Maternal investment for offspring’s growth and survival is widespread among diverse organisms [1-3]. Vertical symbiont transmission via maternal passage is also pivotal for offspring’s growth and survival in many organisms [4-6]. Hence, it is expected that vertical symbiont transmission may co-evolve with various organismal traits concerning maternal investment in offspring. Here we report a novel phenotypic syndrome entailing morphological, histological, behavioral and ecological specializations for maternal investment and vertical symbiont transmission in stinkbugs of the family Urostylididae [7-9]. Adult females develop huge ovaries exaggerated for polysaccharide excretion, possess novel ovipositor-associated organs for vertical transmission of a bacterial symbiont (‘Candidatus Tachikawaea gelatinosa’), and lay eggs covered with voluminous symbiont-supplemented jelly. Newborns hatch in mid winter, feed solely on the jelly, acquire the symbiont, and grow during winter. In spring, the insects start feeding on plant sap, wherein the symbiont localizes to a specialized midgut region and supplies essential amino acids deficient in the host’s diet. The reduced symbiont genome and host-symbiont co-speciation indicate their obligate association over evolutionary time. Experimental deprivation of the jelly results in nymphal mortality whereas restoration of the jelly leads to recovered nymphal growth, confirming that the jelly supports nymphal growth in winter. Chemical analyses demonstrate that the galactan-based jelly contains a sufficient quantity of amino acids to sustain nymphal growth to the third instar. The versatile biological roles of the symbiont-containing egg-covering jelly highlight intricate evolutionary interactions between maternal resource investment and vertical symbiont transmission, which are commonly important for offspring’s growth, survival, and ecological adaptation.