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Research article · 2026 · Full text

International Journal of Biology Sciences

Clinical Manifestations and Pathological Features of Lumpy Skin Disease in Naturally Infected Cattle Herds in Ethiopia

Desta Regassa DemissieMulu Habte WondimAbebe Gizaw Mesafint

Volume 8(5) · Pages 204–207 · DOI: 10.33545/26649926.2026.v8.i5c.922 ↗

Research areasPoxvirus research and outbreaksAnimal Disease Management and EpidemiologyVector-Borne Animal Diseases

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Abstract

Author-written

Despite lumpy skin disease being recognized in Ethiopian cattle since the 1970s, detailed characterization of clinical manifestations and pathological features in naturally infected herds under field conditions remains limited. This research examined clinical and pathological features in 156 lumpy skin disease-affected cattle from 24 naturally infected herds across four geographic regions of Ethiopia between March 2023 and August 2024. Clinical examination revealed progressive lesion development beginning with fever and generalized edema (91.7% of animals week 1–2) progressing to macule formation (85.9%), papule development (94.2%), vesiculation (68.6%), pustule formation (78.8%), crust formation (88.5%), and eventual scar tissue (64.1%). Systemic manifestations including lymphadenitis (87.2%), mastitis (42.3%), lameness (56.4%), and in severe cases, systemic infection with respiratory involvement (18.6%) were documented. Histopathologic examination of lesion biopsies revealed characteristic ballooning degeneration of epidermal cells, eosinophilic intracytoplasmic inclusion bodies consistent with poxvirus, and perivascular lymphocytic infiltration in the dermis. Secondary bacterial infections complicating skin lesions occurred in 34.6% of examined animals. Temporal analysis demonstrated complete lesion resolution in 48.1% of animals by 8 weeks post-infection, while 22.4% retained scarring beyond 12 weeks. These findings characterize the clinical and pathological spectrum of naturally acquired lumpy skin disease in Ethiopian cattle and identify factors associated with disease severity and recovery.

Summary

Source-checked

Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Lumpy skin disease (LSD) presents a broad range of clinical manifestations, which can vary from subclinical infections to severe systemic disease that may be fatal. View evidence ↗

      Why it matters

      Lumpy skin disease (LSD) presents a broad range of clinical manifestations, which can vary from subclinical infections to severe systemic disease that may be fatal.

      In the paper's own words

      “An often underappreciated aspect of lumpy skin disease epidemiology is the wide spectrum of clinical manifestations ranging from apparent subclinical infection through severe systemic disease with potentially fatal complications”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Although LSD was first described in African cattle in Ethiopia during the 1970s, there is a lack of systematic documentation regarding its clinical and pathological spectrum in field conditions. View evidence ↗

      Why it matters

      Although LSD was first described in African cattle in Ethiopia during the 1970s, there is a lack of systematic documentation regarding its clinical and pathological spectrum in field conditions.

      In the paper's own words

      “Ethiopia, as the site where lumpy skin disease was first recognized and described in African cattle in the 1970s, has accumulated decades of clinical observation of natural LSDV infections, yet systematic documentation of the clinical and pathological spectrum under field conditions remains sparse in the international veterinary literature”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. The question

    • The study aimed to characterize the clinical and pathological features of naturally infected cattle to create baseline data for evaluating prognosis and disease severity. View evidence ↗

      The question

      The study aimed to characterize the clinical and pathological features of naturally infected cattle to create baseline data for evaluating prognosis and disease severity.

      In the paper's own words

      “The present research aimed to comprehensively characterize clinical manifestations and pathological features in naturally infected cattle using both clinical examination and histopathological analysis to establish baseline data for disease severity assessment and prognostic evaluation.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  3. What they did

    • The research analyzed 156 cattle from 24 naturally infected herds across four regions of Ethiopia from March 2023 to August 2024. View evidence ↗

      What they did

      The research analyzed 156 cattle from 24 naturally infected herds across four regions of Ethiopia from March 2023 to August 2024.

