Maternal gut microbes shape the early-life assembly of gut microbiota in passerine chicks via nests

• Published in: Microbiome Vol. 8; no. 1; pp. 129 - 13
• Main Authors: Chen, Cheng-Yu, Chen, Chih-Kuan, Chen, Yi-Ying, Fang, Andrew, Shaw, Grace Tzun-Wen, Hung, Chih-Ming, Wang, Daryi
• Format: Journal Article
• Language: English
• Published: England BioMed Central 11.09.2020; BMC
• Subjects: Aging; Animals; Animals, Newborn - microbiology; Avian microbiota; Birds; Brood parasitism; Crop; Deoxyribonucleic acid; Digestive system; DNA; Eggs; Evolution; Experiments; Farms; Feces; Female; Finches - microbiology; Gastrointestinal Microbiome - genetics; Gastrointestinal tract; Gut microbiota; Gut microbiota assembly; Host-microbiome interactions; Humidity; Intestinal microflora; Intestine; Juveniles; Lonchura striata; Male; Maternal effects; Maternal microbial transmission; Microbiota; Microorganisms; Neonates; Nesting Behavior; Nests; Neurosciences; Oral cavity; Probiotics; RNA, Ribosomal, 16S - genetics; rRNA 16S; Society; Symbionts; Taeniopygia guttata; Host-microbiome interactions; Maternal effects; Gut microbiota assembly; Avian microbiota; Maternal microbial transmission
• ISSN: 2049-2618; 2049-2618
• DOI: 10.1186/s40168-020-00896-9

Knowledge is growing on how gut microbiota are established, but the effects of maternal symbiotic microbes throughout early microbial successions in birds remain elusive. In this study, we examined the contributions and transmission modes of maternal microbes into the neonatal microbiota of a passerine, the zebra finch (Taeniopygia guttata), based on fostering experiments. Using 16S rRNA amplicon sequencing, we found that zebra finch chicks raised by their biological or foster parents (the society finch Lonchura striata domestica) had gut microbial communities converging with those of the parents that reared them. Moreover, source-tracking models revealed high contribution of zebra finches' oral cavity/crop microbiota to their chicks' early gut microbiota, which were largely replaced by the parental gut microbiota at later stages. The results suggest that oral feeding only affects the early stage of hatchling gut microbial development. Our study indicates that passerine chicks mainly acquire symbionts through indirect maternal transmission-passive environmental uptake from nests that were smeared with the intestinal and cloacal microbes of parents that raised them. Gut microbial diversity was low in hand-reared chicks, emphasizing the importance of parental care in shaping the gut microbiota. In addition, several probiotics were found in chicks fostered by society finches, which are excellent foster parents for other finches in bird farms and hosts of brood parasitism by zebra finches in aviaries; this finding implies that avian species that can transfer probiotics to chicks may become selectively preferred hosts of brood parasitism in nature. Video Abstract.