Acetic Acid Bacteria, Newly Emerging Symbionts of Insects

Author:

Crotti Elena1,Rizzi Aurora1,Chouaia Bessem1,Ricci Irene2,Favia Guido2,Alma Alberto3,Sacchi Luciano4,Bourtzis Kostas5,Mandrioli Mauro6,Cherif Ameur7,Bandi Claudio8,Daffonchio Daniele1

Affiliation:

1. Dipartimento di Scienze e Tecnologie Alimentari e Microbiologiche (DiSTAM), Università degli Studi di Milano, 20133 Milan, Italy

2. Dipartimento di Medicina Sperimentale e Sanità Pubblica (DMSSP), Università degli Studi di Camerino, 62032 Camerino, Italy

3. Dipartimento di Valorizzazione e Protezione delle Risorse Agroforestali (DIVAPRA), Università degli Studi di Torino, 10095 Grugliasco, Italy

4. Dipartimento di Biologia Animale (DBA), Università degli Studi di Pavia, 27100 Pavia, Italy

5. Department of Environmental and Natural Resources Management, University of Ioannina, 30100 Agrinio, Greece

6. Dipartimento di Biologia Animale (DBA), Università degli Studi di Modena e Reggio Emilia, 41125 Modena, Italy

7. Laboratoire des Microrganismes et Biomolecules Actives (LMBA), Université de Tunis El Manar, Tunis, Tunisia

8. Dipartimento di Patologia Animale, Igiene e Sanità Pubblica Veterinaria (DiPAV), Università degli Studi di Milano, 20133 Milan, Italy

Abstract

ABSTRACT Recent research in microbe-insect symbiosis has shown that acetic acid bacteria (AAB) establish symbiotic relationships with several insects of the orders Diptera, Hymenoptera, Hemiptera, and Homoptera, all relying on sugar-based diets, such as nectars, fruit sugars, or phloem sap. To date, the fruit flies Drosophila melanogaster and Bactrocera oleae , mosquitoes of the genera Anopheles and Aedes , the honey bee Apis mellifera , the leafhopper Scaphoideus titanus , and the mealybug Saccharicoccus sacchari have been found to be associated with the bacterial genera Acetobacter , Gluconacetobacter , Gluconobacter , Asaia , and Saccharibacter and the novel genus Commensalibacter . AAB establish symbiotic associations with the insect midgut, a niche characterized by the availability of diet-derived carbohydrates and oxygen and by an acidic pH, selective factors that support AAB growth. AAB have been shown to actively colonize different insect tissues and organs, such as the epithelia of male and female reproductive organs, the Malpighian tubules, and the salivary glands. This complex topology of the symbiosis indicates that AAB possess the keys for passing through body barriers, allowing them to migrate to different organs of the host. Recently, AAB involvement in the regulation of innate immune system homeostasis of Drosophila has been shown, indicating a functional role in host survival. All of these lines of evidence indicate that AAB can play different roles in insect biology, not being restricted to the feeding habit of the host. The close association of AAB and their insect hosts has been confirmed by the demonstration of multiple modes of transmission between individuals and to their progeny that include vertical and horizontal transmission routes, comprising a venereal one. Taken together, the data indicate that AAB represent novel secondary symbionts of insects.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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