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Brucellosis

The Silent Threat to Livestock and Human Health

  • 1st Edition - October 27, 2025
  • Latest edition
  • Editor: Maryam Dadar
  • Language: English

Brucellosis: The Silent Threat to Livestock and Human Health offers an in-depth look into the challenges posed by brucellosis, including its prevention, control, diagnosis, and tr… Read more

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Description

Brucellosis: The Silent Threat to Livestock and Human Health offers an in-depth look into the challenges posed by brucellosis, including its prevention, control, diagnosis, and treatment in animals and humans. This zoonotic disease is a significant concern not only for animal health but also public health, creating an economic burden worldwide. As the first comprehensive reference on brucellosis in decades, this book provides valuable insights into combating and managing the disease in herds and communities. The book emphasizes the importance of the One Health approach, presenting a global perspective on brucellosis.

In addition, it discusses the contagious nature of the disease and its impact on livestock and humans, particularly those working in animal husbandry. The book serves as a foundation for new research, highlighting the need for further studies due to the lack of a cure for animals and the difficulties in treating humans.

Key features

  • Reviews Brucellosis in cattle, goats, sheep, swine, and humans
  • Covers prevention, control, clinical presentation, and treatment
  • Presents diagnostic tools and techniques
  • Identifies zoonotic transmission, epidemiology, and global distribution
  • Includes case studies of outbreaks in both livestock and human populations
  • Explores Brucellosis in food safety and processing

Readership

Veterinarians and Animal Health Professionals working in agriculture, livestock farming, and veterinary medicine - Researchers and Scientists in the fields of livestock science, food safety, epidemiology and infectious disease

