thrived across the tick life cycle. Our qRT-PCR analysis indicated that the transcripts of genes with functions related to redox (selenogenes) were upregulated in ticks infected with R. parkeri. Three differentially expressed proteins, selenoprotein M, selenoprotein O, and selenoprotein S were silenced to examine their functional significance during rickettsial replication within the tick tissues. Gene silencing of the target genes was found to impair R. parkeri colonization in the tick vector. Knockdown of the selenogenes triggered a compensatory response from other selenogenes, as observed by changes in gene expression, but oxidative stress levels and endoplasmic reticulum stress inside the ticks were also found to have heightened. Conclusions: This study illustrates the potential of this new research model for augmenting our understanding of the pathogen interactions occurring within tick hosts and the important roles that symbionts and various tick factors play in regulating pathogen growth.
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