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Journal of the American Association for Laboratory Animal Science : JAALAS logoLink to Journal of the American Association for Laboratory Animal Science : JAALAS
. 2026 Mar;65(2):239–242. doi: 10.30802/AALAS-JAALAS-25-165

Decidual Cell Reaction and Endometritis in a Guinea Pig

Alfonso S Gozalo 1,*, Marisa C St Claire 2, William R Elkins 1
PMCID: PMC13086215  PMID: 41468976

Abstract

A female, research-naive, strain 13 guinea pig with no previous significant health history was noted to have a persistent vaginal discharge. On physical examination a soft mass was noted in the lower abdomen accompanied by a serosanguineous vaginal discharge. Due to a poor prognosis, the animal was euthanized. At necropsy, the left uterine horn was markedly enlarged and contained a large amorphous mass. Light microscopy examination showed that the mass had dense areas containing stromal cells surrounded by connective tissue, congested blood vessels, areas of necrosis, hemorrhage, and occasional cyst formation. In some areas numerous bacteria, both rods and cocci, were noted and the uterine wall showed increased thickness caused by a polymorphonuclear cell inflammatory infiltrate. Bacteriological culture and isolation from the vaginal discharge revealed a mixed infection with Escherichia coli, Bacteroides fragilis, Proteus mirabilis, Enterococcus spp., and α-hemolytic Streptococcus spp. while culture and isolation from the uterus revealed a mixed infection with E. coli, Pseudomonas aeruginosa, B. fragilis, and Globicatella sanguinis. The pathology findings were consistent with decidual cell reaction and endometritis. Vaginal bleeding is not a common clinical sign in decidual cell reaction and usually does not require treatment since the lesion in many cases resolves on its own by apoptosis and resorption. However, in this case, systemic antibiotics may have been beneficial to treat the endometrial infection. These findings suggest that decidual cell reactions may occur accompanied by, or as a result of, intrauterine infections in guinea pigs. The potential role of bacteria in decidual cell reaction should be further explored in guinea pigs.

Abbreviations and Acronyms: AVMA, American Veterinary Medical Association; CO2, Carbon Dioxide; IACUC, Institutional Animal Care and Use Committee; NIH, National Institutes of Health

Introduction

Decidual stromal cells are specialized cells in the endometrium essential for the implantation and maintenance of pregnancy, preventing fetal rejection by the maternal immune system.1 They are thought to originate from fibroblast-like cells within the endometrium, which maintain their progesterone receptors in the presence of progesterone.1 Decidual cell reaction is a focal, nonneoplastic, proliferative response of stromal endometrial cells histologically similar to decidua implantation sites.2 Referred to as a deciduoma in earlier human literature because the lesion was originally regarded as neoplastic, the term pseudo-placentational endometrial hyperplasia has been proposed more recently to describe the deciduoma/decidual reaction.3 Spontaneous as well as experimentally induced decidual cell reactions have been reported in various species of animals including mice, rats, hamsters, guinea pigs, rabbits, and dogs.1,3–21 Herein, we report a case of decidual cell reaction accompanied by endometritis in a guinea pig.

