This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sakurai, M.
Right arrow Articles by Fukatsu, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sakurai, M.
Right arrow Articles by Fukatsu, T.
Agricola
Right arrow Articles by Sakurai, M.
Right arrow Articles by Fukatsu, T.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, July 2005, p. 4069-4075, Vol. 71, No. 7
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.7.4069-4075.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Rickettsia Symbiont in the Pea Aphid Acyrthosiphon pisum: Novel Cellular Tropism, Effect on Host Fitness, and Interaction with the Essential Symbiont Buchnera

Makiko Sakurai, Ryuichi Koga, Tsutomu Tsuchida, Xian-Ying Meng, and Takema Fukatsu*

Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8566, Japan

Received 6 January 2005/ Accepted 2 February 2005

In natural populations of the pea aphid Acyrthosiphon pisum, a facultative bacterial symbiont of the genus Rickettsia has been detected at considerable infection frequencies worldwide. We investigated the effects of the Rickettsia symbiont on the host aphid and also on the coexisting essential symbiont Buchnera. In situ hybridization revealed that the Rickettsia symbiont was specifically localized in two types of host cells specialized for endosymbiosis: secondary mycetocytes and sheath cells. Electron microscopy identified bacterial rods, about 2 µm long and 0.5 µm thick, in sheath cells of Rickettsia-infected aphids. Virus-like particles were sometimes observed in association with the bacterial cells. By an antibiotic treatment, we generated Rickettsia-infected and Rickettsia-eliminated aphid strains with an identical genetic background. Comparison of these strains revealed that Rickettsia infection negatively affected some components of the host fitness. Quantitative PCR analysis of the bacterial population dynamics identified a remarkable interaction between the coexisting symbionts: Buchnera population was significantly suppressed in the presence of Rickettsia, particularly at the young adult stage, when the aphid most actively reproduces. On the basis of these results, we discussed the possible mechanisms that enable the prevalence of Rickettsia infection in natural host populations in spite of the negative fitness effects observed in the laboratory.


* Corresponding author. Mailing address: Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8566, Japan. Phone: 81-29-861-6087. Fax: 81-29-861-6080. E-mail: t-fukatsu{at}aist.go.jp.


Applied and Environmental Microbiology, July 2005, p. 4069-4075, Vol. 71, No. 7
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.7.4069-4075.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Pais, R., Lohs, C., Wu, Y., Wang, J., Aksoy, S. (2008). The Obligate Mutualist Wigglesworthia glossinidia Influences Reproduction, Digestion, and Immunity Processes of Its Host, the Tsetse Fly. Appl. Environ. Microbiol. 74: 5965-5974 [Abstract] [Full Text]  
  • Kono, M., Koga, R., Shimada, M., Fukatsu, T. (2008). Infection Dynamics of Coexisting Beta- and Gammaproteobacteria in the Nested Endosymbiotic System of Mealybugs. Appl. Environ. Microbiol. 74: 4175-4184 [Abstract] [Full Text]  
  • Fukatsu, T., Koga, R., Smith, W. A., Tanaka, K., Nikoh, N., Sasaki-Fukatsu, K., Yoshizawa, K., Dale, C., Clayton, D. H. (2007). Bacterial Endosymbiont of the Slender Pigeon Louse, Columbicola columbae, Allied to Endosymbionts of Grain Weevils and Tsetse Flies. Appl. Environ. Microbiol. 73: 6660-6668 [Abstract] [Full Text]  
  • Kikuchi, Y., Graf, J. (2007). Spatial and Temporal Population Dynamics of a Naturally Occurring Two-Species Microbial Community inside the Digestive Tract of the Medicinal Leech. Appl. Environ. Microbiol. 73: 1984-1991 [Abstract] [Full Text]  
  • Perotti, M. A., Clarke, H. K., Turner, B. D., Braig, H. R. (2006). Rickettsia as obligate and mycetomic bacteria. FASEB J. 20: 2372-2374 [Abstract] [Full Text]  
  • Kageyama, D., Anbutsu, H., Watada, M., Hosokawa, T., Shimada, M., Fukatsu, T. (2006). Prevalence of a Non-Male-Killing Spiroplasma in Natural Populations of Drosophila hydei.. Appl. Environ. Microbiol. 72: 6667-6673 [Abstract] [Full Text]  
  • Perlman, S. J, Hunter, M. S, Zchori-Fein, E. (2006). The emerging diversity of Rickettsia. Proc R Soc B 273: 2097-2106 [Abstract] [Full Text]  
  • Goto, S., Anbutsu, H., Fukatsu, T. (2006). Asymmetrical Interactions between Wolbachia and Spiroplasma Endosymbionts Coexisting in the Same Insect Host.. Appl. Environ. Microbiol. 72: 4805-4810 [Abstract] [Full Text]  
  • Gottlieb, Y., Ghanim, M., Chiel, E., Gerling, D., Portnoy, V., Steinberg, S., Tzuri, G., Horowitz, A. R., Belausov, E., Mozes-Daube, N., Kontsedalov, S., Gershon, M., Gal, S., Katzir, N., Zchori-Fein, E. (2006). Identification and Localization of a Rickettsia sp. in Bemisia tabaci (Homoptera: Aleyrodidae).. Appl. Environ. Microbiol. 72: 3646-3652 [Abstract] [Full Text]