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1.
Cir. Esp. (Ed. impr.) ; 99(5): 368-373, mayo 2021. tab, graf
Article in Spanish | IBECS | ID: ibc-192543

ABSTRACT

INTRODUCCIÓN: La pandemia por SARS-CoV-2 ha causado un importante impacto en nuestro medio, con la necesidad de demorar la cirugía programada y urgente. Las cifras referentes a la disminución de la actividad quirúrgica y el impacto del periodo aún no se conocen con exactitud. Se estima una mortalidad de hasta un 20% en los pacientes operados con infección peroperatoria por SARS-CoV-2 MÉTODOS: Del 14/03 al 11/05 del 2020 se han recogido los datos de los pacientes ingresados en el servicio de Cirugía General y Digestiva del Hospital Universitari Dr. Josep Trueta de Girona, para analizar el impacto de la pandemia sobre la cirugía electiva y urgente. RESULTADOS: Durante el periodo de ocupación pico de la Unidad de Medicina Intensiva de nuestro centro (con un máximo de 303,8%), la cirugía electiva y la urgente se redujeron un 93,8% y un 72,7%, respectivamente. La mortalidad de los pacientes operados con infección por SARS-CoV-2 en nuestro estudio (n = 10) fue del 10%; las complicaciones fueron del 80% (siendo graves un 30%). CONCLUSIONES: El presente estudio muestra una reducción global de la actividad quirúrgica tanto electiva como urgente durante la pandemia. La mortalidad global de los pacientes operados con infección por SARS-CoV-2 ha sido baja, pero la tasa de complicaciones graves ha sido superior a la global


INTRODUCTION: SARS-CoV-2 pandemic has caused an important impact in our country and elective surgery has been postponed in most cases. There's not known information about the decreasing and impact on surgery. Mortality of surgical patients with SARS-CoV-2 infection is estimated to be around 20%. METHODS: We conducted prospective data recruitment of people inpatient in our Digestive and General Surgery section of Girona's University Hospital Dr. Josep Trueta from 03/14 to 05/11. Our objective is to analyze the impact that SARS-CoV-2 pandemic over elective and urgent surgery. RESULTS: During the peak occupation of our center Intensive Care Unit (303.8%) there was a reduction on elective (93.8%) and urgent (72.7%) surgery. Mortality of patients with SARS-CoV-2 infection who underwent surgery (n=10) is estimated to be a 10%. An 80% of these patients suffer complications (sever complications in 30%). CONCLUSIONS: The actual study shows a global reduction of the surgical activity (elective and urgent) during de SARS-CoV-2 pandemic. Global mortality of patients with SARS-CoV-2 infection are low, but the severe complications have been over the usual


Subject(s)
Humans , Male , Female , Middle Aged , Coronaviridae Infections/epidemiology , Pneumonia, Viral/epidemiology , Pandemics , Surgical Procedures, Operative/statistics & numerical data , Emergencies , Elective Surgical Procedures/statistics & numerical data , Coronaviridae Infections/mortality , Pneumonia, Viral/mortality , Tertiary Healthcare , Prospective Studies
2.
Porto Alegre; CEVS/RS; 7 abr. 2021. 1-33 p. ilus., graf., tab., mapas.
Monography in Portuguese | Coleciona SUS, CONASS, SES-RS | ID: biblio-1178004

ABSTRACT

Neste boletim são apresentados: situação mundial, ocorrência de hospitalizações confirmadas para sars-cov-2, perfil das pessoas, distribuição espacial, Síndrome Inflamatória Multissistêmica Pediátrica (SIM-P), povos indígenas, descrição de surtos, trabalhadores da saúde, Vigilância sentinela de síndrome gripal e tabelas de descrição do surto. (AU)


Subject(s)
Humans , Male , Female , Pregnancy , Infant, Newborn , Infant , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Aged , Aged, 80 and over , Health Profile , Hospital Mortality/ethnology , Health Personnel/statistics & numerical data , Coronavirus Infections/epidemiology , Sentinel Surveillance , Diagnostic Techniques and Procedures , Population Groups/statistics & numerical data , Health of Indigenous Peoples/statistics & numerical data , Hospitalization/statistics & numerical data , Child Health/statistics & numerical data , Disease Outbreaks , Coronavirus Infections/complications , Coronaviridae Infections/mortality , Adolescent Health/statistics & numerical data , Betacoronavirus
3.
J Virol ; 84(5): 2511-21, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20032190

