Umanzor Edwin F, Kelly Suzanne E, Ravenscraft Alison, Matsuura Yu, Hunter Martha S
Entomology and Insect Science Graduate Interdisciplinary Program, The University of Arizona, Tucson, AZ, United States.
Department of Entomology, The University of Arizona, Tucson, AZ, United States.
Front Microbiol. 2025 Jul 10;16:1595917. doi: 10.3389/fmicb.2025.1595917. eCollection 2025.
The maternally-inherited, intracellular bacterium (Alphaproteobacteria: Midichloreaceae) has been widely detected in arthropods including true bugs, beetles, a wasp, a moth, and pathogen-vectoring fleas and ticks. Despite its prevalence, its role in the biology of its hosts has been unknown. We set out to determine the role of this symbiont in the leaffooted bug, (Hempitera: Coreidae). To examine the effects of on bug performance and reproduction as well as in possible interactions with the bug's obligate nutritional symbiont, , bugs were reared in a factorial experiment with both and positive and negative treatments. Lifetime survival analysis (~120 days) showed significant developmental delays and decrease in survival for bugs that lacked and -free bugs did not reproduce. However, among the carrying treatments, there were no significant differences in lifetime survival or reproduction in treatments with and without , suggesting this symbiont is neutral for overall bug fitness. To test for reproductive manipulation, crossing among positive and negative individuals was performed. When negative females were mated with positive males, fewer eggs survived early embryogenesis, consistent with a cytoplasmic incompatibility (CI) phenotype. Wild from California and Arizona showed high but not fixed infection rates. Within individuals, titer was low during early development (1st-3rd instar), followed by an increase that coincided with development of reproductive tissues. Our results reveal to be among a growing number of microbial symbionts that cause CI, a phenotype that increases the relative fitness of females harboring the symbiont. Understanding the mechanism of how manipulates reproduction can provide insights into the evolution of reproductive manipulators and may eventually provide tools for management of hosts of , including pathogen-vectoring ticks and fleas.
这种母系遗传的细胞内细菌(α-变形菌纲:米氏菌科)已在包括臭虫、甲虫、黄蜂、飞蛾以及病原体传播媒介跳蚤和蜱虫在内的节肢动物中被广泛检测到。尽管其分布广泛,但其在宿主生物学中的作用一直未知。我们着手确定这种共生菌在角肩蝽(半翅目:缘蝽科)中的作用。为了研究该共生菌对角肩蝽生长性能和繁殖的影响以及与角肩蝽专性营养共生菌的可能相互作用,我们通过一个析因实验饲养角肩蝽,设置该共生菌和专性营养共生菌的阳性和阴性处理。寿命生存分析(约120天)表明,缺乏该共生菌的角肩蝽发育显著延迟且存活率降低,无菌的角肩蝽不繁殖。然而,在携带该共生菌的处理组中,有无专性营养共生菌的处理组在寿命生存或繁殖方面没有显著差异,这表明这种共生菌对整体角肩蝽的适合度是中性的。为了测试生殖操纵情况,进行了阳性和阴性个体之间的杂交。当阴性雌虫与携带该共生菌的阳性雄虫交配时,早期胚胎发育中存活的卵较少,这与细胞质不亲和(CI)表型一致。来自加利福尼亚州和亚利桑那州的野生角肩蝽显示出较高但不固定的该共生菌感染率。在个体内部,该共生菌滴度在早期发育(1龄至3龄若虫)时较低,随后随着生殖组织的发育而增加。我们的结果表明,该共生菌属于越来越多导致CI的微生物共生菌之一,这种表型会增加携带该共生菌雌虫的相对适合度。了解该共生菌操纵繁殖的机制可以为生殖操纵者的进化提供见解,并最终可能为管理该共生菌的宿主(包括病原体传播媒介蜱虫和跳蚤)提供工具。