Table of contents

1. Historical context and background of
brucellosis in the world

1.1. History and spread of brucellosis across
the world

1.2. Conclusion
References

2. Brucellosis throughout human history

2.1. Introduction

2.2. Early evidence of human brucellosis

2.3. Discovery of Brucella

2.3.1. An investigation on the island of
Malta

2.4. Three diseases in one

2.5. Conclusion
References

3. The genetic diversity of Brucella species
Marcela Sua´rez-Esquivel, Jeffrey T. Foster and
Carine Rodrigues Pereira

3.1. Introduction

3.2. General characteristics of Brucella spp

3.3. Techniques to assess Brucella genetic
diversity

3.3.1. Multiple-Locus Variable Number
Tandem Repeat Analysis

3.3.2. WGS (Pangenome and SNP)

3.4. Evolution of Brucella from Ochrobactrum

3.5. Division into classical and atypical

3.6. Classical Brucella

3.6.1. Brucella melitensis

3.6.2. Brucella abortus

3.6.3. Brucella suis

3.6.4. Brucella ovis

3.6.5. Brucella neotomae

3.6.6. Brucella canis

3.6.7. Brucella ceti

3.6.8. Brucella pinnipedialis

3.6.9. Brucella microti

3.6.10. Brucella papionis

3.6.11. Brucella amazoniensis sp. nov

3.6.12. Brucella sp. F5/99

3.6.13. Brucella sp. BCCN84-3 and
B. nosferati

3.7. Atypical Brucella

3.7.1. Brucella inopinata

3.7.2. BO2

3.7.3. Australian rodent Brucella strains

3.7.4. 09RB8471 and 10RB9215

3.7.5. Brucella vulpis

3.7.6. 141012304

3.7.7. B13-0095

3.7.8. 191011898

3.7.9. BO3

3.8. Conclusions
References
Part II
Pathogenesis and immunobiology of
brucellosis

4. Pathogenesis and immunopathological
phenomena around Brucella infections

4.1. Clinical manifestations of human
brucellosis

4.2. Inflammation induced by Brucella
infections

4.3. Osteoarticular brucellosis

4.3.1. Bone structure: Interplay between
forming and resorbing cells

4.3.2. Brucella and osteoblasts/
osteocytes: Dangerous liaisons

4.3.3. Brucella and synoviocytes:
Beyond bone

4.3.4. Osteoclast activation by Brucella

4.4. Interactions of immune cells with bone
cells in the context of Brucella infection

4.5. Brucella placental infection and
pathological findings in the female
reproductive tract

4.5.1. Trophoblasts at the center of the
stage

4.5.2. In vitro approaches to understand
Brucella abortion in humans

4.5.3. Immune response to Brucella
infection in the maternal—fetal
interface

4.6. Neurobrucellosis

4.6.1. Getting there: Brucella and the
Trojan horse mechanism

4.6.2. Once inside: The negative loop
between glial cells and BBB

4.6.3. Inflammation in the middle of the
scene

4.6.4. Neurons as the ultimate target of
the inflammation storm or neurons
as the victim of this crime

4.7. Epididymoorchitis

4.8. Hepatic brucellosis

4.9. Cardiovascular brucellosis

4.10. Conclusion
References

5. Immunopathology in osteoarticular
Brucella infection

5.1. Clinical aspect of osteoarticular human
brucellosis

5.2. Spinal brucellosis

5.2.1. Spondylitis, spondylodiscitis, and
discitis

5.2.2. Sacroiliitis

5.2.3. Peripheral skeleton

5.3. Bone and immune system cross-talk

5.4. Classical pathways in bone cells
formation

5.5. Nonclassical pathways in bone cell
formation

5.6. Interaction between Brucella and bone
cells

5.6.1. Osteoclasts

5.6.2. Mesenchymal stem cells

5.6.3. Osteoblasts

5.6.4. Osteocytes

5.6.5. Synoviocytes

5.7. Animal model insights

5.8. Concluding remarks
References
Part III
Brucellosis in animals

6. Brucellosis in livestock and companion
animals

6.1. Introduction

6.2. Public health significance

6.3. Brucellosis in livestock

6.3.1. Cattle

6.3.2. Goat

6.3.3. Sheep

6.3.4. Pig

6.3.5. Camel

6.3.6. Horse

6.4. Brucellosis in companion animal species

6.4.1. Dog

6.5. Etiology

6.6. Pathogenesis

6.6.1. Brucella invasion strategies and
intracellular niche establishment

6.6.2. Target tissues and cellular tropism

6.6.3. Sialic acid-mediated adherence
and invasion: A gateway for
Brucella pathogenesis

6.6.4. Orchestrating cellular entry:
The role of cytoskeletal dynamics
in Brucella invasion

6.6.5. Divergent host inflammatory
responses to Brucella invasion
routes

6.6.6. Oxidative stress and immune
modulation

6.7. Intracellular survival and replication

6.7.1. Modulating phagosomal
acidification

6.7.2. Inhibiting macrophage apoptosis

6.8. Brucella’s atypical virulence arsenal

6.8.1. Type IV secretion system (virB
T4SS)

6.8.2. Brucella lipopolysaccharide

6.8.3. Pathogen-associated molecular
patterns

6.8.4. Two-component sensory and
regulatory system (BvrS/BvrR)

6.8.5. Cyclic β-glucan