ABSTRACT

Viruses of the family Coronaviridae have recently emerged through zoonotic transmission to become serious human pathogens. The pathogenic agent responsible for severe acute respiratory syndrome (SARS), the SARS coronavirus (SARS-CoV), is a member of this large family of positive-strand RNA viruses that cause a spectrum of disease in humans, other mammals, and birds. Since the publicized outbreaks of SARS in China and Canada in 2002-2003, significant efforts successfully identified the causative agent, host cell receptor(s), and many of the pathogenic mechanisms underlying SARS. With this greater understanding of SARS-CoV biology, many researchers have sought to identify agents for the treatment of SARS. Here we report the utility of the potent antiviral protein griffithsin (GRFT) in the prevention of SARS-CoV infection both in vitro and in vivo. We also show that GRFT specifically binds to the SARS-CoV spike glycoprotein and inhibits viral entry. In addition, we report the activity of GRFT against a variety of additional coronaviruses that infect humans, other mammals, and birds. Finally, we show that GRFT treatment has a positive effect on morbidity and mortality in a lethal infection model using a mouse-adapted SARS-CoV and also specifically inhibits deleterious aspects of the host immunological response to SARS infection in mammals.


Subject(s)
Algal Proteins , Antiviral Agents , Coronaviridae Infections/drug therapy , Coronaviridae/drug effects , Lectins , Algal Proteins/pharmacology , Algal Proteins/therapeutic use , Amino Acid Sequence , Animals , Antiviral Agents/pharmacology , Antiviral Agents/therapeutic use , Calorimetry , Cell Line , Coronaviridae/genetics , Coronaviridae/immunology , Coronaviridae/pathogenicity , Coronaviridae Infections/immunology , Coronaviridae Infections/mortality , Coronaviridae Infections/prevention & control , Cytokines/immunology , Female , Humans , Lectins/pharmacology , Lectins/therapeutic use , Lung/pathology , Lung/virology , Membrane Glycoproteins/metabolism , Mice , Mice, Inbred BALB C , Models, Molecular , Molecular Sequence Data , Plant Lectins , Protein Binding , Protein Conformation , Severe acute respiratory syndrome-related coronavirus/drug effects , Severe acute respiratory syndrome-related coronavirus/metabolism , Spike Glycoprotein, Coronavirus , Viral Envelope Proteins/metabolism , Zoonoses
4.
Virology ; 385(2): 358-67, 2009 Mar 15.
Article in English | MEDLINE | ID: mdl-19141357

ABSTRACT

C57BL/6 mice infected with mouse hepatitis virus, strain JHM (JHMV) develop a rapidly fatal acute encephalitis. Previously, we showed that this disease is partially CD4 T cell-mediated since infection with a recombinant JHMV (rJ) mutated in only a single immunodominant CD4 T cell epitope (epitope M133, rJ.M(Y135Q)) results in a nonlethal disease. Increased mortality correlated with a greater number of JHMV-specific CD4 T cells in the brains of rJ compared to rJ.M(Y135Q)-infected mice. Here, we extend these results to show that the diminished number of virus-specific T cells correlates with a reduced cytokine/chemokine response in the infected brain. We also show that regulatory CD4 T cells (Tregs) are critical for mild disease in rJ.M(Y135Q)-infected mice because their depletion results in increased mortality. Further, a relative paucity of Tregs characterizes lethal infection because adoptive transfer of Tregs into rJ-infected mice increases survival from 0% to 50%. These results support the notion that clinical disease in coronavirus-induced acute encephalitis results from a balance between factors critical for virus clearance, such as virus-specific effector T cells and anti-inflammatory elements, such as Tregs. These findings also show that unlike chronic infections, in which an excessive number of Tregs contributes to pathogen persistence, Tregs in the setting of acute encephalitis may help to limit immunopathological disease without delaying virus clearance.