      In the paper's own words

      “This research examined clinical and pathological features in 156 lumpy skin disease-affected cattle from 24 naturally infected herds across four geographic regions of Ethiopia between March 2023 and August 2024.”

      Page 1

      Found in: Material

      Read it in the full textOpen PDF at page 1 ↗
    • Animals were included in the study if they had a PCR-confirmed LSDV infection, with stages ranging from acute (≤2 weeks) to chronic (>8 weeks). View evidence ↗

      What they did

      Animals were included in the study if they had a PCR-confirmed LSDV infection, with stages ranging from acute (≤2 weeks) to chronic (>8 weeks).

      In the paper's own words

      “Inclusion criteria comprised animals with confirmed LSDV infection by PCR and stage of infection ranging from acute (≤2 weeks post-infection presumed onset) through chronic (>8 weeks).”

      Page 2

      Found in: Material

      Read it in the full textOpen PDF at page 2 ↗
    • Skin biopsies of papules, pustules, and crusts were collected, fixed in 10% neutral buffered formalin, and stained with hematoxylin and eosin for histopathological analysis. View evidence ↗

      What they did

      Skin biopsies of papules, pustules, and crusts were collected, fixed in 10% neutral buffered formalin, and stained with hematoxylin and eosin for histopathological analysis.

      In the paper's own words

      “Skin lesion biopsies were collected from consenting herd owners for histopathological examination.”

      Page 2

      “Biopsies of representative lesions at different clinical stages (papules, pustules, crusts) were fixed in 10% neutral buffered formalin, processed for histopathology, and stained with hematoxylin and eosin.”

      Page 2

      Found in: Material

      Read it in the full textOpen PDF at page 2 ↗
    • The researchers used anti-vaccinia virus antibodies for immunohistochemistry to locate viral antigens and performed bacterial cultures on purulent pustule samples. View evidence ↗

      What they did

      The researchers used anti-vaccinia virus antibodies for immunohistochemistry to locate viral antigens and performed bacterial cultures on purulent pustule samples.

      In the paper's own words

      “Poxvirus-specific immunohistochemistry was performed using anti-vaccinia virus antibodies to facilitate viral antigen localization. Secondary bacterial culture was performed on samples from pustules appearing to have purulent content.”

      Page 2

      Found in: Methods

      Read it in the full textOpen PDF at page 2 ↗
  4. What they found

    • During the acute prodromal phase (weeks 1–2), 91.7% of animals had a fever, with a mean temperature of 39.8 °C (range 39.2–40.4 °C). View evidence ↗

      What they found

      During the acute prodromal phase (weeks 1–2), 91.7% of animals had a fever, with a mean temperature of 39.8 °C (range 39.2–40.4 °C).

      In the paper's own words

      “In the acute prodromal phase (week 1–2 post-infection), animals exhibited fever (mean temperature 39.8 °C; range 39.2–40.4 °C) in 91.7% of cases”

      Page 2

      Found in: Discussion

      Read it in the full textOpen PDF at page 2 ↗
    • Skin lesions progressed from macules (85.9%) and papules (94.2%) to vesiculation (68.6%), pustules (78.8%), crusts (88.5%), and finally scar tissue (64.1%). View evidence ↗

      What they found

      Skin lesions progressed from macules (85.9%) and papules (94.2%) to vesiculation (68.6%), pustules (78.8%), crusts (88.5%), and finally scar tissue (64.1%).

      In the paper's own words

      “Clinical examination revealed progressive lesion development beginning with fever and generalized edema (91.7% of animals week 1–2) progressing to macule formation (85.9%), papule development (94.2%), vesiculation (68.6%), pustule formation (78.8%), crust formation (88.5%), and eventual scar tissue (64.1%).”

      Page 1

      Found in: Methods

      Read it in the full textOpen PDF at page 1 ↗
    • Systemic signs were common, including lymphadenitis (87.2%), lameness (56.4%), mastitis (42.3%), and respiratory involvement in severe cases (18.6%). View evidence ↗

      What they found

      Systemic signs were common, including lymphadenitis (87.2%), lameness (56.4%), mastitis (42.3%), and respiratory involvement in severe cases (18.6%).

