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Wolbachia endosymbiont of Brugia malayi elicits a T helper type 17‐mediated pro‐inflammatory immune response through Wolbachia surface protein
Author(s) -
Pathak Manisha,
Verma Meenakshi,
Srivastava Mrigank,
MisraBhattacharya Shailja
Publication year - 2015
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/imm.12364
Subject(s) - brugia malayi , wolbachia , biology , immune system , lymphatic filariasis , immunology , interleukin 10 , microbiology and biotechnology , helminths , host (biology) , filariasis , ecology
Summary Wolbachia is an endosymbiotic bacterium of the filarial nematode Brugia malayi . The symbiotic relationship between Wolbachia and its filarial host is dependent on interactions between the proteins of both organisms. However, little is known about Wolbachia proteins that are involved in the inflammatory pathology of the host during lymphatic filariasis. In the present study, we cloned, expressed and purified Wolbachia surface protein (r‐wsp) from Wolbachia and administered it to mice, either alone or in combination with infective larvae of B. malayi (Bm‐L3) and monitored the developing immune response in infected animals. Our results show that spleens and mesenteric lymph nodes of mice immunized with either r‐wsp or infected with Bm‐L3 show increased percentages of CD4 + T helper type 17 (Th17) cells and Th1 cytokines like interferon‐ γ and interleukin‐2 (IL‐2) along with decreased percentages of regulatory T cells, Th2 cytokines like IL‐4 and IL‐10 and transforming growth factor β (TGF‐ β ) levels in culture supernatants of splenocytes. These observations were stronger in mice immunized with r‐wsp alone. Interestingly, when mice were first immunized with r‐wsp and subsequently infected with Bm‐L3, percentages of CD4 + Th17 cells and Th1 cytokines increased even further while that of regulatory T cells, Th2 cytokines and TGF‐ β levels decreased. These results for the first time show that r‐wsp acts synergistically with Bm‐L3 in promoting a pro‐inflammatory response by increasing Th17 cells and at the same time diminishes host immunological tolerance by decreasing regulatory T cells and TGF‐ β secretion.