Facultatively intrabacterial localization of a planthopper endosymbiont as an adaptation to its vertical transmission

被引:2
作者
Michalik, Anna [1 ]
Franco, Diego C. [1 ,2 ]
Szklarzewicz, Teresa [1 ]
Stroinski, Adam [3 ]
Lukasik, Piotr [2 ]
机构
[1] Jagiellonian Univ, Inst Zool & Biomed Res, Fac Biol, Dept Dev Biol & Morphol Invertebrates, Krakow, Poland
[2] Jagiellonian Univ, Inst Environm Sci, Fac Biol, Krakow, Poland
[3] Polish Acad Sci, Museum & Inst Zool, Warsaw, Poland
关键词
transovarial transmission; nested symbiosis; facultative endosymbiont; genome reduction; Auchenorrhyncha; Alphaproteobacteria; Sodalis; BOVINE RESPIRATORY-DISEASE; HEALTHY FEEDLOT CATTLE; MANNHEIMIA-HAEMOLYTICA; BACTERIAL MICROBIOTA; BEEF-CALVES; NASOPHARYNGEAL; DIVERSITY; TRACT; NOV; COWS;
D O I
10.1128/msystems.00634-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Transovarial transmission is the most reliable way of passing on essential nutrient-providing endosymbionts from mothers to offspring. However, not all endosymbiotic microbes follow the complex path through the female host tissues to oocytes on their own. Here, we demonstrate an unusual transmission strategy adopted by one of the endosymbionts of the planthopper Trypetimorpha occidentalis (Hemiptera: Tropiduchidae) from Bulgaria. In this species, an Acetobacteraceae endosymbiont is transmitted transovarially within deep invaginations of cellular membranes of an ancient endosymbiont Sulcia-strikingly resembling recently described plant virus transmission. However, in males, Acetobacteraceae colonizes the same bacteriocytes as Sulcia but remains unenveloped. Then, the unusual endobacterial localization of Acetobacteraceae observed in females appears to be a unique adaptation to maternal transmission. Further, the symbiont's genomic features, including encoding essential amino acid biosynthetic pathways and its similarity to a recently described psyllid symbiont, suggest a unique combination of the ability to horizontally transmit among species and confer nutritional benefits. The close association with Acetobacteraceae symbiont correlates with the so-far-unreported level of genomic erosion of ancient nutritional symbionts of this planthopper. In Sulcia, this is reflected in substantial changes in genomic organization, reported for the first time in the symbiont renowned for its genomic stability. In Vidania, substantial gene loss resulted in one of the smallest genomes known, at 108.6 kb. Thus, the symbionts of T. occidentalis display a combination of unusual adaptations and genomic features that expand our understanding of how insect-microbe symbioses may transmit and evolve. IMPORTANCE Reliable transmission across host generations is a major challenge for bacteria that associate with insects, and independently established symbionts have addressed this challenge in different ways. The facultatively endobacterial localization of Acetobacteraceae symbiont, enveloped by cells of ancient nutritional endosymbiont Sulcia in females but not males of the planthopper Trypetimorpha occidentalis, appears to be a unique adaptation to maternal transmission. Acetobacteraceae's genomic features indicate its unusual evolutionary history, and the genomic erosion experienced by ancient nutritional symbionts demonstrates the apparent consequences of such close association. Combined, this multi-partite symbiosis expands our understanding of the diversity of strategies that insect symbioses form and some of their evolutionary consequences.
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页数:18
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共 81 条
[1]   SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing [J].
Bankevich, Anton ;
Nurk, Sergey ;
Antipov, Dmitry ;
Gurevich, Alexey A. ;
Dvorkin, Mikhail ;
Kulikov, Alexander S. ;
Lesin, Valery M. ;
Nikolenko, Sergey I. ;
Son Pham ;
Prjibelski, Andrey D. ;
Pyshkin, Alexey V. ;
Sirotkin, Alexander V. ;
Vyahhi, Nikolay ;
Tesler, Glenn ;
Alekseyev, Max A. ;
Pevzner, Pavel A. .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2012, 19 (05) :455-477
[2]   Biology of bacteriocyte-associated endosymbionts of plant sap-sucking insects [J].
Baumann, P .
ANNUAL REVIEW OF MICROBIOLOGY, 2005, 59 :155-189
[3]   Comparative genomics of a quadripartite symbiosis in a planthopper host reveals the origins and rearranged nutritional responsibilities of anciently diverged bacterial lineages [J].
Bennett, Gordon M. ;
Mao, Meng .
ENVIRONMENTAL MICROBIOLOGY, 2018, 20 (12) :4461-4472
[4]   Heritable symbiosis: The advantages and perils of an evolutionary rabbit hole [J].
Bennett, Gordon M. ;
Moran, Nancy A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (33) :10169-10176
[5]   Small, Smaller, Smallest: The Origins and Evolution of Ancient Dual Symbioses in a Phloem-Feeding Insect [J].
Bennett, Gordon M. ;
Moran, Nancy A. .
GENOME BIOLOGY AND EVOLUTION, 2013, 5 (09) :1675-1688
[6]   A complex journey: transmission of microbial symbionts [J].
Bright, Monika ;
Bulgheresi, Silvia .
NATURE REVIEWS MICROBIOLOGY, 2010, 8 (03) :218-230
[7]   Genomic erosion and extensive horizontal gene transfer in gut-associated Acetobacteraceae [J].
Brown, Bryan P. ;
Wernegreen, Jennifer J. .
BMC GENOMICS, 2019, 20 (1)
[8]   Peptidoglycan Production by an Insect-Bacterial Mosaic [J].
Bublitz, DeAnna C. ;
Chadwick, Grayson L. ;
Magyar, John S. ;
Sandoz, Kelsi M. ;
Brooks, Diane M. ;
Mesnage, Stephane ;
Ladinsky, Mark S. ;
Garber, Arkadiy, I ;
Bjorkman, Pamela J. ;
Orphan, Victoria J. ;
McCutcheon, John P. .
CELL, 2019, 179 (03) :703-+
[9]  
Buchner P, 1965, ENDOSYMBIOSIS ANIMAL
[10]  
Campbell MA, 2018, MBIO, V9, DOI [10.1128/mBio.02104-18, 10.1128/mbio.02104-18]