6.9. Brucella dissemination, target tissues,
and manipulation of host processes

6.9.1. Dissemination and tissue tropism

6.9.2. A selective tropism for the reproductive
tract

6.9.3. Brucella—host interactions in the
placenta

6.9.4. Erythritol: A complex role in
pathogenesis

6.9.5. Targeted replication and placental
disruption

6.9.6. Endothelial invasion and villous
necrosis

6.9.7. A cascade culminating in
pregnancy loss

6.10. Clinical signs

6.10.1. Factors influencing clinical
presentation

6.10.2. Reproductive sequelae in
female animals

6.10.3. Mammary gland pathology

6.10.4. Testicular inflammation and
impaired fertility

6.10.5. Musculoskeletal manifestations

6.10.6. Reproductive disruption in doe
and ewe

6.10.7. Reproductive pathology in buck
and ram

6.10.8. Equine brucellosis

6.10.9. Porcine brucellosis

6.10.10. Canine brucellosis

6.11. Epidemiology

6.12. Geographic distribution of Brucella
species and biovars

6.12.1. Asia

6.12.2. Africa

6.12.3. America

6.12.4. Europe

6.13. Risk factors

6.13.1. Livestock production practices
and brucellosis prevalence

6.13.2. Seasonal and sex-based
epidemiological patterns in
brucellosis

6.13.3. Breed and brucellosis
susceptibility: A complex
relationship

6.13.4. Age-dependent susceptibility in
bovine brucellosis

6.14. Transmission

6.14.1. Ingestion: The predominant
route in livestock

6.14.2. Inhalation

6.14.3. Direct contact and fomite
transmission

6.14.4. Introduction of infected animals:
A critical consideration

6.14.5. Vertical and perinatal
transmission: A potential
concern

6.14.6. Venereal transmission

6.14.7. Per-conjunctival transmission

6.14.8. Urinary excretion

6.14.9. B. abortus shedding in equine
hosts

6.14.10. Wildlife reservoirs

6.14.11. Ticks as vectors

6.15. Economic impact of brucellosis

6.15.1. Direct production losses

6.15.2. Indirect economic consequences

6.15.3. Economic modeling and impact
on individual animals

6.15.4. Reproductive losses in ovine
herds

6.15.5. Distinct challenges in swine
production

6.15.6. Economic considerations for
brucellosis control programs

6.15.7. Global economic significance
of brucellosis control

6.16. Prevention and control

6.17. Success stories and ongoing challenges

6.18. Challenges and future directions: Novel
strategies and data exploration
AI disclosure
References

7. Brucellosis in dogs: epidemiology,
diagnosis, and public health concerns

7.1. Introduction

7.2. Epidemiology

7.3. The pathogenesis of B. canis

7.4. Clinical manifestations

7.5. Diagnosis

7.6. Prognosis and treatment in dogs

7.7. Control and prevention

7.8. Risk factor

7.9. Public health concerns

7.10. Conclusion
References

8. Brucellosis in aquatic mammals

8.1. Introduction

8.2. Brucella infection in aquatic mammals

8.2.1. Marine Brucella in other species

8.3. Distribution

8.4. Impact on the health of aquatic mammals

8.4.1. Clinical signs

8.4.2. Lesions

8.4.3. Consequences for populations

8.5. Transmission

8.5.1. Transmission routes

8.5.2. Risk factors

8.6. Diagnosis of Brucella in aquatic mammals

8.6.1. Direct diagnosis

8.6.2. Indirect diagnosis

8.6.3. Diagnostic challenges

8.7. Zoonosis and health surveillance

8.8. Conclusions
AI disclosure
References

9. Wildlife as reservoirs of brucellosis and
its transmission

9.1. Introduction

9.2. Diagnosis of Brucella in wildlife

9.3. Wildlife as a potential reservoir

9.4. Terrestrial reservoirs

9.4.1. Brucellosis in wild avian species

9.4.2. Brucellosis in amphibians

9.4.3. Brucellosis in large terrestrial
animals

9.4.4. Brucellosis in small and mediumsized
terrestrial animals

9.4.5. Brucellosis in bovidae

9.4.6. Brucellosis in cervidae

9.4.7. Brucellosis in wild snake

9.4.8. Brucellosis in rodents

9.4.9. Ticks as biological carrier

9.5. Aquatic reservoir

9.6. Transmission

9.6.1. Transmission of brucellosis between
animals

9.6.2. Factors influencing susceptibility
and transmission in wildlife
populations

9.6.3. Interactions between infected
wildlife and domestic animals

9.6.4. Strategies for minimizing
transmission within and
between wildlife
populations

9.7. Human health concerns

9.7.1. Routes of transmission from
wildlife to humans

9.7.2. Epidemiology of human
brucellosis cases linked to
wildlife exposure

9.7.3. Prevention and control measures
for at-risk populations

9.8. Conclusion
References
Part IV
Zoonotic transmission

10. Occupational exposure to Brucella spp.
and risk behaviors in exposed
professions
Elaine Dorneles, Andrey Lage and Carine
Rodrigues Pereira

