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Invertebrate Microbiology

Purine Biosynthesis, Biofilm Formation, and Persistence of an Insect-Microbe Gut Symbiosis

Jiyeun Kate Kim, Jeong Yun Kwon, Soo Kyoung Kim, Sang Heum Han, Yeo Jin Won, Joon Hee Lee, Chan-Hee Kim, Takema Fukatsu, Bok Luel Lee
C. R. Lovell, Editor
Jiyeun Kate Kim
aGlobal Research Laboratory, Pusan National University, Pusan, South Korea
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Jeong Yun Kwon
aGlobal Research Laboratory, Pusan National University, Pusan, South Korea
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Soo Kyoung Kim
bCollege of Pharmacy, Pusan National University, Pusan, South Korea
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Sang Heum Han
aGlobal Research Laboratory, Pusan National University, Pusan, South Korea
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Yeo Jin Won
aGlobal Research Laboratory, Pusan National University, Pusan, South Korea
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Joon Hee Lee
bCollege of Pharmacy, Pusan National University, Pusan, South Korea
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Chan-Hee Kim
aGlobal Research Laboratory, Pusan National University, Pusan, South Korea
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Takema Fukatsu
cBioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan
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Bok Luel Lee
aGlobal Research Laboratory, Pusan National University, Pusan, South Korea
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C. R. Lovell
Roles: Editor
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DOI: 10.1128/AEM.00739-14
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ABSTRACT

The Riptortus-Burkholderia symbiotic system is an experimental model system for studying the molecular mechanisms of an insect-microbe gut symbiosis. When the symbiotic midgut of Riptortus pedestris was investigated by light and transmission electron microscopy, the lumens of the midgut crypts that harbor colonizing Burkholderia symbionts were occupied by an extracellular matrix consisting of polysaccharides. This observation prompted us to search for symbiont genes involved in the induction of biofilm formation and to examine whether the biofilms are necessary for the symbiont to establish a successful symbiotic association with the host. To answer these questions, we focused on purN and purT, which independently catalyze the same step of bacterial purine biosynthesis. When we disrupted purN and purT in the Burkholderia symbiont, the ΔpurN and ΔpurT mutants grew normally, and only the ΔpurT mutant failed to form biofilms. Notably, the ΔpurT mutant exhibited a significantly lower level of cyclic-di-GMP (c-di-GMP) than the wild type and the ΔpurN mutant, suggesting involvement of the secondary messenger c-di-GMP in the defect of biofilm formation in the ΔpurT mutant, which might operate via impaired purine biosynthesis. The host insects infected with the ΔpurT mutant exhibited a lower infection density, slower growth, and lighter body weight than the host insects infected with the wild type and the ΔpurN mutant. These results show that the function of purT of the gut symbiont is important for the persistence of the insect gut symbiont, suggesting the intricate biological relevance of purine biosynthesis, biofilm formation, and symbiosis.

FOOTNOTES

    • Received 5 March 2014.
    • Accepted 2 May 2014.
    • Accepted manuscript posted online 9 May 2014.
  • Supplemental material for this article may be found at http://dx.doi.org/10.1128/AEM.00739-14.

  • Copyright © 2014, American Society for Microbiology. All Rights Reserved.
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Purine Biosynthesis, Biofilm Formation, and Persistence of an Insect-Microbe Gut Symbiosis
Jiyeun Kate Kim, Jeong Yun Kwon, Soo Kyoung Kim, Sang Heum Han, Yeo Jin Won, Joon Hee Lee, Chan-Hee Kim, Takema Fukatsu, Bok Luel Lee
Applied and Environmental Microbiology Jun 2014, 80 (14) 4374-4382; DOI: 10.1128/AEM.00739-14

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Purine Biosynthesis, Biofilm Formation, and Persistence of an Insect-Microbe Gut Symbiosis
Jiyeun Kate Kim, Jeong Yun Kwon, Soo Kyoung Kim, Sang Heum Han, Yeo Jin Won, Joon Hee Lee, Chan-Hee Kim, Takema Fukatsu, Bok Luel Lee
Applied and Environmental Microbiology Jun 2014, 80 (14) 4374-4382; DOI: 10.1128/AEM.00739-14
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