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Bacterial Community and Nitrogen Fixation in the Red Turpentine Beetle, Dendroctonus Valens LeConte (Coleoptera: Curculionidae: Scolytinae)

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Journal Microb Ecol
Date 2009 Jun 23
PMID 19543937
Citations 76
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Abstract

The red turpentine beetle, Dendroctonus valens LeConte (Coleoptera: Curculionidae: Scolytinae), colonizes all pines species within its native range throughout North and Central America. Recently, this species was accidentally introduced to China, where it has caused severe damage in pine forests. It belongs to a group of beetles that spend most of their lives between the tree bark and sapwood, where it feeds on phloem: a poor substrate with very low nutritional value of nitrogen and toxic properties due to its high content of secondary defensive compounds. The aim of this study was to characterize the bacterial community of the D. valens gut by culture-dependent and -independent methods. Polymerase chain reaction denaturing gradient gel electrophoresis and ribosomal gene library analyses revealed that species diversity in the D. valens gut was relatively low, containing between six and 17 bacterial species. The bacterial community associated with larvae and adults was dominated by members of the following genera: Lactococcus, Acinetobacter, Pantoea, Rahnella, Stenothrophomonas, Erwinia, Enterobacter, Serratia, Janibacter, Leifsonia, Cellulomonas, and Cellulosimicrobium. The members of the last four genera showed cellulolytic activity in vitro and could be involved in cellulose breakdown in the insect gut. Finally, nitrogen fixation was demonstrated in live larvae and adults; however, capacity of nitrogen fixing in vitro was not found among enterobacterial species isolated in nitrogen-free media; neither were nifD nor nifH genes detected. In contrast, nifD gen was detected in metagenomic DNA from insect guts. The identification of bacterial species and their potential physiological capacities will allow exploring the role of gut symbiotic bacteria in the adaptation and survival of D. valens in a harsh chemical habitat poor in nitrogen sources.

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References
1.
Dixon R, Kahn D . Genetic regulation of biological nitrogen fixation. Nat Rev Microbiol. 2004; 2(8):621-31. DOI: 10.1038/nrmicro954. View

2.
Rivas R, Trujillo M, Mateos P, Martinez-Molina E, Velazquez E . Cellulomonas xylanilytica sp. nov., a cellulolytic and xylanolytic bacterium isolated from a decayed elm tree. Int J Syst Evol Microbiol. 2004; 54(Pt 2):533-536. DOI: 10.1099/ijs.0.02866-0. View

3.
Tokuda G, Watanabe H, Lo N . Does correlation of cellulase gene expression and cellulolytic activity in the gut of termite suggest synergistic collaboration of cellulases?. Gene. 2007; 401(1-2):131-4. DOI: 10.1016/j.gene.2007.06.028. View

4.
Cruden D, Markovetz A . Microbial aspects of the cockroach hindgut. Arch Microbiol. 1984; 138(2):131-9. DOI: 10.1007/BF00413013. View

5.
Noda S, Inoue T, Hongoh Y, Kawai M, Nalepa C, Vongkaluang C . Identification and characterization of ectosymbionts of distinct lineages in Bacteroidales attached to flagellated protists in the gut of termites and a wood-feeding cockroach. Environ Microbiol. 2005; 8(1):11-20. DOI: 10.1111/j.1462-2920.2005.00860.x. View