10.1. History, epidemiology, and
contextualization

10.2. Occupational character

10.2.1. Farmers, rural workers, and
cowboys

10.2.2. Butchers

10.2.3. Veterinarians

10.2.4. Vaccine industry workers

10.2.5. Microbiologists

10.2.6. Kennel employees and animal
shelter workers

10.2.7. Hunters

10.3. Clinical signs

10.4. Diagnosis

10.5. Treatment

10.6. Control and prevention

10.7. Health education

10.8. Conclusions
References

11. Brucellosis in Tanzania and Rwanda:
Current status, challenges, and control
strategies

11.1. Introduction

11.2. Epidemiology and prevalence of
brucellosis in Tanzania and Rwanda

11.3. Economic impact of brucellosis in
Tanzania and Rwanda

11.4. Risk factors and transmission of
brucellosis in Tanzania and Rwanda

11.4.1. Limited community awareness
and education

11.4.2. Diverse livestock management
practices

11.4.3. Wildlife-livestock interface and
brucellosis transmission

11.4.4. Lack of biosecurity practices

11.4.5. Cross-border livestock
movement and trade

11.4.6. Cultural considerations and
gender roles

11.5. Current control strategies for
brucellosis

11.5.1. Test-and-slaughter programs

11.5.2. Vaccination programs

11.6. Proposed control strategies

11.7. Research and funding needs

11.8. Implementation challenges and critical
requirements for brucellosis control

11.9. Conclusion
AI disclosure
References
Part V
Diagnostic tools and techniques

12. Diagnostic tools and techniques for
Brucella detection

12.1. Introduction

12.2. Safety considerations

12.3. Indirect diagnosis

12.3.1. Acidified antigen
modifications (RBT and BPAT)

12.3.2. Serum agglutination test (SAT)

12.3.3. Complement fixation test

12.3.4. Rivanol precipitation

12.3.5. Milk ring test

12.3.6. Fluorescence polarization
assay (FPA)

12.3.7. Native hapten test (NHT)

12.3.8. Enzyme-linked immunosorbent
assay (ELISA)

12.3.9. Precipitation tests

12.3.10. Brucellin skin test (BST)

12.4. Direct methods

12.4.1. Culture methods

12.4.2. Polymerase chain reaction
(PCR)

12.4.3. Real-time PCR (RT-PCR)

12.4.4. Nested and seminested PCR

12.5. Advanced techniques

12.5.1. Matrix-assisted laser
desorption/ionization time-offlight
mass spectrometry
(MALDI-TOF MS)

12.5.2. Next-generation sequencing
(NGS)

12.6. Detection of smooth and rough
isolates of Brucella spp

12.7. Sensitivity and specificity of tests

12.8. Conclusion
References

13. Pathology of brucellosis in livestock

13.1. Introduction

13.2. Pathology of brucellosis in small
ruminants

13.2.1. Brucella melitensis

13.2.2. Brucella ovis

13.2.3. Brucella abortus

13.3. Pathology of brucellosis in cattle and
other domestic bovids

13.3.1. Brucella abortus

13.3.2. Brucella suis

13.3.3. Brucella melitensis

13.4. Pathology of brucellosis in pigs

13.4.1. Brucella suis

13.4.2. Brucella melitensis and
B. abortus

13.5. Pathology of brucellosis in domestic
camelids

13.5.1. Brucella melitensis

13.5.2. Brucella abortus

13.5.3. Brucella suis

13.6. Pathology of brucellosis in other
animals raised for human consumption

13.6.1. Brucella abortus and Brucella
suis in horses

13.6.2. Brucella microti-like infection
in frogs raised for human
consumption

13.6.3. A note on Brucella spp.
infection in the hunting and
fishing context
References
Part VI
Clinical manifestations in humans

