As a C
2
H
2
type zinc finger transcription factor,
CreA
is the key in Carbon Catabolism Repression (CCR) pathway, which negatively regulates the genes in carbon sources utilization. As conidiation in filamentous fungi is affected by nutritional conditions,
CreA
may contribute to fungal conidiation, which has been well studied in filamentous fungi, especially
Aspergillus
spp., but researches on entomopathogenic fungi are not enough. In this study, we found a homologous gene
MaCreA
in
Metarhizium acridum
, and the
MaCreA
deletion strain showed delayed conidiation, significant decrease in conidial yield, and 96.88% lower conidial production, when compared with the wild-type strain, and the normal conidiation and microcycle conidiation pattern shift was blocked. RT-qPCR showed that the transcription levels of the genes
FlbD
and
LaeA
(related to asexual development) were significantly altered, and those of most of the conidiation-related genes were higher in Δ
MaCreA
strain. The results of RNA-Seq revealed that
MaCreA
regulated the two conidiation patterns by mediating genes related to cell cycle, cell division, cell wall, and cell polarity. In conclusion,
CreA
, as a core regulatory gene in conidiation, provides new insight into the mechanism of conidiation in entomopathogenic fungi.