Horses naturally infected with EIAV harbor 2 distinct SU populations but are monophyletic with respect to IN

• Published in: Virus genes Vol. 52; no. 1; pp. 71 - 80
• Main Authors: Cervantes, Diana T., Ball, Judith M., Edwards, John, Payne, Susan
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.02.2016; Springer Nature B.V
• Subjects: Amino Acid Sequence; Animals; Base Sequence; Biomedical and Life Sciences; Biomedicine; Equine Infectious Anemia - virology; Genetic Variation; Genome, Viral; Horses; Infectious Anemia Virus, Equine - classification; Infectious Anemia Virus, Equine - enzymology; Infectious Anemia Virus, Equine - genetics; Integrases - chemistry; Integrases - genetics; Medical Microbiology; Molecular Sequence Data; Phylogeny; Plant Sciences; Sequence Alignment; Texas; Virology; Texas; Equine infectious anemia virus; Retrovirus; EIAV; Lentivirus; Swamp fever; Horse
• ISSN: 0920-8569; 1572-994X
• DOI: 10.1007/s11262-015-1280-z

Equine infectious anemia virus (EIAV) causes lifelong infections ranging from acutely fatal, to chronic, to asymptomatic. Within infected animals, EIAV is found as a quasispecies. Many experimental studies on EIAV, carried out in the U.S. over the past 70 years, have used either the highly virulent Wyoming (EIAVWYO) field strain or various derivatives of that strain. These infections have provided insights into the variety of genetic changes that accumulate in the env gene and LTR in experimentally infected horses. In the current study, we obtained EIAV sequences from blood samples collected from naturally infected Texas horses between 2000 and 2002. We found surface (SU) and long terminal repeat (LTR) sequences clearly related to EIAVWYO and its cell culture-adapted derivatives. Some blood samples yielded SU or LTR sequences belonging to 2 discrete clusters. In these cases, SU and LTR variation between animals was no greater than sequence variation within animals. In contrast, a portion of integrase (IN) was more homogeneous within animals than between animals. These results suggest that specific selective pressures are applied to SU and LTR sequences, potentially driving generation of two distinct sequence clusters within a horse. We speculate that viruses in one cluster may be more highly expressed and easily transmitted while those in the second cluster support long-term inapparent infection. The presence of homogeneous IN sequences within a horse supports the hypothesis that SU and LTR sequences diverged after the initial infection.