14. Brucellosis: Clinical manifestations
in humans

14.1. Introduction

14.2. Systemic brucellosis

14.3. Focal brucellosis

14.3.1. Osteoarticular infections

14.3.2. Genitourinary infections

14.3.3. Skin and soft tissue
manifestations

14.3.4. Neurobrucellosis

14.3.5. Cardiovascular infections

14.3.6. Digestive system infections

14.3.7. Respiratory infections

14.3.8. Ocular manifestations

14.4. Relapses and chronic brucellosis

14.5. Brucellosis in children

14.6. Brucellosis in pregnant women

14.7. Brucellosis in the immunocompromised
and transplanted patient

14.8. Differential diagnosis of brucellosis

14.9. Conclusion
References

15. Rare cases of human brucellosis

15.1. Introduction

15.2. Rare clinical cases of brucellosis

15.2.1. Focal osteoarticular disease

15.2.2. Cardiovascular rare cases

15.2.3. Pulmonary rare cases

15.2.4. Neurological rare cases

15.2.5. Rare hematological cases

15.2.6. Skin lesions

15.2.7. Rare cases of the digestive
system

15.2.8. Focal hepatic disease

15.2.9. Focal ophthalmologic disease

15.2.10. Urogenital brucellosis

15.2.11. Miscellaneous

15.3. Brucella in the immunocompromised
host

15.4. Rare ways of Brucella transmission to
humans

15.5. Human infection by rare Brucella
species

15.6. Conclusion
References
Part VII
Prevention and control in animals

16. The science of brucellosis
elimination

16.1. Introduction

16.2. Historical examples of brucellosis
elimination

16.3. Principles of brucellosis control

16.4. Animal—human brucellosis
transmission models

16.5. Framework conditions for elimination

16.6. Case studies on brucellosis control

16.6.1. Brucellosis control in
Mongolia

16.6.2. Brucellosis control in Armenia

16.6.3. Brucellosis control in the
Middle East

16.6.4. Brucellosis in Ethiopia

16.7. Cross-sector economics of brucellosis
control

16.8. Toward a game-theoretical approach
to brucellosis elimination

16.9. Assessment of freedom of brucellosis

16.10. Conclusion
Acknowledgments
References

17. Brucellosis control, eradication,
and prevention

17.1. Introduction

17.2. Definitions

17.3. Choosing an appropriate strategy

17.3.1. Factors influencing strategy
selection
electronic versions of this book.

17.3.2. Strategy selection framework

17.3.3. One Health perspective

17.3.4. Adaptive management

17.3.5. Statement of objectives and
definition of indicators to
evaluate activities and
achievements

17.3.6. Planning of activities and data
flows

17.4. Prevention of human infection

17.5. Control program

17.5.1. Vaccination programs

17.5.2. Vaccination strategies

17.5.3. Challenges in brucellosis
vaccination

17.5.4. Integration with other control
measures

17.5.5. Transition to test-and-slaughter
policies

17.5.6. Herd accreditation and
separation

17.6. Eradication program

17.6.1. Test-and-slaughter policies

17.6.2. Implementation steps for a brucellosis
eradication program

17.6.3. Addressing challenges in
caprine and ovine brucellosis

17.6.4. Movement control and
restrictions

17.6.5. Surveillance of human
brucellosis

17.6.6. Special topics for eradication
programs

17.7. Conclusions

17.7.1. Main requirements for
brucellosis control and
eradication

17.7.2. Main constraints in brucellosis
control and eradication

17.8. Recommendations
References

18. Comprehensive strategies for
brucellosis control in endemic
areas

18.1. Introduction

18.2. Veterinary strategies for control of
brucellosis in endemic areas

18.3. Serological diagnoses of infected
animals as the critical part of the
test-and-slaughter policy

18.4. Animal vaccination in control
program of brucellosis

18.5. Supplementary measures in the
control program of brucellosis

18.6. Human health interventions

18.7. Integrated one-health approach

18.8. Community engagement and social
mobilization

18.9. Addressing challenges and gaps

18.10. Conclusion
References

19. Efficacy of Brucella vaccine strains: S19,
RB51, and Rev-1

19.1. Introduction

19.2. How to evaluate vaccine efficacy

19.3. Ideal vaccine for brucellosis

19.4. History, characteristics, and efficacy