      In the paper's own words

      “Systemic manifestations including lymphadenitis (87.2%), mastitis (42.3%), lameness (56.4%), and in severe cases, systemic infection with respiratory involvement (18.6%) were documented.”

      Page 1

      Found in: Methods

      Read it in the full textOpen PDF at page 1 ↗
    • Histopathology of lesions showed ballooning degeneration of epidermal cells, perivascular lymphocytic infiltration in the dermis, and eosinophilic intracytoplasmic inclusion bodies typical of poxviruses. View evidence ↗

      What they found

      Histopathology of lesions showed ballooning degeneration of epidermal cells, perivascular lymphocytic infiltration in the dermis, and eosinophilic intracytoplasmic inclusion bodies typical of poxviruses.

      In the paper's own words

      “Histopathologic examination of lesion biopsies revealed characteristic ballooning degeneration of epidermal cells, eosinophilic intracytoplasmic inclusion bodies consistent with poxvirus, and perivascular lymphocytic infiltration in the dermis.”

      Page 1

      Found in: Material

      Read it in the full textOpen PDF at page 1 ↗
    • Secondary bacterial infections occurred in 34.6% of animals, most commonly caused by Staphylococcus aureus and Corynebacterium pseudotuberculosis. View evidence ↗

      What they found

      Secondary bacterial infections occurred in 34.6% of animals, most commonly caused by Staphylococcus aureus and Corynebacterium pseudotuberculosis.

      In the paper's own words

      “Secondary bacterial infections complicating LSDV skin lesions were documented in 34.6% of examined animals, with Staphylococcus aureus and Corynebacterium pseudotuberculosis being the most frequently isolated species.”

      Page 3

      Found in: Secondary Bacterial Complications

      Read it in the full textOpen PDF at page 3 ↗
    • Secondary bacterial infections increased the likelihood of permanent scarring from 22.4% to 48.6% and extended healing times by an average of 2-3 weeks. View evidence ↗

      What they found

      Secondary bacterial infections increased the likelihood of permanent scarring from 22.4% to 48.6% and extended healing times by an average of 2-3 weeks.

      In the paper's own words

      “These secondary bacterial infections prolonged healing times by an average of 2-3 weeks and increased the probability of permanent scarring from 22.4% to 48.6%”

      Page 3

      Found in: Secondary Bacterial Complications

      Read it in the full textOpen PDF at page 3 ↗
    • By 8 weeks post-infection, 48.1% of animals had complete lesion resolution, while 22.4% still had scars after 12 weeks. View evidence ↗

      What they found

      By 8 weeks post-infection, 48.1% of animals had complete lesion resolution, while 22.4% still had scars after 12 weeks.

      In the paper's own words

      “Temporal analysis demonstrated complete lesion resolution in 48.1% of animals by 8 weeks post-infection, while 22.4% retained scarring beyond 12 weeks.”

      Page 1

      Found in: Methods

      Read it in the full textOpen PDF at page 1 ↗
  5. What it means

    • The authors conclude that because fever and systemic signs can precede skin lesions by up to a week, health workers must increase surveillance sensitivity during the prodromal phase. View evidence ↗

      What it means

      The authors conclude that because fever and systemic signs can precede skin lesions by up to a week, health workers must increase surveillance sensitivity during the prodromal phase.

      In the paper's own words

      “The practical message is that field veterinarians and pastoral animal health workers should recognize that fever and systemic signs may precede visible skin lesions by up to a week, necessitating heightened surveillance sensitivity during prodromal phases.”

      Page 3

      Found in: Discussion

      Read it in the full textOpen PDF at page 3 ↗
    • The authors state that future research is needed to investigate host factors that determine disease severity and how early supportive care affects recovery and lesion progression. View evidence ↗

      What it means

      The authors state that future research is needed to investigate host factors that determine disease severity and how early supportive care affects recovery and lesion progression.