Subject(s)
Coronaviridae Infections/complications , Coronaviridae Infections/immunology , Coronavirus/immunology , Encephalitis, Viral/etiology , Encephalitis, Viral/immunology , T-Lymphocytes, Regulatory/immunology , Animals , Brain/immunology , Brain/virology , Coronaviridae Infections/cerebrospinal fluid , Coronaviridae Infections/mortality , Disease Models, Animal , Fibroblasts , Mice , Mice, Inbred BALB C , Survival Analysis , T-Lymphocyte Subsets/immunology
5.
Avian Pathol ; 33(6): 605-9, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15763730

ABSTRACT

Infectious bronchitis is a respiratory disease of chickens that is caused by the coronavirus infectious bronchitis virus (IBV). Virtually all broiler and layer breeder flocks are routinely vaccinated against IBV. Two hatches of 1-day-old chicks from four lines were mistakenly vaccinated for infectious bronchitis using a moderately attenuated vaccine designed for chicks of an older age. The vaccination resulted in high mortality, and chicks from three of four lines died with signs typical of infectious bronchitis. The mortality that occurred using this less-attenuated vaccine was significantly influenced by the genetic line, and the MHC (B) haplotype in chickens of three B congenic lines. B congenic chickens possessing the B*15 haplotype were resistant in contrast to chickens possessing the B*13 or B*21 haplotypes. Chicks from two further hatches of the four lines were vaccinated appropriately with a more attenuated IBV vaccine, and only limited chick mortality was seen. These retrospective data from two repeated hatches confirm earlier data indicating chicken genes influence resistance to IBV, and indicate for the first time that genes tightly linked to the B haplotype are relevant in resistance to IBV. Due to extenuating circumstances it was not possible to verify results with chicks from F2 matings. Factors that may enhance definition of the role of the B haplotype in immune response to IBV, and the desirability for further analysis of a B haplotype-linked influence on immunity to IBV are discussed.


Subject(s)
Chickens/genetics , Coronaviridae Infections/veterinary , Major Histocompatibility Complex/genetics , Poultry Diseases/genetics , Vaccines, Attenuated/adverse effects , Viral Vaccines/adverse effects , Animals , Coronaviridae Infections/mortality , Coronaviridae Infections/pathology , Coronaviridae Infections/prevention & control , Genetic Predisposition to Disease , Infectious bronchitis virus/immunology , Poultry Diseases/mortality , Retrospective Studies , Trachea/pathology
6.
Dis Aquat Organ ; 39(3): 183-92, 2000 Feb 09.
Article in English | MEDLINE | ID: mdl-10768286

ABSTRACT

A new virus disease that displays dermal ulceration and high mortality has been occurring since 1996 in color carp Cyprinus carpio reared in warm water in Japan. In histological examinations, initial erosive lesions displayed necrosis, hemorrhage and fibrin deposition in the dermal loose connective tissue and were accompanied by the partial destruction of the epidermis. Developed ulcerative lesions involved the lateral musculature with bacterial invasions. In visceral organs, necrotic cells were observed in the hematopoietic tissue, the spleen and the intestinal tissues as well as in cardiac muscle fibers which showed no signs of bacterial invasion. Electron microscopy revealed corona-like virus particles in these necrotic cells. The necrotic cells of the hematopoietic tissue and the spleen were accompanied by the formation of tubular structures and crystalline inclusions. The putative virus was isolated and cultured in epithelioma papillosum cyprini (EPC) cells. Carp experimentally inoculated with the cultured virus showed virus transmission, and the same pathological signs of the disease and mortalities as in natural infections.


Subject(s)
Carps , Coronaviridae Infections/veterinary , Coronavirus/isolation & purification , Disease Outbreaks/veterinary , Fish Diseases/virology , Viremia/veterinary , Animals , Anti-Bacterial Agents/therapeutic use , Coronaviridae Infections/mortality , Coronaviridae Infections/pathology , Coronavirus/pathogenicity , Coronavirus/ultrastructure , Cytopathogenic Effect, Viral/physiology , Fish Diseases/mortality , Fish Diseases/pathology , Histocytochemistry , Japan , Microscopy, Electron/veterinary , Muscle, Smooth, Vascular/pathology , Muscle, Smooth, Vascular/virology , Oxytetracycline/therapeutic use , Skin/pathology , Skin/virology , Skin Ulcer/pathology , Skin Ulcer/veterinary , Spleen/pathology , Spleen/virology , Viremia/mortality , Viremia/pathology , Virion/ultrastructure
7.
Arch Virol ; 118(3-4): 225-34, 1991.
Article in English | MEDLINE | ID: mdl-1648896

ABSTRACT

White Leghorn line C chicks were surgically bursectomised (Bx) in ovo to eliminate antibody production. After inoculation with infectious bronchitis virus (IBV) at 14 days after hatching, Bx chicks experienced a more severe and longer lasting infection than intact chicks. The severity and duration of clinical infection in the Bx chicks resembled that previously observed in the highly susceptible line 15I chicks, however no increase in mortality was observed, in contrast to the high levels of mortality recorded in IBV-inoculated line 15I chicks. After secondary challenge the degree of damage to the ciliated epithelium of the trachea was greater in the Bx chicks than in the intact chicks. The results indicate that, although antibodies play an important role in recovery from IBV infection, other immunological factor(s) may also be involved.


