The major protein in the midgut of teneral Glossina morsitans morsitans is a molecular chaperone from the endosymbiotic bacterium Wigglesworthia glossinidia

• Published in: Insect biochemistry and molecular biology Vol. 32; no. 11; pp. 1429 - 1438
• Main Authors: Haines, L.R., Haddow, J.D., Aksoy, S., Gooding, R.H., Pearson, T.W.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.11.2002
• Subjects: Amino Acid Sequence; Animals; Cloning, Molecular; Digestive System - chemistry; Enterobacteriaceae - physiology; Insect Proteins - chemistry; Insect Proteins - genetics; Insect Proteins - isolation & purification; Life Cycle Stages; Mass Spectrometry; Midgut; Molecular chaperone; Molecular Chaperones - chemistry; Molecular Chaperones - genetics; Molecular Chaperones - isolation & purification; Molecular Sequence Data; Peptide Fragments - chemistry; Peptide Fragments - isolation & purification; Sequence Alignment; Sequence Homology, Amino Acid; Sodalis glossinidius; Symbionts; Symbiosis; Tsetse; Tsetse Flies - growth & development; Tsetse Flies - microbiology; Tsetse Flies - physiology; Wigglesworthia glossinidia; Symbionts; Midgut; Sodalis glossinidius; Wigglesworthia glossinidia; Tsetse; Mass spectrometry; Molecular chaperone
• DOI: 10.1016/S0965-1748(02)00063-2
• ISSN: 0965-1748

Molecules in the midgut of the tsetse fly (Diptera: Glossinidiae) are thought to play an important role in the life cycle of African trypanosomes by influencing their initial establishment in the midgut and subsequent differentiation events that ultimately affect parasite transmission. It is thus important to determine the molecular composition of the tsetse midgut to aid in understanding disease transmission by these medically important insect vectors. Here, we report that the most abundant protein in the midguts of teneral (unfed) Glossina morsitans morsitans is a 60 kDa molecular chaperone of bacterial origin. Two species of symbiotic bacteria reside in the tsetse midgut, Sodalis glossinidius and Wigglesworthia glossinidia. To determine the exact origin of the 60 kDa molecule, a protein microchemical approach involving two-dimensional (2-D) gel electrophoresis and mass spectrometry was used. Peptide mass maps were compared to virtual peptide maps predicted for S. glossinidius and W. glossinidia 60 kDa chaperone sequences. Four signature peptides were identified, revealing that the source of the chaperone was W. glossinidia. Comparative 2-D gel electrophoresis and immunoblotting further revealed that this protein was localized to the bacteriome and not the distal portion of the tsetse midgut. The possible function of this highly abundant endosymbiont chaperone in the tsetse midgut is discussed.