of the vaccine strains currently used
for brucellosis control

19.4.1. S19 vaccine strain

19.4.2. RB51 vaccine strain

19.4.3. Rev.1 vaccine strain

19.4.4. Other live vaccines

19.5. Factors that may impact efficacy and
other vaccination aspects of brucellosis

19.5.1. Intrinsic host factors

19.5.2. Vaccine and administration
factors

19.6. Final considerations: Beyond vaccine
efficacy
References
Part VIII
Prevention and control in humans

20. Therapeutic advances in human
brucellosis

20.1. Introduction

20.2. Pharmacology of antibiotics

20.2.1. Doxycycline

20.2.2. Rifampicin

20.2.3. Aminoglycosides

20.2.4. Fluoroquinolones

20.2.5. Trimethoprimsulfamethoxazole


20.2.6. Streptomycin

20.2.7. Tigecycline

20.3. Antibiotic treatment

20.3.1. Proposed regimens for
uncomplicated brucellosis

20.3.2. Proposed regimens for focal
disease

20.3.3. Proposed regimens for
pregnant women

20.3.4. Proposed regimens for
children

20.4. Complications

20.4.1. Osteoarticular complications

20.4.2. Neurological complications

20.4.3. Cardiovascular complications

20.4.4. Other complications

20.5. Prophylaxis and general
recommendations

20.5.1. Avoiding the consumption
of unpasteurized dairy
products

20.5.2. Implementing vaccination
campaigns for livestock in
endemic regions

20.5.3. Promoting the use of
personal protective
equipment

20.5.4. Public health education

20.5.5. Screening and monitoring
of at-risk populations

20.6. Brucellosis in children

20.7. Brucellosis in pregnant women

20.8. Recurrent or resistant brucellosis

20.8.1. Management of relapses and
resistance

20.9. Treatment strategies for severe or
chronic infections

20.10. New therapeutic approaches

20.11. Monitoring and follow-up of
patients

20.11.1. Serological testing

20.11.2. Imaging studies

20.11.3. Reevaluation of treatment

20.11.4. Long-term follow-up

20.11.5. Monitoring for adverse
effects

20.12. Conclusions and future perspectives

20.12.1. Advances in treatment

20.12.2. Challenges in treatment
adherence

20.12.3. Public health and vaccination
programs

20.12.4. Future perspectives
References

21. Medicinal plants used in the treatment
of brucellosis

21.1. Brucellosis: An overview

21.1.1. History

21.1.2. Pathogen

21.1.3. Routes of transmission

21.1.4. Clinical signs and symptoms

21.1.5. Diagnosis

21.1.6. Geographical distribution and
negative effects

21.2. Brucellosis treatment and surveillance

21.3. Brucellosis treatment by medicinal
plants and their derived products

21.3.1. Ethnobotany investigations

21.3.2. In vitro investigations

21.3.3. In vivo investigations

21.4. Future prospects and challenges in
the treatment of brucellosis

21.5. Conclusion
References
Part IX
One health approach

22. Knowledge, attitudes, and practices
(KAP) relating to brucellosis:
Unveiling the vital role of public
awareness

22.1. Introduction

22.2. Knowledge of brucellosis that is
important for farmers

22.2.1. Understanding the disease by
farmers

22.2.2. Symptoms and complications
of animal disease in farm

22.2.3. Modes of transmission in
animal brucellosis

22.2.4. Preventive measures

22.3. Attitudes toward brucellosis

22.3.1. Perceived severity and
susceptibility

22.3.2. Cultural beliefs and stigma

22.3.3. Trust in healthcare systems for
control of animal brucellosis

22.4. Public awareness

22.4.1. Public education on
transmission routes and
prevention of animal
brucellosis

22.4.2. Media campaigns

22.4.3. Community engagement

22.5. Improved livestock management
practices

22.6. Collaborative efforts

22.6.1. Government policies and
programs

22.6.2. Healthcare and veterinary
services

22.6.3. International cooperation

22.7. Knowledge, attitude, and practice
among high-risk occupations

22.8. Knowledge, attitude, and practice
among pastoral and rural
communities

22.9. Conclusion
References

23. One health approach to brucellosis
in SE Europe

23.1. Introduction

23.2. Researched geographical and time
frames

23.3. An overview of historical brucellosis
data, as well as surveillance and
eradication strategies

23.4. Country-by-country insights on
