Physical and Chemical Barriers in the Larval Midgut Confer Developmental Resistance to Virus Infection in Drosophila

• Published in: Viruses Vol. 13; no. 5; p. 894
• Main Authors: Villegas-Ospina, Simon, Merritt, David J, Johnson, Karyn N
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 12.05.2021; MDPI
• Subjects: Animals; antiviral mechanisms; Crystallin; Developmental stages; Dicistroviridae - pathogenicity; dicistrovirus; Digestive System - chemistry; Digestive System - virology; Disease resistance; Drosophila; Drosophila - virology; Eggs; Enzymes; Epithelium; Feeding behavior; Female; Food; Hydrogen-Ion Concentration; Infections; Infectivity; Insects; Larva - anatomy & histology; Larva - virology; Larvae; larval development; Male; Midgut; Mortality; peritrophic matrix; Permeability; Pest resistance; pH effects; Phenotypes; Physiology; Viral infections; Virions; Virus Diseases - prevention & control; Viruses; United States > US; Germany; larval development; peritrophic matrix; antiviral mechanisms; Drosophila; dicistrovirus; midgut; gut pH
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v13050894

Insects can become lethally infected by the oral intake of a number of insect-specific viruses. Virus infection commonly occurs in larvae, given their active feeding behaviour; however, older larvae often become resistant to oral viral infections. To investigate mechanisms that contribute to resistance throughout the larval development, we orally challenged larvae at different stages of their development with Drosophila C virus (DCV, ). Here, we showed that DCV-induced mortality is highest when infection initiates early in larval development and decreases the later in development the infection occurs. We then evaluated the peritrophic matrix as an antiviral barrier within the gut using a Crystallin-deficient fly line ( ), whose PM is weakened and becomes more permeable to DCV-sized particles as the larva ages. This phenotype correlated with increasing mortality the later in development oral challenge occurred. Lastly, we tested in vitro the infectivity of DCV after incubation at pH conditions that may occur in the midgut. DCV virions were stable in a pH range between 3.0 and 10.5, but their infectivity decreased at least 100-fold below (1.0) and above (12.0) this range. We did not observe such acidic conditions in recently hatched larvae. We hypothesise that, in larvae, the PM is essential for containing ingested virions separated from the gut epithelium, while highly acidic conditions inactivate the majority of the virions as they transit.