Subject(s)
Bursa of Fabricius/surgery , Chickens , Coronaviridae Infections/veterinary , Infectious bronchitis virus , Poultry Diseases/microbiology , Animals , Antibodies, Viral/biosynthesis , Antibodies, Viral/immunology , Bursa of Fabricius/embryology , Chick Embryo , Chickens/immunology , Chickens/surgery , Cilia , Coronaviridae Infections/immunology , Coronaviridae Infections/microbiology , Coronaviridae Infections/mortality , Enzyme-Linked Immunosorbent Assay/veterinary , Immunoglobulin G/biosynthesis , Immunoglobulin G/immunology , Postmortem Changes , Poultry Diseases/immunology , Poultry Diseases/mortality , Viral Vaccines/administration & dosage
8.
Am J Vet Res ; 51(5): 726-33, 1990 May.
Article in English | MEDLINE | ID: mdl-2159739

ABSTRACT

Seventy-four cats (52 treated and 22 untreated) were evaluated in efficacy studies of interferon (IFN), Propionibacterium acnes, or a combination of these drugs against experimentally induced feline infectious peritonitis (FIP). Cats were given doses of recombinant human leukocyte (alpha) IFN (rHuIFN-alpha), feline fibroblastic (beta) IFN (FIFN-beta) or P acnes at regular intervals before and after inoculation of virulent FIP virus (FIPV). Prophylactic and therapeutic administration of high doses (10(6) U/kg of body weight) or moderate doses (10(4) U/kg) of rHuIFN-alpha, FIFN-beta (10(3) u/kg), or P acnes (0.4 or 4 mg) did not significantly reduce mortality in treated vs untreated cats. However, the mean survival time in cats treated with 10(6) U of rHuIFN-alpha-/kg alone or combined with doses of P acnes was significantly (P = 0.03) increased after inoculation of highly lethal amounts (200 LD100) of FIPV vs survival time in untreated cats. Although P acnes alone was ineffective, there was some indication that a combination of P acnes and high doses of rHuIFN-alpha was more effective than rHuIFN-alpha alone. Seemingly, the efficacy of rHuIFn-alpha treatment was improved in cats challenge-exposed with less FIPV; in 1 trial, 4 of 5 cats (80%) treated with high doses of rHuIFN-alpha survived after inoculation of minimal lethal amounts (0.6 LD100) of FIPV, whereas only 2 of 5 untreated cats (40%) survived. Pretreatment of cats with 10(6) U of rHuIFN-alpha/kg resulted in detectable serum IFN activity 24 hours later; serum IFN activity was not detected in cats pretreated with P acnes, FIFN-beta, or 10(4) U of rHuIFn-alpha/kg.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Adjuvants, Immunologic/pharmacology , Cat Diseases/prevention & control , Coronaviridae Infections/prevention & control , Interferon Type I/pharmacology , Peritonitis/veterinary , Propionibacterium acnes , Animals , Antibody Formation , Cat Diseases/metabolism , Cat Diseases/microbiology , Cat Diseases/mortality , Cats , Coronaviridae , Coronaviridae Infections/metabolism , Coronaviridae Infections/microbiology , Coronaviridae Infections/mortality , Humans , Interferon Type I/blood , Peritonitis/metabolism , Peritonitis/microbiology , Peritonitis/mortality , Random Allocation , Specific Pathogen-Free Organisms , Time Factors
9.
J Virol ; 64(3): 1407-9, 1990 Mar.
Article in English | MEDLINE | ID: mdl-2154621

ABSTRACT

The gene encoding the fusogenic spike protein of the coronavirus causing feline infectious peritonitis was recombined into the genome of vaccinia virus. The recombinant induced spike-protein-specific, in vitro neutralizing antibodies in mice. When kittens were immunized with the recombinant, low titers of neutralizing antibodies were obtained. After challenge with feline infectious peritonitis virus, these animals succumbed earlier than did the control group immunized with wild-type vaccinia virus (early death syndrome).