      In the paper's own words

      “Future research should investigate the host factors determining disease severity and the impact of early supportive care interventions on lesion progression and recovery.”

      Page 3

      Found in: Introduction

      Read it in the full textOpen PDF at page 3 ↗

Visual summary

3 visuals

Illustrations explain the paper; charts are replotted from the paper's own table values.

AI-generated illustration
AI-generated conceptual illustration (Bovine cattle). It explains the idea and does not show study data.↗ Enlarge
Timeline of LSD Progression
AI-generated conceptual illustration (Bovine cattle). It explains the idea and does not show study data.

AI-generated conceptual illustration (Bovine cattle). It explains the idea and does not show study data.

Open full-size image ↗

Timeline of LSD Progression

AI-generated conceptual illustration (Bovine cattle). It explains the idea and does not show study data.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.↗ Enlarge
1-2: Fever (%) vs Lesion Present (%) vs Systemic Signs (%)
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

1-2: Fever (%) vs Lesion Present (%) vs Systemic Signs (%)

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.↗ Enlarge
3-4: Fever (%) vs Lesion Present (%) vs Systemic Signs (%)
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

3-4: Fever (%) vs Lesion Present (%) vs Systemic Signs (%)

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

View source evidence ↗

Figures & tables

From the original paper
Temporal progression of clinical manifestations and their frequency among 156 cattle naturally infected with lumpy skin diseaseTable 1Page 2Temporal progression of clinical manifestations across disease stages in lumpy skin disease-infected cattleFigure 1Page 2Frequency and severity of complications by anatomical site in lumpy skin disease-infected cattleFigure 2Page 3
FULL TEXT Original article · reflowed for reading

Introduction

An often underappreciated aspect of lumpy skin disease epidemiology is the wide spectrum of clinical manifestations ranging from apparent subclinical infection through severe systemic disease with potentially fatal complications, reflecting substantial variation in host immune responses, viral virulence, and secondary complicating infections [1] . The classical clinical description of lumpy skin disease emphasizes the distinctive skin lesions that define the disease clinically and epidemiologically, yet systemic manifestations including fever, lymphadenopathy, and multi-organ involvement frequently exceed the apparent severity suggested by examination of skin lesions alone [2] . Ethiopia, as the site where lumpy skin disease was first recognized and described in African cattle in the 1970s, has accumulated decades of clinical observation of natural LSDV infections, yet systematic documentation of the clinical and pathological spectrum under field conditions remains sparse in the international veterinary literature [3] . The present research aimed to comprehensively characterize clinical manifestations and pathological features in naturally infected cattle using both clinical examination and histopathological analysis to establish baseline data for disease severity assessment and prognostic evaluation.

Material and Methods

Material and Methods

Material

This cross-sectional research was conducted at the Addis Ababa Research Institute for Tropical Animal Diseases, Addis Ababa, Ethiopia, between March 2023 and August 2024. A total of 156 cattle with clinical signs consistent with lumpy skin disease from 24 affected herds distributed across four geographic regions (Oromia, Amhara, Somali, and Southern Nations) were examined. Inclusion criteria comprised animals with confirmed LSDV infection by PCR and stage of infection ranging from acute (≤2 weeks post-infection presumed onset) through chronic (>8 weeks). The research was approved by the Institutional Ethics Committee (Protocol No. AARITAD-IEC-2023-0031). Skin lesion biopsies were collected from consenting herd owners for histopathological examination.

Methods

Clinical examination documented the progressive stages of lesion development, concurrent systemic manifestations, and recovery timeline. Biopsies of representative lesions at different clinical stages (papules, pustules, crusts) were fixed in 10% neutral buffered formalin, processed for histopathology, and stained with hematoxylin and eosin. Poxvirus-specific immunohistochemistry was performed using anti-vaccinia virus antibodies to facilitate viral antigen localization. Secondary bacterial culture was performed on samples from pustules appearing to have purulent content. Clinical staging was based on temporal documentation: week 1-2 (acute), weeks 3-4 (developing), weeks 5-6 (mature), weeks 7-8 (resolving), and weeks 9-12 (late recovery). Lesion severity was graded on a 5-point scale (minimal to severe based on surface area involvement). Statistical analysis employed descriptive epidemiology and Kaplan-Meier survival analysis to characterize lesion persistence and resolution patterns. Figure 2 shows that limb lesions most frequently progressed to scarring (52.8%), while udder involvement most frequently complicated with mastitis (81.4%), indicating that complication risks vary substantially by anatomical site of primary infection.

