In July 2025, two loblolly pines (Pinus taeda L.) growing within the 761-acre coastal Carolina Beach State Park (New Hanover County, NC) were observed with conspicuous growth abnormalities. One tree displayed a large witches’ broom arising from the main stem approximately 7 meters above the ground, immediately below the primary canopy, whereas the second showed extensive proliferation of epicormic shoots bearing needles along much of its 12-meter trunk, accompanied by reduced crown development. Needle tissues were collected from both trees, along with samples from four asymptomatic loblolly pines in the same area for the investigation of the possible phytoplasma presence. Total DNA was extracted using a Qiagen DNeasy Plant Pro Kit according to the manufacturer’s instructions. DNA extracts were screened by phytoplasma-specific real-time PCR (Hodgetts et al. 2009), which resulted in detection of phytoplasmas only in samples from the symptomatic trees. The full-length 16S rRNA gene (1,531 bp) was amplified with PCR primers flanking the gene: Tyr-F2 (5’-CAGTCTGTAAAACTGYTCCG-3’) and Ile-R2 (5’-TATCAGGCGTGTGCTCTAAC-3’). Amplicons of the expected size (~1.9 kb) were purified and sequenced using Oxford Nanopore sequencing. Identical consensus sequences were obtained and deposited in GenBank as strains PES-NC3 and PWB-NC4 (accession numbers PZ173280–PZ173281). BLASTn analysis of the 16S rRNA gene sequence showed the highest identity (1,530/1,531 bp; 99.93%) with a ‘Candidatus Phytoplasma pini’-related strain MDPP4 from Maryland (GenBank acc. no. OR147379), and 98.43% identity with the reference strain of ‘Ca. P. pini’ Pin127S from Spain (subgroup 16SrXXI-A; GenBank acc. no. AJ632155). Virtual RFLP analysis of the F2n/R2 region using iPhyClassifier (Zhao et al. 2009) produced a restriction pattern identical to that of the designated reference strain of subgroup 16SrXXI-B (GenBank acc. no. KU242428), supporting assignment to subgroup 16SrXXI-B. To further characterize the phytoplasma strains, a 1960 bp fragment of the secA gene was amplified from each symptomatic tree as previously described by Valiunas et al. (2015). The secA sequences differed by 10 nucleotides and were deposited in GenBank under acc. nos. PZ184669 (PES-NC3) and PZ184670 (PWB-NC4). BLASTn analysis showed 99.64% identity (1,932/1,939 bp) for PES-NC3 and 99.74% identity (1,934/1,939 bp) for PWB-NC4 to the corresponding locus of ‘Ca. P. pini’ strain MDPP (GenBank acc. no. KU242429). Phylogenetic analyses based on both the 16S rRNA and secA gene sequences indicated that the two strains detected in North Carolina cluster with previously reported strains from Maryland, forming a distinct, well-supported clade that is clearly separated from European ‘Ca. P. pini’ strains. This is the first report of ‘Ca. P. pini’-related strains infecting loblolly pine in North Carolina and only the second documented occurrence of this phytoplasma in the United States of America, following its detection in mountain pine (P. pungens Lamb.) in Maryland (Costanzo et al. 2016). The 16S rRNA gene sequences of the Maryland and North Carolina strains differ by a single nucleotide, whereas both U.S. strains differed from the European reference strain of ‘Ca. P. pini’ by 24 nucleotides across the 1,531-bp 16S rRNA gene sequence. These findings expand the known host range and geographic distribution of phytoplasmas associated with pines and suggest that they may be more widespread in the U.S.A. than previously recognized.