Subject(s)
Cat Diseases/microbiology , Coronaviridae Infections/veterinary , Immunization, Passive , Peritonitis/veterinary , Animals , Antibodies, Viral/immunology , Antibody Formation , Cat Diseases/immunology , Cat Diseases/mortality , Cats , Coronaviridae/genetics , Coronaviridae/immunology , Coronaviridae Infections/immunology , Coronaviridae Infections/mortality , Genes, Viral , Mice , Neutralization Tests , Peritonitis/immunology , Peritonitis/mortality , Recombinant Proteins/immunology , Vaccinia virus/genetics , Viral Proteins/genetics , Viral Proteins/immunology
10.
Vet Immunol Immunopathol ; 21(3-4): 293-309, 1989 Jul.
Article in English | MEDLINE | ID: mdl-2552650

ABSTRACT

Delayed-type hypersensitivity (DTH)-like reactions to feline infectious peritonitis (FIP) virus (FIPV) were induced in the skin of nine cats that were asymptomatic after a previous challenge-exposure with FIPV. Four of the nine previously challenge-exposed cats were negative for virus-neutralizing antibodies against FIPV at the time of intradermal (ID) testing for DTH. Two other cats tested for DTH when acutely ill with clinical FIP did not have cutaneous DTH responses to FIPV. Gross skin reactions to FIPV injected ID were observed in six of nine asymptomatic cats (67%) at postintradermal inoculation hours (PIH) 24, 48, and/or 72. The reactions consisted of focal, 1-5-mm to 2.5-cm diameter indurated or semi-firm, nonerythematous, slightly raised nodules. Microscopically, DTH-like reactions were observed in biopsies taken from the FIPV-inoculated skin of asymptomatic cats at PIH 24 to 72. The lesions consisted of perivascular and diffuse dermal infiltrations by macrophages, lymphocytes, and polymorphonuclear leukocytes (PMN). The dermal infiltrates, which were maximal at PIH 48 or 72, were predominantly mixed inflammatory cells (five of nine cats) or PMN (four of nine cats) at PIH 24, but later were predominantly mononuclear cells (six of nine cats) or mixed inflammatory cells (two of nine cats) at PIH 72. Five of nine cats (56%) with positive DTH skin responses had increased survival times after lethal ID challenge-exposure with FIPV compared to mean survival times in FIPV-naive, non-immune control cats that were DTH-negative when ID challenge-exposed. Four of nine DTH-positive cats (44%) resisted an ID challenge-exposure dose of FIPV that was fatal in both control cats, and two of the four remaining DTH-positive cats survived a third challenge-exposure with highly lethal doses of FIPV given intraperitoneally. Four of the six DTH-positive cats (67%) that died after re-challenge and were necropsied had lesions of noneffusive FIP, suggesting that cellular immunity may also be involved in the pathogenesis of noneffusive disease, whereas both control cats and both DTH-negative cats with clinical disease succumbed to effusive FIP. Seemingly, DTH responses to FIPV can be associated with an increased level of resistance to disease; however, this state of immunity is variable and apparently can be lost with time in some cats.


Subject(s)
Cat Diseases/immunology , Coronaviridae Infections/veterinary , Hypersensitivity, Delayed/veterinary , Peritonitis/veterinary , Skin/immunology , Animals , Cat Diseases/pathology , Cats , Coronaviridae Infections/immunology , Coronaviridae Infections/mortality , Coronaviridae Infections/pathology , Immunity, Cellular , Immunity, Innate , Intradermal Tests , Neutralization Tests , Peritonitis/immunology , Peritonitis/mortality , Peritonitis/pathology , Skin/pathology
12.
J Gen Virol ; 66 ( Pt 4): 777-86, 1985 Apr.
Article in English | MEDLINE | ID: mdl-2984320

ABSTRACT

By inoculating chickens intranasally with a collection of strains of infectious bronchitis virus (IBV) of the Massachusetts serotype and of Escherichia coli of different serotypes, a pool of viral and bacterial strains was selected which, on inoculation, consistently produced a highly lethal disease closely resembling the natural disease produced by these two organisms. The conditions for reproducing the experimental disease were not rigorous in that, within broad limits, the size of the viral and bacterial inocula were not important; neither were the times at which both organisms were administered in relation to each other. The breed or strain of chicken used was important and the resistance of chickens to fatal infection increased with age. When the E. coli strains of the pool were inoculated intranasally without the IBV component, the chickens remained well; bacteriological examination of chickens inoculated with one of the E. coli strains, O18, revealed little evidence of invasion of the tissues or even of persistence of the inoculated E. coli strain in the upper respiratory tract. A minority of the IBV strains examined were lethal for chickens when inoculated without E. coli but many of them only produced a substantial mortality when the E. coli were included in the inoculum; IBV strains in this latter category included the vaccine strains H52 and H120. High concentrations of IBV strain M41 and E. coli O18 persisted in the upper respiratory tract for a number of days after they had been inoculated together. Much lower concentrations of IBV M41 were found in the internal organs, such as the spleen; E. coli O18 was only found in these sites in some of the inoculated chickens. Coliform organisms proliferated in the upper respiratory tract of chickens inoculated with IBV alone; they were rarely found in their internal organs.