Case Report

A 7-month-old female, research-naive, tricolor, strain 13 guinea pig, born in-house, with no previous significant health history was noted to have a persistent vaginal discharge. The animal was part of a strain 13 guinea pig closed breeding colony housed in a National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH; Bethesda, MD) animal facility accredited by AAALAC International. The female guinea pig was paired with a male but had not produced pups. The animal was housed and cared for according to the Guide for the Care and Use of Laboratory Animals, Public Health Service Policy on Humane Care and Use of Laboratory Animals, the Animal Welfare Act, and Animal Welfare Act Regulations22–24 and was enrolled in an IACUC-approved breeding protocol. Standard husbandry procedures included housing in ventilated microisolation cage setups (Thoren Caging Systems, Hazleton, PA) with autoclaved paper-based bedding (Teklad 7089 diamond soft bedding; Envigo, Indianapolis, IN), food (LabDiet 5025; LabDiet, St. Louis, MO), and tap water ad libitum. In addition, fresh fruits (apple and orange slices), vegetables (cabbage), and/or food treats (Bio-Serv, Flemington, NJ) were provided at least once a week. A dumbbell and tube were provided per cage as environmental enrichment. The colony was tested annually for specific pathogens and found free of lymphocytic choriomeningitis, pneumonia virus of mice, reovirus 3, Sendai virus, and simian virus 5. Culled animals were also tested and found free of ectoparasites and endoparasites, except for intestinal nonpathogenic flagellates. On physical examination the guinea pig had a soft mass in the lower abdomen accompanied by serosanguineous vaginal discharge of 2-day duration. Due to a poor prognosis, the animal was euthanized using CO2 overdose, as per the AVMA guidelines on euthanasia, and the carcass was submitted for pathologic evaluation.25 At necropsy, the left uterine horn was markedly enlarged and purple (Figure 1A). Upon opening the left uterine horn, a 2.5- by 2.5- by 8-cm soft amorphous tissue mass was found (Figure 1B). The mass was red with darker areas and resembled an autolyzed fetus. The right uterine horn was mildly enlarged and congested. The spleen was moderately enlarged. All other organs were within normal limits. Tissue samples were fixed in 10% neutral buffered formalin, paraffin embedded, and processed routinely for histopathologic examination. In addition, uterine tissue and vaginal discharge samples were collected aseptically and submitted to the NIH Division of Veterinary Resources Microbiology Laboratory for routine bacteriological culture, isolation, and sensitivity tests. Light microscopy examination showed that the mass had dense areas containing stromal cells surrounded by connective tissue, congested blood vessels, areas of necrosis, hemorrhage, and occasional cyst formation (Figure 1C). Higher magnification showed areas with densely packed stromal cells next to areas of necrosis and hemorrhage (Figure 1D). The stromal cells were large, round to oval, with abundant eosinophilic cytoplasm, large round nuclei, and in some cases with a prominent nucleolus (Figure 1E). Very few mitotic figures were observed. In some areas, bacteria, both rods and cocci, were noted. Histologic examination of the left uterine wall showed increased thickness caused by a polymorphonuclear cell inflammatory infiltrate (Figure 1F). The right uterine horn was congested and contained multifocal small cysts and mild endometrial hyperplasia. No microscopic abnormalities were noted in other organs. Bacteriological culture and isolation of the vaginal discharge revealed a mixed infection with Escherichia coli, Bacteroides fragilis, Proteus mirabilis, Enterococcus spp., and α-hemolytic Streptococcus spp. while culture and isolation from the uterus revealed a mixed infection with E. coli, B. fragilis, Pseudomonas aeruginosa, and Globicatella sanguinis. The pathology findings were consistent with decidual cell reaction and endometritis.

Figure 1.


Figure 1.

Guinea Pig. (A) Gross image showing a markedly enlarged and discolored left uterine horn (white asterisk). The right uterine horn (R) is mildly enlarged and congested. (B) Gross image showing an amorphous soft tissue mass in the left uterine horn. The mass was red with darker areas and resembled an autolyzed fetus (white asterisk). (C) Mass cross-section. Low-power image of the mass showing dense areas containing stromal cells (S) surrounded by connective tissue, congested blood vessels, areas of necrosis (N), hemorrhage (H), and occasional cyst (Cy) formation. Hematoxylin and eosin stain; original magnification ×12.5. (D) Mass cross-section. Higher magnification showing areas with densely packet stromal cells (S) next to areas of necrosis and hemorrhage (N). Hematoxylin and eosin stain; original magnification ×100. (E) Mass cross-section. Higher magnification showing large stromal cells, round to oval, with abundant eosinophilic cytoplasm and a large round nucleus. Hematoxylin and eosin stain; original magnification ×400. (F) Left uterine horn. Image showing marked thickening of the uterine wall due to a polymorphonuclear cell inflammatory infiltrate (Pm). Note smooth muscle cells (U) and stromal cells (S). Hematoxylin and eosin stain; original magnification ×200.

