The fine structure of the exciton spectrum, containing optically allowed (bright) and forbidden (dark) exciton states, determines the radiation efficiency in nanostructures. We study timeresolved micro-photoluminescence in MoS2 monolayers and bilayers, both unstrained and compressively strained, in a wide temperature range (10-300 K) to distinguish between exciton states optically allowed and forbidden, both in spin and momentum, as well as to estimate their characteristic decay times and contributions to the total radiation intensity. The decay times were found to either increase or decrease with increasing temperature, indicating the lowest bright or lowest dark state, respectively. Our results unambiguously show that, in an unstrained film, the spin-allowed state is the lowest for a series of A excitons (1.9 eV) with the dark state being about 2 meV higher, and that the splitting energy can increase several times at compression. In contrast, in the indirect exciton series in bilayers (1.5 eV), the spinforbidden state is the lowest, being ~ 4 meV below the bright one. The strong effect of strain on the exciton spectrum can explain the large scatter among the published data and must be taken into account to realize the desired optical properties of 2D MoS2.