» Articles » PMID: 11404467

A Novel Application of Gene Arrays: Escherichia Coli Array Provides Insight into the Biology of the Obligate Endosymbiont of Tsetse Flies

Overview
Specialty Science
Date 2001 Jun 19
PMID 11404467
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Symbiotic associations with microorganisms are pivotal in many insects. Yet, the functional roles of obligate symbionts have been difficult to study because it has not been possible to cultivate these organisms in vitro. The medically important tsetse fly (Diptera: Glossinidae) relies on its obligate endosymbiont, Wigglesworthia glossinidia, a member of the Enterobacteriaceae, closely related to Escherichia coli, for fertility and possibly nutrition. We show here that the intracellular Wigglesworthia has a reduced genome size smaller than 770 kb. In an attempt to understand the composition of its genome, we used the gene arrays developed for E. coli. We were able to identify 650 orthologous genes in Wigglesworthia corresponding to approximately 85% of its genome. The arrays were also applied for expression analysis using Wigglesworthia cDNA and 61 gene products were detected, presumably coding for some of its most abundant products. Overall, genes involved in cell processes, DNA replication, transcription, and translation were found largely retained in the small genome of Wigglesworthia. In addition, genes coding for transport proteins, chaperones, biosynthesis of cofactors, and some amino acids were found to comprise a significant portion, suggesting an important role for these proteins in its symbiotic life. Based on its expression profile, we predict that Wigglesworthia may be a facultative anaerobic organism that utilizes ammonia as its major source of nitrogen. We present an application of E. coli gene arrays to obtain broad genome information for a closely related organism in the absence of complete genome sequence data.

Citing Articles

The Rickettsia Endosymbiont of Ixodes pacificus Contains All the Genes of De Novo Folate Biosynthesis.

Hunter D, Torkelson J, Bodnar J, Mortazavi B, Laurent T, Deason J PLoS One. 2015; 10(12):e0144552.

PMID: 26650541 PMC: 4674097. DOI: 10.1371/journal.pone.0144552.


Insight into the transmission biology and species-specific functional capabilities of tsetse (Diptera: glossinidae) obligate symbiont Wigglesworthia.

Rio R, Symula R, Wang J, Lohs C, Wu Y, Snyder A mBio. 2012; 3(1).

PMID: 22334516 PMC: 3280448. DOI: 10.1128/mBio.00240-11.


Microbiome influences on insect host vector competence.

Weiss B, Aksoy S Trends Parasitol. 2011; 27(11):514-22.

PMID: 21697014 PMC: 3179784. DOI: 10.1016/j.pt.2011.05.001.


Microarrays for bacterial pathogens - hope or hype?.

Wren B Comp Funct Genomics. 2008; 3(4):330-2.

PMID: 18629265 PMC: 2448428. DOI: 10.1002/cfg.180.


Comparative genomics of Streptomyces avermitilis, Streptomyces cattleya, Streptomyces maritimus and Kitasatospora aureofaciens using a Streptomyces coelicolor microarray system.

Hsiao N, Kirby R Antonie Van Leeuwenhoek. 2007; 93(1-2):1-25.

PMID: 17588127 PMC: 2140096. DOI: 10.1007/s10482-007-9175-1.


References
1.
Moloo S . Aspects of the nutrition of adult female Glossina morsitans during pregnancy. J Insect Physiol. 1976; 22(4):563-7. DOI: 10.1016/0022-1910(76)90177-3. View

2.
Moloo S . Nutrition of Glossina morsitans: metabolism of U-14C threonine during pregnancy. Acta Trop. 1976; 33(2):133-42. View

3.
Bandi C, Damiani G, Magrassi L, Grigolo A, Fani R, Sacchi L . Flavobacteria as intracellular symbionts in cockroaches. Proc Biol Sci. 1994; 257(1348):43-8. DOI: 10.1098/rspb.1994.0092. View

4.
Pinnock D, Hess R . The occurrence of intracellular rickettsia-like organisms in the tsetse flies, Glossina morsitans, G. fuscipes, G. brevipalpis and G. pallidipes. Acta Trop. 1974; 31(1):70-9. View

5.
Moloo S . An artificial feeding technique for Glossina. Parasitology. 1971; 63(3):507-12. DOI: 10.1017/s0031182000080021. View