Search bioRxiv⌕ Search

Biology subjects

Cavanagh, D.

Publications and source records attributed to Cavanagh, D..

2 recordsLinked to original sources

Insights into the Contribution of Type VI Secretion Towards AHPND Pathogenesis

The Type VI Secretion System (T6SS) is a contractile injection apparatus which delivers effector toxins in a contact-dependent manner, and has drawn considerable attention as a determinant of pathogenicity and environmental fitness in diverse bacterial taxa. Past reports have noted that many strains of Vibrio parahaemolyticus which cause Acute Hepatopancreatic Necrosis Disease (AHPND) in shrimp harbor two functional T6SSs (T6SS1 and T6SS2), leading to speculation that these systems may contribute to virulence. Here, we evaluate the involvement of Type VI Secretion (T6S) as a pathogenicity factor during shrimp infection by two geographically distinct isolates of AHPND-causing V. parahaemolyticus (VpAHPND). Combining in vitro contact-killing assays with comparative genomic analysis, we demonstrate that these strains -- 13-306/D4 (Mexico) and 12-297/B (Vietnam) -- leverage overlapping yet distinct effector arsenals to antagonize bacterial and fungal prey under warm, high-salinity conditions. Moreover, our in silico analyses reveal a predicted T6SS effector/immunity (E/I) module encoded in proximity to the pirAB-Tn903 composite transposon on pVA1-type plasmids. We demonstrate that acquisition of a plasmid expressing this module allows the non-AHPND isolate V. parahaemolyticus BB22OP to antagonize its parental strain in a T6SS1-dependent fashion. In turn, prey equipped with a plasmid expressing only the immunity gene gain protection against BB22OP attackers armed with the full E/I module. Employing an immersion bioassay, we show that both D4 and 297B require T6S functionality for full virulence against whiteleg shrimp (Litopenaeus vannamei) postlarvae under warm, marine-like conditions, and provide preliminary evidence that T6SS-dependent interactions with host-associated bacteria may contribute to virulence. Our findings offer empirical evidence supporting the involvement of T6S in AHPND pathogenesis under conditions relevant to commercial aquaculture, inviting further studies to decipher the role/s of T6S as a virulence determinant.

microbiology↗

Plasmodium falciparum and helminth coinfections increase IgE and parasite-specific IgG responses

Coinfection with Plasmodium falciparum and helminths may impact the immune response to these parasites since they induce different immune profiles. We studied the effects of coinfections on the antibody profile in a cohort of 715 Mozambican children and adults using the Luminex technology with a panel of 16 antigens from P. falciparum and 11 antigens from helminths (Ascaris lumbricoides, hookworm, Trichuris trichiura, Strongyloides stercoralis and Schistosoma spp.) and measured antigen-specific IgG and total IgE responses. We compared the antibody profile between groups defined by P. falciparum and helminth previous exposure (based on serology) and/or current infection (determined by microscopy and/or qPCR). In multivariable regression models adjusted by demographic, socioeconomic, water and sanitation variables, individuals exposed/infected with P. falciparum and helminths had significantly higher total IgE and antigen-specific IgG levels, magnitude (sum of all levels) and breadth of response to both types of parasites compared to individuals exposed/infected with only one type of parasite (p[≤] 0.05). There was a positive association between exposure/infection to P. falciparum and exposure/infection to helminths or the number of helminth species, and vice versa (p[≤] 0.001). In addition, children coexposed/coinfected tended (p= 0.062) to have higher P. falciparum parasitemia than those single exposed/infected. Our results suggest that an increase in the antibody responses in coexposed/coinfected individuals may reflect higher exposure and be due to a more permissive immune environment to infection in the host. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=117 SRC="FIGDIR/small/445753v1_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@a1dc3corg.highwire.dtl.DTLVardef@82128corg.highwire.dtl.DTLVardef@18fcd98org.highwire.dtl.DTLVardef@2d5bb_HPS_FORMAT_FIGEXP M_FIG C_FIG

immunology↗