Discussion

On histologic examination, the left uterus in this guinea pig showed a proliferative response of stromal endometrial cells similar to decidua implantation sites and consistent with the diagnosis of decidual cell reaction. The lesion can be induced experimentally in ovariectomized guinea pigs by daily progesterone treatment followed by minute amounts of estradiol.11 Focal decidualization in nonpregnant guinea pigs may also occur associated with primary uterine neoplasia, intrauterine trauma, or irritation.9,12,13 In rats, decidual cell reaction has been reported associated with vitamin E deficiency and intrauterine trauma.5,6 In dogs, decidual reaction may be induced by introducing a silk suture into the uteri in the nonpregnant luteal stage of the estrous cycle.17 Canine decidual cell reaction has been induced by intrauterine inoculation of E. coli isolated from a naturally occurring canine pyometra.19 In addition, more recently, decidual cell reactions have been reported associated with pyometra in bitches.20 The presence of bacteria in the uterus of the guinea pig in the present case report suggests this may have contributed to endometritis and, possibly, decidual cell reaction. It may be possible that the female had an abortion during early pregnancy that went unnoticed, or embryonic death, with retained membranes that became infected with enterobacteria. Escherichia coli is the most commonly isolated bacteria from pyometra cases in dogs and cats, followed by Staphylococcus spp. and Streptococcus spp.,26 while Pseudomonas spp., Proteus spp., and Enterococcus spp. are occasionally reported as a cause of pyometra in dogs.26 In humans, B. fragilis, E. coli, Streptococcus spp., and Enterococcus spp. are commonly isolated from uterine infections.27,28 Mixed infections appear to be common in both human and veterinary medicine. All bacteria isolated from the guinea pig in this case have been reported in the literature as a cause of pyometra/endometritis in humans and small animals, with the exception, to our knowledge, of G. sanguinis. Globicatella sanguinis was first reported in 1992 as G. sanguis, a new genus and species of catalase-negative, facultatively anaerobic, gram-positive cocci related to the streptococci.29 In 1997 the species was renamed G. sanguinis and has been occasionally isolated from human patients with meningitis, bacteremia, endocarditis, urinary tract infections, osteomyelitis, and endophthalmitis.30–40 In animals, G. sanguinis infections are even rarer, with only one report of its isolation from lambs with meningoencephalitis.41 Vaginal bleeding is not a common clinical sign in decidual cell reaction. Differentials for female reproductive tract bleeding are diverse and mostly include complications of pregnancy, reproductive tract infections, tumors, or traumatic lesions, endometriosis, systemic conditions, and hormonal and coagulation disorders.42

Decidual cell reactions usually do not require treatment since the lesion in many cases resolves on its own by apoptosis and resorption.13 However, in the case described here, systemic antibiotics may have been beneficial to treat the endometrial infection. These findings suggest decidual cell reactions may occur accompanied by, or a result of, intrauterine infections in guinea pigs. The potential role of bacteria in decidual cell reaction should be further explored in guinea pigs. This is to our knowledge the first report of G. sanguinis infection in a guinea pig.

Acknowledgments

This research was supported by the NIH. The contributions of the NIH authors were made as part of their official duties as NIH federal employees, are in compliance with agency policy requirements, and are considered Works of the United States Government. However, the findings and conclusions presented in this paper are those of the authors and do not necessarily reflect the views of the NIH or the U.S. Department of Health and Human Services.

Conflict of Interest

The authors have no conflicts of interest to declare.

Funding

This work was funded by the Intramural Research Program of the NIH.

Data availability

Study materials are available upon reasonable request.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Study materials are available upon reasonable request.


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