Figure 2. Frequency and severity of complications by anatomical site in lumpy skin disease-infected cattle
Frequency and severity of complications by anatomical site in lumpy skin disease-infected cattle↗ Enlarge
Figure 2
Frequency and severity of complications by anatomical site in lumpy skin disease-infected cattle

Frequency and severity of complications by anatomical site in lumpy skin disease-infected cattle

Open full-size image ↗
Original paper figureSource PDF · page 3 ↗

Results

Results

Discussion

The detailed clinical characterization documented in this research demonstrates that lumpy skin disease in naturally infected Ethiopian cattle exhibits a predictable clinical progression distinct from descriptions in experimental or recently infected populations. The prominence of systemic manifestations, particularly fever preceding visible skin lesions by 5-7 days and systemic lymphadenitis affecting 87.2% of animals, underscore that LSDV causes generalized systemic infection rather than the superficial dermatitis suggested by the disease name.

The delayed appearance of skin lesions relative to systemic signs (mean 8.2 days post-fever onset) has important implications for surveillance and early disease detection, as animals may pose a transmission risk to susceptible contacts during the febrile prodromal phase before diagnostic skin lesions appear.

Secondary Bacterial Complications

Secondary bacterial infections complicating LSDV skin lesions were documented in 34.6% of examined animals, with Staphylococcus aureus and Corynebacterium pseudotuberculosis being the most frequently isolated species. These secondary bacterial infections prolonged healing times by an average of 2-3 weeks and increased the probability of permanent scarring from 22.4% to 48.6%, indicating that management strategies to prevent secondary infection through good hygiene and anti-inflammatory care may substantially improve recovery outcomes.

Conclusion

Conclusion

Acknowledgement

AcknowledgementsThe Addis Ababa Research Institute for Tropical Animal Diseases provided laboratory facilities and pathology infrastructure. D.R.D. conceptualized and supervised the research; M.H.W. performed clinical examinations and specimen collection; A.G.M. conducted histopathological analysis and interpretation. Financial support was provided by the Ethiopian Ministry of Agriculture through Research.

Figures and tables from the paper

Table 1. Temporal progression of clinical manifestations and their frequency among 156 cattle naturally infected with lumpy skin disease
Clinical StageWeek Post-InfectionFever (%)Lesion Present (%)Systemic Signs (%)
Acute prodromal1-291.728.258.4
Early lesion development3-462.385.974.2
Mature lesion5-618.694.268.0
Late lesion/resolving7-84.288.532.6
Post-acute/recovery9-120.042.38.4

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

View original table image
Temporal progression of clinical manifestations and their frequency among 156 cattle naturally infected with lumpy skin disease↗ Enlarge
Table 1
Temporal progression of clinical manifestations and their frequency among 156 cattle naturally infected with lumpy skin disease

Temporal progression of clinical manifestations and their frequency among 156 cattle naturally infected with lumpy skin disease

Open full-size image ↗
Original paper tableSource PDF · page 2 ↗
Figure 1. Temporal progression of clinical manifestations across disease stages in lumpy skin disease-infected cattle
Temporal progression of clinical manifestations across disease stages in lumpy skin disease-infected cattle↗ Enlarge
Figure 1
Temporal progression of clinical manifestations across disease stages in lumpy skin disease-infected cattle

Temporal progression of clinical manifestations across disease stages in lumpy skin disease-infected cattle

Open full-size image ↗
Original paper figureSource PDF · page 2 ↗

References

14 in the original paper
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