Scholarlink

<p>Mosquito reproduction and immunity hold tradeoffs that directly impact vector competence, yet the physiological mechanisms linking mating, immunity, and arbovirus infection remain poorly understood under natural conditions. We previously showed in laboratory strains of <i>Aedes aegypti</i> that mating induces gut growth, suppresses immune responses, and promotes microbiota expansion. Here, we extend these findings to field-collected mosquitoes. Mated females displayed significantly enlarged midguts compared to virgins. In gravid individuals, mating was associated with reduced expression of antimicrobial peptide genes (<i>gambicin</i> and <i>attacin</i>) and increased bacterial abundance. Laboratory-reared adults from field-collected immature stages exhibited the same mating-dependent patterns, confirming the robustness of this physiological trade-off across ecological contexts. Our results demonstrate that mating-dependent gut remodeling and immune modulation persist in natural populations, with a trend toward higher Zika virus infection probability in mated females, suggesting reproductive physiology as an underappreciated determinant of vector competence.</p><p></p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Mating-dependent gut enlargement and immune suppression in field-caught Aedes aegypti

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年7月14日

查看全文
  • Alessandra Girard,
  • Adriana Echeverría,
  • Miguel Santos,
  • Norma Padilla,
  • Mabel L. Taracena-Agarwal

摘要

Mosquito reproduction and immunity hold tradeoffs that directly impact vector competence, yet the physiological mechanisms linking mating, immunity, and arbovirus infection remain poorly understood under natural conditions. We previously showed in laboratory strains of Aedes aegypti that mating induces gut growth, suppresses immune responses, and promotes microbiota expansion. Here, we extend these findings to field-collected mosquitoes. Mated females displayed significantly enlarged midguts compared to virgins. In gravid individuals, mating was associated with reduced expression of antimicrobial peptide genes (gambicin and attacin) and increased bacterial abundance. Laboratory-reared adults from field-collected immature stages exhibited the same mating-dependent patterns, confirming the robustness of this physiological trade-off across ecological contexts. Our results demonstrate that mating-dependent gut remodeling and immune modulation persist in natural populations, with a trend toward higher Zika virus infection probability in mated females, suggesting reproductive physiology as an underappreciated determinant of vector competence.