brucellosis, 1999—2024

23.4.1. Albania

23.4.2. Bosnia and Herzegovina

23.4.3. Bulgaria

23.4.4. Croatia

23.4.5. Greece

23.4.6. Kosovo

23.4.7. Montenegro

23.4.8. North Macedonia

23.4.9. Romania

23.4.10. Serbia

23.5. Brucella canis, a zoonotic agent reborn
in the COVID era

23.6. Conclusion and perspectives
References
Part X
Emerging trends and future prospects

24. Challenges posed by antibiotic
resistance in human and animal
brucellosis

24.1. Introduction

24.2. Epidemiology of brucellosis and
Brucella control program

24.3. Antibiotic treatment of animal
brucellosis

24.3.1. Antibiotic treatment in
livestock

24.3.2. Antibiotic treatment in
companion animals

24.4. Antibiotic treatment of human
brucellosis

24.5. Antibiotic resistances in animal and
human brucellosis

24.6. Factors contributing to antibiotic
resistance

24.7. One Health approach to antibiotic
resistance

24.8. Future directions and research
priorities

24.9. Conclusion
References

25. Antimicrobial resistance of Brucella
melitensis

25.1. Introduction

25.2. AMR―Principles, mechanisms, and
contributing factors

25.3. The basics of antimicrobial resistance

25.4. Resistance mechanisms

25.5. Factors contributing to the occurrence
and spread of AMR

25.6. Antimicrobial susceptibility testing

25.6.1. Phenotypic methods

25.6.2. Broth microdilution

25.6.3. Agar dilution

25.6.4. Antimicrobial gradient method

25.6.5. Disc diffusion method

25.6.6. Molecular-based methods

25.6.7. PCR-based assays

25.6.8. Sequencing techniques

25.7. Phenotypic resistance in B. melitensis

25.8. Patterns and drivers of phenotypic
AMR in B. melitensis

25.8.1. Tetracyclines

25.8.2. Rifampin

25.8.3. Aminoglycosides

25.8.4. Trimethoprim/sulfamethoxazole

25.8.5. Fluoroquinolones

25.8.6. Cephalosporins

25.8.7. Macrolides

25.9. Future perspectives and conclusions
References
Part XI
Brucellosis in food safety and
processing

26. Brucellosis in food safety

26.1. Introduction

26.2. Brucella spp. and foodborne
transmission

26.2.1. Pathways of transmission to
humans

26.2.2. Risk factors for foodborne
transmission

26.3. Detection and identification of
Brucella spp. in food

26.3.1. Microbiological techniques

26.3.2. Molecular techniques

26.3.3. Serological techniques

26.3.4. Emerging technologies

26.4. Survival of Brucella spp. in food

26.4.1. Brucella survival in culture
media

26.4.2. Brucella survival in food
products

26.5. Reservoirs of infection

26.5.1. Animals

26.5.2. Milk products and retail

26.5.3. Meat and slaughter practices

26.5.4. Interhuman
transmission―Breastfeeding

26.6. Prevention and control measures

26.6.1. Farm-level interventions

26.6.2. Food industry practices

26.6.3. Public awareness campaigns

26.6.4. International guidelines

26.7. Conclusions

Product details

  • Edition: 1
  • Latest edition
  • Published: October 29, 2025
  • Language: English

About the editor

MD

Maryam Dadar

Maryam Dadar, DVM, PhD, is currently a researcher at the Veterinary Council of Iran, Tehran, Iran. She s an Assistant Professor in the Department of Brucellosis at the Razi Vaccine and Serum Research Institute in Iran. Her extensive expertise lies in the field of microbiology and molecular biology, with main areas of research in zoonotic diseases, microbial risk assessments, Brucellosis prevention and control, and One Health. She has published articles in numerous international journals, edited books including an Elsevier title on brucellosis, and serves as an editor and is on the editorial board of a number of journals such as Microbial Risk Analysis (Elsevier). Dr. Dadar actively participates in international, multidisciplinary research collaborations with colleagues in Germany, United Kingdom, United States, and Pakistan and in educational initiatives aimed at advancing the scientific foundations of zoonotic infections, veterinary science, and molecular medicine.

Affiliations and expertise
Researcher, Department of Brucellosis at the Razi Vaccine and Serum Research Institute, Karaj, IranIran

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