The extensional rheology of dilute suspensions of spheres in viscoelastic/polymeric liquids is studied computationally. At low polymer concentration 
$c$ and Deborah number 
$\textit{De}$ (imposed extension rate times polymer relaxation time), a wake of highly stretched polymers forms downstream of the particles due to larger local velocity gradients than the imposed flow, indicated by 
$\Delta \textit{De}_{\textit{local}}\gt 0$. This increases the suspension’s extensional viscosity with time and 
$\textit{De}$ for 
$De \lt 0.5$. When 
$\textit{De}$ exceeds 0.5, the coil-stretch transition value, the fully stretched polymers from the far-field collapse in regions with 
$\Delta \textit{De}_{\textit{local}} \lt 0$ (lower velocity gradient) around the particle’s stagnation points, reducing suspension viscosity relative to the particle-free liquid. The interaction between local flow and polymers intensifies with increasing 
$c$. Highly stretched polymers impede local flow, reducing 
$\Delta \textit{De}_{\textit{local}}$, while 
$\Delta \textit{De}_{\textit{local}}$ increases in regions with collapsed polymers. Initially, increasing 
$c$ aligns 
$\Delta \textit{De}_{\textit{local}}$ and local polymer stretch with far-field values, diminishing particle–polymer interaction effects. However, beyond a certain 
$c$, a new mechanism emerges. At low 
$c$, fluid three particle radii upstream exhibits 
$\Delta \textit{De}_{\textit{local}} \gt 0$, stretching polymers beyond their undisturbed state. As 
$c$ increases, however, 
$\Delta \textit{De}_{\textit{local}}$ in this region becomes negative, collapsing polymers and resulting in increasingly negative stress from particle–polymer interactions at large 
$\textit{De}$ and time. At high 
$c$, this negative interaction stress scales as 
$c^2$, surpassing the linear increase of particle-free polymer stress, making dilute sphere concentrations more effective at reducing the viscosity of viscoelastic liquids at larger 
$\textit{De}$ and 
$c$.