# Co-Infection and Phylogenetic Evolution of CIAV in Marek’s Disease Tumour-Bearing Flocks in Central China

**Authors:** Fang Han, Bin Shi, Lu-Ping Zheng, Man Teng, Shu-Ge Wang, Wen-Kai Zhang, Zhi-Feng Peng, Qin Luo, Gui-Xi Li, Yong-Xu Zhao, Zhen Yang, Yongxiu Yao, Zu-Hua Yu, Jun Luo

PMC · DOI: 10.3390/v18020227 · Viruses · 2026-02-11

## TL;DR

This study investigates the role of chicken infectious anemia virus (CIAV) in tumor outbreaks among vaccinated chicken flocks in central China, revealing a shift in co-infection patterns and the emergence of a new pathogenic lineage.

## Contribution

The study identifies a rising trend in CIAV mono-infections and a new high-pathogenicity marker in CIAV isolates from China.

## Key findings

- CIAV positivity rate was 59.2% in tumor-bearing flocks from central China between 2021–2023.
- CIAV mono-infections increased from 0% in 2021 to 23.7% in 2023, while CIAV + MDV co-infections decreased.
- New CIAV isolates predominantly clustered in subclade C1 and carried a Q394 marker linked to high pathogenicity.

## Abstract

The avian immunosuppressive and neoplastic diseases are great threats to the poultry industry, causing huge economic losses worldwide. Most recently, the emerging hypervirulent variants of Marek’s disease virus (HV-MDV), partially co-infected with avian leukosis virus (ALV) and/or reticuloendotheliosis virus (REV), have been identified as the key driver of tumour outbreaks in vaccinated chicken flocks, but the role of chicken infectious anemia virus (CIAV) remains unclear. Herein, we have investigated the prevalence and co-infection of CIAV in 71 clinical tumour-bearing flocks collected from central China during 2021–2023, which has shown a CIAV positivity rate of 59.2% (42/71). Notably, the incidence of CIAV mono-infection increased significantly from 0% (0/29) in 2021 to 23.7% (9/38) in 2023, whereas CIAV + MDV co-infection decreased from 65.5% (19/29) to 31.6% (12/38). A total of 20 viral genomes of epidemic CIAV isolates from diverse sources were obtained, and the phylogenetic analysis, including 91 reference isolates were clustered into four major lineages (A–D), with clade C further subdivided into subclades C1 and C2. Clade C1 consisted predominantly of Asian isolates, with 88.5% (46/52) of the isolates originating from mainland China. Among the 20 new isolates, 17 were clustered in subclade C1, two in C2, and one in B. The VP1 gene phylogeny showed a topology largely consistent with that of the whole-genome analysis. Moreover, all newly characterized isolates contained glutamine (Q) at VP1 residue 394, a molecular marker associated with high pathogenicity. Collectively, our data suggest that prevalent HV-MDV variants together with CIAV co-infections are the primary drivers of the ongoing tumour outbreaks in Chinese poultry flocks. Notably, the significantly increased CIAV mono-infections, possibly resulting from an independently evolving lineage among circulating Chinese strains, are likely to pose a new challenge for future control of disease.

## Linked entities

- **Proteins:** VP1 (pyrophosphate-energized vacuolar membrane proton pump 1)
- **Diseases:** Marek’s disease (MONDO:0016101), avian leukosis (MONDO:0025381), reticuloendotheliosis (MONDO:0010721)
- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** SP1 (Sp1 transcription factor) [NCBI Gene 395303]
- **Diseases:** hemorrhages (MESH:D006470), MD tumour (MESH:D008380), CIA (MESH:D004859), growth retardation (MESH:D006130), injury to (MESH:D014947), immunosuppressive and neoplastic diseases (MESH:D004194), atrophy (MESH:D001284), lymphoid hyperplasia (MESH:D019310), Tumour (MESH:D009369), neural damage (MESH:D015441), AL (MESH:D001353), aplastic anemia (MESH:D000741), infectious diseases (MESH:D003141), deaths (MESH:D003643), anemia (MESH:D000740), Co-Infection (MESH:D060085), RE (MESH:C538362), immune dysfunction (MESH:D007154), Infection (MESH:D007239)
- **Chemicals:** water (MESH:D014867), agarose (MESH:D012685), PBS (MESH:D007854), phosphate-buffered saline (-)
- **Species:** Chicken anemia virus (no rank) [taxon 12618], Arthrospira sp. LV (species) [taxon 2231211], Avian leukosis virus (no rank) [taxon 11864], Canis lupus familiaris (dog, subspecies) [taxon 9615], Gallus gallus (bantam, species) [taxon 9031], Reticuloendotheliosis virus (no rank) [taxon 11636], Gallid alphaherpesvirus 2 (Marek disease virus type 1, no rank) [taxon 10390], Escherichia coli DH5[alpha] (strain) [taxon 668369], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** glutamine (Q) at position 394

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944903/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944903/full.md

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Source: https://tomesphere.com/paper/PMC12944903