Subject(s)
Chickens , Coronaviridae Infections/veterinary , Escherichia coli Infections/veterinary , Poultry Diseases/microbiology , Animals , Coronaviridae Infections/mortality , Escherichia coli Infections/immunology , Infectious bronchitis virus , Poultry Diseases/immunology , Poultry Diseases/mortality
13.
Tierarztl Prax ; 12(3): 369-82, 1984.
Article in German | MEDLINE | ID: mdl-6093284

ABSTRACT

The post mortem investigation of 4561 cats during 14 years is analysed according to the diagnosis. The age of the cats necropsied ranged from 1 day to 22 years, with an average of 3,3 years. The sex distribution was about 1:1. The most common disease is feline panleucopenia (16,6%) followed by traumata (11,5%), disorders of the urinary tract (7,0%), feline infectious peritonitis (6,0%), disorders of the circulatory system (5,8%), and diseases of the digestive tract (5,3%). The majority of kittens died of virus diseases, mainly feline panleucopenia. Feline leucosis is found among all groups of age. In middle aged animals (5-10 years) feline leucosis and diseases of the urinary tract are the main causes of death. Cats older than eight years show a high rate of tumor incidence, especially those of non lymphatic origin. Among siamese cats congestive cardiomyopathy is very common. A sexual disposition is notable for the feline urologic syndrome, occurring predominantly in male individuals.


Subject(s)
Cat Diseases/mortality , Age Factors , Animals , Autopsy , Cardiovascular Diseases/mortality , Cardiovascular Diseases/veterinary , Cats , Coronaviridae Infections/mortality , Coronaviridae Infections/veterinary , Digestive System Diseases/mortality , Digestive System Diseases/veterinary , Feline Panleukopenia/mortality , Female , Germany, West , Leukemia/mortality , Leukemia/veterinary , Male , Peritonitis/mortality , Peritonitis/veterinary , Sex Factors , Urologic Diseases/mortality , Urologic Diseases/veterinary , Wounds and Injuries/mortality , Wounds and Injuries/veterinary
15.
J Am Vet Med Assoc ; 173(5 Pt 2): 573-6, 1978 Sep 01.
Article in English | MEDLINE | ID: mdl-212403

ABSTRACT

Methods for estimating the economic impact of disease agents were developed and utilized to assess the relative economic importance of rotavirus and other disease agents in calves. Based on incidence data from 2 sources, Escherichia coli was responsible for the most devastating economic losses (50.9% and 74.6%). Coronaviral (17.5% and 29.7% loss) and rotaviral (3.2% and 9.1% loss) infections ranked 2nd and 3rd, respectively. In one study, cryptosporidial infections (6.5% loss) were estimated to be similar in economic impact to rotaviral infection. Salmonellosis, mycotic gastroenteritis, infectious bovine rhinotracheitis, and bovine viral diarrhea infections accounted for minor losses. The estimated average annual loss of calves for the 7-year period, 1970 through 1976, was $95,500,000/year. Based on data from 2 studies, the estimated average annual loss from E coli was $48.6 and 71.2 million; from coronaviral infection, $16.7 and 28.4 million; from rotaviral infection, $3.1 and $8.7 million; and from cryptosporidial infection, from 1 study, $6.2 million. Estimates of economic impact of disease agents on calves, and likely in other species, indicate that rotaviral infections have a relatively minor role with respect to E coli and coronaviral infections.


Subject(s)
Animals, Newborn , Cattle Diseases/economics , Virus Diseases/veterinary , Animals , Cattle , Cattle Diseases/mortality , Coccidiosis/economics , Coccidiosis/mortality , Coccidiosis/veterinary , Coronaviridae Infections/economics , Coronaviridae Infections/mortality , Coronaviridae Infections/veterinary , Escherichia coli Infections/economics , Escherichia coli Infections/mortality , Escherichia coli Infections/veterinary , Rotavirus , United States , Virus Diseases/economics , Virus Diseases/mortality
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